Colon Cancer: Gene >> STAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124057954:124057954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>T
AA Mutation	p.Val465Phe(p.V465F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124031012:124031012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175G>A
AA Mutation	p.Gly59Arg(p.G59R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124081485:124081485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2881C>T
AA Mutation	p.Leu961Phe(p.L961F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124083531:124083531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3035G>A
AA Mutation	p.Arg1012Gln(p.R1012Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124056156:124056156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773224655
CDS Mutation	c.1225G>T
AA Mutation	p.Asp409Tyr(p.D409Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124086690:124086690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3197G>A
AA Mutation	p.Arg1066Gln(p.R1066Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371144
Start	124047406:124047406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371144
Start	124042603:124042603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371144
Start	124051171:124051171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371144
Start	124037596:124037596(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.363delT
AA Mutation	p.Phe121LeufsTer24(p.F121Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371144
Start	124095400:124095400(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3623delC
AA Mutation	p.Thr1208LysfsTer3(p.T1208Kfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371144
Start	124045351:124045351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650A>G
AA Mutation	p.His217Arg(p.H217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371144
Start	124031080:124031080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371144
Start	124050192:124050192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757136748
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript