Mutation

Primary Site >> Stomach Cancer

Gene >> SPTBN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54646228:54646228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4619G>A
AA Mutation	p.Arg1540His(p.R1540H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356805
Start	54653610:54653610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5579T>G
AA Mutation	p.Val1860Gly(p.V1860G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54649967:54649967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5555A>T
AA Mutation	p.Asp1852Val(p.D1852V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54649675:54649675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779986830
CDS Mutation	c.5263G>A
AA Mutation	p.Val1755Met(p.V1755M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54626211:54626211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200538825
CDS Mutation	c.1621A>G
AA Mutation	p.Met541Val(p.M541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54612185:54612185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Cys(p.R109C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54630913:54630913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2866A>G
AA Mutation	p.Ser956Gly(p.S956G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54657879:54657879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760421103
CDS Mutation	c.6076G>A
AA Mutation	p.Ala2026Thr(p.A2026T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54655978:54655978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762333666
CDS Mutation	c.6026G>A
AA Mutation	p.Arg2009Gln(p.R2009Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54649633:54649633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750537630
CDS Mutation	c.5221C>T
AA Mutation	p.Arg1741Trp(p.R1741W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54649673:54649673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5261G>A
AA Mutation	p.Arg1754His(p.R1754H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54622364:54622364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941T>C
AA Mutation	p.Leu314Pro(p.L314P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54629014:54629014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557616559
CDS Mutation	c.1880C>T
AA Mutation	p.Ala627Val(p.A627V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54668388:54668388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6914C>T
AA Mutation	p.Ala2305Val(p.A2305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54629202:54629202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2068C>T
AA Mutation	p.Arg690Cys(p.R690C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54629200:54629200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066G>A
AA Mutation	p.Gly689Asp(p.G689D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54645356:54645356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4397A>C
AA Mutation	p.Lys1466Thr(p.K1466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54629622:54629622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2488C>T
AA Mutation	p.Arg830Trp(p.R830W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54632739:54632739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3738C>G
AA Mutation	p.Ile1246Met(p.I1246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54631045:54631045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2998G>A
AA Mutation	p.Gly1000Ser(p.G1000S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54624824:54624824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203A>C
AA Mutation	p.Lys401Asn(p.K401N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54625983:54625983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393G>A
AA Mutation	p.Glu465Lys(p.E465K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54631198:54631198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3151C>A
AA Mutation	p.Leu1051Met(p.L1051M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000356805
Start	54643052:54643052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3928C>T
AA Mutation	p.His1310Tyr(p.H1310Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54629198:54629198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749471660
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54631362:54631362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3315G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54628243:54628243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551964268
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54668386:54668386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147084588
CDS Mutation	c.6912C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54612262:54612262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765480147
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54653683:54653683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5652G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54666041:54666041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773456466
CDS Mutation	c.6786C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54668449:54668449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779397892
CDS Mutation	c.6975C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54647244:54647244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748639736
CDS Mutation	c.4980C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54629132:54629132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773513812
CDS Mutation	c.1998C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54668473:54668473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199584027
CDS Mutation	c.6999C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356805
Start	54631119:54631119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3072C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356805
Start	54631333:54631340(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3288_3295delGGCTGAGA
AA Mutation	p.Glu1098AlafsTer86(p.E1098Afs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356805
Start	54668558:54668558(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7088delA
AA Mutation	p.Lys2363ArgfsTer59(p.K2363Rfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356805
Start	54637744:54637744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3799delC
AA Mutation	p.Leu1267PhefsTer2(p.L1267Ffs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript