Colon Cancer: Gene >> ANAPC7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000455511
Start	110387790:110387790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768592404
CDS Mutation	c.725C>T
AA Mutation	p.Ala242Val(p.A242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000455511
Start	110377516:110377516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1336C>A
AA Mutation	p.Leu446Ile(p.L446I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000455511
Start	110388565:110388565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>T
AA Mutation	p.Thr190Ile(p.T190I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000455511
Start	110381797:110381797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Trp(p.R397W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455511
Start	110381798:110381798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455511
Start	110396308:110396308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455511
Start	110403706:110403706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455511
Start	110377421:110377421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000455511
Start	110395161:110395161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.450delA
AA Mutation	p.Lys150AsnfsTer22(p.K150Nfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000455511
Start	110382931:110382931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Ter(p.R317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANAPC7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000455511
Start	110374147:110374147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000455511
Start	110396356:110396356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300T>G
AA Mutation	p.Tyr100Ter(p.Y100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000455511
Start	110403526:110403526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111908272
CDS Mutation	c.203+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript