Variant #0000561454 (NC_000017.10:g.40265812C>T, NM_024119.2:c.-1284G>A (DHX58))

Chromosome 17
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.40265812C>T
DNA change (hg38) g.42113794C>T
Published as KAT2A(NM_021078.2):c.2369G>A (p.(Arg790Gln))
ISCN -
DB-ID DHX58_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT2A NM_021078.2 -?/. - c.2369G>A r.(?) p.(Arg790Gln)
DHX58 NM_024119.2 -?/. - c.-1284G>A r.(?) p.(=)


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