Colon Cancer: Gene >> ENG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127824939:127824939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>T
AA Mutation	p.Glu284Asp(p.E284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127819956:127819956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751787590
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Cys(p.R406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127843137:127843137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176A>T
AA Mutation	p.Asn59Ile(p.N59I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127825320:127825320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761827492
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127818145:127818145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748966307
CDS Mutation	c.1661G>A
AA Mutation	p.Arg554His(p.R554H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373203
Start	127824305:127824305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143054595
CDS Mutation	c.1133C>T
AA Mutation	p.Ala378Val(p.A378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373203
Start	127843124:127843124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189A>C
AA Mutation	p.Glu63Asp(p.E63D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373203
Start	127826580:127826580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373203
Start	127818135:127818135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369135742
CDS Mutation	c.1671C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373203
Start	127829770:127829770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.277delC
AA Mutation	p.Arg93GlufsTer9(p.R93Efs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373203
Start	127819973:127819973(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1199delG
AA Mutation	p.Gly400ValfsTer21(p.G400Vfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373203
Start	127824934:127824934(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.857delA
AA Mutation	p.Asn286ThrfsTer73(p.N286Tfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373203
Start	127825275:127825276(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.771dupC
AA Mutation	p.Tyr258LeufsTer76(p.Y258Lfs*76)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ENG

No Mutation Annotation!