Mutation

Primary Site >> Stomach Cancer

Gene >> ARID1B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206912:157206912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5732G>T
AA Mutation	p.Arg1911Met(p.R1911M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157084795:157084795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563771544
CDS Mutation	c.2132C>T
AA Mutation	p.Ala711Val(p.A711V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157181110:157181110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3238G>C
AA Mutation	p.Val1080Leu(p.V1080L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157190196:157190196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3809G>T
AA Mutation	p.Gly1270Val(p.G1270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350026
Start	157201486:157201486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4853T>A
AA Mutation	p.Ile1618Asn(p.I1618N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207007:157207007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5827T>C
AA Mutation	p.Ser1943Pro(p.S1943P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157174091:157174091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3070A>G
AA Mutation	p.Thr1024Ala(p.T1024A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157203883:157203883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4873C>T
AA Mutation	p.Arg1625Cys(p.R1625C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157148740:157148740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2629C>T
AA Mutation	p.Pro877Ser(p.P877S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156935570:156935570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1992T>G
AA Mutation	p.Ser664Arg(p.S664R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157084741:157084741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762908553
CDS Mutation	c.2078C>T
AA Mutation	p.Thr693Met(p.T693M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157207803:157207803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6623G>A
AA Mutation	p.Arg2208Gln(p.R2208Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157201041:157201041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4408G>T
AA Mutation	p.Gly1470Cys(p.G1470C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157206945:157206945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5765C>T
AA Mutation	p.Ala1922Val(p.A1922V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157201056:157201056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4423C>G
AA Mutation	p.Pro1475Ala(p.P1475A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	156901403:156901403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1765G>A
AA Mutation	p.Val589Met(p.V589M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000350026
Start	157167159:157167159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750810656
CDS Mutation	c.2960C>T
AA Mutation	p.Ala987Val(p.A987V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157206622:157206622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753997383
CDS Mutation	c.5442C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207795:157207795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183572405
CDS Mutation	c.6615C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157206361:157206361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759473238
CDS Mutation	c.5181C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157207735:157207735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754242891
CDS Mutation	c.6555G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350026
Start	157190101:157190101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3714G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157206264:157206264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5088delA
AA Mutation	p.Ala1697HisfsTer56(p.A1697Hfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157206683:157206683(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5508delC
AA Mutation	p.Leu1837Ter(p.L1837*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157190195:157190195(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3812delG
AA Mutation	p.Gly1271GlufsTer2(p.G1271Efs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157207150:157207150(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749055122
CDS Mutation	c.5974delG
AA Mutation	p.Val1992TrpfsTer16(p.V1992Wfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157201056:157201056(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4427delC
AA Mutation	p.Pro1476LeufsTer5(p.P1476Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157148755:157148755(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2647delC
AA Mutation	p.Leu883TrpfsTer18(p.L883Wfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157201335:157201335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4702C>T
AA Mutation	p.Gln1568Ter(p.Q1568*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157200951:157200951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4318C>T
AA Mutation	p.Gln1440Ter(p.Q1440*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000350026
Start	157196275:157196275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3934C>T
AA Mutation	p.Gln1312Ter(p.Q1312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157201088:157201089(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4456dupA
AA Mutation	p.Met1486AsnfsTer11(p.M1486Nfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350026
Start	157084819:157084820(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2162dupG
AA Mutation	p.Ser723IlefsTer27(p.S723Ifs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	34
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000350026
Start	157167038:157167038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2841-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript