Variant #0000805860 (NC_000012.11:g.56625155G>C, NM_173596.2:c.97G>C (SLC39A5))

Chromosome 12
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.56625155G>C
DNA change (hg38) -
Published as SLC39A5(NM_173596.2):c.97G>C (p.E33Q)
ISCN -
DB-ID ANKRD52_000010
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
NABP2 NM_024068.3 ?/. - c.*2158G>C r.(=) p.(=)
ANKRD52 NM_173595.3 ?/. - c.*11771C>G r.(=) p.(=)
SLC39A5 NM_173596.2 ?/. - c.97G>C r.(?) p.(Glu33Gln)


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