Variant #0000564308 (NC_000018.9:g.28650748A>C, NM_004949.3:c.2194T>G (DSC2))
| 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.28650748A>C |
| DNA change (hg38) |
g.31070782A>C |
| Published as |
DSC2(NM_004949.3):c.2194T>G (p.L732V), DSC2(NM_004949.5):c.2194T>G (p.L732V), DSC2(NM_024422.4):c.2194T>G (p.L732V) |
| ISCN |
- |
| DB-ID |
DSC2_000021 See all 9 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) |
0.00117 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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