Variant #0000040772 (NC_000009.11:g.35078601C>G, FANCG(NM_004629.1):c.307+1G>C)
Individual ID |
00020195 |
Chromosome |
9 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35078601C>G |
DNA change (hg38) |
g.35078604C>G |
Published as |
- |
ISCN |
- |
DB-ID |
FANCG_000019 See all 27 reported entries |
Variant remarks |
- |
Reference |
PubMed: Yamada 2000 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
? |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
Johan de Winter |
Database submission license |
No license selected |
Created by |
Myungshin Kim |

Variant on transcripts
Screenings
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