Variant #0000611528 (NC_000008.10:g.145640746T>A, NM_130849.2:c.532A>T (SLC39A4))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.145640746T>A
DNA change (hg38) g.144415362T>A
Published as SLC39A4(NM_001280557.1):c.-1870A>T (p.(=))
ISCN -
DB-ID SLC39A4_000028
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) 0.00117 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A4 NM_017767.2 ?/. - c.457A>T r.(?) p.(Ser153Cys)
SLC39A4 NM_130849.2 ?/. - c.532A>T r.(?) p.(Ser178Cys)


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