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

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2372435	NM_002209.3(ITGAL):c.65C>T (p.Pro22Leu)	ITGAL (P22L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362317	NM_002209.3(ITGAL):c.713A>G (p.Asn238Ser)	ITGAL (N155S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111352	NM_002209.3(ITGAL):c.957G>C (p.Lys319Asn)	ITGAL (K236N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111353	NM_002209.3(ITGAL):c.965A>T (p.Asp322Val)	ITGAL (D239V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310745	NM_002209.3(ITGAL):c.1087G>A (p.Ala363Thr)	ITGAL (A280T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407452	NM_002209.3(ITGAL):c.1222G>C (p.Val408Leu)	ITGAL (V325L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213411	NM_002209.3(ITGAL):c.1241G>A (p.Arg414Gln)	ITGAL (R414Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2340105	NM_002209.3(ITGAL):c.1282C>G (p.Gln428Glu)	ITGAL (Q345E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367537	NM_002209.3(ITGAL):c.1399G>A (p.Val467Ile)	ITGAL (V384I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3286796	NM_002209.3(ITGAL):c.1424C>T (p.Thr475Ile)	ITGAL (T475I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286795	NM_002209.3(ITGAL):c.1486A>G (p.Ile496Val)	ITGAL (I496V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3286798	NM_002209.3(ITGAL):c.1558C>T (p.Arg520Trp)	ITGAL (R520W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400215	NM_002209.3(ITGAL):c.1559G>A (p.Arg520Gln)	ITGAL (R520Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394975	NM_002209.3(ITGAL):c.1579G>T (p.Ala527Ser)	ITGAL (A527S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376632	NM_002209.3(ITGAL):c.1642C>G (p.Gln548Glu)	ITGAL (Q465E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111345	NM_002209.3(ITGAL):c.1657A>C (p.Ile553Leu)	ITGAL (I470L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385908	NM_002209.3(ITGAL):c.1715C>A (p.Thr572Asn)	ITGAL (T489N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314915	NM_002209.3(ITGAL):c.1825G>A (p.Val609Met)	ITGAL (V609M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111346	NM_002209.3(ITGAL):c.1930A>C (p.Met644Leu)	ITGAL, ITGAL-AS1 (M561L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219484	NM_002209.3(ITGAL):c.1954A>G (p.Ile652Val)	ITGAL, ITGAL-AS1 (I569V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2302656	NM_002209.3(ITGAL):c.1970A>C (p.Lys657Thr)	ITGAL, ITGAL-AS1 (K574T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286801	NM_002209.3(ITGAL):c.2240G>A (p.Gly747Asp)	ITGAL (G663D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111347	NM_002209.3(ITGAL):c.2276A>G (p.His759Arg)	ITGAL (H759R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286792	NM_002209.3(ITGAL):c.2279C>T (p.Ser760Leu)	ITGAL (S676L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111348	NM_002209.3(ITGAL):c.2334G>C (p.Glu778Asp)	ITGAL (E778D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111349	NM_002209.3(ITGAL):c.2473C>A (p.Pro825Thr)	ITGAL (P741T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111350	NM_002209.3(ITGAL):c.2474C>T (p.Pro825Leu)	ITGAL (P741L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286799	NM_002209.3(ITGAL):c.2651T>C (p.Val884Ala)	ITGAL (V884A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618973	NM_002209.3(ITGAL):c.2835G>C (p.Lys945Asn)	ITGAL (K945N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286793	NM_002209.3(ITGAL):c.2861A>G (p.Gln954Arg)	ITGAL (Q954R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459583	NM_002209.3(ITGAL):c.2972A>G (p.Gln991Arg)	ITGAL (Q907R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623080	NM_002209.3(ITGAL):c.2980C>T (p.Pro994Ser)	ITGAL (P994S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344015	NM_002209.3(ITGAL):c.3214G>A (p.Ala1072Thr)	ITGAL (A1072T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559517	NM_002209.3(ITGAL):c.3375G>A (p.Met1125Ile)	ITGAL (M1125I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286794	NM_002209.3(ITGAL):c.3379G>C (p.Ala1127Pro)	ITGAL (A1127P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3111351	NM_002209.3(ITGAL):c.3394C>T (p.Pro1132Ser)	ITGAL (P1048S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3286791	NM_002209.3(ITGAL):c.3457G>A (p.Gly1153Ser)	ITGAL (G1069S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345770	NM_002209.3(ITGAL):c.3483G>T (p.Lys1161Asn)	ITGAL (K1161N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286800	NM_002209.3(ITGAL):c.3491A>G (p.Glu1164Gly)	ITGAL (E1164G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 39