Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MYO10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701612:16701612(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747241037
CDS Mutation c.2783G>A
AA Mutation p.Arg928His(p.R928H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16704607:16704607(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200913263
CDS Mutation c.2248C>T
AA Mutation p.Arg750Trp(p.R750W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16758147:16758147(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374278677
CDS Mutation c.1819C>T
AA Mutation p.Arg607Trp(p.R607W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16779571:16779571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.904G>T
AA Mutation p.Asp302Tyr(p.D302Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16681935:16681935(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4125G>T
AA Mutation p.Trp1375Cys(p.W1375C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16794703:16794703(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.410C>T
AA Mutation p.Ala137Val(p.A137V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16681342:16681342(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142263783
CDS Mutation c.4351G>A
AA Mutation p.Val1451Ile(p.V1451I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701123:16701123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3272A>G
AA Mutation p.Tyr1091Cys(p.Y1091C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701519:16701519(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192857675
CDS Mutation c.2876G>A
AA Mutation p.Arg959Gln(p.R959Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000513610
Start 16780741:16780741(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.728A>C
AA Mutation p.Tyr243Ser(p.Y243S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701828:16701828(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561148130
CDS Mutation c.2567C>T
AA Mutation p.Thr856Met(p.T856M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16680081:16680081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4408G>A
AA Mutation p.Gly1470Arg(p.G1470R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701615:16701615(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2780T>A
AA Mutation p.Leu927His(p.L927H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000513610
Start 16762546:16762546(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753136237
CDS Mutation c.1586C>T
AA Mutation p.Ala529Val(p.A529V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16702551:16702551(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs550120876
CDS Mutation c.2548G>A
AA Mutation p.Ala850Thr(p.A850T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16674947:16674947(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4870G>A
AA Mutation p.Gly1624Ser(p.G1624S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701267:16701267(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3128C>T
AA Mutation p.Thr1043Ile(p.T1043I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16699506:16699506(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3500A>G
AA Mutation p.Asp1167Gly(p.D1167G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16680082:16680082(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781121509
CDS Mutation c.4407C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16701017:16701017(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3378G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16699487:16699487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3519C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16818105:16818105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200910595
CDS Mutation c.183C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16701419:16701419(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2976G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16681433:16681433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4260A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16685792:16685792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369230260
CDS Mutation c.3936G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16668316:16668316(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760058971
CDS Mutation c.6036C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16672718:16672718(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5280C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16681385:16681385(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775759246
CDS Mutation c.4308G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16670973:16670973(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777584439
CDS Mutation c.5436C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16701638:16701638(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2757G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000513610
Start 16672807:16672807(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771074228
CDS Mutation c.5191C>T
AA Mutation p.Arg1731Ter(p.R1731*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000513610
Start 16794755:16794755(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.358C>T
AA Mutation p.Gln120Ter(p.Q120*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000513610
Start 16762612:16762613(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1519_1520insTGTG
AA Mutation p.Asn507MetfsTer2(p.N507Mfs*2)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000513610
Start 16694504:16694505(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3666dupA
AA Mutation p.Gly1223ArgfsTer28(p.G1223Rfs*28)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000513610
Start 16763679:16763680(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1402dupT
AA Mutation p.Ser468PhefsTer8(p.S468Ffs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 36
Mutation Consequence frameshift_variant
Transcription ID ENST00000513610
Start 16762613:16762614(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1518_1519insCA
AA Mutation p.Asn507GlnfsTer30(p.N507Qfs*30)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 37
Mutation Consequence frameshift_variant
Transcription ID ENST00000513610
Start 16764326:16764327(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1249_1250insCAGAGATTTGT
AA Mutation p.Ile417ThrfsTer39(p.I417Tfs*39)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 38
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000513610
Start 16711024:16711024(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2055-2A>G
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> MYO10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16680050:16680050(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4439A>G
AA Mutation p.Lys1480Arg(p.K1480R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16702998:16702998(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2437G>C
AA Mutation p.Ala813Pro(p.A813P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16766155:16766155(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1104G>T
AA Mutation p.Gln368His(p.Q368H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16680025:16680025(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4464G>T
AA Mutation p.Trp1488Cys(p.W1488C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16679982:16679982(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4507G>A
AA Mutation p.Asp1503Asn(p.D1503N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16701403:16701403(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2992G>A
AA Mutation p.Glu998Lys(p.E998K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000513610
Start 16794796:16794796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.317A>G
AA Mutation p.Tyr106Cys(p.Y106C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16670544:16670544(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371241992
CDS Mutation c.5865G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16703140:16703140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2295C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000513610
Start 16701545:16701545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2850C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000513610
Start 16779646:16779646(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.829G>T
AA Mutation p.Glu277Ter(p.E277*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript