Variant #0000576610 (NC_000023.10:g.53432736C>T, NM_006306.2:c.1698G>A (SMC1A))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53432736C>T |
| DNA change (hg38) |
g.53405804C>T |
| Published as |
SMC1A(NM_001281463.1):c.1632G>A (p.E544=) |
| ISCN |
- |
| DB-ID |
SMC1A_000088 |
| 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) |
0.00121 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-20 09:52:08 +02:00 (CEST) |

Variant on transcripts
|