Variant #0000568206 (NC_000019.9:g.50905173C>T, NM_001256849.1:c.455C>T (POLD1))

Chromosome 19
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.50905173C>T
DNA change (hg38) g.50401916C>T
Published as POLD1(NM_001256849.1):c.455C>T (p.A152V, p.(Ala152Val)), POLD1(NM_001308632.1):c.455C>T (p.A152V), POLD1(NM_002691.4):c.455C>T (p.A152V)
ISCN -
DB-ID POLD1_000018 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) 0.00048 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLD1 NM_001256849.1 -?/. - c.455C>T r.(?) p.(Ala152Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.