Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TCF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57232362:57232362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>A
AA Mutation	p.Leu253Met(p.L253M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57273147:57273147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791C>A
AA Mutation	p.Phe597Leu(p.F597L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57273122:57273122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs730880016
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589His(p.R589H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57282511:57282511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973C>T
AA Mutation	p.Ser658Leu(p.S658L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57273128:57273128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1772G>T
AA Mutation	p.Arg591Leu(p.R591L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57262106:57262106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408C>T
AA Mutation	p.Arg470Trp(p.R470W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57232781:57232781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772390979
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57273127:57273127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757369824
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Trp(p.R591W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267811
Start	57262114:57262123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1419_1428delTGTCAGTCTC
AA Mutation	p.Val474MetfsTer18(p.V474Mfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000267811
Start	57273220:57273220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1864C>T
AA Mutation	p.Gln622Ter(p.Q622*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267811
Start	57197785:57197786(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.546dupA
AA Mutation	p.Val183SerfsTer21(p.V183Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267811
Start	57263207:57263208(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1606_1607insC
AA Mutation	p.Asp536AlafsTer2(p.D536Afs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267811
Start	57234074:57234075(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1002_1003insTT
AA Mutation	p.Thr335LeufsTer71(p.T335Lfs*71)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000267811
Start	57234108:57234108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000267811
Start	57273255:57273256(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1900_1902dupGTC
AA Mutation	p.Val634dup(p.V634dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000267811
Start	57234073:57234074(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1001_1002insTCT
AA Mutation	p.Gln334delinsHisLeu(p.Q334delinsHL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	56921029:56921029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79T>C
AA Mutation	p.Phe27Leu(p.F27L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57232781:57232781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772390979
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57273127:57273127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757369824
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Trp(p.R591W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267811
Start	57282501:57282501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1963T>C
AA Mutation	p.Ser655Pro(p.S655P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267811
Start	57197785:57197786(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.546dupA
AA Mutation	p.Val183SerfsTer21(p.V183Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript