Mutation

Primary Site >> Stomach Cancer

Gene >> CUX1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102170532:102170532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>G
AA Mutation	p.Ile270Met(p.I270M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102201743:102201743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2446C>T
AA Mutation	p.Arg816Cys(p.R816C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102196724:102196724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313C>T
AA Mutation	p.Pro438Leu(p.P438L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102248953:102248953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4429C>A
AA Mutation	p.Arg1477Ser(p.R1477S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000437600
Start	102278006:102278006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782760993
CDS Mutation	c.1621C>T
AA Mutation	p.Arg541Cys(p.R541C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102193855:102193855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090A>G
AA Mutation	p.Met364Val(p.M364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102201389:102201389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782786732
CDS Mutation	c.2092G>A
AA Mutation	p.Gly698Ser(p.G698S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102227415:102227415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3179C>T
AA Mutation	p.Pro1060Leu(p.P1060L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102195511:102195511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130C>T
AA Mutation	p.Ala377Val(p.A377V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000437600
Start	102278055:102278055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670A>G
AA Mutation	p.Tyr557Cys(p.Y557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	101916128:101916128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Ala15Val(p.A15V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000437600
Start	102273491:102273491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782181844
CDS Mutation	c.1381G>A
AA Mutation	p.Glu461Lys(p.E461K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102178630:102178630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990G>T
AA Mutation	p.Gln330His(p.Q330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102201617:102201617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141755950
CDS Mutation	c.2320G>A
AA Mutation	p.Gly774Ser(p.G774S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102227637:102227637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782309779
CDS Mutation	c.3401G>A
AA Mutation	p.Arg1134Gln(p.R1134Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	102204500:102204500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3017T>C
AA Mutation	p.Leu1006Pro(p.L1006P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000292535
Start	101916145:101916145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000437600
Start	102274293:102274293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433C>T
AA Mutation	p.Ala478Val(p.A478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102196692:102196692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782186138
CDS Mutation	c.1281G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102202195:102202195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782042169
CDS Mutation	c.2898C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102201838:102201838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375527499
CDS Mutation	c.2541C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102196680:102196680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570594920
CDS Mutation	c.1269G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102201835:102201835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115507543
CDS Mutation	c.2538G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000437600
Start	102280054:102280054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1698C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102178519:102178519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139114802
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	101916189:101916189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145317607
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292535
Start	102201826:102201826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102195519:102195519(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1141delC
AA Mutation	p.Leu381TrpfsTer26(p.L381Wfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102196694:102196694(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1289delC
AA Mutation	p.Pro430LeufsTer27(p.P430Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102196725:102196725(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1318delG
AA Mutation	p.Glu440SerfsTer17(p.E440Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102227471:102227471(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3240delC
AA Mutation	p.Ile1081SerfsTer39(p.I1081Sfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102201637:102201637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2345delC
AA Mutation	p.Pro782ArgfsTer26(p.P782Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000292535
Start	102201485:102201485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188C>T
AA Mutation	p.Gln730Ter(p.Q730*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102227503:102227504(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3269dupC
AA Mutation	p.Glu1091ArgfsTer4(p.E1091Rfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102196693:102196694(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs782381199
CDS Mutation	c.1289dupC
AA Mutation	p.Pro431SerfsTer16(p.P431Sfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292535
Start	102202023:102202024(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2731dupC
AA Mutation	p.Leu911ProfsTer43(p.L911Pfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	37
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000292535
Start	102193892:102193892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript