Variant #0000566123 (NC_000019.9:g.12917523C>T, NM_006397.2:c.36C>T (RNASEH2A))

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.12917523C>T
DNA change (hg38) g.12806709C>T
Published as RNASEH2A(NM_006397.2):c.36C>T (p.G12=), RNASEH2A(NM_006397.3):c.36C>T (p.(Gly12=), p.G12=)
ISCN -
DB-ID RNASEH2A_000044 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) 0.00014 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRDX2 NM_005809.4 -?/. - c.-4979G>A r.(?) p.(=)
RNASEH2A NM_006397.2 -?/. - c.36C>T r.(?) p.(Gly12=)


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