Variant #0000815726 (NC_000007.13:g.107312690G>T, NM_000441.1:c.412G>T (SLC26A4))
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.107312690G>T |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
SLC26A4_000072 See all 13 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs111033199 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00017 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2021-10-21 18:26:01 +02:00 (CEST) |
Date last edited |
2022-09-26 12:22:42 +02:00 (CEST) |

Variant on transcripts
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