chr22:29130389 A>T
Annotations
GeneCHEK2
TranscriptNM_007194.3
cDNAc.319+2T>A
Protein
Functionsplicing
Localizationsplice site
hg19chr22:29130389 A>T
dbSNPrs587782401
Synonyms
TranscriptcDNAProtein
NM_001257387.1UTR5
NM_145862.2c.319+2T>A
NM_001005735.1c.319+2T>A
NM_001349956.1c.319+2T>A
Frequency in gnomAD
GenomeExome
MAX0.00060.00004484
AFR00
AMR00
ASJ00
EAS00
FIN0.00090.0006
NFE0.00060.00004484
SAS–0
ClinVar
IDPhenotypeEffect
RCV000515447.1Likely pathogenic
HGMD
IDPhenotypeEffect
CS1617635Breast cancerDM