Variant #0000614308 (NC_000012.11:g.56625114T>C, NM_173596.2:c.56T>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.56625114T>C
DNA change (hg38) g.56231330T>C
Published as SLC39A5(NM_173596.2):c.56T>C (p.L19S)
ISCN -
DB-ID ANKRD52_000002
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) 0.00559 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NABP2 NM_024068.3 -?/. - c.*2117T>C r.(=) p.(=)
ANKRD52 NM_173595.3 -?/. - c.*11812A>G r.(=) p.(=)
SLC39A5 NM_173596.2 -?/. - c.56T>C r.(?) p.(Leu19Ser)


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