Colon Cancer: Gene >> ORM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259396
Start	114325112:114325112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139631990
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259396
Start	114324790:114324790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370750676
CDS Mutation	c.329T>A
AA Mutation	p.Val110Glu(p.V110E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259396
Start	114323152:114323152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>A
AA Mutation	p.Leu7Ile(p.L7I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259396
Start	114323722:114323722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143769852
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259396
Start	114324884:114324884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771853505
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259396
Start	114323794:114323794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259396
Start	114323797:114323797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259396
Start	114324809:114324809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141250386
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000259396
Start	114324894:114324895(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.433_434insTAC
AA Mutation	p.Tyr145delinsLeuHis(p.Y145delinsLH)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ORM1

No Mutation Annotation!