Mutation

Primary Site >> Stomach Cancer

Gene >> OGT

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71557572:71557572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1502G>A
AA Mutation	p.Arg501Lys(p.R501K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71538004:71538004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394G>A
AA Mutation	p.Ala132Thr(p.A132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71563155:71563155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2174C>T
AA Mutation	p.Ser725Phe(p.S725F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71555245:71555245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784C>T
AA Mutation	p.His262Tyr(p.H262Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71567540:71567540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2630G>A
AA Mutation	p.Arg877His(p.R877H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373719
Start	71559333:71559333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759414360
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Cys(p.R557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373719
Start	71547939:71547939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764536052
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373719
Start	71547987:71547987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373719
Start	71562975:71562975(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2112delT
AA Mutation	p.Phe704LeufsTer12(p.F704Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373719
Start	71567611:71567612(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2707dupT
AA Mutation	p.Ser903PhefsTer6(p.S903Ffs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript