Variant #0000995785 (NC_000006.11:g.43582176C>A, NM_006502.2:c.2024C>A (POLH))

Chromosome 6
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.43582176C>A
DNA change (hg38) -
Published as POLH(NM_006502.2):c.2024C>A (p.S675Y), POLH(NM_006502.3):c.2024C>A (p.S675Y)
ISCN -
DB-ID GTPBP2_000014 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) 0.00175 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLH NM_006502.2 -?/. - c.2024C>A r.(?) p.(Ser675Tyr)
GTPBP2 NM_019096.3 -?/. - c.*7175G>T r.(=) p.(=)


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