Mutation

Primary Site >> Stomach Cancer

Gene >> PCDH9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225467:67225467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773838866
CDS Mutation	c.2974A>G
AA Mutation	p.Ser992Gly(p.S992G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227540:67227540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901A>G
AA Mutation	p.Arg301Gly(p.R301G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225885:67225885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2556A>C
AA Mutation	p.Gln852His(p.Q852H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227883:67227883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.558T>G
AA Mutation	p.Ser186Arg(p.S186R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67226918:67226918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523T>C
AA Mutation	p.Leu508Pro(p.L508P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227268:67227268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173G>T
AA Mutation	p.Lys391Asn(p.K391N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227074:67227074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367G>C
AA Mutation	p.Arg456Thr(p.R456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225676:67225676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199964981
CDS Mutation	c.2765C>T
AA Mutation	p.Pro922Leu(p.P922L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67228292:67228292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149C>A
AA Mutation	p.Ser50Tyr(p.S50Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	66304785:66304785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199877381
CDS Mutation	c.3584G>A
AA Mutation	p.Arg1195His(p.R1195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67228244:67228244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197T>G
AA Mutation	p.Leu66Arg(p.L66R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	66305014:66305014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3355C>G
AA Mutation	p.Pro1119Ala(p.P1119A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67228320:67228320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Gly41Arg(p.G41R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67226117:67226117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2324A>C
AA Mutation	p.Asn775Thr(p.N775T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225958:67225958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2483T>C
AA Mutation	p.Val828Ala(p.V828A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225509:67225509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755751696
CDS Mutation	c.2932G>A
AA Mutation	p.Asp978Asn(p.D978N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225977:67225977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2464G>A
AA Mutation	p.Gly822Ser(p.G822S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227789:67227789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652T>C
AA Mutation	p.Tyr218His(p.Y218H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	66304891:66304891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3478A>C
AA Mutation	p.Thr1160Pro(p.T1160P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227578:67227578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778185688
CDS Mutation	c.863G>A
AA Mutation	p.Arg288Gln(p.R288Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67227470:67227470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778004717
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000377865
Start	67225631:67225631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2810A>G
AA Mutation	p.Lys937Arg(p.K937R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66903543:66903543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773530084
CDS Mutation	c.3099G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67227280:67227280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67227673:67227673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67227228:67227228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1213A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67227813:67227813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67226143:67226143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769828344
CDS Mutation	c.2298G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67226653:67226653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66631229:66631229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3321C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67226221:67226221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2220A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67228261:67228261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66631256:66631256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3294T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67226407:67226407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2034A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66631241:66631241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3309T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66304682:66304682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3687T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	67227547:67227547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377865
Start	66304709:66304709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3660G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377865
Start	67226939:67226939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1502delA
AA Mutation	p.Asn501MetfsTer24(p.N501Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377865
Start	67225862:67225862(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2579delA
AA Mutation	p.Asn860ThrfsTer23(p.N860Tfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377865
Start	67228183:67228184(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.257dupT
AA Mutation	p.Thr87HisfsTer19(p.T87Hfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377865
Start	67226220:67226221(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2220dupA
AA Mutation	p.Pro741ThrfsTer5(p.P741Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	43
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000377865
Start	66903606:66903606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3037-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	44
Mutation Consequence	stop_lost
Transcription ID	ENST00000377865
Start	66304655:66304655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3714A>C
AA Mutation	p.Ter1238TyrextTer26(p.1238Yext26)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript