Mutation

Primary Site >> Stomach Cancer

Gene >> RAG2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593066:36593066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103C>T
AA Mutation	p.Ser368Leu(p.S368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593167:36593167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002C>A
AA Mutation	p.Asp334Glu(p.D334E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593634:36593634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>A
AA Mutation	p.Leu179Met(p.L179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593683:36593683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767924789
CDS Mutation	c.486G>A
AA Mutation	p.Met162Ile(p.M162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593328:36593328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841A>C
AA Mutation	p.Asn281His(p.N281H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36592934:36592934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235A>G
AA Mutation	p.Glu412Gly(p.E412G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311485
Start	36594016:36594016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772223078
CDS Mutation	c.153G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311485
Start	36592645:36592645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1524delA
AA Mutation	p.Gly509ValfsTer6(p.G509Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311485
Start	36592673:36592673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1496delA
AA Mutation	p.Lys499SerfsTer4(p.K499Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript