Colon Cancer: Gene >> STK26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394334
Start	132054769:132054769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Glu61Lys(p.E61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394334
Start	132068266:132068266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382A>T
AA Mutation	p.Ile128Phe(p.I128F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394334
Start	132074148:132074148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240G>A
AA Mutation	p.Glu414Lys(p.E414K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394334
Start	132072352:132072352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394334
Start	132069577:132069577(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.701delA
AA Mutation	p.Asn234ThrfsTer22(p.N234Tfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STK26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394334
Start	132054665:132054665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77A>C
AA Mutation	p.Lys26Thr(p.K26T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394334
Start	132074147:132074147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757926287
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000394334
Start	132068218:132068218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Ter(p.R112*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript