Variant #0000913911 (NC_000012.11:g.56631364T>C, NC_000012.11(NM_173596.2):c.1480-8T>C (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.56631364T>C
DNA change (hg38) -
Published as SLC39A5(NM_173596.3):c.1480-8T>C
ISCN -
DB-ID ANKRD52_000017
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) 0.00187 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     
ANKRD52 NM_173595.3 -?/. - c.*5562A>G r.(=) p.(=)
SLC39A5 NM_173596.2 -?/. - c.1480-8T>C r.(=) p.(=)


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