Variant #0000403892 (NC_000023.10:g.53449568G>A, NM_006306.2:c.-19C>T (SMC1A))
| Chromosome |
X |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53449568G>A |
| DNA change (hg38) |
g.53422619G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SMC1A_000012 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs1264011 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.14-0.64 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.52412 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-09-04 16:50:35 +02:00 (CEST) |
| Date last edited |
2009-12-24 09:24:37 +01:00 (CET) |

Variant on transcripts
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