Variant #0000403894 (NC_000023.10:g.53449468T>G, NM_006306.2:c.82A>C (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.53449468T>G |
DNA change (hg38) |
g.53422519T>G |
Published as |
- |
ISCN |
- |
DB-ID |
SMC1A_000013 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs34530151 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.00-0.10 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
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 |
2020-07-20 09:57:35 +02:00 (CEST) |

Variant on transcripts
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