Colon Cancer: Gene >> PDE3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14867707:14867707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782615223
CDS Mutation	c.3088G>A
AA Mutation	p.Gly1030Ser(p.G1030S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14835039:14835039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264G>T
AA Mutation	p.Arg755Leu(p.R755L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14818332:14818332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672G>A
AA Mutation	p.Ala558Thr(p.A558T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14859170:14859170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146384818
CDS Mutation	c.2648G>A
AA Mutation	p.Arg883His(p.R883H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14830824:14830824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1934C>T
AA Mutation	p.Ala645Val(p.A645V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14644392:14644392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317C>A
AA Mutation	p.Ala106Asp(p.A106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14644547:14644547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472C>G
AA Mutation	p.Pro158Ala(p.P158A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14859112:14859112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2590T>C
AA Mutation	p.Ser864Pro(p.S864P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14818233:14818233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1573T>G
AA Mutation	p.Ser525Ala(p.S525A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14832821:14832821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2194C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14867661:14867661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3042A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14861261:14861261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2781G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14844011:14844011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2505T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14803953:14803953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000282096
Start	14818266:14818266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606G>T
AA Mutation	p.Glu536Ter(p.E536*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000282096
Start	14859248:14859248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2724+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000282096
Start	14843934:14843935(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2428_2429insCACATA
AA Mutation	p.Glu810delinsAlaHisLys(p.E810delinsAHK)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDE3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14831764:14831764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2081G>C
AA Mutation	p.Arg694Thr(p.R694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14859164:14859164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369209287
CDS Mutation	c.2642G>A
AA Mutation	p.Arg881His(p.R881H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14869546:14869546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782627306
CDS Mutation	c.3225C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000282096
Start	14861313:14861313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2833C>T
AA Mutation	p.Arg945Ter(p.R945*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript