Colon Cancer: Gene >> GSPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744242:51744242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782167047
CDS Mutation	c.616G>A
AA Mutation	p.Val206Ile(p.V206I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744837:51744837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211T>C
AA Mutation	p.Phe404Ser(p.F404S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744178:51744178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552G>T
AA Mutation	p.Glu184Asp(p.E184D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744419:51744419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793A>G
AA Mutation	p.Lys265Glu(p.K265E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51743775:51743775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744171:51744171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141788007
CDS Mutation	c.545A>G
AA Mutation	p.Glu182Gly(p.E182G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340438
Start	51743722:51743722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340438
Start	51745237:51745237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340438
Start	51744088:51744088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340438
Start	51745313:51745313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1692delA
AA Mutation	p.Lys564AsnfsTer13(p.K564Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340438
Start	51744357:51744357(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.737delA
AA Mutation	p.Asn246ThrfsTer11(p.N246Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340438
Start	51743943:51743943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.322delG
AA Mutation	p.Ala108HisfsTer11(p.A108Hfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340438
Start	51744171:51744171(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.549delA
AA Mutation	p.Glu184ArgfsTer3(p.E184Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GSPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340438
Start	51744134:51744134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>T
AA Mutation	p.Gly170Trp(p.G170W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript