Variant #0000403896 (NC_000023.10:g.53436051C>T, NM_006306.2:c.1487G>A (SMC1A))
Chromosome |
X |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53436051C>T |
DNA change (hg38) |
g.53409120C>T |
Published as |
- |
ISCN |
- |
DB-ID |
SMC1A_000004 See all 8 reported entries |
Variant remarks |
increased affinity of SMC hinge dimers for DNA binding |
Reference |
PubMed: Revenkova 2009, OMIM:var0004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
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 09:52:27 +02:00 (CEST) |

Variant on transcripts
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