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 InternationalCreative Commons License
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A8 NM_022154.5 +/. 1i c.220-5T>A r.spl? p.?


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