Variant #0000915133 (NC_000019.9:g.12921186T>C, NM_006397.2:c.605T>C (RNASEH2A))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.12921186T>C
DNA change (hg38) -
Published as RNASEH2A(NM_006397.2):c.605T>C (p.L202S), RNASEH2A(NM_006397.3):c.605T>C (p.(Leu202Ser), p.L202S)
ISCN -
DB-ID RNASEH2A_000032 See all 5 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) 0.04696 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 2023-01-11 15:44:22 +01:00 (CET)
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     
RNASEH2A NM_006397.2 -/. - c.605T>C r.(?) p.(Leu202Ser)


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