Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP1A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522354:43522354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.881C>T
AA Mutation p.Ala294Val(p.A294V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522697:43522697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1224G>T
AA Mutation p.Lys408Asn(p.K408N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43524270:43524270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369269035
CDS Mutation c.2797T>C
AA Mutation p.Ser933Pro(p.S933P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43527298:43527298(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746342958
CDS Mutation c.5825C>T
AA Mutation p.Ala1942Val(p.A1942V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43524421:43524421(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763883565
CDS Mutation c.2948G>A
AA Mutation p.Arg983Gln(p.R983Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43524065:43524065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2592G>T
AA Mutation p.Lys864Asn(p.K864N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43523826:43523826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2353G>A
AA Mutation p.Glu785Lys(p.E785K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43526101:43526101(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4628T>C
AA Mutation p.Val1543Ala(p.V1543A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522316:43522316(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.843A>C
AA Mutation p.Glu281Asp(p.E281D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522321:43522321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.848T>A
AA Mutation p.Leu283His(p.L283H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43523493:43523493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376517161
CDS Mutation c.2020G>A
AA Mutation p.Ala674Thr(p.A674T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43525627:43525627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4154C>T
AA Mutation p.Thr1385Ile(p.T1385I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43527781:43527781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6308A>G
AA Mutation p.Asp2103Gly(p.D2103G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43529805:43529805(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8191G>A
AA Mutation p.Glu2731Lys(p.E2731K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43528767:43528767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7294G>T
AA Mutation p.Ala2432Ser(p.A2432S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43526842:43526842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762403007
CDS Mutation c.5369G>A
AA Mutation p.Arg1790His(p.R1790H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522714:43522714(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746796501
CDS Mutation c.1241A>G
AA Mutation p.Glu414Gly(p.E414G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43524768:43524768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3295G>A
AA Mutation p.Val1099Ile(p.V1099I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43523422:43523422(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1949A>G
AA Mutation p.Glu650Gly(p.E650G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43525453:43525453(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3980C>T
AA Mutation p.Pro1327Leu(p.P1327L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43526784:43526784(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5311C>T
AA Mutation p.Arg1771Cys(p.R1771C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522942:43522942(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750529589
CDS Mutation c.1469G>A
AA Mutation p.Arg490His(p.R490H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43530094:43530094(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759132366
CDS Mutation c.8282C>T
AA Mutation p.Thr2761Met(p.T2761M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522321:43522321(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.848T>G
AA Mutation p.Leu283Arg(p.L283R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43528441:43528441(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6968G>T
AA Mutation p.Ser2323Ile(p.S2323I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43525117:43525117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3644A>T
AA Mutation p.Lys1215Met(p.K1215M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43525141:43525141(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3668G>A
AA Mutation p.Gly1223Asp(p.G1223D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43528731:43528731(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200292939
CDS Mutation c.7258G>A
AA Mutation p.Gly2420Arg(p.G2420R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43525094:43525094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3621G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43522415:43522415(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.942A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43528190:43528190(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6717T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43521836:43521836(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs552869456
CDS Mutation c.363C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43527971:43527971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6498A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43526723:43526723(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5250C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43524770:43524770(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3297C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43526603:43526603(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5130C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43525975:43525975(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4506delA
AA Mutation p.Val1503SerfsTer16(p.V1503Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43527660:43527660(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6193delC
AA Mutation p.Arg2065ValfsTer5(p.R2065Vfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43526107:43526107(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4637delA
AA Mutation p.Lys1546ArgfsTer6(p.K1546Rfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43528722:43528722(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7253delG
AA Mutation p.Gly2418AlafsTer36(p.G2418Afs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43528844:43528845(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.7376dupC
AA Mutation p.Ser2460IlefsTer4(p.S2460Ifs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43527180:43527181(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.5713dupC
AA Mutation p.Leu1905ProfsTer9(p.L1905Pfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 43
Mutation Consequence inframe_insertion
Transcription ID ENST00000300231
Start 43524039:43524040(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2567_2568insAGGGAGCTCTTGCCTGTC
AA Mutation p.Ala856_Pro857insGlySerSerCysLeuSer(p.A856_P857insGSSCLS)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> MAP1A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43521603:43521603(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.130C>T
AA Mutation p.Pro44Ser(p.P44S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43525413:43525413(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3940G>A
AA Mutation p.Glu1314Lys(p.E1314K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43523713:43523713(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2240A>G
AA Mutation p.Glu747Gly(p.E747G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522291:43522291(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.818A>C
AA Mutation p.Gln273Pro(p.Q273P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43521494:43521494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.21C>A
AA Mutation p.Phe7Leu(p.F7L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43526093:43526093(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4620G>T
AA Mutation p.Lys1540Asn(p.K1540N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43526418:43526418(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4945G>A
AA Mutation p.Glu1649Lys(p.E1649K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43527442:43527442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5969T>G
AA Mutation p.Leu1990Arg(p.L1990R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000300231
Start 43522323:43522323(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768730706
CDS Mutation c.850C>T
AA Mutation p.Arg284Trp(p.R284W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43522163:43522163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.690G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43525556:43525556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4083G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43522061:43522061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.588C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000300231
Start 43525211:43525211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3738C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000300231
Start 43524366:43524379(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2893_2906delGCCCCTGGGCATGC
AA Mutation p.Ala965ProfsTer17(p.A965Pfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000300231
Start 43523229:43523229(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1756G>T
AA Mutation p.Glu586Ter(p.E586*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript