Mutation

Primary Site >> Stomach Cancer

Gene >> TET2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105236184:105236184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771091424
CDS Mutation	c.2242T>A
AA Mutation	p.Leu748Ile(p.L748I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105235252:105235252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310A>G
AA Mutation	p.Tyr437Cys(p.Y437C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105234016:105234016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762289112
CDS Mutation	c.74G>T
AA Mutation	p.Cys25Phe(p.C25F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105235820:105235820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1878G>T
AA Mutation	p.Gln626His(p.Q626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105235474:105235474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532A>G
AA Mutation	p.His511Arg(p.H511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105234777:105234777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835A>C
AA Mutation	p.Thr279Pro(p.T279P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105235092:105235092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150A>G
AA Mutation	p.Ser384Gly(p.S384G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380013
Start	105235924:105235924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1982A>G
AA Mutation	p.His661Arg(p.H661R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380013
Start	105236036:105236036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380013
Start	105234500:105234500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380013
Start	105237308:105237308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3366A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380013
Start	105234504:105234504(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.565delA
AA Mutation	p.Ser189ValfsTer18(p.S189Vfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380013
Start	105235779:105235779(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763386429
CDS Mutation	c.1842delG
AA Mutation	p.Leu615SerfsTer24(p.L615Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000380013
Start	105236745:105236745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2803G>T
AA Mutation	p.Gly935Ter(p.G935*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380013
Start	105236951:105236952(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3014dupA
AA Mutation	p.Val1006GlyfsTer3(p.V1006Gfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380013
Start	105236391:105236392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2453dupC
AA Mutation	p.Tyr819LeufsTer2(p.Y819Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	17
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000380013
Start	105237353:105237353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3409+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript