Colon Cancer: Gene >> ARAF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47566719:47566719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>T
AA Mutation	p.Thr213Met(p.T213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47567326:47567326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773318953
CDS Mutation	c.970G>A
AA Mutation	p.Val324Met(p.V324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47563256:47563256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Asp43Asn(p.D43N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47571357:47571357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1721T>C
AA Mutation	p.Leu574Pro(p.L574P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47567312:47567312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47569613:47569613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754787460
CDS Mutation	c.1375G>A
AA Mutation	p.Gly459Arg(p.G459R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47564861:47564861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265G>A
AA Mutation	p.Glu89Lys(p.E89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47571437:47571437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1801G>A
AA Mutation	p.Ala601Thr(p.A601T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47566706:47566706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Cys(p.R209C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47568742:47568742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47567349:47567349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47570913:47570913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47565335:47565335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.547delC
AA Mutation	p.Gln183ArgfsTer109(p.Q183Rfs*109)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47567016:47567016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.763delC
AA Mutation	p.Arg255GlyfsTer37(p.R255Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47562985:47562985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.23delC
AA Mutation	p.Pro8LeufsTer26(p.P8Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000377045
Start	47564798:47564798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Ter(p.R68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47568732:47568733(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1092_1098dupCAACATC
AA Mutation	p.Leu367GlnfsTer22(p.L367Qfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARAF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47564855:47564855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259A>C
AA Mutation	p.Ile87Leu(p.I87L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47570913:47570913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47565089:47565089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47569630:47569630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript