Mutation

Primary Site >> Stomach Cancer

Gene >> CUL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148730217:148730217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95A>G
AA Mutation	p.Tyr32Cys(p.Y32C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148792775:148792775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856C>T
AA Mutation	p.Ala619Val(p.A619V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148792759:148792759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1840T>C
AA Mutation	p.Tyr614His(p.Y614H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148730159:148730159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37A>C
AA Mutation	p.Lys13Gln(p.K13Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148767684:148767684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018T>G
AA Mutation	p.Leu340Val(p.L340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148800560:148800560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309A>G
AA Mutation	p.Asp770Gly(p.D770G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148788651:148788651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574T>C
AA Mutation	p.Leu525Ser(p.L525S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148798661:148798661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2120G>A
AA Mutation	p.Arg707His(p.R707H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148788593:148788593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516C>A
AA Mutation	p.Arg506Ser(p.R506S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000325222
Start	148799276:148799276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138C>T
AA Mutation	p.Ala713Val(p.A713V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148800523:148800523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2272G>C
AA Mutation	p.Glu758Gln(p.E758Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148787032:148787032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391A>C
AA Mutation	p.Lys464Thr(p.K464T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148788594:148788594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148787101:148787101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460G>A
AA Mutation	p.Ser487Asn(p.S487N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148757103:148757103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436C>T
AA Mutation	p.Arg146Cys(p.R146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000325222
Start	148757106:148757106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Cys(p.R147C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325222
Start	148787087:148787087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774670924
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325222
Start	148790375:148790375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764499381
CDS Mutation	c.1740G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325222
Start	148788565:148788565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750560055
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325222
Start	148792758:148792758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761975125
CDS Mutation	c.1839G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325222
Start	148760439:148760440(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.734_776dupCCAGAGAGAGTACTGAATTCTTGCAGCAGAACCCAGTTACTGA
AA Mutation	p.Glu259AspfsTer6(p.E259Dfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325222
Start	148767674:148767675(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1014dupA
AA Mutation	p.Leu339ThrfsTer8(p.L339Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325222
Start	148759302:148759302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	24
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325222
Start	148756982:148756982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000325222
Start	148759356:148759356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript