Variant #0000096445 (NC_000023.10:g.113818520=, NM_001256760.1:c.-850C= (HTR2C))
| Chromosome |
X |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.113818520= |
| DNA change (hg38) |
g.114584047= |
| Published as |
C-759T (NM_000868.3) |
| ISCN |
- |
| DB-ID |
HTR2C_000000 See all 3 reported entries |
| Variant remarks |
reference haplotype HTR2C 2-1-1 |
| Reference |
Reference haplotype |
| ClinVar ID |
- |
| dbSNP ID |
rs3813929 |
| Origin |
SUMMARY record |
| 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 |
2016-05-09 17:25:47 +02:00 (CEST) |
| Date last edited |
2020-07-21 08:59:14 +02:00 (CEST) |

Variant on transcripts
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