Colon Cancer: Gene >> KIAA0391

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35123949:35123949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704A>G
AA Mutation	p.Asp235Gly(p.D235G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35123352:35123352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107G>C
AA Mutation	p.Arg36Pro(p.R36P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35123561:35123561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35123913:35123913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>T
AA Mutation	p.Ser223Leu(p.S223L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35180716:35180716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214A>T
AA Mutation	p.Asp405Val(p.D405V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534898
Start	35266858:35266858(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1413delT
AA Mutation	p.Phe471LeufsTer30(p.F471Lfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KIAA0391

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000534898
Start	35123385:35123385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>A
AA Mutation	p.Ser47Tyr(p.S47Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534898
Start	35123665:35123665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420C>T
Mutation Classification	Silent
Feature Type	Transcript