Colon Cancer: Gene >> HRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154841:49154841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Gly133Arg(p.G133R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154843:49154843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763236818
CDS Mutation	c.395G>A
AA Mutation	p.Arg132His(p.R132H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154026:49154026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212G>T
AA Mutation	p.Glu404Asp(p.E404D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154751:49154751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751086318
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49153577:49153577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1661A>G
AA Mutation	p.Glu554Gly(p.E554G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154254:49154254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>T
AA Mutation	p.Glu328Asp(p.E328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49155177:49155177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>T
AA Mutation	p.Leu21Phe(p.L21F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252825
Start	49153603:49153603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252825
Start	49154452:49154452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252825
Start	49154302:49154302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252825
Start	49153954:49153954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252825
Start	49153600:49153600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252825
Start	49153781:49153781(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1457delA
AA Mutation	p.Lys486ArgfsTer45(p.K486Rfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252825
Start	49153841:49153841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1397delC
AA Mutation	p.Pro466GlnfsTer12(p.P466Qfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000252825
Start	49154346:49154346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148629919
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Ter(p.R298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252825
Start	49154815:49154815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>A
AA Mutation	p.Asp141Glu(p.D141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript