Colon Cancer: Gene >> PDE4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10446316:10446316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419G>A
AA Mutation	p.Ser140Asn(p.S140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10450619:10450619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>A
AA Mutation	p.Gly213Ser(p.G213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10450877:10450877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719G>T
AA Mutation	p.Trp240Leu(p.W240L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10467287:10467287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327C>G
AA Mutation	p.Ala776Gly(p.A776G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10459432:10459432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>A
AA Mutation	p.Asn378Lys(p.N378K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10459663:10459663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269G>T
AA Mutation	p.Glu423Asp(p.E423D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10467538:10467538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777713898
CDS Mutation	c.2578A>G
AA Mutation	p.Ser860Gly(p.S860G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10458010:10458010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>T
AA Mutation	p.Gly337Trp(p.G337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10466915:10466915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1955C>T
AA Mutation	p.Pro652Leu(p.P652L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10446343:10446343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201316500
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380702
Start	10467367:10467367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200409316
CDS Mutation	c.2407G>A
AA Mutation	p.Val803Met(p.V803M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380702
Start	10446302:10446302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199755060
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380702
Start	10463912:10463912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202169888
CDS Mutation	c.1863C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380702
Start	10467366:10467366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202005713
CDS Mutation	c.2406C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380702
Start	10467471:10467471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2511G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380702
Start	10457927:10457927(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.930delA
AA Mutation	p.Lys310AsnfsTer29(p.K310Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000380702
Start	10457923:10457923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Ter(p.R308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000380702
Start	10461651:10461651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591C>T
AA Mutation	p.Gln531Ter(p.Q531*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PDE4A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380702
Start	10461087:10461087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449G>A
Mutation Classification	Silent
Feature Type	Transcript