Variant #0000617358 (NC_000019.9:g.12917597G>A, NM_006397.2:c.110G>A (RNASEH2A))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.12917597G>A
DNA change (hg38) g.12806783G>A
Published as RNASEH2A(NM_006397.2):c.110G>A (p.G37D)
ISCN -
DB-ID RNASEH2A_000049 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-5053C>T r.(?) p.(=)
RNASEH2A NM_006397.2 ?/. - c.110G>A r.(?) p.(Gly37Asp)


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