Variant #0000534232 (NC_000008.10:g.145639675C>T, NM_013291.2:c.-5017G>A (CPSF1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145639675C>T
DNA change (hg38) g.144414291C>T
Published as SLC39A4(NM_130849.4):c.1120G>A (p.G374R)
ISCN -
DB-ID SLC39A4_000006 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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 +?/. - c.-5017G>A r.(?) p.(=)
SLC39A4 NM_017767.2 +?/. - c.1045G>A r.(?) p.(Gly349Arg)
SLC39A4 NM_130849.2 +?/. - c.1120G>A r.(?) p.(Gly374Arg)


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