Variant #0000951339 (NC_000019.9:g.50905151G>A, NM_001256849.1:c.433G>A (POLD1))

Chromosome 19
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.50905151G>A
DNA change (hg38) -
Published as POLD1(NM_001256849.1):c.433G>A (p.A145T, p.(Ala145Thr)), POLD1(NM_001308632.1):c.433G>A (p.A145T)
ISCN -
DB-ID POLD1_000017 See all 5 reported entries
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) 0.00276 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
POLD1 NM_001256849.1 ?/. - c.433G>A r.(?) p.(Ala145Thr)


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