Variant #0000600573 (NC_000005.9:g.172662297G>A, NM_004387.3:c.-211C>T (NKX2-5))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.172662297G>A |
DNA change (hg38) |
g.173235294G>A |
Published as |
- |
ISCN |
- |
DB-ID |
NKX2-5_001345 |
Variant remarks |
rs974080535 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Liliana Dain |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2019-10-29 14:46:57 +01:00 (CET) |
Date last edited |
2021-09-09 14:48:34 +02:00 (CEST) |

Variant on transcripts
|