Mutation

Primary Site >> Stomach Cancer

Gene >> RAB12

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329286
Start	8633245:8633245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344C>T
AA Mutation	p.Ala115Val(p.A115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329286
Start	8609944:8609944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769658729
CDS Mutation	c.217T>C
AA Mutation	p.Ser73Pro(p.S73P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329286
Start	8635549:8635549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443C>T
AA Mutation	p.Ala148Val(p.A148V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329286
Start	8636340:8636340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>A
AA Mutation	p.Asp202Asn(p.D202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329286
Start	8609921:8609921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194A>T
AA Mutation	p.Asp65Val(p.D65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329286
Start	8635598:8635598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329286
Start	8638259:8638259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370554407
CDS Mutation	c.732T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329286
Start	8633210:8633210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329286
Start	8609830:8609830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.108delC
AA Mutation	p.Arg37GlyfsTer22(p.R37Gfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329286
Start	8636352:8636352(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.620delA
AA Mutation	p.Lys207ArgfsTer7(p.K207Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript