Variant #0000267560 (NC_000018.9:g.29122618G>A, NM_001943.3:c.2137G>A (DSG2))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.29122618G>A |
DNA change (hg38) |
g.31542655G>A |
Published as |
DSG2(NM_001943.3):c.2137G>A (p.E713K), DSG2(NM_001943.5):c.2137G>A (p.E713K), DSG2-AS1(NR_045216.1):n.1811-334C>T |
ISCN |
- |
DB-ID |
DSG2_000045 See all 8 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) |
0.0531 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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