"Ambry Genetics"[submitter] AND "ALDH9A1"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2376219	NM_000696.4(ALDH9A1):c.1492A>G (p.Ile498Val)	ALDH9A1 (I404V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344977	NM_000696.4(ALDH9A1):c.1484G>A (p.Arg495His)	ALDH9A1 (R401H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283748	NM_000696.4(ALDH9A1):c.1480G>A (p.Gly494Ser)	ALDH9A1 (G494S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253276	NM_000696.4(ALDH9A1):c.1468G>C (p.Gly490Arg)	ALDH9A1 (G490R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110161	NM_000696.4(ALDH9A1):c.1310A>G (p.Asn437Ser)	ALDH9A1 (N437S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207108	NM_000696.4(ALDH9A1):c.1278T>G (p.Phe426Leu)	ALDH9A1 (F332L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513303	NM_000696.4(ALDH9A1):c.1265C>T (p.Ser422Phe)	ALDH9A1 (S328F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110145	NM_000696.4(ALDH9A1):c.1263G>A (p.Met421Ile)	ALDH9A1 (M327I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366022	NM_000696.4(ALDH9A1):c.1178A>G (p.Asp393Gly)	ALDH9A1 (D299G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283811	NM_000696.4(ALDH9A1):c.1157C>A (p.Pro386His)	ALDH9A1 (P386H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275518	NM_000696.4(ALDH9A1):c.1147A>C (p.Ile383Leu)	ALDH9A1 (I289L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2593041	NM_000696.4(ALDH9A1):c.1090C>G (p.Leu364Val)	ALDH9A1 (L270V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283757	NM_000696.4(ALDH9A1):c.1085G>A (p.Arg362Gln)	ALDH9A1 (R268Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334876	NM_000696.4(ALDH9A1):c.967G>C (p.Glu323Gln)	ALDH9A1 (E323Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283800	NM_000696.4(ALDH9A1):c.910A>G (p.Asn304Asp)	ALDH9A1 (N210D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312354	NM_000696.4(ALDH9A1):c.820C>T (p.Pro274Ser)	ALDH9A1 (P180S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110211	NM_000696.4(ALDH9A1):c.742G>A (p.Asp248Asn)	ALDH9A1 (D248N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283768	NM_000696.4(ALDH9A1):c.707G>A (p.Gly236Glu)	ALDH9A1 (G236E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283789	NM_000696.4(ALDH9A1):c.641T>C (p.Leu214Ser)	ALDH9A1 (L214S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284514	NM_000696.4(ALDH9A1):c.590G>C (p.Cys197Ser)	ALDH9A1 (C103S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110201	NM_000696.4(ALDH9A1):c.562T>C (p.Ser188Pro)	ALDH9A1 (S188P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110199	NM_000696.4(ALDH9A1):c.550T>G (p.Phe184Val)	ALDH9A1 (F184V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379683	NM_000696.4(ALDH9A1):c.548C>T (p.Pro183Leu)	ALDH9A1 (P183L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110192	NM_000696.4(ALDH9A1):c.485C>T (p.Ser162Leu)	ALDH9A1 (S162L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398868	NM_000696.4(ALDH9A1):c.431A>G (p.Tyr144Cys)	ALDH9A1 (Y50C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110182	NM_000696.4(ALDH9A1):c.232G>A (p.Ala78Thr)	ALDH9A1 (A78T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349334	NM_000696.4(ALDH9A1):c.185G>A (p.Arg62Gln)	ALDH9A1 (R62Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512681	NM_000696.4(ALDH9A1):c.23C>T (p.Ala8Val)	ALDH9A1 (A8V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235834	NM_000696.4(ALDH9A1):c.22G>C (p.Ala8Pro)	ALDH9A1 (A8P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557076	NM_000696.4(ALDH9A1):c.11G>T (p.Arg4Leu)	ALDH9A1 (R4L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283779	NM_000696.4(ALDH9A1):c.10C>G (p.Arg4Gly)	ALDH9A1 (R4G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 31