Colon Cancer: Gene >> ART1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3659627:3659627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>T
AA Mutation	p.Glu36Asp(p.E36D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3659931:3659931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3659698:3659698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179C>T
AA Mutation	p.Ala60Val(p.A60V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3659649:3659649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3660177:3660177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750142725
CDS Mutation	c.658G>A
AA Mutation	p.Gly220Ser(p.G220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250693
Start	3659880:3659880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361T>C
AA Mutation	p.Tyr121His(p.Y121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250693
Start	3660248:3660248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762428866
CDS Mutation	c.735delC
AA Mutation	p.Phe246LeufsTer6(p.F246Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250693
Start	3660109:3660110(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.596dupG
AA Mutation	p.Phe200LeufsTer16(p.F200Lfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ART1

No Mutation Annotation!