Mutation

Primary Site >> Stomach Cancer

Gene >> TRAF2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136925857:136925857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142412558
CDS Mutation	c.1462G>A
AA Mutation	p.Asp488Asn(p.D488N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136900470:136900470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551577118
CDS Mutation	c.316G>A
AA Mutation	p.Val106Ile(p.V106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247668
Start	136921197:136921197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Pro374Ser(p.P374S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247668
Start	136920455:136920455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247668
Start	136920344:136920344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200313379
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247668
Start	136908203:136908203(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.502delG
AA Mutation	p.Ala168HisfsTer8(p.A168Hfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247668
Start	136898760:136898760(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772564887
CDS Mutation	c.26delC
AA Mutation	p.Pro9LeufsTer77(p.P9Lfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247668
Start	136925759:136925760(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1368dupT
AA Mutation	p.Gln457SerfsTer277(p.Q457Sfs*277)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000247668
Start	136925681:136925681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript