Colon Cancer: Gene >> FIP1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53458787:53458787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545Gln(p.R545Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53425900:53425900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775077951
CDS Mutation	c.952G>A
AA Mutation	p.Gly318Ser(p.G318S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53428088:53428088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1079T>C
AA Mutation	p.Phe360Ser(p.F360S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53428102:53428102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093C>A
AA Mutation	p.Pro365Thr(p.P365T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53425943:53425943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995C>A
AA Mutation	p.Ala332Glu(p.A332E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53399818:53399818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794A>C
AA Mutation	p.Lys265Thr(p.K265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000337488
Start	53458655:53458655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502A>C
AA Mutation	p.Asp501Ala(p.D501A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53399800:53399800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>T
AA Mutation	p.Ser259Phe(p.S259F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000337488
Start	53425964:53425964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016A>T
AA Mutation	p.Gln339Leu(p.Q339L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53399806:53399806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782C>A
AA Mutation	p.Pro261His(p.P261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337488
Start	53453049:53453050(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1415_1416insG
AA Mutation	p.Asp472GlufsTer3(p.D472Efs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337488
Start	53453051:53453052(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1417_1418insT
AA Mutation	p.Arg473LeufsTer2(p.R473Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FIP1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53453057:53453057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>T
AA Mutation	p.Arg475Trp(p.R475W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337488
Start	53459316:53459316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1652G>A
AA Mutation	p.Arg551His(p.R551H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript