Variant #0000979754 (NC_000011.9:g.65487707G>A, NC_000011.9(NM_032193.3):c.348+6C>T (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.65487707G>A
DNA change (hg38) -
Published as RNASEH2C(NM_032193.3):c.348+6C>T (p.?)
ISCN -
DB-ID KAT5_000018
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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.*1055G>A r.(=) p.(=)
RNASEH2C NM_032193.3 ?/. - c.348+6C>T r.(=) p.(=)


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