Colon Cancer: Gene >> TPM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300933
Start	16088082:16088082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440C>T
AA Mutation	p.Ala147Val(p.A147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300933
Start	16089098:16089098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>A
AA Mutation	p.Ser170Tyr(p.S170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300933
Start	16081995:16081995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751550419
CDS Mutation	c.215C>T
AA Mutation	p.Thr72Met(p.T72M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300933
Start	16093721:16093721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632C>T
AA Mutation	p.Ala211Val(p.A211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TPM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300933
Start	16081941:16081941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777126031
CDS Mutation	c.161G>A
AA Mutation	p.Arg54Gln(p.R54Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300933
Start	16081939:16081939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript