Variant #0000659337 (NC_000023.10:g.48123357G>C, NC_000023.10(NM_005635.2):c.466+5G>C (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.48123357G>C |
| DNA change (hg38) |
g.48263922G>C |
| Published as |
SSX1(NM_001278691.1):c.466+5G>C (p.?) |
| ISCN |
- |
| DB-ID |
SSX1_000060 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-07-19 20:27:47 +02:00 (CEST) |

Variant on transcripts
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