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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