Variant #0000267581 (NC_000018.9:g.28991180T>C, DSG4(NM_177986.3):c.2138-14T>C)
Chromosome |
18 |
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.28991180T>C |
DNA change (hg38) |
g.31411217T>C |
Published as |
DSG4(NM_001134453.3):c.2181T>C (p.H727=) |
ISCN |
- |
DB-ID |
DSG4_000006 |
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) |
2.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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