Mutation

Primary Site >> Stomach Cancer

Gene >> PCDH7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000511884
Start	31142529:31142529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2493G>A
AA Mutation	p.Glu832Lys(p.E832K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722390:30722390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968C>T
AA Mutation	p.Pro323Leu(p.P323L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723430:30723430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008C>T
AA Mutation	p.Arg670Trp(p.R670W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722818:30722818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396G>A
AA Mutation	p.Val466Met(p.V466M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722413:30722413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Cys(p.R331C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722284:30722284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723464:30723464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042A>G
AA Mutation	p.Asn681Ser(p.N681S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722840:30722840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418C>T
AA Mutation	p.Ala473Val(p.A473V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30724513:30724513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3091G>A
AA Mutation	p.Val1031Met(p.V1031M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723128:30723128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706A>G
AA Mutation	p.Glu569Gly(p.E569G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30721505:30721505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83C>T
AA Mutation	p.Ala28Val(p.A28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000511884
Start	30920292:30920292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2383C>T
AA Mutation	p.Ala795Val(p.A795V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723028:30723028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777309631
CDS Mutation	c.1606G>A
AA Mutation	p.Gly536Ser(p.G536S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722567:30722567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723181:30723181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759G>A
AA Mutation	p.Asp587Asn(p.D587N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723406:30723406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1984A>G
AA Mutation	p.Thr662Ala(p.T662A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30722285:30722285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863G>A
AA Mutation	p.Arg288His(p.R288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30723089:30723089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667C>T
AA Mutation	p.Thr556Met(p.T556M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30721822:30721822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Leu134Phe(p.L134F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000361762
Start	30730756:30730756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367733138
CDS Mutation	c.3178C>T
AA Mutation	p.Arg1060Cys(p.R1060C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30724368:30724368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372075213
CDS Mutation	c.2946C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30722586:30722586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30721938:30721938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544156156
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30722814:30722814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30721539:30721539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30722649:30722649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372895036
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30724008:30724008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2586C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30721572:30721572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361762
Start	30723252:30723252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361762
Start	30724420:30724421(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3002dupC
AA Mutation	p.Leu1002IlefsTer45(p.L1002Ifs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript