Variant #0000298992 (NC_000019.9:g.50902164G>A, NM_001256849.1:c.56G>A (POLD1))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50902164G>A
DNA change (hg38) g.50398907G>A
Published as POLD1(NM_001256849.1):c.56G>A (p.R19H), POLD1(NM_001308632.1):c.56G>A (p.R19H)
ISCN -
DB-ID POLD1_000007 See all 3 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) 0.00527 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLD1 NM_001256849.1 -/. - c.56G>A r.(?) p.(Arg19His)


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