Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> UTP20

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101372954:101372954(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6869C>T
AA Mutation p.Ala2290Val(p.A2290V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101286398:101286398(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147399996
CDS Mutation c.404C>T
AA Mutation p.Ser135Leu(p.S135L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101305983:101305983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1850G>A
AA Mutation p.Gly617Asp(p.G617D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101329372:101329372(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750578552
CDS Mutation c.3340G>A
AA Mutation p.Ala1114Thr(p.A1114T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101290225:101290225(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.686T>G
AA Mutation p.Phe229Cys(p.F229C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101383049:101383049(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7665G>T
AA Mutation p.Lys2555Asn(p.K2555N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101373426:101373426(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6904T>A
AA Mutation p.Ser2302Thr(p.S2302T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101383062:101383062(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770137347
CDS Mutation c.7678G>A
AA Mutation p.Ala2560Thr(p.A2560T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101281155:101281155(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.85G>A
AA Mutation p.Asp29Asn(p.D29N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101366605:101366605(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6173G>T
AA Mutation p.Cys2058Phe(p.C2058F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101363690:101363690(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759472914
CDS Mutation c.5905G>A
AA Mutation p.Gly1969Ser(p.G1969S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101371149:101371149(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6779C>T
AA Mutation p.Ala2260Val(p.A2260V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101379419:101379419(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7445C>T
AA Mutation p.Thr2482Ile(p.T2482I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101379487:101379487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7513A>G
AA Mutation p.Thr2505Ala(p.T2505A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101356987:101356987(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778767258
CDS Mutation c.5596C>T
AA Mutation p.Arg1866Cys(p.R1866C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101367969:101367969(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6377A>G
AA Mutation p.Asp2126Gly(p.D2126G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101285799:101285799(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.244G>A
AA Mutation p.Val82Met(p.V82M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101312056:101312056(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2332A>T
AA Mutation p.Met778Leu(p.M778L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101354868:101354868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5144C>T
AA Mutation p.Ala1715Val(p.A1715V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101338131:101338131(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140749743
CDS Mutation c.3722C>T
AA Mutation p.Ala1241Val(p.A1241V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101285588:101285588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.145T>G
AA Mutation p.Phe49Val(p.F49V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101309772:101309772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2164C>T
AA Mutation p.Arg722Cys(p.R722C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101281126:101281126(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777483339
CDS Mutation c.56T>G
AA Mutation p.Phe19Cys(p.F19C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101329309:101329309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552660501
CDS Mutation c.3277C>T
AA Mutation p.Arg1093Cys(p.R1093C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101342983:101342983(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199880162
CDS Mutation c.4339G>A
AA Mutation p.Asp1447Asn(p.D1447N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101352151:101352151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4981C>A
AA Mutation p.His1661Asn(p.H1661N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101370549:101370549(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6673T>G
AA Mutation p.Phe2225Val(p.F2225V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101344717:101344717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4572G>T
AA Mutation p.Glu1524Asp(p.E1524D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101361978:101361978(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5708T>G
AA Mutation p.Phe1903Cys(p.F1903C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101375657:101375657(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771120382
CDS Mutation c.7297C>T
AA Mutation p.Arg2433Cys(p.R2433C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101383266:101383266(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752995039
CDS Mutation c.7882C>T
AA Mutation p.Arg2628Trp(p.R2628W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101365517:101365517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756791850
CDS Mutation c.6017G>A
AA Mutation p.Arg2006Gln(p.R2006Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101295572:101295572(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1344G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101338159:101338159(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3750T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101343012:101343012(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4368C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101295530:101295530(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1302T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101312043:101312043(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2319A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101383569:101383569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7956C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101317616:101317616(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2691C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101317562:101317562(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138126922
CDS Mutation c.2637C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101373692:101373692(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7056C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101373416:101373416(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201584446
CDS Mutation c.6894C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000261637
Start 101286412:101286412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.418C>T
AA Mutation p.Gln140Ter(p.Q140*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000261637
Start 101356617:101356617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747880391
CDS Mutation c.5458C>T
AA Mutation p.Arg1820Ter(p.R1820*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000261637
Start 101288984:101288985(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.546dupA
AA Mutation p.Leu183ThrfsTer9(p.L183Tfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000261637
Start 101356982:101356983(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5591_5592insATCCTTTAGTC
AA Mutation p.Ala1865SerfsTer12(p.A1865Sfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> UTP20

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101317637:101317637(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2712G>T
AA Mutation p.Lys904Asn(p.K904N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101342476:101342476(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4132C>A
AA Mutation p.Gln1378Lys(p.Q1378K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101365513:101365513(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143153802
CDS Mutation c.6013C>T
AA Mutation p.Arg2005Cys(p.R2005C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101308239:101308239(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2050C>T
AA Mutation p.Leu684Phe(p.L684F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101334445:101334445(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3582G>T
AA Mutation p.Glu1194Asp(p.E1194D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101379433:101379433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7459T>G
AA Mutation p.Phe2487Val(p.F2487V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261637
Start 101334492:101334492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3629G>A
AA Mutation p.Ser1210Asn(p.S1210N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101371093:101371093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6723C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101352184:101352184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5014C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000261637
Start 101342952:101342952(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751110666
CDS Mutation c.4308C>T
Mutation Classification Silent
Feature Type Transcript