Colon Cancer: Gene >> PIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376509
Start	48915034:48915034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581A>C
AA Mutation	p.Tyr194Ser(p.Y194S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376509
Start	48915251:48915251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376509
Start	48914515:48914515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>A
AA Mutation	p.Pro218Thr(p.P218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376509
Start	48914263:48914263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376509
Start	48918802:48918802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375934218
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376509
Start	48918796:48918796(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.39delC
AA Mutation	p.Thr15ProfsTer48(p.T15Pfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376509
Start	48918582:48918582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.125delG
AA Mutation	p.Gly42AlafsTer21(p.G42Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376509
Start	48918795:48918796(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs782496935
CDS Mutation	c.39dupC
AA Mutation	p.Gly14ArgfsTer27(p.G14Rfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PIM2

No Mutation Annotation!