"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1268 - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2781658	NM_006015.6(ARID1A):c.3407-16G>T	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956305	NM_006015.6(ARID1A):c.3407-8G>C	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 521449	NM_006015.6(ARID1A):c.3407C>T (p.Ala1136Val)	ARID1A, LOC126805670 (A1136V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 434322	NM_006015.6(ARID1A):c.3408G>A (p.Ala1136=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1915575	NM_006015.6(ARID1A):c.3421A>G (p.Met1141Val)	ARID1A, LOC126805670 (M1141V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1334642	NM_006015.6(ARID1A):c.3426G>T (p.Gln1142His)	ARID1A, LOC126805670 (Q1142H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2032473	NM_006015.6(ARID1A):c.3441C>A (p.Pro1147=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1974333	NM_006015.6(ARID1A):c.3464C>T (p.Ala1155Val)	ARID1A, LOC126805670 (A1155V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3020283	NM_006015.6(ARID1A):c.3477C>T (p.Asp1159=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2836539	NM_006015.6(ARID1A):c.3485C>T (p.Pro1162Leu)	ARID1A, LOC126805670 (P1162L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2818093	NM_006015.6(ARID1A):c.3499T>C (p.Ser1167Pro)	ARID1A, LOC126805670 (S1167P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 133547	NM_006015.6(ARID1A):c.3524C>T (p.Pro1175Leu)	LOC126805670, ARID1A (P1175L)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1646388	NM_006015.6(ARID1A):c.3539+16G>A	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2961295	NM_006015.6(ARID1A):c.3539+18G>A	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1601463	NM_006015.6(ARID1A):c.3540-12C>T	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2258896	NM_006015.6(ARID1A):c.3613A>G (p.Met1205Val)	ARID1A, LOC126805670 (M1205V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2834644	NM_006015.6(ARID1A):c.3619C>A (p.Pro1207Thr)	ARID1A, LOC126805670 (P1207T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2983526	NM_006015.6(ARID1A):c.3670A>G (p.Met1224Val)	ARID1A, LOC126805670 (M1224V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2984215	NM_006015.6(ARID1A):c.3675C>G (p.Ser1225=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3011031	NM_006015.6(ARID1A):c.3677A>G (p.Tyr1226Cys)	ARID1A, LOC126805670 (Y1226C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1492750	NM_006015.6(ARID1A):c.3692A>T (p.Asp1231Val)	ARID1A, LOC126805670 (D1231V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 518315	NM_006015.6(ARID1A):c.3702C>T (p.Gly1234=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2979740	NM_006015.6(ARID1A):c.3715+10C>G	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3022536	NM_006015.6(ARID1A):c.3716-20G>A	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983010	NM_006015.6(ARID1A):c.3716-10C>T	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1947072	NM_006015.6(ARID1A):c.3716-8A>G	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1206070	NM_006015.6(ARID1A):c.3716-7C>T	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 14 +2 more	GBenign/Likely benign
Select item 2910752	NM_006015.6(ARID1A):c.3716-6G>A	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2791904	NM_006015.6(ARID1A):c.3716-3C>T	ARID1A, LOC126805670	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2976277	NM_006015.6(ARID1A):c.3718C>G (p.Pro1240Ala)	ARID1A, LOC126805670 (P1240A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Items: 30