"Ambry Genetics"[submitter] AND "MFSD10"[gene] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2542442	NM_001146069.2(MFSD10):c.1352C>A (p.Thr451Lys)	MFSD10 (T451K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623321	NM_001146069.2(MFSD10):c.1289C>T (p.Thr430Met)	MFSD10 (R466C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478444	NM_001146069.2(MFSD10):c.1277C>G (p.Ala426Gly)	MFSD10 (P462A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493937	NM_001146069.2(MFSD10):c.1267G>A (p.Gly423Arg)	MFSD10 (G423R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2245507	NM_001146069.2(MFSD10):c.1232G>C (p.Gly411Ala)	MFSD10 (G411A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125753	NM_001146069.2(MFSD10):c.1198C>A (p.Leu400Met)	MFSD10 (H363Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286591	NM_001146069.2(MFSD10):c.1127T>G (p.Val376Gly)	MFSD10 (W340G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406158	NM_001146069.2(MFSD10):c.1120G>A (p.Ala374Thr)	MFSD10 (A374T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125752	NM_001146069.2(MFSD10):c.1082T>C (p.Val361Ala)	MFSD10 (V361A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307069	NM_001146069.2(MFSD10):c.1048T>C (p.Phe350Leu)	MFSD10 (F350L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402210	NM_001146069.2(MFSD10):c.1037T>C (p.Leu346Pro)	MFSD10 (L346P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512275	NM_001146069.2(MFSD10):c.1012G>A (p.Ala338Thr)	MFSD10 (A338T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526454	NM_001146069.2(MFSD10):c.1000G>A (p.Gly334Arg)	MFSD10 (G334R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2284010	NM_001146069.2(MFSD10):c.991C>T (p.His331Tyr)	MFSD10 (H331Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258839	NM_001146069.2(MFSD10):c.977A>G (p.Tyr326Cys)	MFSD10 (Y326C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319082	NM_001146069.2(MFSD10):c.971G>C (p.Gly324Ala)	MFSD10 (G324A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125763	NM_001146069.2(MFSD10):c.962C>T (p.Thr321Ile)	MFSD10 (T321I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216848	NM_001146069.2(MFSD10):c.908T>A (p.Phe303Tyr)	LOC129992084, MFSD10 (F303Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605552	NM_001146069.2(MFSD10):c.905A>C (p.Gln302Pro)	LOC129992084, MFSD10 (Q302P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343483	NM_001146069.2(MFSD10):c.899G>A (p.Arg300His)	LOC129992084, MFSD10 (R300H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125762	NM_001146069.2(MFSD10):c.893A>C (p.His298Pro)	LOC129992084, MFSD10 (H298P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125761	NM_001146069.2(MFSD10):c.875C>T (p.Thr292Met)	LOC129992084, MFSD10 (T292M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482279	NM_001146069.2(MFSD10):c.817C>T (p.Arg273Cys)	MFSD10 (R273C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305639	NM_001146069.2(MFSD10):c.757C>T (p.Arg253Cys)	MFSD10 (R253C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125759	NM_001146069.2(MFSD10):c.695C>T (p.Ala232Val)	MFSD10 (A232V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125758	NM_001146069.2(MFSD10):c.694G>A (p.Ala232Thr)	MFSD10 (A232T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125757	NM_001146069.2(MFSD10):c.691C>T (p.Arg231Trp)	MFSD10 (R231W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552634	NM_001146069.2(MFSD10):c.667C>T (p.Pro223Ser)	MFSD10 (P223S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296382	NM_001146069.2(MFSD10):c.662T>C (p.Phe221Ser)	MFSD10 (F221S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601270	NM_001146069.2(MFSD10):c.640G>A (p.Asp214Asn)	MFSD10 (D214N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454235	NM_001146069.2(MFSD10):c.566C>T (p.Thr189Ile)	MFSD10 (T189I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541097	NM_001146069.2(MFSD10):c.533C>T (p.Ala178Val)	MFSD10 (A178V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325465	NM_001146069.2(MFSD10):c.521G>A (p.Ser174Asn)	MFSD10 (S174N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316195	NM_001146069.2(MFSD10):c.482C>T (p.Thr161Met)	MFSD10 (T161M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597223	NM_001146069.2(MFSD10):c.434C>T (p.Ala145Val)	MFSD10 (A145V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459172	NM_001146069.2(MFSD10):c.412C>T (p.Arg138Trp)	MFSD10 (R138W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486618	NM_001146069.2(MFSD10):c.377G>T (p.Gly126Val)	MFSD10 (G126V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371333	NM_001146069.2(MFSD10):c.311C>T (p.Ala104Val)	LOC129992086, MFSD10 (A104V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281306	NM_001146069.2(MFSD10):c.226G>C (p.Gly76Arg)	MFSD10 (G76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125754	NM_001146069.2(MFSD10):c.205G>C (p.Asp69His)	MFSD10 (D69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222462	NM_001146069.2(MFSD10):c.199G>A (p.Gly67Arg)	MFSD10 (G67R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362534	NM_001146069.2(MFSD10):c.124C>A (p.Leu42Met)	MFSD10 (L42M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125760	NM_001146069.2(MFSD10):c.74T>C (p.Val25Ala)	MFSD10 (V25A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125755	NM_001146069.2(MFSD10):c.35G>A (p.Arg12His)	MFSD10 (R12H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387756	NM_001146069.2(MFSD10):c.14G>C (p.Gly5Ala)	MFSD10 (G5A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2376593	NM_001146069.2(MFSD10):c.14G>A (p.Gly5Glu)	MFSD10 (G5E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 46