Variant #0000948305 (NC_000004.11:g.185599552T>C, NC_000004.11(NM_152683.2):c.1007+4T>C (PRIMPOL))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.185599552T>C
DNA change (hg38) -
Published as PRIMPOL(NM_001345891.2):c.1007+4T>C
ISCN -
DB-ID MLF1IP_000015
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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.*16890A>G r.(=) p.(=)
PRIMPOL NM_152683.2 -?/. - c.1007+4T>C r.spl? p.?


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