Войти
РусскийРусскийEnglish
ГлавнаяВарианты

chr17:41258504 A>C

Основные

ГенBRCA1
ТранскриптNM_007294.3
кДНКc.181T>G
Белокp.C61G
Функцияmissense
Локализацияexon
hg19chr17:41258504 A>C

Синонимы

ТранскрипткДНКБелок
NM_007297.3c.40T>Gp.C14G
NM_007298.3c.181T>Gp.C61G
NM_007299.3c.181T>Gp.C61G
NM_007300.3c.181T>Gp.C61G
NR_027676.1n.342T>G

Частота в gnomAD

GenomeExome
MAX0.00006277
AFR0
AMR0
ASJ0
EAS0
FIN0.00004488
NFE0.00006277
SAS0

ClinVar

IDФенотипЭффект
RCV000131902.5Hereditary cancer-predisposing syndromePathogenic
RCV000047597.13Hereditary breast and ovarian cancer syndromePathogenic
RCV000019229.12Breast-ovarian cancer, familial 1Pathogenic
RCV000506927.1not specifiedPathogenic
RCV000412714.1Neoplasm of the breastPathogenic
RCV000159935.7not providedPathogenic
RCV000415051.1Breast carcinomaPathogenic
RCV000239114.2Familial cancer of breastPathogenic

HGMD

IDФенотипЭффект
CM940172Breast cancerDM