Colon Cancer: Gene >> BMF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354670
Start	40091875:40091875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467A>G
AA Mutation	p.Gln156Arg(p.Q156R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354670
Start	40105830:40105830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257G>A
AA Mutation	p.Cys86Tyr(p.C86Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354670
Start	40105950:40105950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354670
Start	40105943:40105943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>T
AA Mutation	p.Gln48His(p.Q48H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354670
Start	40104247:40104247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386C>T
AA Mutation	p.Ala129Val(p.A129V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354670
Start	40104270:40104270(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.363delC
AA Mutation	p.Glu122LysfsTer51(p.E122Kfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BMF

No Mutation Annotation!