Variant #0000441340 (NC_000006.11:g.7542274T>C, NM_004415.2:c.126T>C (DSP))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7542274T>C |
| DNA change (hg38) |
g.7542041T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DSP_000003 See all 6 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs36087964 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.05458 View details |
| Owner |
Paul van der Zwaag |
| Database submission license |
No license selected |
| Created by |
Paul van der Zwaag |
| Date created |
2009-01-26 15:51:42 +01:00 (CET) |
| Date last edited |
2018-12-24 13:09:58 +01:00 (CET) |

Variant on transcripts
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