Colon Cancer: Gene >> COG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230688549:230688549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758756274
CDS Mutation	c.1781G>A
AA Mutation	p.Arg594Gln(p.R594Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230663157:230663157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766695806
CDS Mutation	c.317T>C
AA Mutation	p.Val106Ala(p.V106A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230691404:230691404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1955A>C
AA Mutation	p.Asp652Ala(p.D652A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230688132:230688132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1640C>A
AA Mutation	p.Ser547Tyr(p.S547Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230685214:230685214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372577276
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453Gln(p.R453Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230679001:230679001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115C>T
AA Mutation	p.Ala372Val(p.A372V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230685115:230685115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259A>G
AA Mutation	p.His420Arg(p.H420R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230678952:230678952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200705175
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Trp(p.R356W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230688441:230688441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673G>T
AA Mutation	p.Ser558Ile(p.S558I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230691509:230691509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2060A>G
AA Mutation	p.Asp687Gly(p.D687G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000366669
Start	230642666:230642666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>G
AA Mutation	p.Asp20Glu(p.D20E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366669
Start	230685200:230685200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366669
Start	230691507:230691507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749263516
CDS Mutation	c.2058C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366669
Start	230663179:230663179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> COG2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366669
Start	230669433:230669433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186499102
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366669
Start	230663213:230663213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.380delA
AA Mutation	p.Lys127ArgfsTer5(p.K127Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000366669
Start	230668716:230668716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>T
AA Mutation	p.Glu176Ter(p.E176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript