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chr22:29120962 T>A

Annotations

GeneCHEK2
TranscriptNM_007194.3
cDNAc.592+3A>T
Protein
Functionsplicing
Localizationsplice site
hg19chr22:29120962 T>A

Synonyms

TranscriptcDNAProtein
NM_001257387.1UTR5
NM_145862.2c.592+3A>T
NM_001005735.1c.721+3A>T
NM_001349956.1c.445-51A>T

Frequency in gnomAD

GenomeExome
MAX0.00005374
AFR0
AMR0
ASJ0
EAS0
FIN0
NFE0.00005374
SAS0.00003249

ClinVar

IDPhenotypeEffect
RCV000132447.7Hereditary cancer-predisposing syndromeVUS
RCV000656830.1not providedVUS
RCV000228472.4Familial cancer of breastConflicting interpretations of pathogenicity
RCV000212430.4not specifiedVUS
RCV000348008.1Neoplasm of the breastVUS
RCV000290615.1Colorectal cancerVUS

HGMD

IDPhenotypeEffect
CS1610907Non-triple negative breast cancerDM