Variant #0000801598 (NC_000004.11:g.185593346T>G, NM_152683.2:c.576T>G (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.185593346T>G
DNA change (hg38) -
Published as PRIMPOL(NM_001345891.1):c.576T>G (p.I192M)
ISCN -
DB-ID MLF1IP_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLF1IP NM_024629.3 ?/. - c.*23096A>C r.(=) p.(=)
PRIMPOL NM_152683.2 ?/. - c.576T>G r.(?) p.(Ile192Met)


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