Colon Cancer: Gene >> IP6K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48692985:48692985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575264529
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Cys(p.R133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48688434:48688434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200712199
CDS Mutation	c.1120G>A
AA Mutation	p.Ala374Thr(p.A374T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48692978:48692978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404A>G
AA Mutation	p.His135Arg(p.H135R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48688467:48688467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1087T>C
AA Mutation	p.Ser363Pro(p.S363P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48688288:48688288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266G>T
AA Mutation	p.Glu422Asp(p.E422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48689683:48689683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372776558
CDS Mutation	c.635G>A
AA Mutation	p.Arg212His(p.R212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328631
Start	48695197:48695197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95T>C
AA Mutation	p.Val32Ala(p.V32A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328631
Start	48693025:48693025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328631
Start	48689673:48689673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328631
Start	48691436:48691436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IP6K2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328631
Start	48688685:48688685(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.869delT
AA Mutation	p.Phe290SerfsTer22(p.F290Sfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript