Colon Cancer: Gene >> PDE3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20637223:20637223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125C>A
AA Mutation	p.Arg709Ser(p.R709S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20613476:20613476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150253039
CDS Mutation	c.1045G>A
AA Mutation	p.Val349Ile(p.V349I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20650466:20650466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2791G>C
AA Mutation	p.Asp931His(p.D931H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20613497:20613497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066C>A
AA Mutation	p.Leu356Ile(p.L356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20634953:20634953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1898G>A
AA Mutation	p.Ser633Asn(p.S633N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20370129:20370129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753232121
CDS Mutation	c.845A>T
AA Mutation	p.Asp282Val(p.D282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20369508:20369508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224C>T
AA Mutation	p.Ala75Val(p.A75V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20369741:20369741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754390819
CDS Mutation	c.457G>A
AA Mutation	p.Ala153Thr(p.A153T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20648836:20648836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2714T>G
AA Mutation	p.Ile905Ser(p.I905S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20369568:20369568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284C>A
AA Mutation	p.Ala95Glu(p.A95E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20654033:20654033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3012C>A
AA Mutation	p.Phe1004Leu(p.F1004L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20369656:20369656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20369482:20369482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20613493:20613493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773971834
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20630089:20630089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20369575:20369575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20369800:20369800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20648738:20648738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2616T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359062
Start	20369789:20369789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.511delG
AA Mutation	p.Glu171LysfsTer36(p.E171Kfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000359062
Start	20650550:20650550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2875G>T
AA Mutation	p.Glu959Ter(p.E959*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359062
Start	20556663:20556664(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.965dupT
AA Mutation	p.Met322IlefsTer82(p.M322Ifs*82)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359062
Start	20634901:20634901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1847-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PDE3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20653995:20653995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974C>T
AA Mutation	p.Arg992Cys(p.R992C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20613582:20613582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151A>T
AA Mutation	p.Gln384Leu(p.Q384L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20613642:20613642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211A>C
AA Mutation	p.Asn404Thr(p.N404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359062
Start	20650591:20650591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2916T>G
AA Mutation	p.Phe972Leu(p.F972L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20634912:20634912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20680058:20680058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3213C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359062
Start	20680220:20680220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3375G>A
Mutation Classification	Silent
Feature Type	Transcript