Mutation

Primary Site >> Stomach Cancer

Gene >> PCDH1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141864127:141864127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370805685
CDS Mutation	c.2204C>T
AA Mutation	p.Thr735Met(p.T735M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141863263:141863263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767284701
CDS Mutation	c.3068G>A
AA Mutation	p.Arg1023His(p.R1023H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141868726:141868726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Thr249Ile(p.T249I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141864065:141864065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2266A>G
AA Mutation	p.Ile756Val(p.I756V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141865045:141865045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286C>T
AA Mutation	p.Ala429Val(p.A429V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287008
Start	141854329:141854329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3427C>A
AA Mutation	p.Arg1143Ser(p.R1143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141863619:141863619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2712G>T
AA Mutation	p.Lys904Asn(p.K904N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141864308:141864308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023C>G
AA Mutation	p.Arg675Gly(p.R675G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287008
Start	141857263:141857263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3308A>G
AA Mutation	p.His1103Arg(p.H1103R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141865385:141865385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770603781
CDS Mutation	c.946G>A
AA Mutation	p.Glu316Lys(p.E316K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141868576:141868576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896T>A
AA Mutation	p.Val299Asp(p.V299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141865366:141865366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374705686
CDS Mutation	c.965C>T
AA Mutation	p.Ala322Val(p.A322V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141863239:141863239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3092G>A
AA Mutation	p.Ser1031Asn(p.S1031N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141863726:141863726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2605G>A
AA Mutation	p.Ala869Thr(p.A869T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000394536
Start	141868906:141868906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566T>C
AA Mutation	p.Ile189Thr(p.I189T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141865386:141865386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375066343
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141864087:141864087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2244C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141863277:141863277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149883982
CDS Mutation	c.3054C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141864321:141864321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141864108:141864108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2223C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394536
Start	141868692:141868692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770186390
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394536
Start	141863250:141863250(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3081delC
AA Mutation	p.Lys1028AsnfsTer7(p.K1028Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394536
Start	141863766:141863767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2564_2565delTT
AA Mutation	p.Phe855TrpfsTer35(p.F855Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394536
Start	141865231:141865231(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1100delA
AA Mutation	p.Lys367ArgfsTer9(p.K367Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript