chr17:7577548 C>T
Annotations
GeneTP53
TranscriptNM_000546.5
cDNAc.733G>A
Proteinp.G245S
Functionmissense
Localizationexon
hg19chr17:7577548 C>T
dbSNPrs28934575
Synonyms
TranscriptcDNAProtein
NM_001126115.1c.337G>Ap.G113S
NM_001126116.1c.337G>Ap.G113S
NM_001126117.1c.337G>Ap.G113S
NM_001276697.1c.256G>Ap.G86S
NM_001276698.1c.256G>Ap.G86S
NM_001276699.1c.256G>Ap.G86S
NM_001126118.1c.616G>Ap.G206S
NM_001126112.2c.733G>Ap.G245S
NM_001126113.2c.733G>Ap.G245S
NM_001126114.2c.733G>Ap.G245S
NM_001276695.1c.616G>Ap.G206S
NM_001276696.1c.616G>Ap.G206S
NM_001276760.1c.616G>Ap.G206S
NM_001276761.1c.616G>Ap.G206S
ENST00000359597.8c.733G>Ap.Gly245Ser
ENST00000413465.6c.733G>Ap.Gly245Ser
Frequency in gnomAD
GenomeExome
MAX0.00010
AFR0.00010
AMR00
ASJ00
EAS00
FIN00
NFE00
SAS–0
ClinVar
IDPhenotypeEffect
RCV000432898.1Likely pathogenic
RCV000588736.1Pathogenic
RCV000226657.5Pathogenic
RCV000587017.1Pathogenic
RCV000438107.1Likely pathogenic
RCV000442506.1Likely pa
HGMD
IDPhenotypeEffect
CM920674OsteosarcomaDM