Colon Cancer: Gene >> KCTD12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885445:76885445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704G>C
AA Mutation	p.Arg235Pro(p.R235P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885338:76885338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811T>C
AA Mutation	p.Tyr271His(p.Y271H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885244:76885244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905T>A
AA Mutation	p.Phe302Tyr(p.F302Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885497:76885497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652T>C
AA Mutation	p.Tyr218His(p.Y218H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885472:76885472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677C>T
AA Mutation	p.Ala226Val(p.A226V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377474
Start	76886108:76886108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.41delG
AA Mutation	p.Gly14AlafsTer25(p.G14Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCTD12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377474
Start	76885311:76885311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>A
AA Mutation	p.Ala280Thr(p.A280T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript