All variants in the CDH1 gene


Information The variants shown are described using the NM_004360.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. - c.233G>A r.(?) p.(Gly78Asp) - VUS g.68835642G>A g.68801739G>A - - CDH1_000205 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs587781404 Germline - 1/12490 controls - 0 - Yukihide Momozawa
?/. - c.233G>A r.(?) p.(Gly78Asp) - NA g.68835642G>A - chr16_68835642_G_A - CDH1_000205 not in 60466 cases; the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 1/53461 controls - 0 - BRIDGES consortium
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This database is one of the InSiGHT gene variant databases