Variant #0000863073 (NC_000012.11:g.56625099G>C, NM_173596.2:c.41G>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.56625099G>C
DNA change (hg38) -
Published as SLC39A5(NM_173596.2):c.41G>C (p.C14S)
ISCN -
DB-ID ANKRD52_000012
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NABP2 NM_024068.3 -?/. - c.*2102G>C r.(=) p.(=)
ANKRD52 NM_173595.3 -?/. - c.*11827C>G r.(=) p.(=)
SLC39A5 NM_173596.2 -?/. - c.41G>C r.(?) p.(Cys14Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.