Colon Cancer: Gene >> PDE10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165543539:165543539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185608480
CDS Mutation	c.67C>A
AA Mutation	p.Leu23Ile(p.L23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165430318:165430318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Glu248Lys(p.E248K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165339332:165339332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2094A>G
AA Mutation	p.Ile698Met(p.I698M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165448935:165448935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359G>A
AA Mutation	p.Cys120Tyr(p.C120Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165388344:165388344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736C>T
AA Mutation	p.Ser579Phe(p.S579F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165388429:165388429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>A
AA Mutation	p.Leu551Met(p.L551M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165433122:165433122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515G>A
AA Mutation	p.Arg172Gln(p.R172Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165388375:165388375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705G>A
AA Mutation	p.Asp569Asn(p.D569N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366882
Start	165396415:165396415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778570347
CDS Mutation	c.1293G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366882
Start	165413633:165413633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777212417
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366882
Start	165388376:165388376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139267725
CDS Mutation	c.1704C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366882
Start	165336194:165336194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35370607
CDS Mutation	c.2166C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366882
Start	165418764:165418764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.839delA
AA Mutation	p.Asn280ThrfsTer3(p.N280Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000366882
Start	165433000:165433000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>T
AA Mutation	p.Glu213Ter(p.E213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000366882
Start	165416188:165416188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PDE10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165395234:165395234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422C>A
AA Mutation	p.Asn474Lys(p.N474K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165450309:165450309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249A>T
AA Mutation	p.Glu83Asp(p.E83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165435331:165435331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>A
AA Mutation	p.Arg138His(p.R138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165343438:165343438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117826255
CDS Mutation	c.2020G>A
AA Mutation	p.Val674Ile(p.V674I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165343395:165343395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2063C>A
AA Mutation	p.Ala688Asp(p.A688D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366882
Start	165343391:165343391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2067G>T
AA Mutation	p.Glu689Asp(p.E689D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366882
Start	165413677:165413677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072T>A
AA Mutation	p.Leu358Met(p.L358M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366882
Start	165396397:165396397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780011165
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000366882
Start	165396327:165396327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1381G>T
AA Mutation	p.Glu461Ter(p.E461*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript