Colon Cancer: Gene >> ANXA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150983345:150983345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112833633
CDS Mutation	c.83C>T
AA Mutation	p.Ala28Val(p.A28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150984389:150984389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376C>A
AA Mutation	p.Leu126Met(p.L126M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150983424:150983424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162T>G
AA Mutation	p.Ile54Met(p.I54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150983420:150983420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158C>A
AA Mutation	p.Ala53Asp(p.A53D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150988172:150988172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779C>T
AA Mutation	p.Ala260Val(p.A260V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368947
Start	150983164:150983164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59T>A
AA Mutation	p.Leu20Gln(p.L20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript