Variant #0000544505 (NC_000011.9:g.47435978C>T, NM_001128225.2:c.738C>T (SLC39A13))

Chromosome 11
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.47435978C>T
DNA change (hg38) g.47414427C>T
Published as SLC39A13(NM_001128225.2):c.738C>T (p.(=))
ISCN -
DB-ID PSMC3_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 15:16:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A13 NM_001128225.2 -?/. - c.738C>T r.(?) p.(Ile246=)
PSMC3 NM_002804.4 -?/. - c.*4408G>A r.(=) p.(=)


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