Colon Cancer: Gene >> STAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4333984:4333984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763722818
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Trp(p.R55W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4338663:4338663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372268872
CDS Mutation	c.91C>T
AA Mutation	p.Pro31Ser(p.P31S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4327371:4327371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605G>A
AA Mutation	p.Arg202Gln(p.R202Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4325503:4325503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770230350
CDS Mutation	c.872C>T
AA Mutation	p.Ala291Val(p.A291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4329982:4329982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746019430
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000594605
Start	4328807:4328807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>A
AA Mutation	p.Cys153Tyr(p.C153Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594605
Start	4326976:4326976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000594605
Start	4327187:4327187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700G>A
AA Mutation	p.Val234Met(p.V234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript