Variant #0000528940 (NC_000006.11:g.43572357G>A, NM_006502.2:c.890G>A (POLH))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43572357G>A
DNA change (hg38) g.43604620G>A
Published as POLH(NM_006502.2):c.890G>A (p.W297*), POLH(NM_006502.3):c.890G>A (p.W297*)
ISCN -
DB-ID GTPBP2_000010 See all 2 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) Retrieve
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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLH NM_006502.2 +/. - c.890G>A r.(?) p.(Trp297Ter)
GTPBP2 NM_019096.3 +/. - c.*16994C>T r.(=) p.(=)


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