ClinVar for MedGen (Select 382625) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3366959	NM_000059.4(BRCA2):c.750_771del (p.Thr251fs)	BRCA2 (T128fs +1 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3341472	NM_000059.4(BRCA2):c.347_350del (p.Ser116fs)	BRCA2 (S116fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3336626	NM_000059.4(BRCA2):c.1625_1626del (p.Ile542fs)	BRCA2 (I542fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3257752	NM_000059.4(BRCA2):c.9458_9459delinsA	BRCA2	Deletion (frameshift variant +2 more)	Neoplasm	OOncogenic
Select item 3255361	NM_000059.4(BRCA2):c.3814del (p.Met1272fs)	BRCA2 (M1272fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254417	NM_000059.4(BRCA2):c.9353_9357del (p.Met3118fs)	BRCA2 (M1474fs +4 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254416	NM_000059.4(BRCA2):c.8154dup (p.Ile2719fs)	BRCA2 (I1075fs +3 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254410	NM_000059.4(BRCA2):c.8926dup (p.Ser2976fs)	BRCA2 (S1332fs +3 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254406	NM_000059.4(BRCA2):c.2886_2907del (p.His962fs)	BRCA2 (H962fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254405	NM_000059.4(BRCA2):c.1275_1276delinsG (p.Asp427fs)	BRCA2 (D427fs)	Indel (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254398	NM_000059.4(BRCA2):c.5447dup (p.Ser1816fs)	BRCA2 (S1816fs)	Duplication (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254395	NM_000059.4(BRCA2):c.5573_5574del (p.Thr1858fs)	BRCA2 (T1858fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2 +1 more	GPathogenic
Select item 3254394	NM_000059.4(BRCA2):c.5949_5962del (p.Lys1984fs)	BRCA2 (K1984fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254391	NM_000059.4(BRCA2):c.4717_4718insAC (p.Cys1573fs)	BRCA2 (C1573fs)	Insertion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254382	NM_000059.4(BRCA2):c.9605dup (p.Tyr3203fs)	BRCA2 (Y1064fs +4 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254379	NM_000059.4(BRCA2):c.6839del (p.Val2280fs)	BRCA2 (V2280fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254374	NM_000059.4(BRCA2):c.8681_8690del (p.Gln2894fs)	BRCA2 (Q1250fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254370	NM_000059.4(BRCA2):c.8103del (p.Glu2702fs)	BRCA2 (E1058fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254325	NM_000059.4(BRCA2):c.331_347delinsC (p.Asn111fs)	BRCA2 (N111fs)	Indel (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3254212	NM_000059.4(BRCA2):c.7005dup (p.Arg2336fs)	BRCA2 (R197fs +3 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3254047	NM_000059.4(BRCA2):c.8185A>T (p.Lys2729Ter)	BRCA2 (K1085* +3 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3242222	NM_000059.4(BRCA2):c.9084del (p.Ala3029fs)	BRCA2 (A1385fs +4 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3236921	NM_000059.4(BRCA2):c.2129C>A (p.Ser710Ter)	BRCA2 (S710*)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3236915	NM_000059.4(BRCA2):c.7165A>T (p.Arg2389Ter)	BRCA2 (R2357* +3 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3236914	NM_000059.4:c.(6841+1_6842-1)_(7805+1_7806-1)del	BRCA2	Deletion	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3236913	NM_000059.4(BRCA2):c.5600_5601del (p.Thr1867fs)	BRCA2 (T1867fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3236849	NM_000059.4(BRCA2):c.8387del (p.Pro2796fs)	BRCA2 (P1152fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3236847	NM_000059.4(BRCA2):c.1397dup (p.Asn466fs)	BRCA2 (N466fs)	Duplication (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3236846	NM_000059.4(BRCA2):c.1363_1369del (p.Glu456fs)	BRCA2 (E456fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3236207	NM_000059.4(BRCA2):c.9016_9021del (p.Tyr3006_Arg3007del)	BRCA2	Deletion (inframe_deletion +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3235765	NM_000059.4(BRCA2):c.5898dup (p.Lys1967Ter)	BRCA2 (K1967*)	Duplication (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148729	NM_000059.4(BRCA2):c.8929del (p.Tyr2977fs)	BRCA2 (Y1333fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148720	NM_000059.4(BRCA2):c.5843del (p.Cys1948fs)	BRCA2 (C1948fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148712	NM_000059.4(BRCA2):c.760_761delinsTG (p.Glu254Ter)	BRCA2 (E131* +1 more)	Indel (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148710	NM_000059.4(BRCA2):c.1850delinsTGA (p.Ser617fs)	BRCA2 (S617fs)	Indel (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148707	NM_000059.4(BRCA2):c.7402dup (p.Val2468fs)	BRCA2 (V824fs +3 more)	Duplication (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3148705	NM_000059.4(BRCA2):c.5828_5829del (p.Val1942_Ser1943insTer)	BRCA2	Deletion (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148703	NM_000059.4(BRCA2):c.9410_9414del (p.Thr3137fs)	BRCA2 (T3137fs +4 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148697	NM_000059.4(BRCA2):c.9097_9098insG (p.Thr3033fs)	BRCA2 (T894fs +4 more)	Insertion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148685	NM_000059.4(BRCA2):c.8821del (p.Gln2941fs)	BRCA2 (Q802fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148683	NM_000059.4(BRCA2):c.3514del (p.Ser1172fs)	BRCA2 (S1172fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148682	NM_000059.4(BRCA2):c.1908del (p.Gly637fs)	BRCA2 (G637fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2 +1 more	GPathogenic/Likely pathogenic
Select item 3148680	NM_000059.4(BRCA2):c.811_824dup (p.Val276fs)	BRCA2 (V276fs)	Duplication (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148670	NM_000059.4(BRCA2):c.6344_6345dup (p.His2116fs)	BRCA2 (H2116fs)	Microsatellite (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148664	NM_000059.4(BRCA2):c.1571dup (p.Met524fs)	BRCA2 (M524fs)	Duplication (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148660	NM_000059.4(BRCA2):c.7660del (p.Ser2554fs)	BRCA2 (S2522fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148650	NM_000059.4(BRCA2):c.4740dup (p.Glu1581Ter)	BRCA2 (E1581*)	Duplication (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148648	NM_000059.4(BRCA2):c.7956_7957del (p.Leu2653fs)	BRCA2 (L2621fs +3 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148589	NM_000059.4(BRCA2):c.1664del (p.Pro555fs)	BRCA2 (P555fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148551	NM_000059.4(BRCA2):c.4370del (p.Leu1457fs)	BRCA2 (L1457fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148338	NM_000059.4(BRCA2):c.760G>T (p.Glu254Ter)	BRCA2 (E131* +1 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3148247	NM_000059.4(BRCA2):c.3222del (p.Ser1074fs)	BRCA2 (S1074fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3075636	NM_000059.4(BRCA2):c.8401_8403del (p.Phe2801del)	BRCA2 (F1157del +3 more)	Deletion (inframe_deletion +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075635	NM_000059.4(BRCA2):c.7210A>G (p.Lys2404Glu)	BRCA2 (K2372E +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2 +1 more	GUncertain significance
Select item 3075634	NM_000059.4(BRCA2):c.6378C>T (p.Cys2126=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075633	NM_000059.4(BRCA2):c.6080G>T (p.Arg2027Ile)	BRCA2 (R2027I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075632	NM_000059.4(BRCA2):c.5962G>T (p.Val1988Leu)	BRCA2 (V1988L)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075631	NM_000059.4(BRCA2):c.5592C>T (p.Asp1864=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075630	NM_000059.4(BRCA2):c.5558G>T (p.Cys1853Phe)	BRCA2 (C1853F)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075629	NM_000059.4(BRCA2):c.5557T>C (p.Cys1853Arg)	BRCA2 (C1853R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075628	NM_000059.4(BRCA2):c.4996A>G (p.Asn1666Asp)	BRCA2 (N1666D)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075627	NM_000059.4(BRCA2):c.4344T>C (p.Asn1448=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075625	NM_000059.4(BRCA2):c.3860A>T (p.Asn1287Ile)	BRCA2 (N1287I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075623	NM_000059.4(BRCA2):c.3726T>C (p.Ser1242=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075622	NM_000059.4(BRCA2):c.2413T>A (p.Ser805Thr)	BRCA2 (S805T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075621	NM_000059.4(BRCA2):c.2296G>A (p.Ala766Thr)	BRCA2 (A766T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075620	NM_000059.4(BRCA2):c.1999C>T (p.Leu667=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075619	NM_000059.4(BRCA2):c.1687T>C (p.Trp563Arg)	BRCA2 (W563R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075618	NM_000059.4(BRCA2):c.1498G>T (p.Gly500Cys)	BRCA2 (G500C)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075453	NM_000059.4(BRCA2):c.2324C>A (p.Ser775Tyr)	BRCA2 (S775Y)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075384	NM_000059.4(BRCA2):c.410_412del (p.Ser137del)	BRCA2 (S137del +1 more)	Deletion (inframe_deletion +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075382	NM_000059.4(BRCA2):c.4152G>C (p.Leu1384Phe)	BRCA2 (L1384F)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075310	NM_000059.4(BRCA2):c.4654G>T (p.Gly1552Cys)	BRCA2 (G1552C)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075180	NM_000059.4(BRCA2):c.3086T>A (p.Met1029Lys)	BRCA2 (M1029K)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075171	NM_000059.4(BRCA2):c.4931A>G (p.Glu1644Gly)	BRCA2 (E1644G)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075159	NM_000059.4(BRCA2):c.9990A>T (p.Glu3330Asp)	BRCA2 (E1191D +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075123	NM_000059.4(BRCA2):c.4690G>C (p.Ala1564Pro)	BRCA2 (A1564P)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075086	NM_000059.4(BRCA2):c.9599C>T (p.Ser3200Leu)	BRCA2 (S1061L +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074768	NM_000059.4(BRCA2):c.9685C>A (p.Pro3229Thr)	BRCA2 (P1090T +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074699	NM_000059.4(BRCA2):c.6387A>G (p.Glu2129=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3074413	NM_000059.4(BRCA2):c.10145T>G (p.Leu3382Arg)	BRCA2 (L1243R +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074170	NM_000059.4(BRCA2):c.1350T>C (p.Ser450=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3074130	NM_000059.4(BRCA2):c.3644_3646delinsTAAAAAGG (p.Gly1215fs)	BRCA2 (G1215fs)	Indel (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3074016	NM_000059.4(BRCA2):c.7991T>C (p.Ile2664Thr)	BRCA2 (I1020T +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073896	NM_000059.4(BRCA2):c.5812G>A (p.Gly1938Arg)	BRCA2 (G1938R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073868	NM_000059.4(BRCA2):c.3419_3421del (p.Ser1140del)	BRCA2 (S1140del)	Deletion (inframe_deletion +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073847	NM_000059.4(BRCA2):c.337A>G (p.Arg113Gly)	BRCA2 (R113G)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073799	NM_000059.4(BRCA2):c.9636A>G (p.Gly3212=)	BRCA2	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3073658	NM_000059.4(BRCA2):c.7089T>A (p.Tyr2363Ter)	BRCA2 (Y224* +3 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3073635	NM_000059.4(BRCA2):c.1068T>G (p.Ser356=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3073618	NM_000059.4(BRCA2):c.8072C>A (p.Ser2691Tyr)	BRCA2 (S1047Y +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073591	NM_000059.4(BRCA2):c.9759T>A (p.Cys3253Ter)	BRCA2 (C1114* +4 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3073463	NM_000059.4(BRCA2):c.2122T>G (p.Ser708Ala)	BRCA2 (S708A)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073424	NM_000059.4(BRCA2):c.8340T>G (p.Ala2780=)	BRCA2	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 3073334	NM_000059.4(BRCA2):c.8755-15C>G	BRCA2	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073227	NM_000059.4(BRCA2):c.6427T>A (p.Ser2143Thr)	BRCA2 (S2143T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073175	NM_000059.4(BRCA2):c.7186T>G (p.Leu2396Val)	BRCA2 (L2364V +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073087	NM_000059.4(BRCA2):c.9318G>C (p.Trp3106Cys)	BRCA2 (W1462C +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072932	NM_000059.4(BRCA2):c.9532A>G (p.Asn3178Asp)	BRCA2 (N1039D +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072828	NM_000059.4(BRCA2):c.5100_5102del (p.Gln1701del)	BRCA2 (Q1701del)	Deletion (inframe_deletion +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance

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