Variant #0000600564 (NC_000005.9:g.172662261G>A, NM_004387.3:c.-175C>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.172662261G>A |
| DNA change (hg38) |
g.173235258G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
NKX2-5_001336 |
| Variant remarks |
rs576540640 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
0.00182 |
| 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
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