Variant #0000534231 (NC_000008.10:g.145639669C>T, NM_013291.2:c.-5011G>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.145639669C>T
DNA change (hg38) g.144414285C>T
Published as SLC39A4(NM_017767.2):c.1051G>A (p.A351T)
ISCN -
DB-ID CPSF1_000018
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) 0.0007 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF1 NM_013291.2 ?/. - c.-5011G>A r.(?) p.(=)
SLC39A4 NM_017767.2 ?/. - c.1051G>A r.(?) p.(Ala351Thr)
SLC39A4 NM_130849.2 ?/. - c.1126G>A r.(?) p.(Ala376Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.