Colon Cancer: Gene >> KRT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52520211:52520211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543574061
CDS Mutation	c.86G>A
AA Mutation	p.Arg29His(p.R29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52517627:52517627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766857995
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352His(p.R352H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52517723:52517723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959A>G
AA Mutation	p.Asp320Gly(p.D320G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52517183:52517183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755300932
CDS Mutation	c.1142A>G
AA Mutation	p.Asn381Ser(p.N381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52520290:52520290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200156424
CDS Mutation	c.7C>T
AA Mutation	p.Arg3Cys(p.R3C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52516665:52516665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267607448
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Cys(p.R471C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52516842:52516842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234A>G
AA Mutation	p.Asn412Asp(p.N412D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52515134:52515134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52515122:52515122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52516728:52516728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774089332
CDS Mutation	c.1348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52517173:52517173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52519976:52519976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376691972
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000252242
Start	52517217:52517217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108C>T
AA Mutation	p.Gln370Ter(p.Q370*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KRT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252242
Start	52519852:52519852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Ile(p.L149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52519976:52519976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376691972
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52520159:52520159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201458850
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252242
Start	52517987:52517987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837A>G
Mutation Classification	Silent
Feature Type	Transcript