Colon Cancer: Gene >> MPP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67302422:67302422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749130375
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67279325:67279325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767964224
CDS Mutation	c.155G>A
AA Mutation	p.Arg52Gln(p.R52Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67321075:67321075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556G>A
AA Mutation	p.Arg519Gln(p.R519Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67279474:67279474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304C>G
AA Mutation	p.Pro102Ala(p.P102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67279219:67279219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781290440
CDS Mutation	c.49G>A
AA Mutation	p.Glu17Lys(p.E17K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261681
Start	67323777:67323777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Trp(p.R606W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261681
Start	67279461:67279461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139355613
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261681
Start	67312682:67312682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1197T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261681
Start	67316895:67316895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1293delA
AA Mutation	p.Lys431AsnfsTer34(p.K431Nfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MPP5

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261681
Start	67279392:67279393(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.227dupA
AA Mutation	p.Gln77AlafsTer4(p.Q77Afs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript