Variant #0000690207 (NC_000008.10:g.145640292C>A, NC_000008.10(NM_130849.2):c.805-12G>T (SLC39A4))

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.145640292C>A
DNA change (hg38) -
Published as SLC39A4(NM_017767.3):c.730-12G>T
ISCN -
DB-ID SLC39A4_000037
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) 0.00044 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC39A4 NM_017767.2 -?/. - c.730-12G>T r.(=) p.(=)
SLC39A4 NM_130849.2 -?/. - c.805-12G>T r.(=) p.(=)


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