Mutation

Primary Site >> Stomach Cancer

Gene >> TF

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133766391:133766391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>A
AA Mutation	p.Pro482Thr(p.P482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133748492:133748492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377691845
CDS Mutation	c.124C>T
AA Mutation	p.Arg42Cys(p.R42C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133746453:133746453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>A
AA Mutation	p.Val5Met(p.V5M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133775559:133775559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1814C>A
AA Mutation	p.Ala605Asp(p.A605D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133748549:133748549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181A>G
AA Mutation	p.Lys61Glu(p.K61E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000402696
Start	133748573:133748573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205A>G
AA Mutation	p.Arg69Gly(p.R69G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402696
Start	133756321:133756321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402696
Start	133777066:133777066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754752269
CDS Mutation	c.1890C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402696
Start	133775527:133775527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778400078
CDS Mutation	c.1782G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402696
Start	133757924:133757924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000402696
Start	133768105:133768105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402696
Start	133777144:133777144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1970delT
AA Mutation	p.Leu657TrpfsTer14(p.L657Wfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402696
Start	133757870:133757870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.978delC
AA Mutation	p.Arg327GlyfsTer35(p.R327Gfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000402696
Start	133775434:133775434(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1694delA
AA Mutation	p.Asn565ThrfsTer9(p.N565Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000402696
Start	133756956:133756956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Ter(p.R273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000402696
Start	133766419:133766420(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1474dupC
AA Mutation	p.His492ProfsTer5(p.H492Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript