Variant #0000001007 (NC_000004.11:g.155533035G>C, NM_021870.2:c.323C>G (FGG))
Individual ID |
00000028 |
Chromosome |
4 |
Allele |
Unknown |
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.155533035G>C |
DNA change (hg38) |
g.154611883G>C |
Published as |
- |
ISCN |
- |
DB-ID |
FGG_000000 See all 5 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00196 View details |
Owner |
Gerard C.P. Schaafsma |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Gerard C.P. Schaafsma |
Date created |
2011-04-06 16:20:25 +02:00 (CEST) |
Date last edited |
2025-07-06 22:55:27 +02:00 (CEST) |

Variant on transcripts
Screenings
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