Genomic variant #0000401442

Individual ID 00177098
Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.76741612C>T
DNA change (hg38) -
Published as missense variant c.2292C>T p.(His767Tyr)
ISCN -
DB-ID KAT6B_000103 See all 3 reported entries
Variant remarks -
Reference PubMed: [Kim 2017]
ClinVar ID -
dbSNP ID -
Origin Not applicable
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Philippe Campeau




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
KAT6B NM_001256468.1 ./. - c.1750C>T - r.(?) p.(His584Tyr)
KAT6B NM_001256469.1 ./. - c.1423C>T - r.(?) p.(His475Tyr)
KAT6B NM_012330.3 +?/. - c.2299C>T - r.(?) p.(His767Tyr)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000177998 DNA SEQ - - KAT6B 1 Philippe Campeau