Colon Cancer: Gene >> INHBB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295228
Start	120349462:120349462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>T
AA Mutation	p.Ser271Leu(p.S271L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295228
Start	120349117:120349117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779417932
CDS Mutation	c.467G>A
AA Mutation	p.Arg156Gln(p.R156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295228
Start	120349778:120349778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000295228
Start	120349383:120349383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Ter(p.R245*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INHBB

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295228
Start	120349322:120349322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777437637
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript