Variant #0000999281 (NC_000011.9:g.65484225G>A, NM_032193.3:c.*3029C>T (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.65484225G>A
DNA change (hg38) -
Published as KAT5(NM_182710.2):c.1117G>A (p.(Val373Ile))
ISCN -
DB-ID KAT5_000023
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) 4.0E-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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT5 NM_006388.3 -?/. - c.1018G>A r.(?) p.(Val340Ile)
RNASEH2C NM_032193.3 -?/. - c.*3029C>T r.(=) p.(=)


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