Mutation

Primary Site >> Stomach Cancer

Gene >> S1PR3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001571:89001571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001597:89001597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001607:89001607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751247905
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001204:89001204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4G>A
AA Mutation	p.Ala2Thr(p.A2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002303:89002303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103A>G
AA Mutation	p.Asn368Ser(p.N368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002224:89002224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024A>G
AA Mutation	p.Ser342Gly(p.S342G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001910:89001910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542433062
CDS Mutation	c.710G>A
AA Mutation	p.Arg237Gln(p.R237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001879:89001879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89002088:89002088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745966943
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89002118:89002118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001800:89001800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001596:89001596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358157
Start	89002162:89002162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.967delG
AA Mutation	p.Ala323ProfsTer84(p.A323Pfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript