Variant #0000913909 (NC_000012.11:g.56626573C>T, NM_173596.2:c.388C>T (SLC39A5))

Chromosome 12
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.56626573C>T
DNA change (hg38) -
Published as SLC39A5(NM_173596.3):c.388C>T (p.R130C)
ISCN -
DB-ID ANKRD52_000015
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) 0.00194 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NABP2 NM_024068.3 -?/. - c.*3576C>T r.(=) p.(=)
ANKRD52 NM_173595.3 -?/. - c.*10353G>A r.(=) p.(=)
SLC39A5 NM_173596.2 -?/. - c.388C>T r.(?) p.(Arg130Cys)


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