Colon Cancer: Gene >> KRT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52904752:52904752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230T>G
AA Mutation	p.Val77Gly(p.V77G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52898830:52898830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764622352
CDS Mutation	c.1051G>A
AA Mutation	p.Ala351Thr(p.A351T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52902063:52902063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>A
AA Mutation	p.Leu112Met(p.L112M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52900631:52900631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.647G>C
AA Mutation	p.Gly216Ala(p.G216A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52898806:52898806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs57626370
CDS Mutation	c.1075G>A
AA Mutation	p.Ala359Thr(p.A359T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293308
Start	52904697:52904697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293308
Start	52898831:52898831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377555703
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293308
Start	52904930:52904930(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.52delC
AA Mutation	p.Arg18GlyfsTer56(p.R18Gfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293308
Start	52898878:52898878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003A>G
AA Mutation	p.Ile335Val(p.I335V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293308
Start	52898867:52898867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112222496
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript