Mutation

Primary Site >> Stomach Cancer

Gene >> RARB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25580663:25580663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748A>G
AA Mutation	p.Thr250Ala(p.T250A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25501279:25501279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425A>C
AA Mutation	p.Tyr142Ser(p.Y142S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25174558:25174558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161G>T
AA Mutation	p.Ser54Ile(p.S54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25594660:25594660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759614000
CDS Mutation	c.1153C>T
AA Mutation	p.Arg385Cys(p.R385C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25461327:25461327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313T>A
AA Mutation	p.Cys105Ser(p.C105S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25580649:25580649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78062701
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25461282:25461282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372338731
CDS Mutation	c.268G>A
AA Mutation	p.Val90Ile(p.V90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25580678:25580678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773216330
CDS Mutation	c.763G>A
AA Mutation	p.Ala255Thr(p.A255T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25461293:25461293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279C>A
AA Mutation	p.Asp93Glu(p.D93E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000383772
Start	25596429:25596429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181G>C
AA Mutation	p.Arg394Pro(p.R394P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383772
Start	25174502:25174502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383772
Start	25569795:25569795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383772
Start	25461235:25461236(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.227dupC
AA Mutation	p.Ser77IlefsTer30(p.S77Ifs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript