Mutation

Primary Site >> Stomach Cancer

Gene >> GPR137

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64289309:64289309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1198C>T
AA Mutation	p.Leu400Phe(p.L400F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64286714:64286714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Ala64Thr(p.A64T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64287010:64287010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Gly135Ser(p.G135S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64286856:64286856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Thr111Met(p.T111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64286603:64286603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79A>G
AA Mutation	p.Thr27Ala(p.T27A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64288391:64288391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835A>G
AA Mutation	p.Ile279Val(p.I279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64288651:64288651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961T>G
AA Mutation	p.Phe321Val(p.F321V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64289235:64289235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124C>A
AA Mutation	p.Pro375His(p.P375H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313074
Start	64289356:64289356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769279910
CDS Mutation	c.1245G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313074
Start	64288100:64288100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147288418
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313074
Start	64287745:64287745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.436delG
AA Mutation	p.Ala146ProfsTer8(p.A146Pfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313074
Start	64287776:64287776(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.463delG
AA Mutation	p.Val155CysfsTer24(p.V155Cfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000313074
Start	64287007:64287007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Ter(p.R134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript