Variant #0000721865 (NC_000008.10:g.145639773G>A, NM_130849.2:c.1022C>T (SLC39A4))

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.145639773G>A
DNA change (hg38) -
Published as SLC39A4(NM_017767.2):c.947C>T (p.A316V), SLC39A4(NM_130849.4):c.1022C>T (p.A341V)
ISCN -
DB-ID SLC39A4_000026 See all 2 reported entries
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) 0.00013 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.947C>T r.(?) p.(Ala316Val)
SLC39A4 NM_130849.2 ?/. - c.1022C>T r.(?) p.(Ala341Val)


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