Variant #0000967004 (NC_000012.11:g.56631012G>C, NM_173596.2:c.1367G>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.56631012G>C
DNA change (hg38) -
Published as SLC39A5(NM_173596.2):c.1367G>C (p.G456A), SLC39A5(NM_173596.3):c.1367G>C (p.G456A)
ISCN -
DB-ID ANKRD52_000014 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) 0.00218 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD52 NM_173595.3 -?/. - c.*5914C>G r.(=) p.(=)
SLC39A5 NM_173596.2 -?/. - c.1367G>C r.(?) p.(Gly456Ala)


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