Colon Cancer: Gene >> F11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186275865:186275865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564T>G
AA Mutation	p.Phe188Leu(p.F188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186280056:186280056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>T
AA Mutation	p.Thr267Ile(p.T267I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186280270:186280270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>A
AA Mutation	p.Glu305Lys(p.E305K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186280360:186280360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>A
AA Mutation	p.Ala335Thr(p.A335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186285692:186285692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359A>C
AA Mutation	p.Glu453Asp(p.E453D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186280272:186280272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915A>C
AA Mutation	p.Glu305Asp(p.E305D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186280016:186280016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>A
AA Mutation	p.Leu254Ile(p.L254I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186276281:186276281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646G>A
AA Mutation	p.Asp216Asn(p.D216N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186287782:186287782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675A>T
AA Mutation	p.Ile559Phe(p.I559F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403665
Start	186287784:186287784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1677C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> F11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186284142:186284142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771896253
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Cys(p.R396C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000403665
Start	186284224:186284224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268A>G
AA Mutation	p.Asn423Ser(p.N423S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000403665
Start	186276268:186276268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633A>C
Mutation Classification	Silent
Feature Type	Transcript