Colon Cancer: Gene >> TCF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1619821:1619821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759970483
CDS Mutation	c.1126G>A
AA Mutation	p.Gly376Ser(p.G376S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1623997:1623997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748050498
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Met(p.T168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1615720:1615720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375552133
CDS Mutation	c.1552A>G
AA Mutation	p.Lys518Glu(p.K518E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1625596:1625596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479G>T
AA Mutation	p.Arg160Ile(p.R160I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1615438:1615438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767680626
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Trp(p.R557W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262965
Start	1615742:1615742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142947854
CDS Mutation	c.1530G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262965
Start	1650216:1650216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262965
Start	1632386:1632386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262965
Start	1621938:1621938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
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

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262965
Start	1620980:1620980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1081delC
AA Mutation	p.Gln361ArgfsTer33(p.Q361Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000262965
Start	1619836:1619836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Ter(p.R371*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262965
Start	1622053:1622053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000262965
Start	1621913:1621915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs748560717
CDS Mutation	c.878_880delTCT
AA Mutation	p.Phe293del(p.F293del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TCF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262965
Start	1625605:1625605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>A
AA Mutation	p.Ser157Tyr(p.S157Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript