Colon Cancer: Gene >> PDE6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	666544:666544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144727865
CDS Mutation	c.2282G>A
AA Mutation	p.Arg761Gln(p.R761Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	626017:626017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145863444
CDS Mutation	c.391G>A
AA Mutation	p.Val131Ile(p.V131I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	625924:625924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537263212
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	634761:634761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Asp185Asn(p.D185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	634714:634714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506A>G
AA Mutation	p.Asp169Gly(p.D169G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	634756:634756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>C
AA Mutation	p.Gly183Ala(p.G183A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	666592:666592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2330T>C
AA Mutation	p.Phe777Ser(p.F777S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	667962:667962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2459C>T
AA Mutation	p.Ala820Val(p.A820V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	625728:625728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142437453
CDS Mutation	c.102G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	654094:654094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	625758:625758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199974771
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	662583:662583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	634784:634784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	626040:626040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748297420
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	656000:656000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768980060
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	664216:664216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144847778
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	667981:667981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2478G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000496514
Start	664196:664196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2104G>T
AA Mutation	p.Glu702Ter(p.E702*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PDE6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	635958:635958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374915809
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Cys(p.R234C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000496514
Start	662161:662161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642A>C
AA Mutation	p.Ser548Arg(p.S548R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	656274:656274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150360174
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000496514
Start	664216:664216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144847778
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript