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chr17:41245845 G>A

Основные

ГенBRCA1
ТранскриптNM_007294.3
кДНКc.1703C>T
Белокp.P568L
Функцияmissense
Локализацияexon
hg19chr17:41245845 G>A

Синонимы

ТранскрипткДНКБелок
NM_007297.3c.1562C>Tp.P521L
NM_007300.3c.1703C>Tp.P568L
NM_007298.3c.787+916C>T
NM_007299.3c.787+916C>T
NR_027676.1n.1839C>T

Частота в gnomAD

GenomeExome
MAX
AFR
AMR
ASJ
EAS
FIN
NFE
SAS

ClinVar

IDФенотипЭффект
RCV000443568.2not specifiedConflicting interpretations of pathogenicity
RCV000588961.1not providedVUS
RCV000047564.7Hereditary breast and ovarian cancer syndromeLikely benign
RCV000131307.4Hereditary cancer-predisposing syndromeLikely benign
RCV000083171.4Breast-ovarian cancer, familial 1Conflicting interpretations of pathogenicity

HGMD

IDФенотипЭффект
CM1619488Breast and/or ovarian cancerDM?