Variant #0000533568 (NC_000008.10:g.11566169C>T, NM_002052.3:c.348C>T (GATA4))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.11566169C>T |
| DNA change (hg38) |
g.11708660C>T |
| Published as |
GATA4(NM_001308093.1):c.348C>T (p.(Ser116=)), GATA4(NM_001308093.3):c.348C>T (p.S116=), GATA4(NM_002052.4):c.348C>T (p.S116=), GATA4(NM_002052.5):c... |
| ISCN |
- |
| DB-ID |
GATA4_000026 See all 5 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00109 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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