Mutation

Primary Site >> Liver Cancer

Gene >> TEP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20384467:20384467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201494870
CDS Mutation	c.3263A>G
AA Mutation	p.Tyr1088Cys(p.Y1088C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20383528:20383528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3827G>T
AA Mutation	p.Gly1276Val(p.G1276V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20406352:20406352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616C>T
AA Mutation	p.Pro206Ser(p.P206S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20403869:20403869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>T
AA Mutation	p.Asp350Tyr(p.D350Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20378845:20378845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111632717
CDS Mutation	c.5261A>G
AA Mutation	p.Gln1754Arg(p.Q1754R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262715
Start	20408169:20408169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271A>C
AA Mutation	p.Met91Leu(p.M91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262715
Start	20382032:20382032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4305G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262715
Start	20408404:20408404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262715
Start	20379037:20379037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764524084
CDS Mutation	c.5196C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262715
Start	20373061:20373067(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6895_6901delAATCAAG
AA Mutation	p.Asn2299LeufsTer4(p.N2299Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262715
Start	20383552:20383552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3803delC
AA Mutation	p.Ala1268ValfsTer4(p.A1268Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262715
Start	20403376:20403376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript