Mutation

Primary Site >> Stomach Cancer

Gene >> RBM4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643494:66643494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>A
AA Mutation	p.Ala153Thr(p.A153T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643722:66643722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643629:66643629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748197738
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643696:66643696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659C>T
AA Mutation	p.Ala220Val(p.A220V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66640057:66640057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368114061
CDS Mutation	c.346G>A
AA Mutation	p.Val116Ile(p.V116I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643723:66643723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768616980
CDS Mutation	c.686G>A
AA Mutation	p.Arg229Gln(p.R229Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310092
Start	66643704:66643704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667A>G
AA Mutation	p.Lys223Glu(p.K223E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66640017:66640017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66643499:66643499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310092
Start	66643904:66643904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867A>T
Mutation Classification	Silent
Feature Type	Transcript