Variant #0001054670 (NC_000013.10:g.51484216G>C, NM_024570.3:c.4G>C (RNASEH2B))

Chromosome 13
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.51484216G>C
DNA change (hg38) -
Published as RNASEH2B(NM_024570.4):c.4G>C (p.(Ala2Pro))
ISCN -
DB-ID RNASEH2B_000078
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNASEH2B NM_024570.3 ?/. - c.4G>C r.(?) p.(Ala2Pro)
RNASEH2B-AS1 NR_046552.1 ?/. - n.230+403C>G r.(?) -


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