Variant #0000619916 (NC_000023.10:g.7811821_7811822del, NM_013452.2:c.385_386del (VCX))
| Chromosome |
X |
| Allele |
Unknown |
| 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.7811821_7811822del |
| DNA change (hg38) |
g.7843780_7843781del |
| Published as |
VCX(NM_013452.2):c.385_386del (p.?), VCX(NM_013452.2):c.385_386delCA (p.Q129Gfs*?) |
| ISCN |
- |
| DB-ID |
VCX_000009 See all 2 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) |
0.00796 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-17 18:05:07 +02:00 (CEST) |

Variant on transcripts
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