Mutation

Primary Site >> Stomach Cancer

Gene >> PCDH8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52848286:52848286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>A
AA Mutation	p.Glu51Lys(p.E51K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846438:52846438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1999C>A
AA Mutation	p.Arg667Ser(p.R667S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52844762:52844762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3011A>G
AA Mutation	p.Tyr1004Cys(p.Y1004C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52845622:52845622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548787593
CDS Mutation	c.2642C>T
AA Mutation	p.Ala881Val(p.A881V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846110:52846110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2327G>A
AA Mutation	p.Arg776His(p.R776H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846216:52846216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2221G>A
AA Mutation	p.Gly741Arg(p.G741R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52848088:52848088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Trp(p.R117W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846767:52846767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670C>A
AA Mutation	p.Ala557Asp(p.A557D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52847463:52847463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.974G>A
AA Mutation	p.Arg325Gln(p.R325Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846296:52846296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141G>A
AA Mutation	p.Gly714Asp(p.G714D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52845583:52845583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2681C>T
AA Mutation	p.Ala894Val(p.A894V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52847941:52847941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52847041:52847041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396A>G
AA Mutation	p.Thr466Ala(p.T466A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846141:52846141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2296G>A
AA Mutation	p.Ala766Thr(p.A766T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846111:52846111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2326C>T
AA Mutation	p.Arg776Cys(p.R776C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846291:52846291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146C>T
AA Mutation	p.Arg716Cys(p.R716C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846708:52846708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729G>A
AA Mutation	p.Val577Ile(p.V577I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52847149:52847149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288G>A
AA Mutation	p.Ala430Thr(p.A430T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52848213:52848213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52847107:52847107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>A
AA Mutation	p.Ala444Thr(p.A444T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52846213:52846213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2224T>C
AA Mutation	p.Ser742Pro(p.S742P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000377942
Start	52844853:52844853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141509995
CDS Mutation	c.2920G>A
AA Mutation	p.Ala974Thr(p.A974T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52846142:52846142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2295C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847924:52847924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369468266
CDS Mutation	c.513C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52846391:52846391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2046C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847864:52847864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52848350:52848350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847981:52847981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52844587:52844587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199906293
CDS Mutation	c.3186G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847015:52847015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1422G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52848041:52848041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847315:52847315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749861077
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847321:52847321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52844683:52844683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3090C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52846922:52846922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761213188
CDS Mutation	c.1515G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52846850:52846850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377942
Start	52847603:52847603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757465623
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377942
Start	52846081:52846081(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2356delG
AA Mutation	p.Ala786ProfsTer151(p.A786Pfs*151)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377942
Start	52848414:52848414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.23delG
AA Mutation	p.Gly8AlafsTer48(p.G8Afs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000377942
Start	52848340:52848340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Ter(p.R33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript