Variant #0000256673 (NC_000010.10:g.54040611A>T, NM_006258.3:c.1466A>T (PRKG1))
| Chromosome |
10 |
| 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.54040611A>T |
| DNA change (hg38) |
g.52280851A>T |
| Published as |
PRKG1(NM_001098512.3):c.1421A>T (p.Y474F), PRKG1(NM_006258.4):c.1466A>T (p.Y489F) |
| ISCN |
- |
| DB-ID |
PRKG1_000028 See all 4 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) |
0.00024 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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