Variant #0000613559 (NC_000011.9:g.65487511C>T, NC_000011.9(NM_032193.3):c.468+5G>A (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.65487511C>T
DNA change (hg38) g.65720040C>T
Published as RNASEH2C(NM_032193.3):c.468+5G>A
ISCN -
DB-ID KAT5_000006
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) 2.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-30 18:14:28 +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.*859C>T r.(=) p.(=)
RNASEH2C NM_032193.3 ?/. - c.468+5G>A r.spl? p.?


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