Colon Cancer: Gene >> KRT80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394815
Start	52173096:52173096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394815
Start	52173045:52173045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950A>G
AA Mutation	p.Lys317Arg(p.K317R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394815
Start	52191855:52191855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394815
Start	52173684:52173684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369613010
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394815
Start	52185435:52185435(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.453delG
AA Mutation	p.Gln152SerfsTer37(p.Q152Sfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394815
Start	52180941:52180941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767920544
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript