Colon Cancer: Gene >> KLK15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50826892:50826892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467G>T
AA Mutation	p.Ser156Ile(p.S156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50826941:50826941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>C
AA Mutation	p.Val140Leu(p.V140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50827109:50827109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Glu84Lys(p.E84K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50827088:50827088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Trp(p.R91W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50827048:50827048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50826991:50826991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>A
AA Mutation	p.Arg123His(p.R123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000598239
Start	50827043:50827043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Asp106Asn(p.D106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000598239
Start	50827065:50827065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000598239
Start	50826711:50826711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLK15

No Mutation Annotation!