Variant #0000040779 (NC_000009.11:g.35077267_35077273del, FANCG(NM_004629.1):c.637_643del)
Individual ID |
00020202 |
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 14 reported entries |
Variant remarks |
- |
Reference |
PubMed: Morgan 2005 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
? |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Arleen D. Auerbach |
Database submission license |
No license selected |
Created by |
Arleen D. Auerbach |

Variant on transcripts
Screenings
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