Colon Cancer: Gene >> TPM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360958
Start	35685752:35685752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360958
Start	35689775:35689775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43A>C
AA Mutation	p.Lys15Gln(p.K15Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360958
Start	35689751:35689751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>A
AA Mutation	p.Glu23Lys(p.E23K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360958
Start	35683185:35683185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371325326
CDS Mutation	c.829G>A
AA Mutation	p.Ala277Thr(p.A277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360958
Start	35689812:35689812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000360958
Start	35684538:35684538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>T
AA Mutation	p.Glu218Ter(p.E218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TPM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360958
Start	35683185:35683185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371325326
CDS Mutation	c.829G>A
AA Mutation	p.Ala277Thr(p.A277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript