Colon Cancer: Gene >> PDE8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310298
Start	85126295:85126295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2174C>T
AA Mutation	p.Ala725Val(p.A725V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310298
Start	85113392:85113392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130G>T
AA Mutation	p.Arg377Leu(p.R377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310298
Start	85116085:85116085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501G>T
AA Mutation	p.Asp501Tyr(p.D501Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310298
Start	85123147:85123147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2039T>G
AA Mutation	p.Phe680Cys(p.F680C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310298
Start	85113411:85113411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310298
Start	85120935:85120935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310298
Start	85123133:85123133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145560886
CDS Mutation	c.2025G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310298
Start	85067109:85067109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310298
Start	85091129:85091129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.806delA
AA Mutation	p.Lys269ArgfsTer8(p.K269Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000310298
Start	85091162:85091162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>A
AA Mutation	p.Ser278Ter(p.S278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000310298
Start	85091134:85091135(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.805_806insCATAAAGTGAATT
AA Mutation	p.Lys269ThrfsTer2(p.K269Tfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000310298
Start	85126315:85126315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748220659
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Ter(p.R732*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PDE8A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310298
Start	85117777:85117777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672T>C
AA Mutation	p.Ser558Pro(p.S558P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript