Related gene-specific medical variations for Gene (Select 170370) - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3277244	NM_001164484.2(FAM170B):c.841G>A (p.Glu281Lys)	FAM170B, FAM170B-AS1 (E281K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3277243	NM_001164484.2(FAM170B):c.587G>C (p.Trp196Ser)	FAM170B, FAM170B-AS1 (W196S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277242	NM_001164484.2(FAM170B):c.569T>C (p.Leu190Pro)	FAM170B, FAM170B-AS1 (L190P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277241	NM_001164484.2(FAM170B):c.214A>G (p.Ser72Gly)	FAM170B, FAM170B-AS1 (S72G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277240	NM_001164484.2(FAM170B):c.800G>A (p.Cys267Tyr)	FAM170B, FAM170B-AS1 (C267Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277239	NM_001164484.2(FAM170B):c.193G>A (p.Asp65Asn)	FAM170B, FAM170B-AS1 (D65N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092001	NM_001164484.2(FAM170B):c.803C>T (p.Ser268Phe)	FAM170B, FAM170B-AS1 (S268F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092000	NM_001164484.2(FAM170B):c.521G>A (p.Ser174Asn)	FAM170B, FAM170B-AS1 (S174N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091999	NM_001164484.2(FAM170B):c.392C>T (p.Pro131Leu)	FAM170B, FAM170B-AS1 (P131L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091998	NM_001164484.2(FAM170B):c.29G>A (p.Gly10Glu)	FAM170B, FAM170B-AS1 (G10E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091997	NM_001164484.2(FAM170B):c.210C>A (p.Asp70Glu)	FAM170B, FAM170B-AS1 (D70E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091996	NM_001164484.2(FAM170B):c.137C>T (p.Ser46Phe)	FAM170B, FAM170B-AS1 (S46F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621748	NM_001164484.2(FAM170B):c.516C>G (p.Asn172Lys)	FAM170B, FAM170B-AS1 (N172K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605997	NM_001164484.2(FAM170B):c.560T>G (p.Leu187Arg)	FAM170B, FAM170B-AS1 (L187R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595798	NM_001164484.2(FAM170B):c.19G>T (p.Asp7Tyr)	FAM170B, FAM170B-AS1 (D7Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590857	NM_001164484.2(FAM170B):c.337G>A (p.Val113Met)	FAM170B, FAM170B-AS1 (V113M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527049	NM_001164484.2(FAM170B):c.124A>G (p.Arg42Gly)	FAM170B, FAM170B-AS1 (R42G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482826	NM_001164484.2(FAM170B):c.289G>A (p.Asp97Asn)	FAM170B, FAM170B-AS1 (D97N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481032	NM_001164484.2(FAM170B):c.619G>A (p.Val207Met)	FAM170B, FAM170B-AS1 (V207M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468618	NM_001164484.2(FAM170B):c.173G>A (p.Gly58Asp)	FAM170B, FAM170B-AS1 (G58D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2462587	NM_001164484.2(FAM170B):c.794G>A (p.Ser265Asn)	FAM170B, FAM170B-AS1 (S265N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460136	NM_001164484.2(FAM170B):c.556T>C (p.Cys186Arg)	FAM170B, FAM170B-AS1 (C186R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402607	NM_001164484.2(FAM170B):c.209A>G (p.Asp70Gly)	FAM170B, FAM170B-AS1 (D70G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2390676	NM_001164484.2(FAM170B):c.817G>A (p.Glu273Lys)	FAM170B, FAM170B-AS1 (E273K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375588	NM_001164484.2(FAM170B):c.819G>C (p.Glu273Asp)	FAM170B, FAM170B-AS1 (E273D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374767	NM_001164484.2(FAM170B):c.168G>C (p.Glu56Asp)	FAM170B, FAM170B-AS1 (E56D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354740	NM_001164484.2(FAM170B):c.734G>A (p.Arg245Gln)	FAM170B, FAM170B-AS1 (R245Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276574	NM_001164484.2(FAM170B):c.434A>T (p.Lys145Met)	FAM170B, FAM170B-AS1 (K145M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264921	NM_001164484.2(FAM170B):c.323C>T (p.Ala108Val)	FAM170B, FAM170B-AS1 (A108V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249830	NM_001164484.2(FAM170B):c.499G>A (p.Glu167Lys)	FAM170B, FAM170B-AS1 (E167K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221273	NM_001164484.2(FAM170B):c.679A>T (p.Ile227Phe)	FAM170B, FAM170B-AS1 (I227F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219895	NM_001164484.2(FAM170B):c.781C>A (p.Pro261Thr)	FAM170B, FAM170B-AS1 (P261T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219653	NM_001164484.2(FAM170B):c.749C>T (p.Ala250Val)	FAM170B, FAM170B-AS1 (A250V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 33