Colon Cancer: Gene >> IMMP2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331762
Start	110886655:110886655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>A
AA Mutation	p.Gly116Ser(p.G116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331762
Start	110663693:110663693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>T
AA Mutation	p.Ala146Val(p.A146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331762
Start	110663630:110663630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200952795
CDS Mutation	c.500G>A
AA Mutation	p.Arg167His(p.R167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331762
Start	110963542:110963542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263A>C
AA Mutation	p.Lys88Thr(p.K88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331762
Start	111487321:111487321(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.156delG
AA Mutation	p.Ser53AlafsTer9(p.S53Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000331762
Start	110886696:110886697(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.306-2_306-1insT
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IMMP2L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331762
Start	110886603:110886603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375048435
CDS Mutation	c.398C>A
AA Mutation	p.Ser133Tyr(p.S133Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript