Variant #0000545015 (NC_000011.9:g.65488180C>G, NM_032193.3:c.50G>C (RNASEH2C))

Chromosome 11
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.65488180C>G
DNA change (hg38) g.65720709C>G
Published as RNASEH2C(NM_032193.4):c.50G>C (p.R17P)
ISCN -
DB-ID KAT5_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT5 NM_006388.3 ?/. - c.*1528C>G r.(=) p.(=)
RNASEH2C NM_032193.3 ?/. - c.50G>C r.(?) p.(Arg17Pro)


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