Variant #0000950685 (NC_000016.9:g.56921879G>A, NM_000339.2:c.2221G>A (SLC12A3))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.56921879G>A |
| DNA change (hg38) |
- |
| Published as |
SLC12A3(NM_000339.2):c.2221G>A (p.G741R), SLC12A3(NM_000339.3):c.2221G>A (p.G741R), SLC12A3(NM_001126108.2):c.2221G>A (p.(Gly741Arg)) |
| ISCN |
- |
| DB-ID |
SLC12A3_000092 See all 9 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) |
0.00038 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-11-27 17:35:39 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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