Colon Cancer: Gene >> PDE4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66363537:66363537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Ser417Leu(p.S417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66257844:66257844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565C>A
AA Mutation	p.Leu189Ile(p.L189I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	65918702:65918702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148T>G
AA Mutation	p.Leu50Val(p.L50V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66247567:66247567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773480022
CDS Mutation	c.389G>A
AA Mutation	p.Arg130His(p.R130H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	65913340:65913340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769931436
CDS Mutation	c.26C>T
AA Mutation	p.Thr9Met(p.T9M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66247627:66247627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370994595
CDS Mutation	c.449C>T
AA Mutation	p.Ser150Leu(p.S150L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66361753:66361753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777377398
CDS Mutation	c.980G>A
AA Mutation	p.Arg327His(p.R327H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66363247:66363247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100T>C
AA Mutation	p.Ile367Thr(p.I367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329654
Start	65913326:65913326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329654
Start	65918797:65918797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780521988
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329654
Start	66368942:66368942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329654
Start	66365688:66365689(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1306_1307insGTATCCTACT
AA Mutation	p.Ile436SerfsTer15(p.I436Sfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDE4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66368794:66368794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116312841
CDS Mutation	c.1670G>A
AA Mutation	p.Arg557His(p.R557H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329654
Start	66372422:66372422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1955A>G
AA Mutation	p.Tyr652Cys(p.Y652C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329654
Start	66372540:66372540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000329654
Start	66257808:66257808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Ter(p.R177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript