Mutation

Primary Site >> Stomach Cancer

Gene >> RORA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60511346:60511346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Ile(p.L234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60514717:60514717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>T
AA Mutation	p.Ser108Phe(p.S108F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60514684:60514684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335670
Start	60499914:60499914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385G>A
AA Mutation	p.Arg462Gln(p.R462Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	61229186:61229186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	60499997:60499997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776035356
CDS Mutation	c.1302A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	60511503:60511503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202109768
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335670
Start	60514677:60514677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335670
Start	60499967:60499967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1332delA
AA Mutation	p.Lys444AsnfsTer8(p.K444Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000335670
Start	60502868:60502868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript