Mutation

Primary Site >> Stomach Cancer

Gene >> TCF3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1627406:1627406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199628190
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1619185:1619185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761036422
CDS Mutation	c.1376T>C
AA Mutation	p.Met459Thr(p.M459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1611783:1611783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1889T>C
AA Mutation	p.Val630Ala(p.V630A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1615408:1615408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781162855
CDS Mutation	c.1699G>A
AA Mutation	p.Glu567Lys(p.E567K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1615420:1615420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148304557
CDS Mutation	c.1687C>T
AA Mutation	p.Arg563Cys(p.R563C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262965
Start	1615429:1615429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1052768
CDS Mutation	c.1678C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262965
Start	1615699:1615699(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1573delC
AA Mutation	p.Arg525GlyfsTer76(p.R525Gfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262965
Start	1611814:1611815(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1857dupA
AA Mutation	p.Arg620ThrfsTer82(p.R620Tfs*82)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262965
Start	1619110:1619110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1450+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript