Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZEB2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398596:144398596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2591T>G
AA Mutation p.Phe864Cys(p.F864C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144401218:144401218(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.897A>C
AA Mutation p.Glu299Asp(p.E299D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404885:144404885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.543G>T
AA Mutation p.Glu181Asp(p.E181D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399905:144399905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761671566
CDS Mutation c.1282G>A
AA Mutation p.Val428Ile(p.V428I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144401210:144401210(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs730881174
CDS Mutation c.905G>A
AA Mutation p.Arg302Gln(p.R302Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144403965:144403965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.758G>A
AA Mutation p.Arg253His(p.R253H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144517304:144517304(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.47A>G
AA Mutation p.Lys16Arg(p.K16R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000409487
Start 144403917:144403917(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.806A>C
AA Mutation p.Gln269Pro(p.Q269P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399772:144399772(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1415C>A
AA Mutation p.Ser472Tyr(p.S472Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400065:144400065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1122G>T
AA Mutation p.Glu374Asp(p.E374D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404070:144404070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.653G>A
AA Mutation p.Arg218Gln(p.R218Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144403953:144403953(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.770A>T
AA Mutation p.Glu257Val(p.E257V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404961:144404961(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.467G>A
AA Mutation p.Arg156His(p.R156H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144389923:144389923(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3173A>C
AA Mutation p.Asp1058Ala(p.D1058A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399452:144399452(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1735A>T
AA Mutation p.Thr579Ser(p.T579S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144389809:144389809(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3287G>A
AA Mutation p.Arg1096His(p.R1096H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400171:144400171(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1016C>A
AA Mutation p.Ser339Tyr(p.S339Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399311:144399311(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs727504224
CDS Mutation c.1876G>A
AA Mutation p.Gly626Arg(p.G626R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399929:144399929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1258C>T
AA Mutation p.Leu420Phe(p.L420F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404020:144404020(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.703G>A
AA Mutation p.Glu235Lys(p.E235K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399737:144399737(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1450T>G
AA Mutation p.Ser484Ala(p.S484A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400108:144400108(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1079C>A
AA Mutation p.Ser360Tyr(p.S360Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398825:144398825(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2362C>A
AA Mutation p.Leu788Ile(p.L788I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144389803:144389803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3293A>C
AA Mutation p.Lys1098Thr(p.K1098T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144389827:144389827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3269C>T
AA Mutation p.Ala1090Val(p.A1090V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399635:144399635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1552C>T
AA Mutation p.His518Tyr(p.H518Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144517324:144517324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.27C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144389664:144389664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768007761
CDS Mutation c.3432C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144399561:144399561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1626C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144399351:144399351(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754916469
CDS Mutation c.1836G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144399528:144399528(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1659T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144399687:144399687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1500A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144398352:144398352(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2835T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000409487
Start 144398477:144398478(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2709_2710insATCCTTG
AA Mutation p.Phe904IlefsTer47(p.F904Ifs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> ZEB2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399008:144399008(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2179T>G
AA Mutation p.Leu727Val(p.L727V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144401220:144401220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.895G>A
AA Mutation p.Glu299Lys(p.E299K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144517308:144517308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.43C>T
AA Mutation p.Arg15Cys(p.R15C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404938:144404938(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771155056
CDS Mutation c.490G>A
AA Mutation p.Glu164Lys(p.E164K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400159:144400159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746958005
CDS Mutation c.1028G>A
AA Mutation p.Arg343Gln(p.R343Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399352:144399352(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1835C>T
AA Mutation p.Ala612Val(p.A612V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144399724:144399724(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1463G>A
AA Mutation p.Gly488Asp(p.G488D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398921:144398921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2266C>T
AA Mutation p.Pro756Ser(p.P756S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398308:144398308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2879G>A
AA Mutation p.Gly960Glu(p.G960E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398318:144398318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2869C>T
AA Mutation p.Arg957Trp(p.R957W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144398329:144398329(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2858G>T
AA Mutation p.Arg953Ile(p.R953I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400001:144400001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186G>A
AA Mutation p.Asp396Asn(p.D396N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144400207:144400207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.980C>T
AA Mutation p.Ser327Leu(p.S327L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144404982:144404982(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.446C>T
AA Mutation p.Ala149Val(p.A149V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000409487
Start 144429971:144429971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.129G>T
AA Mutation p.Lys43Asn(p.K43N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000409487
Start 144400161:144400161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1026C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000409487
Start 144404842:144404842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.586G>T
AA Mutation p.Glu196Ter(p.E196*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript