Colon Cancer: Gene >> RAB11FIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118046106:118046106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>T
AA Mutation	p.Leu20Phe(p.L20F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118045837:118045837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327T>G
AA Mutation	p.Phe109Leu(p.F109L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118040332:118040332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587C>T
AA Mutation	p.Ala196Val(p.A196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118039294:118039294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943T>A
AA Mutation	p.Phe315Ile(p.F315I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118038982:118038982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255C>T
AA Mutation	p.Pro419Ser(p.P419S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355624
Start	118045840:118045840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355624
Start	118046125:118046125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000355624
Start	118040534:118040534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Ter(p.R129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000355624
Start	118039207:118039207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030G>T
AA Mutation	p.Glu344Ter(p.E344*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355624
Start	118040280:118040281(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.638dupA
AA Mutation	p.Pro214AlafsTer17(p.P214Afs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAB11FIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118039116:118039116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1121A>C
AA Mutation	p.Lys374Thr(p.K374T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355624
Start	118040273:118040273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646C>T
AA Mutation	p.Leu216Phe(p.L216F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript