Mutation

Primary Site >> Stomach Cancer

Gene >> CNBD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87353670:87353670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187T>G
AA Mutation	p.Leu396Arg(p.L396R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	86905100:86905100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781715512
CDS Mutation	c.178T>G
AA Mutation	p.Leu60Val(p.L60V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87284712:87284712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.806T>G
AA Mutation	p.Val269Gly(p.V269G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87284710:87284710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804A>C
AA Mutation	p.Glu268Asp(p.E268D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87353670:87353670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187T>C
AA Mutation	p.Leu396Pro(p.L396P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87353670:87353670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187T>A
AA Mutation	p.Leu396His(p.L396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87284765:87284765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370856044
CDS Mutation	c.859G>A
AA Mutation	p.Asp287Asn(p.D287N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	86939693:86939693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370T>G
AA Mutation	p.Leu124Val(p.L124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000518476
Start	87353760:87353760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518476
Start	87353749:87353749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518476
Start	86905152:86905152(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.234delA
AA Mutation	p.Lys78AsnfsTer34(p.K78Nfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000518476
Start	87353645:87353645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Gln388Ter(p.Q388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000518476
Start	87237009:87237009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.668C>A
AA Mutation	p.Ser223Ter(p.S223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript