Variant #0000976239 (NC_000004.11:g.185623284_185623287del, NM_152683.2:c.*7351_*7354del (PRIMPOL))

Chromosome 4
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.185623284_185623287del
DNA change (hg38) -
Published as CENPU(NM_024629.4):c.884_887del (p.(Glu295AlafsTer4))
ISCN -
DB-ID MLF1IP_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLF1IP NM_024629.3 ?/. - c.884_887del r.(?) p.(Glu295Alafs*4)
PRIMPOL NM_152683.2 ?/. - c.*7351_*7354del r.(=) p.(=)


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