Mutation

Primary Site >> Stomach Cancer

Gene >> SORBS2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185624044:185624044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284776
Start	185662104:185662104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Asp32Asn(p.D32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185649545:185649545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139060966
CDS Mutation	c.491C>T
AA Mutation	p.Ala164Val(p.A164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185662133:185662133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65G>A
AA Mutation	p.Ser22Asn(p.S22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185657548:185657548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143C>G
AA Mutation	p.Thr48Ser(p.T48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185614955:185614955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2759T>G
AA Mutation	p.Leu920Arg(p.L920R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185622932:185622932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2485C>T
AA Mutation	p.Arg829Cys(p.R829C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185623087:185623087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376831365
CDS Mutation	c.2330C>T
AA Mutation	p.Ala777Val(p.A777V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185623468:185623468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562339021
CDS Mutation	c.1949A>G
AA Mutation	p.His650Arg(p.H650R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185620140:185620140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376740726
CDS Mutation	c.2515C>T
AA Mutation	p.Pro839Ser(p.P839S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185623325:185623325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2092G>A
AA Mutation	p.Ala698Thr(p.A698T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185624000:185624000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548721156
CDS Mutation	c.1417G>A
AA Mutation	p.Val473Met(p.V473M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185623817:185623817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752193024
CDS Mutation	c.1600G>A
AA Mutation	p.Val534Ile(p.V534I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185624348:185624348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069G>A
AA Mutation	p.Gly357Ser(p.G357S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185657465:185657465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778612065
CDS Mutation	c.226G>A
AA Mutation	p.Gly76Arg(p.G76R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000284776
Start	185611910:185611910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2954G>T
AA Mutation	p.Arg985Ile(p.R985I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185623461:185623461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1956C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185624373:185624373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185611906:185611906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2958A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185614921:185614921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2793A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185623614:185623614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140964722
CDS Mutation	c.1803C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284776
Start	185624295:185624295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532554332
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185624326:185624326(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1091delA
AA Mutation	p.Asn364ThrfsTer25(p.N364Tfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185593890:185593890(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3130delG
AA Mutation	p.Glu1044AsnfsTer65(p.E1044Nfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185657531:185657531(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.160delC
AA Mutation	p.Leu54CysfsTer11(p.L54Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185623285:185623285(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754977280
CDS Mutation	c.2132delA
AA Mutation	p.Asn711IlefsTer65(p.N711Ifs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185623725:185623725(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1692delC
AA Mutation	p.Ala565LeufsTer49(p.A565Lfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284776
Start	185589702:185589702(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3218delA
AA Mutation	p.Lys1073SerfsTer36(p.K1073Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript