Mutation

Primary Site >> Stomach Cancer

Gene >> PTPRH

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55181782:55181782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3320C>T
AA Mutation	p.Ala1107Val(p.A1107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55181894:55181894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140496718
CDS Mutation	c.3208G>A
AA Mutation	p.Val1070Ile(p.V1070I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55185599:55185599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769872554
CDS Mutation	c.2965G>A
AA Mutation	p.Val989Ile(p.V989I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55185914:55185914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2849T>C
AA Mutation	p.Val950Ala(p.V950A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55191720:55191720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2279T>C
AA Mutation	p.Val760Ala(p.V760A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55198711:55198711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622A>G
AA Mutation	p.Tyr541Cys(p.Y541C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55182052:55182052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3162G>C
AA Mutation	p.Lys1054Asn(p.K1054N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55196669:55196669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73619559
CDS Mutation	c.2110C>T
AA Mutation	p.Arg704Trp(p.R704W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55196699:55196699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764109925
CDS Mutation	c.2080G>A
AA Mutation	p.Glu694Lys(p.E694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376350
Start	55203902:55203902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766A>C
AA Mutation	p.Asn256His(p.N256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55203975:55203975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55206804:55206804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376350
Start	55185976:55185976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2787T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376350
Start	55205519:55205519(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.426delC
AA Mutation	p.Asp143ThrfsTer69(p.D143Tfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376350
Start	55182041:55182044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3170_3173delAGAG
AA Mutation	p.Glu1057ValfsTer4(p.E1057Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376350
Start	55197282:55197282(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1825delC
AA Mutation	p.Arg609GlyfsTer44(p.R609Gfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript