Variant #0000721944 (NC_000008.10:g.22269716G>A, NM_001128431.2:c.624G>A (SLC39A14))

Chromosome 8
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.22269716G>A
DNA change (hg38) -
Published as SLC39A14(NM_001351660.1):c.624G>A (p.P208=)
ISCN -
DB-ID SLC39A14_000027
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) 5.0E-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 2021-02-08 18:36:18 +01:00 (CET)
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.624G>A r.(?) p.(Pro208=)
SLC39A14 NM_015359.4 -?/. - c.627+2088G>A r.(=) p.(=)


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