Mutation

Primary Site >> Stomach Cancer

Gene >> PDE3B

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000282096
Start	14771986:14771986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028A>T
AA Mutation	p.Gln343Leu(p.Q343L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14859094:14859094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2572G>A
AA Mutation	p.Ala858Thr(p.A858T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14843956:14843956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2450C>T
AA Mutation	p.Ala817Val(p.A817V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14869562:14869562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3241A>C
AA Mutation	p.Lys1081Gln(p.K1081Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14843944:14843944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2438C>T
AA Mutation	p.Ala813Val(p.A813V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14786560:14786560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153A>G
AA Mutation	p.Ser385Gly(p.S385G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14786507:14786507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100T>C
AA Mutation	p.Leu367Pro(p.L367P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14644911:14644911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836C>T
AA Mutation	p.Ser279Phe(p.S279F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14859200:14859200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201854538
CDS Mutation	c.2678C>T
AA Mutation	p.Thr893Met(p.T893M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14786581:14786581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>A
AA Mutation	p.Gly392Ser(p.G392S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14789150:14789150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323C>G
AA Mutation	p.Ser441Arg(p.S441R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14818378:14818378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718G>A
AA Mutation	p.Ser573Asn(p.S573N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14867647:14867647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028C>A
AA Mutation	p.Pro1010Thr(p.P1010T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14786549:14786549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142G>A
AA Mutation	p.Arg381Gln(p.R381Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14644262:14644262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187C>G
AA Mutation	p.Pro63Ala(p.P63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000282096
Start	14644451:14644451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>A
AA Mutation	p.Ala126Thr(p.A126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14867634:14867634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3015T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282096
Start	14859228:14859228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372887526
CDS Mutation	c.2706C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282096
Start	14859171:14859171(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2654delT
AA Mutation	p.Leu885Ter(p.L885*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282096
Start	14859208:14859208(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2690delA
AA Mutation	p.Lys897SerfsTer16(p.K897Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000282096
Start	14835028:14835028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2253T>A
AA Mutation	p.Tyr751Ter(p.Y751*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000282096
Start	14861313:14861313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2833C>T
AA Mutation	p.Arg945Ter(p.R945*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript