Mutation

Primary Site >> Stomach Cancer

Gene >> RUVBL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49009813:49009813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500A>T
AA Mutation	p.Glu167Val(p.E167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49007140:49007140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>T
AA Mutation	p.Arg130Cys(p.R130C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49015581:49015581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1261G>A
AA Mutation	p.Val421Met(p.V421M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49007032:49007032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280C>A
AA Mutation	p.Leu94Met(p.L94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49011198:49011198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889T>G
AA Mutation	p.Phe297Val(p.F297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49007310:49007310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776647069
CDS Mutation	c.404C>T
AA Mutation	p.Thr135Met(p.T135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000595090
Start	49010023:49010023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762109573
CDS Mutation	c.620G>A
AA Mutation	p.Arg207His(p.R207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595090
Start	49004384:49004384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595090
Start	49004309:49004309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000595090
Start	49010000:49010000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550156979
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000595090
Start	49011309:49011309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000C>T
AA Mutation	p.Arg334Ter(p.R334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000595090
Start	49015686:49015689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1366+2_1366+5delTAAG
Mutation Classification	Splice_Site
Feature Type	Transcript