Colon Cancer: Gene >> KCNK16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373229
Start	39322483:39322483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.58G>A
AA Mutation	p.Ala20Thr(p.A20T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373229
Start	39317793:39317793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556042374
CDS Mutation	c.488G>A
AA Mutation	p.Arg163His(p.R163H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373229
Start	39322347:39322347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194C>T
AA Mutation	p.Ala65Val(p.A65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373229
Start	39319032:39319032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373229
Start	39316930:39316930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373229
Start	39316354:39316354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNK16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373229
Start	39315050:39315050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882A>T
AA Mutation	p.Gln294His(p.Q294H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript