"GeneDx"[submitter] AND "ITGA8"[gene] - ClinVar

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Search results

Items: 89

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59657	GRCh38/hg38 10p15.3-12.31(chr10:69261-19184047)x3	LOC126860819, LOC126860820 +680 more	Copy number gain	See cases	GPathogenic
Select item 58717	GRCh38/hg38 10p15.1-13(chr10:4802753-16823491)x1	LOC130003217, LOC130003218 +482 more	Copy number loss	See cases	GPathogenic
Select item 1290122	NM_003638.3(ITGA8):c.2981T>C (p.Val994Ala)	ITGA8 (V979A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1237225	NM_003638.3(ITGA8):c.2881-55A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277160	NM_003638.3(ITGA8):c.2881-187C>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264028	NM_003638.3(ITGA8):c.2881-216C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232924	NM_003638.3(ITGA8):c.2881-220G>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268226	NM_003638.3(ITGA8):c.2881-248A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279678	NM_003638.3(ITGA8):c.2881-264A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253664	NM_003638.3(ITGA8):c.2880+310C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239658	NM_003638.3(ITGA8):c.2880+102T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250211	NM_003638.3(ITGA8):c.2880+82C>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232286	NM_003638.3(ITGA8):c.2880+47G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227742	NM_003638.3(ITGA8):c.2880+46T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221462	NM_003638.3(ITGA8):c.2766+81A>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175407	NM_003638.3(ITGA8):c.2638-70T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267365	NM_003638.3(ITGA8):c.2478+337C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252693	NM_003638.3(ITGA8):c.2478+305G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270850	NM_003638.3(ITGA8):c.2478+240C>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2497896	NM_003638.3(ITGA8):c.2317A>C (p.Asn773His)	ITGA8 (N758H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 450375	NM_003638.3(ITGA8):c.2174dup (p.Cys726fs)	ITGA8 (C711fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1252376	NM_003638.3(ITGA8):c.2119-113A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228858	NM_003638.3(ITGA8):c.2119-247T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270034	NM_003638.3(ITGA8):c.2119-293T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234514	NM_003638.3(ITGA8):c.1971-104del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1234974	NM_003638.3(ITGA8):c.1971-186G>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276645	NM_003638.3(ITGA8):c.1971-245dup	ITGA8	Duplication (intron variant)	not provided	GBenign
Select item 1283636	NM_003638.3(ITGA8):c.1971-224del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1235715	NM_003638.3(ITGA8):c.1971-225_1971-224del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1220633	NM_003638.3(ITGA8):c.1971-226_1971-224del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1276287	NM_003638.3(ITGA8):c.1971-297C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286910	NM_003638.3(ITGA8):c.1970+245del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1245585	NM_003638.3(ITGA8):c.1902+180C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280317	NM_003638.3(ITGA8):c.1902+41G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234633	NM_003638.3(ITGA8):c.1765-227G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183844	NM_003638.3(ITGA8):c.1742A>C (p.Gln581Pro)	ITGA8 (Q566P +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1238988	NM_003638.3(ITGA8):c.1730C>T (p.Ser577Phe)	ITGA8 (S562F +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1258168	NM_003638.3(ITGA8):c.1610-169G>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258619	NM_003638.3(ITGA8):c.1609+48G>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282029	NM_003638.3(ITGA8):c.1554-134GT[10]	ITGA8	Microsatellite (intron variant)	not provided	GBenign
Select item 1262220	NM_003638.3(ITGA8):c.1554-296A>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259471	NM_003638.3(ITGA8):c.1553+261T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236673	NM_003638.3(ITGA8):c.1553+234C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282911	NM_003638.3(ITGA8):c.1446-275T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289998	NM_003638.3(ITGA8):c.1445+216A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225284	NM_003638.3(ITGA8):c.1400-38C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265946	NM_003638.3(ITGA8):c.1400-101A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244870	NM_003638.3(ITGA8):c.1400-184del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1269689	NM_003638.3(ITGA8):c.1400-217G>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286211	NM_003638.3(ITGA8):c.1399+46T>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230798	NM_003638.3(ITGA8):c.1208-139G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244641	NM_003638.3(ITGA8):c.1001+258_1001+259insAA	ITGA8	Insertion (intron variant)	not provided	GBenign
Select item 1232463	NM_003638.3(ITGA8):c.1001+221G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275552	NM_003638.3(ITGA8):c.1001+157T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295106	NM_003638.3(ITGA8):c.949-273A>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270116	NM_003638.3(ITGA8):c.948+195T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234198	NM_003638.3(ITGA8):c.948+171T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247406	NM_003638.3(ITGA8):c.892-39T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244298	NM_003638.3(ITGA8):c.892-158del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1274654	NM_003638.3(ITGA8):c.892-224A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258317	NM_003638.3(ITGA8):c.891+293T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240922	NM_003638.3(ITGA8):c.891+215T>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274718	NM_003638.3(ITGA8):c.848-71G>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279650	NM_003638.3(ITGA8):c.848-180C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230251	NM_003638.3(ITGA8):c.848-307A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268143	NM_003638.3(ITGA8):c.847+95T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277424	NM_003638.3(ITGA8):c.847+61A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264237	NM_003638.3(ITGA8):c.803-21G>C	ITGA8	Single nucleotide variant (intron variant)	Renal hypodysplasia/aplasia 1 +1 more	GBenign
Select item 1235985	NM_003638.3(ITGA8):c.803-233del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1268799	NM_003638.3(ITGA8):c.803-311T>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244806	NM_003638.3(ITGA8):c.802+192G>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2497952	NM_003638.3(ITGA8):c.707T>A (p.Ile236Asn)	ITGA8 (I236N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1174471	NM_003638.3(ITGA8):c.631-73A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174427	NM_003638.3(ITGA8):c.631-111A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270140	NM_003638.3(ITGA8):c.569-180C>T	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 57883	GRCh38/hg38 10p13(chr10:15680938-16480748)x3	ITGA8, LINC02654 +11 more	Copy number gain	See cases	GUncertain significance
Select item 1229558	NM_003638.3(ITGA8):c.568+332T>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270775	NM_003638.3(ITGA8):c.568+280G>A	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273753	NM_003638.3(ITGA8):c.444+14G>A	ITGA8	Single nucleotide variant (intron variant)	Renal hypodysplasia/aplasia 1 +1 more	GBenign
Select item 3372139	NM_003638.3(ITGA8):c.360dup (p.Val121fs)	ITGA8 (V121fs)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 1703974	NM_003638.3(ITGA8):c.361G>A (p.Val121Ile)	ITGA8 (V121I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1248669	NM_003638.3(ITGA8):c.344-285dup	ITGA8	Duplication (intron variant)	not provided	GBenign
Select item 1177980	NM_003638.3(ITGA8):c.344-285_344-284dup	ITGA8	Duplication (intron variant)	not provided	GBenign
Select item 1289215	NM_003638.3(ITGA8):c.344-265del	ITGA8	Deletion (intron variant)	not provided	GBenign
Select item 1262795	NM_003638.3(ITGA8):c.343+95G>C	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236885	NM_003638.3(ITGA8):c.210-311T>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262407	NM_003638.3(ITGA8):c.209+35A>G	ITGA8	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237012	NM_003638.3(ITGA8):c.24T>A (p.Gly8=)	ITGA8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1281312	NM_003638.3(ITGA8):c.-64dup	ITGA8	Duplication (5 prime UTR variant)	not provided	GBenign

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Items: 89