Colon Cancer: Gene >> PAK1IP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379568
Start	10702635:10702635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439T>G
AA Mutation	p.Leu147Val(p.L147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379568
Start	10704822:10704822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Glu240Lys(p.E240K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379568
Start	10709327:10709327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147437498
CDS Mutation	c.1054C>T
AA Mutation	p.Arg352Cys(p.R352C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379568
Start	10704530:10704530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>A
AA Mutation	p.Pro174Thr(p.P174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379568
Start	10704789:10704789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.690delT
AA Mutation	p.Phe230LeufsTer6(p.F230Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PAK1IP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379568
Start	10704792:10704792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688T>C
AA Mutation	p.Phe230Leu(p.F230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript