Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLX4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3591199:3591199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2439G>T
AA Mutation p.Glu813Asp(p.E813D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3590331:3590331(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200708159
CDS Mutation c.3307C>T
AA Mutation p.Arg1103Cys(p.R1103C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597432:3597432(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1630G>T
AA Mutation p.Asp544Tyr(p.D544Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3590732:3590732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2906G>T
AA Mutation p.Arg969Ile(p.R969I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3602215:3602215(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.853G>T
AA Mutation p.Asp285Tyr(p.D285Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589962:3589962(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142008398
CDS Mutation c.3676C>T
AA Mutation p.Arg1226Trp(p.R1226W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3606525:3606525(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199912910
CDS Mutation c.709C>T
AA Mutation p.Arg237Trp(p.R237W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597941:3597941(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758029323
CDS Mutation c.1222C>T
AA Mutation p.Arg408Trp(p.R408W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3584784:3584784(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4724A>G
AA Mutation p.Lys1575Arg(p.K1575R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3582556:3582556(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5291C>T
AA Mutation p.Pro1764Leu(p.P1764L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3590823:3590823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2815C>T
AA Mutation p.Arg939Trp(p.R939W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3608480:3608480(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140876043
CDS Mutation c.485C>T
AA Mutation p.Thr162Met(p.T162M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3591291:3591291(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771580450
CDS Mutation c.2347G>A
AA Mutation p.Val783Ile(p.V783I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589299:3589299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4339G>T
AA Mutation p.Gly1447Cys(p.G1447C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597389:3597389(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773558127
CDS Mutation c.1673G>A
AA Mutation p.Arg558Gln(p.R558Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589961:3589961(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748607152
CDS Mutation c.3677G>A
AA Mutation p.Arg1226Gln(p.R1226Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3608726:3608726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.239C>T
AA Mutation p.Ala80Val(p.A80V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589736:3589736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3902G>A
AA Mutation p.Gly1301Glu(p.G1301E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589917:3589917(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771835799
CDS Mutation c.3721C>T
AA Mutation p.Arg1241Cys(p.R1241C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589047:3589047(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4591C>T
AA Mutation p.Pro1531Ser(p.P1531S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3583332:3583332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4918G>T
AA Mutation p.Gly1640Trp(p.G1640W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597913:3597913(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1250C>A
AA Mutation p.Pro417Gln(p.P417Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589971:3589971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3667C>T
AA Mutation p.Pro1223Ser(p.P1223S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3590647:3590647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770736311
CDS Mutation c.2991G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3590860:3590860(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375872764
CDS Mutation c.2778C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3602147:3602147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370468973
CDS Mutation c.921C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3589108:3589108(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139254595
CDS Mutation c.4530G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3589798:3589798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767189475
CDS Mutation c.3840C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3582639:3582639(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569225834
CDS Mutation c.5208C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3582465:3582465(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368848191
CDS Mutation c.5382G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3590341:3590341(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3297A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3590698:3590698(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2940C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3589042:3589042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527733303
CDS Mutation c.4596C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3591301:3591301(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2337G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000294008
Start 3589397:3589397(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs748691881
CDS Mutation c.4241delC
AA Mutation p.Pro1414HisfsTer36(p.P1414Hfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000294008
Start 3589379:3589379(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4259delC
AA Mutation p.Pro1420GlnfsTer30(p.P1420Qfs*30)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> SLX4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3582512:3582512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5335C>T
AA Mutation p.Arg1779Trp(p.R1779W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3589899:3589899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3739G>A
AA Mutation p.Glu1247Lys(p.E1247K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597467:3597467(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1595A>T
AA Mutation p.Glu532Val(p.E532V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3590478:3590478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3160T>A
AA Mutation p.Ser1054Thr(p.S1054T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3590007:3590007(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202032197
CDS Mutation c.3631G>A
AA Mutation p.Glu1211Lys(p.E1211K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3597570:3597570(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1492T>A
AA Mutation p.Ser498Thr(p.S498T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000294008
Start 3602139:3602139(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759447034
CDS Mutation c.929G>A
AA Mutation p.Arg310Gln(p.R310Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3597526:3597526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1536G>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3590611:3590611(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3027C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3591292:3591292(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775150046
CDS Mutation c.2346C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000294008
Start 3582468:3582468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5379C>A
Mutation Classification Silent
Feature Type Transcript