Colon Cancer: Gene >> CIR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342016
Start	174378943:174378943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768225837
CDS Mutation	c.464C>T
AA Mutation	p.Ser155Leu(p.S155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342016
Start	174348570:174348570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280A>C
AA Mutation	p.Asp427Ala(p.D427A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342016
Start	174348740:174348740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1110C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342016
Start	174348659:174348659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342016
Start	174349143:174349143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.707delA
AA Mutation	p.Lys236ArgfsTer104(p.K236Rfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000342016
Start	174348625:174348625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373714942
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Ter(p.R409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000342016
Start	174348562:174348562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288A>T
AA Mutation	p.Arg430Ter(p.R430*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CIR1

No Mutation Annotation!