"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ITGA6"[ - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 480

<< First< Prev

Page of 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 743028	NM_000210.4(ITGA6):c.6C>T (p.Ala2=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2972393	NM_000210.4(ITGA6):c.9C>A (p.Ala3=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 332355	NM_000210.4(ITGA6):c.10G>A (p.Ala4Thr)	ITGA6 (A4T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2989180	NM_000210.4(ITGA6):c.12C>G (p.Ala4=)	ITGA6	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2748195	NM_000210.4(ITGA6):c.15G>C (p.Gly5=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2981344	NM_000210.4(ITGA6):c.19C>T (p.Leu7=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2786028	NM_000210.4(ITGA6):c.21G>A (p.Leu7=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2799793	NM_000210.4(ITGA6):c.24C>T (p.Cys8=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2794145	NM_000210.4(ITGA6):c.30C>T (p.Leu10=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2830962	NM_000210.4(ITGA6):c.39G>C (p.Ser13=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2979551	NM_000210.4(ITGA6):c.42G>A (p.Ala14=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2200802	NM_000210.4(ITGA6):c.55C>T (p.Arg19Trp)	ITGA6 (R19W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 3002712	NM_000210.4(ITGA6):c.60C>T (p.Leu20=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2839510	NM_000210.4(ITGA6):c.88G>T (p.Glu30Ter)	ITGA6 (E30*)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2981229	NM_000210.4(ITGA6):c.102C>A (p.Ile34=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1930365	NM_000210.4(ITGA6):c.102C>T (p.Ile34=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2801303	NM_000210.4(ITGA6):c.108A>G (p.Lys36=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2976633	NM_000210.4(ITGA6):c.117C>T (p.Asp39=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2794658	NM_000210.4(ITGA6):c.135C>T (p.Gly45=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2900831	NM_000210.4(ITGA6):c.138C>T (p.Phe46=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 713777	NM_000210.4(ITGA6):c.148A>G (p.Met50Val)	ITGA6 (M50V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2966457	NM_000210.4(ITGA6):c.162G>A (p.Leu54=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2804085	NM_000210.4(ITGA6):c.182+8C>G	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 332356	NM_000210.4(ITGA6):c.182+11A>G	ITGA6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 332357	NM_000210.4(ITGA6):c.182+15C>T	ITGA6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1599744	NM_000210.4(ITGA6):c.183-18714A>G	ITGA6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2834514	NM_000210.4(ITGA6):c.183-20T>G	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2982690	NM_000210.4(ITGA6):c.183-15_183-14del	ITGA6, ITGA6-AS1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2972189	NM_000210.4(ITGA6):c.183-16T>C	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2822301	NM_000210.4(ITGA6):c.183-10T>G	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005841	NM_000210.4(ITGA6):c.183-6C>T	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2857820	NM_000210.4(ITGA6):c.184T>C (p.Leu62=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2998477	NM_000210.4(ITGA6):c.189C>G (p.Leu63=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2721602	NM_000210.4(ITGA6):c.189C>T (p.Leu63=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 745028	NM_000210.4(ITGA6):c.201G>A (p.Pro67=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	Epidermolysis bullosa, junctional 6, with pyloric atresia +1 more	GLikely benign
Select item 2972601	NM_000210.4(ITGA6):c.213G>A (p.Ala71=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2805374	NM_000210.4(ITGA6):c.213G>T (p.Ala71=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2717281	NM_000210.4(ITGA6):c.240G>A (p.Thr80=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 781823	NM_000210.4(ITGA6):c.258C>T (p.Cys86=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2724830	NM_000210.4(ITGA6):c.267C>T (p.Thr89=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2877990	NM_000210.4(ITGA6):c.285G>A (p.Thr95=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2984957	NM_000210.4(ITGA6):c.286C>A (p.Arg96=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2829222	NM_000210.4(ITGA6):c.294G>A (p.Glu98=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2918584	NM_000210.4(ITGA6):c.303C>T (p.Asn101=)	ITGA6, ITGA6-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2419235	NM_000210.4(ITGA6):c.304G>A (p.Asp102Asn)	ITGA6, ITGA6-AS1 (D102N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2771301	NM_000210.4(ITGA6):c.307+1dup	ITGA6, ITGA6-AS1	Duplication (splice donor variant)	not provided	GLikely pathogenic
Select item 2736863	NM_000210.4(ITGA6):c.307+15C>G	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2997445	NM_000210.4(ITGA6):c.307+17C>T	ITGA6, ITGA6-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2845743	NM_000210.4(ITGA6):c.308-16A>G	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2852761	NM_000210.4(ITGA6):c.309T>C (p.Ala103=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2901764	NM_000210.4(ITGA6):c.312C>T (p.Asp104=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2957892	NM_000210.4(ITGA6):c.318G>A (p.Thr106=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2827871	NM_000210.4(ITGA6):c.333A>G (p.Glu111=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2043614	NM_000210.4(ITGA6):c.343A>T (p.Met115Leu)	ITGA6 (M1L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2861210	NM_000210.4(ITGA6):c.372dup (p.Gly125fs)	ITGA6 (G11fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2704237	NM_000210.4(ITGA6):c.372A>G (p.Pro124=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2781938	NM_000210.4(ITGA6):c.377del (p.Gly126fs)	ITGA6 (G12fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2704157	NM_000210.4(ITGA6):c.378del (p.Lys127fs)	ITGA6 (K127fs +1 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2740735	NM_000210.4(ITGA6):c.384C>T (p.Val128=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2696567	NM_000210.4(ITGA6):c.387+1G>A	ITGA6	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2983813	NM_000210.4(ITGA6):c.387+9A>G	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000708	NM_000210.4(ITGA6):c.387+11A>C	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2786384	NM_000210.4(ITGA6):c.387+11A>T	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2807846	NM_000210.4(ITGA6):c.387+16_387+17del	ITGA6	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2970411	NM_000210.4(ITGA6):c.387+14C>T	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2806926	NM_000210.4(ITGA6):c.387+17A>C	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002427	NM_000210.4(ITGA6):c.387+19G>A	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2832314	NM_000210.4(ITGA6):c.388-17C>A	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 332358	NM_000210.4(ITGA6):c.388-13C>A	ITGA6	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2856904	NM_000210.4(ITGA6):c.388-8G>A	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 591460	NM_000210.4(ITGA6):c.400C>T (p.Arg134Ter)	ITGA6 (R134* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 1949351	NM_000210.4(ITGA6):c.405T>C (p.Tyr135=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1940413	NM_000210.4(ITGA6):c.428C>T (p.Thr143Met)	ITGA6 (T29M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2960698	NM_000210.4(ITGA6):c.429G>A (p.Thr143=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957673	NM_000210.4(ITGA6):c.435G>A (p.Gln145=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 870820	NM_000210.4(ITGA6):c.442C>T (p.Arg148Ter)	ITGA6 (R148* +1 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1940602	NM_000210.4(ITGA6):c.458G>A (p.Arg153Gln)	ITGA6 (R153Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2794417	NM_000210.4(ITGA6):c.465T>C (p.Tyr155=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2754861	NM_000210.4(ITGA6):c.471G>C (p.Leu157=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2711765	NM_000210.4(ITGA6):c.495C>T (p.Asp165=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1942319	NM_000210.4(ITGA6):c.513T>C (p.Asp171=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2708839	NM_000210.4(ITGA6):c.532C>A (p.Arg178=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2793179	NM_000210.4(ITGA6):c.535T>C (p.Leu179=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2841581	NM_000210.4(ITGA6):c.555T>C (p.Phe185=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2751462	NM_000210.4(ITGA6):c.579A>T (p.Ala193=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2822039	NM_000210.4(ITGA6):c.611dup (p.Phe205fs)	ITGA6 (F205fs +1 more)	Duplication (frameshift variant)	Epidermolysis bullosa, junctional 6, with pyloric atresia +1 more	GPathogenic/Likely pathogenic
Select item 2985922	NM_000210.4(ITGA6):c.633T>C (p.Tyr211=)	ITGA6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780337	NM_000210.4(ITGA6):c.643+8C>T	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2800837	NM_000210.4(ITGA6):c.643+12G>A	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2803221	NM_000210.4(ITGA6):c.644-12T>C	ITGA6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2888129	NM_000210.4(ITGA6):c.657A>G (p.Val219=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3014960	NM_000210.4(ITGA6):c.675T>G (p.Thr225=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2745821	NM_000210.4(ITGA6):c.702T>C (p.Asp234=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2898868	NM_000210.4(ITGA6):c.705G>A (p.Gly235=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 727885	NM_000210.4(ITGA6):c.729T>C (p.Thr243=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	Epidermolysis bullosa, junctional 6, with pyloric atresia +1 more	GLikely benign
Select item 2796667	NM_000210.4(ITGA6):c.735T>C (p.His245=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1932383	NM_000210.4(ITGA6):c.738T>C (p.Asp246=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 748327	NM_000210.4(ITGA6):c.747C>T (p.Leu249=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2799676	NM_000210.4(ITGA6):c.756T>A (p.Val252=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 893154	NM_000210.4(ITGA6):c.759T>G (p.Pro253=)	ITGA6	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity

<< First< Prev

Page of 5