"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "TAPT1"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1628203	NM_153365.3(TAPT1):c.1614G>A (p.Thr538=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1441031	NM_153365.3(TAPT1):c.1613C>T (p.Thr538Met)	TAPT1 (T538M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1710654	NM_153365.3(TAPT1):c.1599C>G (p.Asp533Glu)	TAPT1 (D533E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1513469	NM_153365.3(TAPT1):c.1599C>A (p.Asp533Glu)	TAPT1 (D533E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 719092	NM_153365.3(TAPT1):c.1599C>T (p.Asp533=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1539236	NM_153365.3(TAPT1):c.1581G>A (p.Leu527=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1525915	NM_153365.3(TAPT1):c.1581G>C (p.Leu527Phe)	TAPT1 (L527F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 770900	NM_153365.3(TAPT1):c.1565A>G (p.Asn522Ser)	TAPT1 (N522S)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2004952	NM_153365.3(TAPT1):c.1522A>G (p.Ile508Val)	TAPT1 (I508V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1642980	NM_153365.3(TAPT1):c.1512C>G (p.Thr504=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1522735	NM_153365.3(TAPT1):c.1499C>T (p.Ser500Phe)	TAPT1 (S500F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3006665	NM_153365.3(TAPT1):c.1497G>A (p.Leu499=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3021560	NM_153365.3(TAPT1):c.1474+13C>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667230	NM_153365.3(TAPT1):c.1474+12C>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1207054	NM_153365.3(TAPT1):c.1474+10G>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 1985093	NM_153365.3(TAPT1):c.1474G>A (p.Gly492Ser)	TAPT1 (G492S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1443191	NM_153365.3(TAPT1):c.1468T>G (p.Ser490Ala)	TAPT1 (S490A)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3002138	NM_153365.3(TAPT1):c.1467C>T (p.Pro489=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 737831	NM_153365.3(TAPT1):c.1437G>A (p.Pro479=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1498587	NM_153365.3(TAPT1):c.1414G>A (p.Ala472Thr)	TAPT1 (A472T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 781846	NM_153365.3(TAPT1):c.1413C>T (p.Pro471=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1941753	NM_153365.3(TAPT1):c.1411C>G (p.Pro471Ala)	TAPT1 (P471A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1520058	NM_153365.3(TAPT1):c.1408C>G (p.Pro470Ala)	TAPT1 (P470A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 794163	NM_153365.3(TAPT1):c.1401G>A (p.Leu467=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2806565	NM_153365.3(TAPT1):c.1395G>A (p.Glu465=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 786035	NM_153365.3(TAPT1):c.1393G>A (p.Glu465Lys)	TAPT1 (E465K)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1912060	NM_153365.3(TAPT1):c.1362G>A (p.Ser454=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 736272	NM_153365.3(TAPT1):c.1350G>A (p.Leu450=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2096875	NM_153365.3(TAPT1):c.1322C>T (p.Ser441Phe)	TAPT1 (S441F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2191025	NM_153365.3(TAPT1):c.1317G>A (p.Leu439=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1673399	NM_153365.3(TAPT1):c.1314-14G>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965895	NM_153365.3(TAPT1):c.1314-15T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1497049	NM_153365.3(TAPT1):c.1314-18T>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2419378	NM_153365.3(TAPT1):c.1269G>A (p.Val423=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2197708	NM_153365.3(TAPT1):c.1252A>T (p.Thr418Ser)	TAPT1 (T418S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2800477	NM_153365.3(TAPT1):c.1209C>T (p.Gly403=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1500552	NM_153365.3(TAPT1):c.1190C>T (p.Ser397Phe)	TAPT1 (S397F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2030968	NM_153365.3(TAPT1):c.1168-10C>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1599470	NM_153365.3(TAPT1):c.1168-15T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1568385	NM_153365.3(TAPT1):c.1168-19T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1658552	NM_153365.3(TAPT1):c.1167+20G>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1895539	NM_153365.3(TAPT1):c.1167+11A>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1525596	NM_153365.3(TAPT1):c.1161G>C (p.Gln387His)	TAPT1 (Q387H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1926781	NM_153365.3(TAPT1):c.1119A>G (p.Glu373=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2794225	NM_153365.3(TAPT1):c.1107+1_1107+8del	TAPT1	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 1517161	NM_153365.3(TAPT1):c.1090A>T (p.Asn364Tyr)	TAPT1 (N364Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1497927	NM_153365.3(TAPT1):c.1057G>A (p.Asp353Asn)	TAPT1 (D353N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1464378	NM_153365.3(TAPT1):c.1054G>A (p.Val352Met)	TAPT1 (V352M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2985474	NM_153365.3(TAPT1):c.1053C>T (p.Ala351=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2735728	NM_153365.3(TAPT1):c.1044A>G (p.Ser348=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 690289	NM_153365.3(TAPT1):c.1032G>T (p.Met344Ile)	TAPT1 (M344I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2986419	NM_153365.3(TAPT1):c.998-17_998-9dup	TAPT1	Duplication (intron variant)	not provided	GLikely benign
Select item 1604568	NM_153365.3(TAPT1):c.998-15T>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2824392	NM_153365.3(TAPT1):c.998-17C>T	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011082	NM_153365.3(TAPT1):c.997+20A>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 791973	NM_153365.3(TAPT1):c.997+7C>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 2978568	NM_153365.3(TAPT1):c.954G>C (p.Leu318=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 718513	NM_153365.3(TAPT1):c.942T>C (p.Tyr314=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 721256	NM_153365.3(TAPT1):c.917-3T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2982661	NM_153365.3(TAPT1):c.917-7C>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2187944	NM_153365.3(TAPT1):c.917-8dup	TAPT1	Duplication (intron variant)	not provided	GBenign
Select item 2033381	NM_153365.3(TAPT1):c.917-7C>T	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1618984	NM_153365.3(TAPT1):c.917-8del	TAPT1	Deletion (intron variant)	not provided	GBenign
Select item 2191026	NM_153365.3(TAPT1):c.915C>T (p.Ser305=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 1661465	NM_153365.3(TAPT1):c.867T>C (p.Ser289=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2101893	NM_153365.3(TAPT1):c.852T>C (p.Val284=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1913502	NM_153365.3(TAPT1):c.847-13T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2957897	NM_153365.3(TAPT1):c.846+18C>T	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2807453	NM_153365.3(TAPT1):c.846+17T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1675040	NM_153365.3(TAPT1):c.846+8T>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1350797	NM_153365.3(TAPT1):c.837G>A (p.Met279Ile)	TAPT1 (M279I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1647244	NM_153365.3(TAPT1):c.831C>T (p.Ile277=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2044226	NM_153365.3(TAPT1):c.829A>G (p.Ile277Val)	TAPT1 (I277V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2183440	NM_153365.3(TAPT1):c.815A>G (p.Lys272Arg)	TAPT1 (K272R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1573157	NM_153365.3(TAPT1):c.763C>T (p.Leu255Phe)	TAPT1 (L255F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1903090	NM_153365.3(TAPT1):c.749-5A>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 755733	NM_153365.3(TAPT1):c.748+10T>C	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1088247	NM_153365.3(TAPT1):c.741C>G (p.Leu247=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1370040	NM_153365.3(TAPT1):c.706_708del (p.Ile236del)	TAPT1 (I236del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 1416810	NM_153365.3(TAPT1):c.707T>G (p.Ile236Ser)	TAPT1 (I236S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1509408	NM_153365.3(TAPT1):c.694A>C (p.Lys232Gln)	TAPT1 (K232Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 786884	NM_153365.3(TAPT1):c.675A>G (p.Ala225=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1956733	NM_153365.3(TAPT1):c.650T>C (p.Ile217Thr)	TAPT1 (I217T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 753979	NM_153365.3(TAPT1):c.615A>G (p.Val205=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1574142	NM_153365.3(TAPT1):c.613-3dup	TAPT1	Duplication (intron variant)	not provided	GBenign
Select item 1602004	NM_153365.3(TAPT1):c.613-3del	TAPT1	Deletion (intron variant)	not provided	GBenign
Select item 1473490	NM_153365.3(TAPT1):c.613-6_613-3del	TAPT1	Deletion (intron variant)	not provided	GUncertain significance
Select item 1268405	NM_153365.3(TAPT1):c.613-13T>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2067740	NM_153365.3(TAPT1):c.612+20C>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1605378	NM_153365.3(TAPT1):c.612+20C>T	TAPT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1638536	NM_153365.3(TAPT1):c.612+19C>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2109551	NM_153365.3(TAPT1):c.612+14_612+16dup	TAPT1	Duplication (intron variant)	not provided	GLikely benign
Select item 1976321	NM_153365.3(TAPT1):c.604A>G (p.Met202Val)	TAPT1 (M202V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2782774	NM_153365.3(TAPT1):c.588C>G (p.Leu196=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976425	NM_153365.3(TAPT1):c.576C>T (p.Ser192=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708783	NM_153365.3(TAPT1):c.496G>T (p.Gly166Cys)	TAPT1 (G166C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1461067	NM_153365.3(TAPT1):c.478G>T (p.Val160Leu)	TAPT1 (V160L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2125271	NM_153365.3(TAPT1):c.474C>A (p.Ala158=)	TAPT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693981	NM_153365.3(TAPT1):c.450-9A>G	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1564483	NM_153365.3(TAPT1):c.449+15G>A	TAPT1	Single nucleotide variant (intron variant)	not provided	GLikely benign

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