Variant #0000760939 (NC_000004.11:g.103236992A>T, NC_000004.11(NM_022154.5):c.220-5T>A (SLC39A8))
Chromosome |
4 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103236992A>T |
DNA change (hg38) |
- |
Published as |
c.220-5T>A /p.? |
ISCN |
- |
DB-ID |
SLC39A8_000007 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Cynthia Silveira |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Cynthia Silveira |
Date created |
2021-03-30 16:46:20 +02:00 (CEST) |
Date last edited |
2021-07-21 13:30:17 +02:00 (CEST) |

Variant on transcripts
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