Colon Cancer: Gene >> TNNI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344887
Start	55151892:55151892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs104894729
CDS Mutation	c.575G>A
AA Mutation	p.Arg192His(p.R192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344887
Start	55154805:55154805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371000425
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344887
Start	55157076:55157076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNNI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344887
Start	55154094:55154094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397516354
CDS Mutation	c.485G>A
AA Mutation	p.Arg162Gln(p.R162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344887
Start	55154176:55154176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403C>A
AA Mutation	p.Leu135Ile(p.L135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript