Colon Cancer: Gene >> KLK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908379:50908379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>T
AA Mutation	p.Asp198Tyr(p.D198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908641:50908641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413C>T
AA Mutation	p.Ala138Val(p.A138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908391:50908391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580G>A
AA Mutation	p.Gly194Ser(p.G194S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908481:50908481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777659052
CDS Mutation	c.490G>A
AA Mutation	p.Val164Met(p.V164M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908606:50908606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448G>A
AA Mutation	p.Val150Ile(p.V150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908760:50908760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
AA Mutation	p.Glu98Asp(p.E98D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324041
Start	50908392:50908392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762955905
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324041
Start	50910682:50910682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324041
Start	50907072:50907072(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.627delG
AA Mutation	p.Leu211Ter(p.L211*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000324041
Start	50909411:50909411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65C>A
AA Mutation	p.Ser22Ter(p.S22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324041
Start	50908638:50908638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>T
AA Mutation	p.Ser139Leu(p.S139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript