FAM13B[gene] and "single gene"[properties] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091856	NM_001385994.1(FAM13B):c.2561G>A (p.Arg854Gln)	FAM13B (R572Q +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545745	NM_001385994.1(FAM13B):c.2511C>G (p.Asn837Lys)	FAM13B (N555K +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327727	NM_001385994.1(FAM13B):c.2497T>C (p.Ser833Pro)	FAM13B (S811P +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288029	NM_001385994.1(FAM13B):c.2417A>C (p.Glu806Ala)	FAM13B (E660A +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251255	NM_001385994.1(FAM13B):c.2362A>G (p.Arg788Gly)	FAM13B (R496G +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494816	NM_001385994.1(FAM13B):c.2353A>C (p.Thr785Pro)	FAM13B (T573P +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238553	NM_001385994.1(FAM13B):c.2345C>G (p.Ser782Cys)	FAM13B (S542C +16 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551101	NM_001385994.1(FAM13B):c.2324G>C (p.Ser775Thr)	FAM13B (S607T +14 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3277181	NM_001385994.1(FAM13B):c.2022C>G (p.Asp674Glu)	FAM13B (D622E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390401	NM_001385994.1(FAM13B):c.2015C>T (p.Ser672Phe)	FAM13B (S532F +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2338587	NM_001385994.1(FAM13B):c.1975C>A (p.Arg659Ser)	FAM13B (R447S +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2285002	NM_001385994.1(FAM13B):c.1975C>T (p.Arg659Cys)	FAM13B (R607C +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3277178	NM_001385994.1(FAM13B):c.1926T>G (p.Ile642Met)	FAM13B (I378M +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091854	NM_001385994.1(FAM13B):c.1856A>G (p.Tyr619Cys)	FAM13B (Y407C +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614524	NM_001385994.1(FAM13B):c.1810C>G (p.Gln604Glu)	FAM13B (Q464E +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537092	NM_001385994.1(FAM13B):c.1721T>G (p.Ile574Ser)	FAM13B (I292S +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536142	NM_001385994.1(FAM13B):c.1696T>C (p.Ser566Pro)	FAM13B (S302P +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223065	NM_001385994.1(FAM13B):c.1399C>T (p.His467Tyr)	FAM13B (H207Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091851	NM_001385994.1(FAM13B):c.1313G>A (p.Cys438Tyr)	FAM13B (C178Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384211	NM_001385994.1(FAM13B):c.1301G>A (p.Ser434Asn)	FAM13B (S382N +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481179	NM_001385994.1(FAM13B):c.1282C>T (p.His428Tyr)	FAM13B (H238Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510913	NM_001385994.1(FAM13B):c.1243A>T (p.Arg415Trp)	FAM13B (R225W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246195	NM_001385994.1(FAM13B):c.1183G>A (p.Val395Ile)	FAM13B (V395I +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249057	NM_001385994.1(FAM13B):c.1153G>T (p.Val385Leu)	FAM13B (V125L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091850	NM_001385994.1(FAM13B):c.1096T>G (p.Cys366Gly)	FAM13B (C124G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570154	NM_001385994.1(FAM13B):c.1061A>T (p.Asp354Val)	FAM13B (D164V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378028	NM_001385994.1(FAM13B):c.856A>G (p.Ile286Val)	FAM13B (I286V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228770	NM_001385994.1(FAM13B):c.847A>G (p.Ser283Gly)	FAM13B (S23G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091860	NM_001385994.1(FAM13B):c.746A>T (p.Glu249Val)	FAM13B (E59V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3091859	NM_001385994.1(FAM13B):c.722A>G (p.Asp241Gly)	FAM13B (D123G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3091858	NM_001385994.1(FAM13B):c.691G>T (p.Val231Phe)	FAM13B (V41F +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2480523	NM_001385994.1(FAM13B):c.488A>G (p.His163Arg)	FAM13B (H163R +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3091857	NM_001385994.1(FAM13B):c.476A>G (p.Asn159Ser)	FAM13B (N41S +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2408032	NM_001385994.1(FAM13B):c.341T>C (p.Leu114Ser)	FAM13B (L114S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2263693	NM_001385994.1(FAM13B):c.310G>A (p.Glu104Lys)	FAM13B (E104K)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2550604	NM_001385994.1(FAM13B):c.133G>A (p.Val45Ile)	FAM13B (V45I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2314660	NM_001385994.1(FAM13B):c.121A>G (p.Ile41Val)	FAM13B (I41V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3277179	NM_001385994.1(FAM13B):c.107A>G (p.Asn36Ser)	FAM13B (N36S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 38