Variant #0000655696 (NC_000007.13:g.107302221G>T, NM_000441.1:c.135G>T (SLC26A4))
| Chromosome |
7 |
| 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.107302221G>T |
| DNA change (hg38) |
g.107661776G>T |
| Published as |
SLC26A4(NM_000441.1):c.135G>T (p.T45=) |
| ISCN |
- |
| DB-ID |
SLC26A4_000234 |
| 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) |
0.00028 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-06-23 13:20:55 +02:00 (CEST) |

Variant on transcripts
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