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chr22:29130389 A>T

Annotations

GeneCHEK2
TranscriptNM_007194.3
cDNAc.319+2T>A
Protein
Functionsplicing
Localizationsplice site
hg19chr22:29130389 A>T

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
SAS0

ClinVar

IDPhenotypeEffect
RCV000131434.9Hereditary cancer-predisposing syndromeLikely pathogenic
RCV000545158.2Familial cancer of breastLikely pathogenic
RCV000515447.1Likely pathogenic
RCV000212411.2not providedLikely pathogenic

HGMD

IDPhenotypeEffect
CS1617635Breast cancerDM