Mutation

Primary Site >> Stomach Cancer

Gene >> UBTD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570204:97570204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746293748
CDS Mutation	c.365C>T
AA Mutation	p.Pro122Leu(p.P122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570412:97570412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573G>T
AA Mutation	p.Trp191Cys(p.W191C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570288:97570288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>A
AA Mutation	p.Pro150Gln(p.P150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570299:97570299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752369963
CDS Mutation	c.460C>T
AA Mutation	p.Arg154Cys(p.R154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570320:97570320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546233811
CDS Mutation	c.481G>A
AA Mutation	p.Val161Met(p.V161M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370664
Start	97570446:97570446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536025967
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Trp(p.R203W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370664
Start	97570289:97570289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370664
Start	97570251:97570251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.417delC
AA Mutation	p.Glu140SerfsTer12(p.E140Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript