Mutation

Primary Site >> Stomach Cancer

Gene >> SPHK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76386053:76386053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79A>G
AA Mutation	p.Lys27Glu(p.K27E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76387003:76387003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76387376:76387376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945A>T
AA Mutation	p.Glu315Asp(p.E315D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76386939:76386939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76387395:76387395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746200388
CDS Mutation	c.964G>A
AA Mutation	p.Val322Met(p.V322M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76386430:76386430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>T
AA Mutation	p.Thr99Ile(p.T99I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76387521:76387521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201780441
CDS Mutation	c.1090G>A
AA Mutation	p.Gly364Ser(p.G364S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76387569:76387569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>T
AA Mutation	p.Pro380Ser(p.P380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392496
Start	76386068:76386068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94C>A
AA Mutation	p.Gln32Lys(p.Q32K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392496
Start	76386869:76386869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript