Variant #0000548697 (NC_000012.11:g.56631126_56631129del, NC_000012.11(NM_173596.2):c.1479+2_1479+5del (SLC39A5))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56631126_56631129del
DNA change (hg38) g.56237342_56237345del
Published as SLC39A5(NM_173596.2):c.1479+2_1479+5delTGAG
ISCN -
DB-ID SLC39A5_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) Retrieve
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 2020-07-02 16:29:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD52 NM_173595.3 +?/. - c.*5798_*5801del r.(=) p.(=)
SLC39A5 NM_173596.2 +?/. - c.1479+2_1479+5del r.spl? p.?


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