Colon Cancer: Gene >> EXOC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	489001:489001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2659C>T
AA Mutation	p.Leu887Phe(p.L887F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	486720:486720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2726T>C
AA Mutation	p.Leu909Ser(p.L909S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	576760:576760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146558148
CDS Mutation	c.1315G>A
AA Mutation	p.Asp439Asn(p.D439N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	637784:637784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35G>A
AA Mutation	p.Gly12Asp(p.G12D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	619449:619449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Glu173Lys(p.E173K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230449
Start	549246:549246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373080488
CDS Mutation	c.2167C>T
AA Mutation	p.Arg723Cys(p.R723C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	564658:564658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114105090
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	532566:532566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	556550:556550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1866A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	564562:564562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779200539
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230449
Start	637794:637794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.25delC
AA Mutation	p.Val10Ter(p.V10*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000230449
Start	532500:532500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2349T>G
AA Mutation	p.Tyr783Ter(p.Y783*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EXOC2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	497484:497484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230449
Start	637729:637729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90T>C
Mutation Classification	Silent
Feature Type	Transcript