Mutation

Primary Site >> Stomach Cancer

Gene >> SPTAN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128632250:128632250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6871G>A
AA Mutation	p.Ala2291Thr(p.A2291T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128566962:128566962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>G
AA Mutation	p.Asp74Glu(p.D74E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128588866:128588866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2929G>A
AA Mutation	p.Asp977Asn(p.D977N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128626611:128626611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6485T>C
AA Mutation	p.Val2162Ala(p.V2162A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128584382:128584382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765His(p.R765H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128632699:128632699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7126G>A
AA Mutation	p.Asp2376Asn(p.D2376N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128593003:128593003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3176C>T
AA Mutation	p.Ala1059Val(p.A1059V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128605303:128605303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3872C>T
AA Mutation	p.Ser1291Phe(p.S1291F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128582549:128582549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753283021
CDS Mutation	c.1643G>A
AA Mutation	p.Arg548Gln(p.R548Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128575235:128575235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541C>A
AA Mutation	p.Leu181Met(p.L181M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128625151:128625151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6026C>A
AA Mutation	p.Ser2009Tyr(p.S2009Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128632869:128632869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7207G>A
AA Mutation	p.Val2403Ile(p.V2403I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128624358:128624358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5848A>G
AA Mutation	p.Lys1950Glu(p.K1950E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128584355:128584355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2267A>C
AA Mutation	p.Lys756Thr(p.K756T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128608959:128608959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182272113
CDS Mutation	c.4577G>A
AA Mutation	p.Arg1526His(p.R1526H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128566748:128566748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>A
AA Mutation	p.Pro3Gln(p.P3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128626608:128626608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200834733
CDS Mutation	c.6482G>A
AA Mutation	p.Arg2161His(p.R2161H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128617737:128617737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777267488
CDS Mutation	c.5440G>C
AA Mutation	p.Ala1814Pro(p.A1814P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128587655:128587655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2828G>A
AA Mutation	p.Gly943Asp(p.G943D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000372731
Start	128626610:128626610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371095095
CDS Mutation	c.6484G>A
AA Mutation	p.Val2162Ile(p.V2162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128633319:128633319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375649697
CDS Mutation	c.7404G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128584482:128584482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768271102
CDS Mutation	c.2394G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128630342:128630342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140856932
CDS Mutation	c.6714G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128577411:128577411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128613401:128613401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5049C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128591500:128591500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202129574
CDS Mutation	c.3030C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128591527:128591527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759833805
CDS Mutation	c.3057G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128633238:128633238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374405583
CDS Mutation	c.7323C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128566752:128566752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128591521:128591521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140279996
CDS Mutation	c.3051G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372731
Start	128607673:128607673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148554113
CDS Mutation	c.4116C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372731
Start	128609232:128609232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4710delA
AA Mutation	p.Lys1570AsnfsTer67(p.K1570Nfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000372731
Start	128566873:128566873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Ter(p.R45*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372731
Start	128576927:128576928(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.760dupG
AA Mutation	p.Ala254GlyfsTer8(p.A254Gfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript