Mutation

Primary Site >> Stomach Cancer

Gene >> PDE2A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72580909:72580909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2110A>T
AA Mutation	p.Asn704Tyr(p.N704Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72577449:72577449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770991809
CDS Mutation	c.2761G>A
AA Mutation	p.Glu921Lys(p.E921K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72581462:72581462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940A>C
AA Mutation	p.Lys647Thr(p.K647T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584205:72584205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646C>A
AA Mutation	p.Ala549Asp(p.A549D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72579373:72579373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759387435
CDS Mutation	c.2267G>A
AA Mutation	p.Arg756His(p.R756H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584218:72584218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1633G>A
AA Mutation	p.Gly545Ser(p.G545S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584886:72584886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345G>A
AA Mutation	p.Val449Met(p.V449M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72588832:72588832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022A>T
AA Mutation	p.Asp341Val(p.D341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72578932:72578932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2434C>A
AA Mutation	p.Gln812Lys(p.Q812K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72577475:72577475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2735C>T
AA Mutation	p.Ser912Leu(p.S912L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334456
Start	72584206:72584206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645G>A
AA Mutation	p.Ala549Thr(p.A549T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72584648:72584648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72584564:72584564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1524G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72584893:72584893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202070484
CDS Mutation	c.1338C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72577588:72577588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2622G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334456
Start	72597538:72597538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334456
Start	72583498:72583498(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1668delA
AA Mutation	p.Val557Ter(p.V557*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000334456
Start	72674165:72674165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Gln15Ter(p.Q15*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334456
Start	72596612:72596613(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.469dupG
AA Mutation	p.Ala157GlyfsTer15(p.A157Gfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript