Colon Cancer: Gene >> TCF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376255
Start	31162614:31162614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>A
AA Mutation	p.Gly312Asp(p.G312D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376255
Start	31161680:31161680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472G>A
AA Mutation	p.Ala158Thr(p.A158T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376255
Start	31161870:31161870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662G>T
AA Mutation	p.Arg221Leu(p.R221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376255
Start	31161764:31161764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762889350
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Trp(p.R186W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376255
Start	31162543:31162543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369152415
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376255
Start	31161871:31161871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376255
Start	31161875:31161875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376255
Start	31161841:31161841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.636delG
AA Mutation	p.Thr213ProfsTer45(p.T213Pfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376255
Start	31161533:31161533(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.329delC
AA Mutation	p.Pro110GlnfsTer65(p.P110Qfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376255
Start	31159534:31159535(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs763666737
CDS Mutation	c.72dupC
AA Mutation	p.Ala25ArgfsTer17(p.A25Rfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCF19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376255
Start	31161824:31161824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761157384
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript