"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1300 - ClinVar

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Search results

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1601156	NM_018670.4(MESP1):c.687T>G (p.Pro229=)	LOC130057888, MESP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1629584	NM_018670.4(MESP1):c.669C>G (p.Phe223Leu)	LOC130057888, MESP1 (F223L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2197719	NM_018670.4(MESP1):c.661G>T (p.Ala221Ser)	LOC130057888, MESP1 (A221S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1561757	NM_018670.4(MESP1):c.657G>T (p.Pro219=)	LOC130057888, MESP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1600508	NM_018670.4(MESP1):c.650G>A (p.Arg217His)	LOC130057888, MESP1 (R217H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2057836	NM_018670.4(MESP1):c.627A>G (p.Gly209=)	LOC130057888, MESP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2192063	NM_018670.4(MESP1):c.624C>T (p.Pro208=)	LOC130057888, MESP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1426113	NM_018670.4(MESP1):c.568G>T (p.Gly190Cys)	LOC130057888, MESP1 (G190C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2780279	NM_018670.4(MESP1):c.561C>T (p.Arg187=)	LOC130057888, MESP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2067619	NM_018670.4(MESP1):c.560G>T (p.Arg187Leu)	LOC130057888, MESP1 (R187L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2698155	NM_018670.4(MESP1):c.542AGGGGC[2] (p.183QG[1])	LOC130057888, MESP1	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1633924	NM_018670.4(MESP1):c.526A>T (p.Thr176Ser)	LOC130057888, MESP1 (T176S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1537845	NM_018670.4(MESP1):c.520A>G (p.Met174Val)	LOC130057888, MESP1 (M174V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1654286	NM_018670.4(MESP1):c.503A>G (p.Asp168Gly)	LOC130057888, MESP1 (D168G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2751389	NM_018670.4(MESP1):c.499C>G (p.Pro167Ala)	LOC130057888, MESP1 (P167A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2704626	NM_018670.4(MESP1):c.469G>T (p.Ala157Ser)	LOC130057888, MESP1 (A157S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2068273	NM_018670.4(MESP1):c.459G>C (p.Gln153His)	LOC130057888, MESP1 (Q153H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1574446	NM_018670.4(MESP1):c.453C>G (p.Cys151Trp)	LOC130057888, MESP1 (C151W)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1926231	NM_018670.4(MESP1):c.449G>A (p.Arg150Gln)	LOC130057888, MESP1 (R150Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1528118	NM_018670.4(MESP1):c.435G>T (p.Glu145Asp)	LOC130057888, MESP1 (E145D)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar

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Items: 20