Variant #0000040782 (NC_000009.11:g.35077267_35077273del, FANCG(NM_004629.1):c.637_643del)

Individual ID 00020205
Chromosome 9
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35077267_35077273del
DNA change (hg38) g.35077270_35077276del
Published as -
ISCN -
DB-ID FANCG_000037 See all 13 reported entries
Variant remarks -
Reference PubMed: Morgan 2005
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Arleen D. Auerbach
Database submission license No license selected
Created by Arleen D. Auerbach
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FANCG NM_004629.1 ?/. 5 c.637_643del r.(?) p.(fs*) FA



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000020202 DNA SEQ - - FANCG 2 Arleen D. Auerbach