Mutation

Primary Site >> Stomach Cancer

Gene >> ETV5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186079892:186079892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779639231
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186064464:186064464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923G>A
AA Mutation	p.Cys308Tyr(p.C308Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186079913:186079913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554G>T
AA Mutation	p.Gly185Val(p.G185V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186048835:186048835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337A>C
AA Mutation	p.Lys446Thr(p.K446T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186081140:186081140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Trp(p.R90W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306376
Start	186052038:186052038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303A>G
AA Mutation	p.Met435Val(p.M435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306376
Start	186079948:186079948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765841912
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306376
Start	186080046:186080046(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.421delC
AA Mutation	p.Leu141SerfsTer66(p.L141Sfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000306376
Start	186105304:186105304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript