Colon Cancer: Gene >> KCNK17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373231
Start	39304620:39304620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747130965
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Cys(p.R130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373231
Start	39304631:39304631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376144090
CDS Mutation	c.377C>T
AA Mutation	p.Thr126Met(p.T126M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373231
Start	39304003:39304003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140940240
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373231
Start	39314108:39314108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373231
Start	39304505:39304505(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.503delG
AA Mutation	p.Gly168AlafsTer61(p.G168Afs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373231
Start	39303972:39303972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745795187
CDS Mutation	c.673G>A
AA Mutation	p.Gly225Ser(p.G225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373231
Start	39304606:39304606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373231
Start	39304546:39304546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
Mutation Classification	Silent
Feature Type	Transcript