Variant #0000973883 (NC_000001.10:g.27440500G>A, NM_003047.4:c.630C>T (SLC9A1))
| Chromosome |
1 |
| 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.27440500G>A |
| DNA change (hg38) |
- |
| Published as |
SLC9A1(NM_003047.4):c.630C>T (p.A210=), SLC9A1(NM_003047.5):c.630C>T (p.(Ala210=)) |
| ISCN |
- |
| DB-ID |
SLC9A1_000024 See all 2 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) |
0.00067 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2024-04-19 20:20:39 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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