Colon Cancer: Gene >> ANAPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121308547:121308547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115934510
CDS Mutation	c.2201C>T
AA Mutation	p.Ala734Val(p.A734V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121335713:121335713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770G>A
AA Mutation	p.Ser257Asn(p.S257N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121319704:121319704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>A
AA Mutation	p.Val544Ile(p.V544I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121319784:121319784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550A>G
AA Mutation	p.Asp517Gly(p.D517G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121328365:121328365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>A
AA Mutation	p.Asp419Asn(p.D419N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121352301:121352301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40A>G
AA Mutation	p.Met14Val(p.M14V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261819
Start	121327132:121327132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114730469
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANAPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261819
Start	121335578:121335578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905A>G
AA Mutation	p.Tyr302Cys(p.Y302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261819
Start	121352146:121352146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript