Variant #0000721863 (NC_000008.10:g.145638778G>T, NM_013291.2:c.-4120C>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.145638778G>T
DNA change (hg38) -
Published as SLC39A4(NM_130849.4):c.1475-5C>A
ISCN -
DB-ID CPSF1_000027
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) Retrieve
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     
CPSF1 NM_013291.2 ?/. - c.-4120C>A r.(?) p.(=)
SLC39A4 NM_017767.2 ?/. - c.1400-5C>A r.spl? p.?
SLC39A4 NM_130849.2 ?/. - c.1475-5C>A r.spl? p.?


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