Mutation

Primary Site >> Stomach Cancer

Gene >> ELMO3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67203578:67203578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753617002
CDS Mutation	c.2104C>T
AA Mutation	p.Arg702Trp(p.R702W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67202041:67202041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274T>C
AA Mutation	p.Leu425Ser(p.L425S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67202007:67202007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375789407
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Met(p.V414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67200247:67200247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754967465
CDS Mutation	c.458G>A
AA Mutation	p.Arg153His(p.R153H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393997
Start	67202455:67202455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760145785
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393997
Start	67199194:67199194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767577798
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393997
Start	67202010:67202010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781430251
CDS Mutation	c.1248delC
AA Mutation	p.Gly417ValfsTer44(p.G417Vfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393997
Start	67203827:67203827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2277delC
AA Mutation	p.Thr760ProfsTer31(p.T760Pfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000393997
Start	67203163:67203163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879C>T
AA Mutation	p.Gln627Ter(p.Q627*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript