Variant #0000658242 (NC_000017.10:g.71204547C>G, NM_018714.2:c.2900C>G (COG1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71204547C>G |
DNA change (hg38) |
g.73208408C>G |
Published as |
COG1(NM_018714.2):c.2900C>G (p.P967R, p.(Pro967Arg)) |
ISCN |
- |
DB-ID |
COG1_000026 See all 2 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.0005 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
|