Mutation

Primary Site >> Stomach Cancer

Gene >> PCDHB1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052803:141052803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333G>A
AA Mutation	p.Val445Ile(p.V445I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052221:141052221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>A
AA Mutation	p.Val251Ile(p.V251I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141051898:141051898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>T
AA Mutation	p.Pro143Leu(p.P143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053691:141053691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2221G>T
AA Mutation	p.Val741Leu(p.V741L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053188:141053188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718G>A
AA Mutation	p.Cys573Tyr(p.C573Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053286:141053286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816C>A
AA Mutation	p.His606Asn(p.H606N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053373:141053373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903G>T
AA Mutation	p.Asp635Tyr(p.D635Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053017:141053017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116101801
CDS Mutation	c.1547C>T
AA Mutation	p.Ala516Val(p.A516V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141051966:141051966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Gly166Ser(p.G166S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052017:141052017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Cys(p.R183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052369:141052369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899A>T
AA Mutation	p.Glu300Val(p.E300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052197:141052197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782654150
CDS Mutation	c.727T>A
AA Mutation	p.Ser243Thr(p.S243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052370:141052370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900A>C
AA Mutation	p.Glu300Asp(p.E300D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141053802:141053802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332T>A
AA Mutation	p.Phe778Ile(p.F778I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052111:141052111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>T
AA Mutation	p.Ala214Val(p.A214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306549
Start	141052889:141052889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419A>T
AA Mutation	p.Lys473Asn(p.K473N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141051611:141051611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141053468:141053468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1998C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141053567:141053567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2097C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141051818:141051818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141053714:141053714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2244C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141053210:141053210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1740T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141052673:141052673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141052130:141052130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782104351
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141051767:141051767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782180084
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141051938:141051938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306549
Start	141053261:141053261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306549
Start	141051526:141051526(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.60delT
AA Mutation	p.Leu21CysfsTer28(p.L21Cfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript