Variant #0000912450 (NC_000006.11:g.31911055G>A, NM_000063.4:c.1414G>A (C2))
Chromosome |
6 |
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.31911055G>A |
DNA change (hg38) |
- |
Published as |
C2(NM_000063.4):c.1414G>A (p.A472T) |
ISCN |
- |
DB-ID |
C2_000033 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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|