Variant #0000548696 (NC_000012.11:g.56625097C>G, NM_173596.2:c.39C>G (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.56625097C>G
DNA change (hg38) g.56231313C>G
Published as SLC39A5(NM_173596.2):c.39C>G (p.F13L)
ISCN -
DB-ID ANKRD52_000001
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NABP2 NM_024068.3 ?/. - c.*2100C>G r.(=) p.(=)
ANKRD52 NM_173595.3 ?/. - c.*11829G>C r.(=) p.(=)
SLC39A5 NM_173596.2 ?/. - c.39C>G r.(?) p.(Phe13Leu)


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