Colon Cancer: Gene >> ESM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54985316:54985316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202A>G
AA Mutation	p.Thr68Ala(p.T68A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54982077:54982077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>A
AA Mutation	p.Arg124Lys(p.R124K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54979397:54979397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490G>A
AA Mutation	p.Glu164Lys(p.E164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54985244:54985244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274T>C
AA Mutation	p.Phe92Leu(p.F92L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54982069:54982069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Gly127Arg(p.G127R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381405
Start	54982071:54982071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201100866
CDS Mutation	c.377C>T
AA Mutation	p.Thr126Met(p.T126M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381405
Start	54981999:54981999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367904025
CDS Mutation	c.449C>T
AA Mutation	p.Thr150Met(p.T150M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381405
Start	54982124:54982124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000381405
Start	54982038:54982039(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.409_410insCCACATCTTATTCTACTCACAGATATTTTCTAAGTTATTCACACTGAAATTCCCCTTCTTCCAAT
AA Mutation	p.Tyr137SerfsTer16(p.Y137Sfs*16)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ESM1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381405
Start	54981999:54981999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367904025
CDS Mutation	c.449C>T
AA Mutation	p.Thr150Met(p.T150M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript