"PreventionGenetics, part of Exact Sciences"[submitter] AND "CDH15"[ge - ClinVar

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

Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 210623	NM_004933.3(CDH15):c.107G>A (p.Arg36Gln)	CDH15 (R36Q)	Single nucleotide variant (missense variant)	CDH15-related condition +1 more	GConflicting classifications of pathogenicity
Select item 3025587	NM_004933.3(CDH15):c.111G>A (p.Ala37=)	CDH15	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3026436	NM_004933.3(CDH15):c.255C>A (p.Pro85=)	CDH15	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2629850	NM_004933.3(CDH15):c.277G>A (p.Gly93Ser)	CDH15 (G93S)	Single nucleotide variant (missense variant)	CDH15-related condition	GUncertain significance
Select item 17644	NM_004933.3(CDH15):c.365C>T (p.Ala122Val)	CDH15 (A122V)	Single nucleotide variant (missense variant)	CDH15-related condition +1 more	GLikely benign
Select item 2629984	NM_004933.3(CDH15):c.404C>A (p.Pro135His)	CDH15 (P135H)	Single nucleotide variant (missense variant)	CDH15-related condition	GUncertain significance
Select item 2633342	NM_004933.3(CDH15):c.520G>T (p.Ala174Ser)	CDH15 (A174S)	Single nucleotide variant (missense variant)	CDH15-related condition	GUncertain significance
Select item 717425	NM_004933.3(CDH15):c.1095T>C (p.His365=)	CDH15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 434628	NM_004933.3(CDH15):c.1211C>T (p.Thr404Ile)	CDH15 (T404I)	Single nucleotide variant (missense variant)	CDH15-related condition +1 more	GLikely benign
Select item 3050308	NM_004933.3(CDH15):c.1338C>T (p.Gly446=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 3051282	NM_004933.3(CDH15):c.1376-8G>A	CDH15	Single nucleotide variant (intron variant)	CDH15-related condition	GLikely benign
Select item 788313	NM_004933.3(CDH15):c.1410C>T (p.Ser470=)	CDH15	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3044669	NM_004933.3(CDH15):c.1653C>T (p.Pro551=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 3042731	NM_004933.3(CDH15):c.1665C>T (p.His555=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 434629	NM_004933.3(CDH15):c.1680G>T (p.Leu560=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition +2 more	GLikely benign
Select item 2628873	NM_004933.3(CDH15):c.1796dup (p.Thr600fs)	CDH15, LOC130059794 (T600fs)	Duplication (frameshift variant)	CDH15-related condition	GUncertain significance
Select item 3035019	NM_004933.3(CDH15):c.1851G>A (p.Leu617=)	CDH15, LOC130059794	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 3034413	NM_004933.3(CDH15):c.1980G>C (p.Gly660=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 3039040	NM_004933.3(CDH15):c.1989C>T (p.Asp663=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign
Select item 3047872	NM_004933.3(CDH15):c.2152-9T>C	CDH15	Single nucleotide variant (intron variant)	CDH15-related condition	GLikely benign
Select item 3049285	NM_004933.3(CDH15):c.2436G>A (p.Arg812=)	CDH15	Single nucleotide variant (synonymous variant)	CDH15-related condition	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 21