Colon Cancer: Gene >> PSIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15465538:15465538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575T>G
AA Mutation	p.Asp525Glu(p.D525E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15479659:15479659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485C>T
AA Mutation	p.Ala162Val(p.A162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15506624:15506624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86C>A
AA Mutation	p.Pro29His(p.P29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15468722:15468722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328C>A
AA Mutation	p.Ser443Tyr(p.S443Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15486916:15486916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304T>C
AA Mutation	p.Ser102Pro(p.S102P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380733
Start	15474181:15474181(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.686delA
AA Mutation	p.Lys229SerfsTer36(p.K229Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380733
Start	15465558:15465561(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768872267
CDS Mutation	c.1552_1555delGAGA
AA Mutation	p.Glu518LeufsTer5(p.E518Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380733
Start	15490116:15490116(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.158delT
AA Mutation	p.Leu53Ter(p.L53*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000380733
Start	15474032:15474034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757199981
CDS Mutation	c.833_835delAAG
AA Mutation	p.Glu278del(p.E278del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PSIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380733
Start	15510171:15510171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18A>T
AA Mutation	p.Lys6Asn(p.K6N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380733
Start	15479606:15479606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538A>C
Mutation Classification	Silent
Feature Type	Transcript