Colon Cancer: Gene >> TROAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49325581:49325581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418C>T
AA Mutation	p.His140Tyr(p.H140Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49325775:49325775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>T
AA Mutation	p.Pro175Leu(p.P175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49330358:49330358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1513C>T
AA Mutation	p.Leu505Phe(p.L505F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49327290:49327290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762827543
CDS Mutation	c.851G>A
AA Mutation	p.Arg284Gln(p.R284Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49330491:49330491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1646C>A
AA Mutation	p.Pro549His(p.P549H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49331355:49331355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2240C>T
AA Mutation	p.Thr747Ile(p.T747I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257909
Start	49330287:49330287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257909
Start	49329001:49329001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257909
Start	49330411:49330411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1566C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000257909
Start	49329939:49329941(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758361197
CDS Mutation	c.1249_1251delTCT
AA Mutation	p.Ser417del(p.S417del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TROAP

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000257909
Start	49325846:49325846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Ter(p.R199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257909
Start	49326701:49326702(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.753_754dupGA
AA Mutation	p.Thr252ArgfsTer37(p.T252Rfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript