Mutation

Primary Site >> Stomach Cancer

Gene >> CD248

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316219:66316219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Ser270Asn(p.S270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316648:66316648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>T
AA Mutation	p.Pro127Leu(p.P127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316900:66316900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128C>A
AA Mutation	p.Thr43Asn(p.T43N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316264:66316264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764C>T
AA Mutation	p.Ser255Phe(p.S255F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315079:66315079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>A
AA Mutation	p.Gly650Asp(p.G650D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66316763:66316763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Trp(p.R89W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315208:66315208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1820C>A
AA Mutation	p.Ser607Tyr(p.S607Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311330
Start	66315661:66315661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539641105
CDS Mutation	c.1367C>T
AA Mutation	p.Thr456Met(p.T456M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66316107:66316107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547491652
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311330
Start	66315801:66315801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311330
Start	66316487:66316487(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.541delA
AA Mutation	p.Thr181ArgfsTer34(p.T181Rfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311330
Start	66316143:66316144(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.878_884dupGCTGCCA
AA Mutation	p.His295GlnfsTer14(p.H295Qfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript