Mutation

Primary Site >> Stomach Cancer

Gene >> ITSN2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24210833:24210833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4204T>G
AA Mutation	p.Ser1402Ala(p.S1402A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24284767:24284767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940T>G
AA Mutation	p.Leu647Arg(p.L647R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24208290:24208290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201345506
CDS Mutation	c.4625C>T
AA Mutation	p.Ala1542Val(p.A1542V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24302076:24302076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>A
AA Mutation	p.Gly295Glu(p.G295E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24258047:24258047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2729C>T
AA Mutation	p.Thr910Ile(p.T910I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24286291:24286291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784T>G
AA Mutation	p.Leu595Arg(p.L595R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24270750:24270750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2276T>C
AA Mutation	p.Leu759Ser(p.L759S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24310606:24310606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439A>T
AA Mutation	p.Thr147Ser(p.T147S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24261119:24261119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669C>A
AA Mutation	p.Pro890His(p.P890H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24300156:24300156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097A>C
AA Mutation	p.Lys366Thr(p.K366T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24298787:24298787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775911766
CDS Mutation	c.1372C>T
AA Mutation	p.Arg458Cys(p.R458C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355123
Start	24261727:24261727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377521295
CDS Mutation	c.2371G>A
AA Mutation	p.Val791Ile(p.V791I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355123
Start	24310532:24310532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760514011
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355123
Start	24203698:24203698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5022G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355123
Start	24271853:24271853(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2170delA
AA Mutation	p.Thr724HisfsTer23(p.T724Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355123
Start	24261652:24261652(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2446delA
AA Mutation	p.Met816CysfsTer41(p.M816Cfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355123
Start	24271841:24271841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2182delA
AA Mutation	p.Ile728PhefsTer19(p.I728Ffs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355123
Start	24261730:24261730(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2368delA
AA Mutation	p.Thr790ProfsTer2(p.T790Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355123
Start	24286226:24286227(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1848dupT
AA Mutation	p.Asn617Ter(p.N617*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	20
Mutation Consequence	stop_lost
Transcription ID	ENST00000355123
Start	24203626:24203626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5094G>T
AA Mutation	p.Ter1698TyrextTer3(p.1698Yext3)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript