Variant #0000766027 (NC_000017.10:g.48244779C>A, NM_000023.2:c.88C>A (SGCA))
Chromosome |
17 |
Allele |
Unknown |
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.48244779C>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
SGCA_000063 See all 3 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1327595249 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2021-04-30 11:07:02 +02:00 (CEST) |
Date last edited |
2022-09-26 12:22:42 +02:00 (CEST) |

Variant on transcripts
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