Colon Cancer: Gene >> KRT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41567547:41567547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598G>T
AA Mutation	p.Gly533Val(p.G533V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41567283:41567283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1862C>A
AA Mutation	p.Ser621Tyr(p.S621Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41568365:41568365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>A
AA Mutation	p.Ser397Arg(p.S397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41568261:41568261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199526457
CDS Mutation	c.1295G>A
AA Mutation	p.Cys432Tyr(p.C432Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41568235:41568235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>A
AA Mutation	p.Leu441Ile(p.L441I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41567293:41567293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776803750
CDS Mutation	c.1852G>A
AA Mutation	p.Gly618Arg(p.G618R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41567478:41567478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667G>A
AA Mutation	p.Gly556Asp(p.G556D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41571553:41571553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Gly147Asp(p.G147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246662
Start	41567741:41567741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147473954
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246662
Start	41569510:41569510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000246662
Start	41567578:41567578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1567G>T
AA Mutation	p.Gly523Ter(p.G523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KRT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41567305:41567305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765577453
CDS Mutation	c.1840G>A
AA Mutation	p.Gly614Arg(p.G614R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41568378:41568378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246662
Start	41569959:41569959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143907766
CDS Mutation	c.782G>A
AA Mutation	p.Arg261Gln(p.R261Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000246662
Start	41569906:41569906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835G>T
AA Mutation	p.Glu279Ter(p.E279*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript