Variant #0000530150 (NC_000007.13:g.103015002A>G, NM_198999.2:c.2079T>C (SLC26A5))
| 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.103015002A>G |
| DNA change (hg38) |
g.103374555A>G |
| Published as |
SLC26A5(NM_198999.2):c.2079T>C (p.F693=) |
| ISCN |
- |
| DB-ID |
PSMC2_000003 |
| 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-23 13:02:25 +02:00 (CEST) |

Variant on transcripts
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