Variant #0000826633 (NC_000018.9:g.29099821G>A, NM_001943.3:c.137G>A (DSG2))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.29099821G>A |
DNA change (hg38) |
g.31519858G>A |
Published as |
Arg46Gln |
ISCN |
- |
DB-ID |
DSG2_000006 See all 11 reported entries |
Variant remarks |
- |
Reference |
PubMed: Vissing 2021 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2021-11-30 15:04:38 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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