Colon Cancer: Gene >> API5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43342471:43342471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1536G>T
AA Mutation	p.Trp512Cys(p.W512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43323457:43323457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571T>G
AA Mutation	p.Phe191Val(p.F191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43323598:43323598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712C>T
AA Mutation	p.Leu238Phe(p.L238F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43329994:43329994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157T>C
AA Mutation	p.Val386Ala(p.V386A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43321452:43321452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367A>C
AA Mutation	p.Ser123Arg(p.S123R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43330011:43330011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174C>T
AA Mutation	p.Arg392Cys(p.R392C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43318689:43318689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119A>G
AA Mutation	p.Lys40Arg(p.K40R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000531273
Start	43330046:43330046(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1213delA
AA Mutation	p.Thr405GlnfsTer11(p.T405Qfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> API5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43320870:43320870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>T
AA Mutation	p.Asn94Ile(p.N94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000531273
Start	43323613:43323613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Trp(p.R243W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript