Colon Cancer: Gene >> KRT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52245544:52245544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758674885
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Cys(p.R373C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52248687:52248687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1337G>A
AA Mutation	p.Ser446Asn(p.S446N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52243105:52243105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952C>A
AA Mutation	p.Leu318Met(p.L318M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52243058:52243058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52233526:52233526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762446937
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331817
Start	52235310:52235310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331817
Start	52245465:52245465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775241475
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331817
Start	52241477:52241477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745420332
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331817
Start	52243038:52243038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331817
Start	52241579:52241580(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.802dupT
AA Mutation	p.Tyr268LeufsTer2(p.Y268Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331817
Start	52241581:52241582(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.804dupT
AA Mutation	p.Glu269Ter(p.E269*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KRT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52248629:52248629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279G>A
AA Mutation	p.Gly427Ser(p.G427S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331817
Start	52243074:52243074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921G>T
AA Mutation	p.Glu307Asp(p.E307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript