Colon Cancer: Gene >> MUT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49441885:49441885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141829043
CDS Mutation	c.1763G>A
AA Mutation	p.Arg588His(p.R588H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49451641:49451641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157A>G
AA Mutation	p.His386Arg(p.H386R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49459334:49459334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133G>A
AA Mutation	p.Ala45Thr(p.A45T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49459189:49459189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121918251
CDS Mutation	c.278G>A
AA Mutation	p.Arg93His(p.R93H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000274813
Start	49431854:49431854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2127T>A
AA Mutation	p.Asp709Glu(p.D709E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000274813
Start	49459406:49459406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61G>T
AA Mutation	p.Glu21Ter(p.E21*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274813
Start	49457899:49457900(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs746556715
CDS Mutation	c.544dupA
AA Mutation	p.Met182AsnfsTer29(p.M182Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MUT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49444700:49444700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763417266
CDS Mutation	c.1615G>A
AA Mutation	p.Glu539Lys(p.E539K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49451672:49451672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126G>T
AA Mutation	p.Ala376Ser(p.A376S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49457773:49457773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671A>C
AA Mutation	p.Glu224Ala(p.E224A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49459094:49459094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373G>A
AA Mutation	p.Asp125Asn(p.D125N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274813
Start	49459452:49459452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>T
AA Mutation	p.Lys5Asn(p.K5N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript