Variant #0000872180 (NC_000013.10:g.51517529A>G, NM_024570.3:c.509A>G (RNASEH2B))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51517529A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RNASEH2B_000072
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1475724702
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-07-12 15:42:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNASEH2B NM_024570.3 +?/. - c.509A>G r.(?) p.(Lys170Arg)


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