Variant #0000927382 (NC_000023.10:g.48123311dup, NM_005635.2:c.425dup (SSX1))
| 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.48123311dup |
| DNA change (hg38) |
- |
| Published as |
SSX1(NM_001278691.1):c.419_420insC (p.(Gly143ArgfsTer7)), SSX1(NM_001278691.1):c.425dupC (p.G143Rfs*7), SSX1(NM_005635.4):c.425dupC (p.G143Rfs*7) |
| ISCN |
- |
| DB-ID |
SSX1_000049 See all 3 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) |
Retrieve |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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