Colon Cancer: Gene >> TMC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19038040:19038040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172T>C
AA Mutation	p.Met391Thr(p.M391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19009343:19009343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239G>T
AA Mutation	p.Arg80Ile(p.R80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19061784:19061784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2113C>T
AA Mutation	p.Arg705Cys(p.R705C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19047125:19047125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1616C>T
AA Mutation	p.Ala539Val(p.A539V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19040431:19040431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441His(p.R441H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19038037:19038037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169A>G
AA Mutation	p.His390Arg(p.H390R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304381
Start	19009376:19009376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TMC7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304381
Start	19045421:19045421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566960043
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript