Variant #0000611525 (NC_000008.10:g.145638181C>T, NM_013291.2:c.-3523G>A (CPSF1))

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.145638181C>T
DNA change (hg38) g.144412797C>T
Published as SLC39A4(NM_001280557.1):c.283G>A (p.(Ala95Thr))
ISCN -
DB-ID CPSF1_000019
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) 0.00011 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.-3523G>A r.(?) p.(=)
SLC39A4 NM_017767.2 ?/. - c.1702G>A r.(?) p.(Ala568Thr)
SLC39A4 NM_130849.2 ?/. - c.1777G>A r.(?) p.(Ala593Thr)


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