Colon Cancer: Gene >> PRSS8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317508
Start	31132200:31132200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841A>G
AA Mutation	p.Ile281Val(p.I281V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317508
Start	31132463:31132463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778802523
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317508
Start	31132239:31132239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
AA Mutation	p.Pro268Ser(p.P268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317508
Start	31132791:31132791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317508
Start	31133381:31133381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776511670
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317508
Start	31133368:31133368(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.124delC
AA Mutation	p.Gln42LysfsTer64(p.Q42Kfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317508
Start	31132158:31132158(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.883delC
AA Mutation	p.Gln295LysfsTer27(p.Q295Kfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRSS8

No Mutation Annotation!