Colon Cancer: Gene >> UGP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63856359:63856359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>T
AA Mutation	p.Arg25Trp(p.R25W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63891195:63891195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495G>A
AA Mutation	p.Val499Met(p.V499M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63856320:63856320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34A>T
AA Mutation	p.Met12Leu(p.M12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63885872:63885872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Cys(p.R287C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63882511:63882511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301A>C
AA Mutation	p.Ile101Leu(p.I101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63886471:63886471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004C>A
AA Mutation	p.Ser335Tyr(p.S335Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63885783:63885783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337130
Start	63882615:63882615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337130
Start	63890167:63890167(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1406delA
AA Mutation	p.Asn469MetfsTer4(p.N469Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337130
Start	63884032:63884032(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.520delA
AA Mutation	p.Ile174TyrfsTer10(p.I174Yfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337130
Start	63890166:63890167(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1406dupA
AA Mutation	p.Asn469LysfsTer16(p.N469Kfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UGP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63884070:63884070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552A>C
AA Mutation	p.Lys184Asn(p.K184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337130
Start	63885776:63885776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.763C>A
AA Mutation	p.Leu255Met(p.L255M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript