Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ORM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114330004:114330004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748201206
CDS Mutation	c.100G>A
AA Mutation	p.Ala34Thr(p.A34T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114331666:114331666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>A
AA Mutation	p.Ser143Tyr(p.S143Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114330517:114330517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.198C>A
AA Mutation	p.Phe66Leu(p.F66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000431067
Start	114331607:114331607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000431067
Start	114331917:114331917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146039808
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000431067
Start	114330524:114330524(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.207delT
AA Mutation	p.Phe69LeufsTer29(p.F69Lfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ORM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114329909:114329909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768724177
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114330546:114330546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227A>C
AA Mutation	p.Asp76Ala(p.D76A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000431067
Start	114329987:114329987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83C>T
AA Mutation	p.Pro28Leu(p.P28L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript