Colon Cancer: Gene >> PDE2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72605176:72605176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285G>T
AA Mutation	p.Glu95Asp(p.E95D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72583491:72583491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>A
AA Mutation	p.Glu559Lys(p.E559K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584206:72584206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645G>A
AA Mutation	p.Ala549Thr(p.A549T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72579373:72579373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759387435
CDS Mutation	c.2267G>A
AA Mutation	p.Arg756His(p.R756H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72578317:72578317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2531C>T
AA Mutation	p.Pro844Leu(p.P844L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72590195:72590195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753A>T
AA Mutation	p.Gln251His(p.Q251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72578248:72578248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2600C>T
AA Mutation	p.Ala867Val(p.A867V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72579316:72579316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771749226
CDS Mutation	c.2324G>A
AA Mutation	p.Arg775His(p.R775H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584937:72584937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1294G>A
AA Mutation	p.Val432Met(p.V432M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72597552:72597552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391C>G
AA Mutation	p.Pro131Ala(p.P131A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72577488:72577488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2722C>T
AA Mutation	p.Pro908Ser(p.P908S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72578997:72578997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754739546
CDS Mutation	c.2369G>A
AA Mutation	p.Arg790Gln(p.R790Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72582506:72582506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789G>T
AA Mutation	p.Asp597Tyr(p.D597Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584647:72584647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1441G>A
AA Mutation	p.Ala481Thr(p.A481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334456
Start	72578898:72578898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2468C>T
AA Mutation	p.Ala823Val(p.A823V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72584720:72584720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72596611:72596611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201081600
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334456
Start	72605168:72605168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.293delC
AA Mutation	p.Pro98HisfsTer53(p.P98Hfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PDE2A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72591300:72591300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000334456
Start	72578499:72578499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485G>T
AA Mutation	p.Glu829Ter(p.E829*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript