Variant #0000534580 (NC_000008.10:g.22269540C>T, NC_000008.10(NM_001128431.2):c.458-10C>T (SLC39A14))

Chromosome 8
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.22269540C>T
DNA change (hg38) g.22412027C>T
Published as SLC39A14(NM_001135153.2):c.458-10C>T
ISCN -
DB-ID SLC39A14_000005
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A14 NM_001128431.2 ?/. - c.458-10C>T r.(=) p.(=)
SLC39A14 NM_015359.4 ?/. - c.627+1912C>T r.(=) p.(=)


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