"Ambry Genetics"[submitter] AND "FUT2"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2336717	NM_000511.6(FUT2):c.10G>A (p.Val4Ile)	FUT2, LOC105447645 (V4I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2621709	NM_000511.6(FUT2):c.65T>C (p.Val22Ala)	FUT2, LOC105447645 (V22A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2325732	NM_000511.6(FUT2):c.92G>A (p.Arg31Gln)	FUT2, LOC105447645 (R31Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097477	NM_000511.6(FUT2):c.212G>A (p.Arg71His)	FUT2, LOC105447645 (R71H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2410136	NM_000511.6(FUT2):c.242C>T (p.Thr81Ile)	FUT2, LOC105447645 (T81I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2309754	NM_000511.6(FUT2):c.247T>C (p.Tyr83His)	FUT2, LOC105447645 (Y83H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2216219	NM_000511.6(FUT2):c.297G>A (p.Met99Ile)	FUT2, LOC105447645 (M99I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3280185	NM_000511.6(FUT2):c.308T>C (p.Leu103Pro)	FUT2, LOC105447645 (L103P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097478	NM_000511.6(FUT2):c.353C>T (p.Thr118Met)	FUT2, LOC105447645 (T118M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097479	NM_000511.6(FUT2):c.413G>A (p.Arg138His)	FUT2, LOC105447645 (R138H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2617742	NM_000511.6(FUT2):c.431A>T (p.Tyr144Phe)	FUT2, LOC105447645 (Y144F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097480	NM_000511.6(FUT2):c.517C>T (p.His173Tyr)	FUT2, LOC105447645 (H173Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2223420	NM_000511.6(FUT2):c.523C>T (p.Arg175Trp)	FUT2, LOC105447645 (R175W)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GUncertain significance
Select item 2220632	NM_000511.6(FUT2):c.587T>G (p.Val196Gly)	FUT2, LOC105447645 (V196G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2599580	NM_000511.6(FUT2):c.659G>A (p.Arg220Gln)	FUT2, LOC105447645 (R220Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2381435	NM_000511.6(FUT2):c.744G>C (p.Trp248Cys)	FUT2, LOC105447645 (W248C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097481	NM_000511.6(FUT2):c.758T>C (p.Ile253Thr)	FUT2, LOC105447645 (I253T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2559775	NM_000511.6(FUT2):c.851C>G (p.Thr284Ser)	FUT2, LOC105447645 (T284S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3097482	NM_000511.6(FUT2):c.853A>G (p.Ile285Val)	FUT2, LOC105447645 (I285V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2215059	NM_000511.6(FUT2):c.971C>T (p.Ala324Val)	FUT2 (A324V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560159	NM_000511.6(FUT2):c.994G>C (p.Gly332Arg)	FUT2 (G332R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369673	NM_000511.6(FUT2):c.1003G>T (p.Ala335Ser)	FUT2 (A335S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353267	NM_000511.6(FUT2):c.1003G>A (p.Ala335Thr)	FUT2 (A335T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280186	NM_000511.6(FUT2):c.1010T>C (p.Leu337Pro)	FUT2 (L337P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 24