Colon Cancer: Gene >> PAK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77392426:77392426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95G>A
AA Mutation	p.Gly32Glu(p.G32E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77392441:77392441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80G>A
AA Mutation	p.Gly27Asp(p.G27D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77343882:77343882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>G
AA Mutation	p.Ile312Ser(p.I312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77379324:77379324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356A>G
AA Mutation	p.Lys119Arg(p.K119R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77336269:77336269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>A
AA Mutation	p.Phe410Leu(p.F410L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77392354:77392354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356341
Start	77379321:77379321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.359delA
AA Mutation	p.Asn120ThrfsTer24(p.N120Tfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000356341
Start	77355668:77355668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201726311
CDS Mutation	c.772C>T
AA Mutation	p.Arg258Ter(p.R258*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000356341
Start	77374326:77374326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PAK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77336269:77336269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230C>A
AA Mutation	p.Phe410Leu(p.F410L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356341
Start	77343882:77343882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>G
AA Mutation	p.Ile312Ser(p.I312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript