Mutation

Primary Site >> Stomach Cancer

Gene >> SELPLG

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623157:108623157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746961402
CDS Mutation	c.1151T>C
AA Mutation	p.Leu384Pro(p.L384P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108624223:108624223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776843709
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623703:108623703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605A>C
AA Mutation	p.Gln202Pro(p.Q202P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623394:108623394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914T>G
AA Mutation	p.Val305Gly(p.V305G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108624160:108624160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>T
AA Mutation	p.Asp50Tyr(p.D50Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623178:108623178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130C>T
AA Mutation	p.Ser377Phe(p.S377F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623302:108623302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771908051
CDS Mutation	c.1006G>A
AA Mutation	p.Val336Met(p.V336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623989:108623989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000550948
Start	108623261:108623261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000550948
Start	108624107:108624107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201T>G
Mutation Classification	Silent
Feature Type	Transcript