Variant #0000001884 (NC_000017.11:g.43094023_43094027delTTTAA, NM_007294.3:c.1504_1508delTTAAA (BRCA1))

Individual ID 00000406
Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43094023_43094027delTTTAA
Published as -
Reference Wei Xiong Wen et al. (2018), dbSNP, ClinVar
DB-ID BRCA1_000089
dbSNP ID rs80357888
Frequency 1/1726
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-02-09 10:41:28 +08:00 (CST)
Date last edited 2021-09-05 09:54:28 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA1 NM_007294.3 +/. - c.1504_1508delTTAAA - r.(?) p.(Leu502Alafs*2) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000419 DNA MLPA;SEQ-NG-I BRCA1 20 Nuur Athirah Binti Mohd Daud