Variant #0000009203 (NC_000016.10:g.68810223C>T, CDH1(NM_004360.3):c.714C>T)

Individual ID 00001793
Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.68810223C>T
Reference -
DB-ID CDH1_000019
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Laura Vargas Roig-IMBECU
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

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Co_ocurrence     

RNA change     

Review status     
CDH1 NM_004360.3 -?/-? 6 c.714C>T p.(=) Not available BRCA2 r.(=) -



Screenings


AscendingScreening ID     

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Technique     

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Date of test     

Type of test     

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Variants found     

Owner     
0000002078 DNA SEQ-NG Biogenotec Panel Multigénico (21 genes) APC, ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN,NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53 10-oct-2019 Multigenetic panel - 4 Laura Vargas Roig-IMBECU