Related gene-specific medical variations for Gene (Select 388931) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294546	NM_001346880.2(MFSD2B):c.1276G>C (p.Gly426Arg)	LOC122756669, MFSD2B (G426R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125783	NM_001346880.2(MFSD2B):c.1325A>G (p.Tyr442Cys)	LOC122756669, MFSD2B (Y442C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125782	NM_001346880.2(MFSD2B):c.1282T>C (p.Cys428Arg)	LOC122756669, MFSD2B (C428R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125780	NM_001346880.2(MFSD2B):c.1186G>A (p.Val396Met)	LOC122756669, MFSD2B (V396M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597103	NM_001346880.2(MFSD2B):c.1387G>A (p.Ala463Thr)	LOC122756669, MFSD2B (A463T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594571	NM_001346880.2(MFSD2B):c.1435G>A (p.Gly479Ser)	LOC122756669, MFSD2B (G479S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567732	NM_001346880.2(MFSD2B):c.1202A>C (p.Gln401Pro)	LOC122756669, MFSD2B (Q401P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544305	NM_001346880.2(MFSD2B):c.1460G>C (p.Arg487Pro)	LOC122756669, MFSD2B (R487P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495544	NM_001346880.2(MFSD2B):c.1342A>G (p.Lys448Glu)	LOC122756669, MFSD2B (K448E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471927	NM_001346880.2(MFSD2B):c.1235C>A (p.Thr412Asn)	LOC122756669, MFSD2B (T412N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460960	NM_001346880.2(MFSD2B):c.1336G>T (p.Val446Phe)	LOC122756669, MFSD2B (V446F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459255	NM_001346880.2(MFSD2B):c.1487G>A (p.Arg496Gln)	LOC122756669, MFSD2B (R496Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330706	NM_001346880.2(MFSD2B):c.1486C>T (p.Arg496Trp)	LOC122756669, MFSD2B (R496W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325540	NM_001346880.2(MFSD2B):c.1447A>G (p.Lys483Glu)	LOC122756669, MFSD2B (K483E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243938	NM_001346880.2(MFSD2B):c.1348G>A (p.Ala450Thr)	LOC122756669, MFSD2B (A450T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226582	NM_001346880.2(MFSD2B):c.1409T>C (p.Leu470Pro)	LOC122756669, MFSD2B (L470P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance