Variant #0000528938 (NC_000006.11:g.43565568G>T, NM_006502.2:c.626G>T (POLH))

Chromosome 6
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.43565568G>T
DNA change (hg38) g.43597831G>T
Published as POLH(NM_006502.2):c.626G>T (p.G209V, p.(Gly209Val)), POLH(NM_006502.3):c.626G>T (p.G209V)
ISCN -
DB-ID POLH_000016 See all 4 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) 0.00383 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +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     
POLH NM_006502.2 -/. - c.626G>T r.(?) p.(Gly209Val)
GTPBP2 NM_019096.3 -/. - c.*23783C>A r.(=) p.(=)


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