Variant #0000999124 (NC_000011.9:g.47434984G>A, NM_001128225.2:c.571G>A (SLC39A13))

Chromosome 11
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.47434984G>A
DNA change (hg38) -
Published as SLC39A13(NM_001128225.2):c.571G>A (p.(Ala191Thr)), SLC39A13(NM_001128225.3):c.571G>A (p.A191T)
ISCN -
DB-ID SLC39A13_000008 See all 2 reported entries
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) 0.00012 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A13 NM_001128225.2 -?/. - c.571G>A r.(?) p.(Ala191Thr)


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