Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RAB11FIP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258098
Start	73075537:73075537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772145463
CDS Mutation	c.1946C>T
AA Mutation	p.Pro649Leu(p.P649L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258098
Start	73088561:73088561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202050559
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Trp(p.R353W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258098
Start	73088934:73088934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758076621
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258098
Start	73075677:73075677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201443945
CDS Mutation	c.1806C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258098
Start	73088155:73088155(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1463delG
AA Mutation	p.Gly488ValfsTer25(p.G488Vfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258098
Start	73075537:73075537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1946delC
AA Mutation	p.Pro649ArgfsTer111(p.P649Rfs*111)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258098
Start	73075527:73075527(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1956delC
AA Mutation	p.Lys653AsnfsTer107(p.K653Nfs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RAB11FIP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258098
Start	73088105:73088105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513G>A
AA Mutation	p.Ala505Thr(p.A505T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript