Variant #0000254235 (NC_000011.9:g.65488169A>G, NM_032193.3:c.61T>C (RNASEH2C))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65488169A>G
DNA change (hg38) g.65720698A>G
Published as RNASEH2C(NM_032193.3):c.61T>C (p.L21=)
ISCN -
DB-ID RNASEH2C_000028
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) 0.0023 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 18:15:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT5 NM_006388.3 -?/. - c.*1517A>G r.(=) p.(=)
RNASEH2C NM_032193.3 -?/. - c.61T>C r.(?) p.(Leu21=)


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