Variant #0000803600 (NC_000008.10:g.22262321T>C, NM_001128431.2:c.98T>C (SLC39A14))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.22262321T>C
DNA change (hg38) -
Published as SLC39A14(NM_001351660.2):c.98T>C (p.L33P)
ISCN -
DB-ID SLC39A14_000029
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) 0.52532 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A14 NM_001128431.2 -/. - c.98T>C r.(?) p.(Leu33Pro)
SLC39A14 NM_015359.4 -/. - c.98T>C r.(?) p.(Leu33Pro)


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