FAM110B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091637	NM_001377989.1(FAM110B):c.100C>G (p.Pro34Ala)	FAM110B (P34A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232587	NM_001377989.1(FAM110B):c.232G>T (p.Ala78Ser)	FAM110B (A78S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551189	NM_001377989.1(FAM110B):c.250C>T (p.Pro84Ser)	FAM110B (P84S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543491	NM_001377989.1(FAM110B):c.251C>T (p.Pro84Leu)	FAM110B (P84L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277081	NM_001377989.1(FAM110B):c.319A>T (p.Thr107Ser)	FAM110B (T107S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349909	NM_001377989.1(FAM110B):c.425G>A (p.Arg142His)	FAM110B (R142H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228363	NM_001377989.1(FAM110B):c.443G>A (p.Arg148Gln)	FAM110B (R148Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393395	NM_001377989.1(FAM110B):c.466C>T (p.Arg156Cys)	FAM110B (R156C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277080	NM_001377989.1(FAM110B):c.478G>C (p.Ala160Pro)	FAM110B (A160P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277079	NM_001377989.1(FAM110B):c.485C>G (p.Ser162Cys)	FAM110B (S162C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264668	NM_001377989.1(FAM110B):c.564G>C (p.Gln188His)	FAM110B (Q188H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243449	NM_001377989.1(FAM110B):c.571G>A (p.Glu191Lys)	FAM110B (E191K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323733	NM_001377989.1(FAM110B):c.584A>C (p.His195Pro)	FAM110B (H195P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616280	NM_001377989.1(FAM110B):c.611G>T (p.Arg204Leu)	FAM110B (R204L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213771	NM_001377989.1(FAM110B):c.640G>A (p.Ala214Thr)	FAM110B (A214T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550959	NM_001377989.1(FAM110B):c.898A>G (p.Asn300Asp)	FAM110B (N300D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624211	NM_001377989.1(FAM110B):c.952T>G (p.Cys318Gly)	FAM110B (C318G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339095	NM_001377989.1(FAM110B):c.1099G>T (p.Val367Phe)	FAM110B (V367F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance