Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MYH9

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36292110:36292110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4220C>T
AA Mutation p.Ala1407Val(p.A1407V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36304080:36304080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2305G>A
AA Mutation p.Ala769Thr(p.A769T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36284123:36284123(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5735G>A
AA Mutation p.Arg1912His(p.R1912H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36322451:36322451(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772134801
CDS Mutation c.683A>G
AA Mutation p.Lys228Arg(p.K228R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36285738:36285738(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5194G>A
AA Mutation p.Ala1732Thr(p.A1732T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36284501:36284501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5494G>A
AA Mutation p.Ala1832Thr(p.A1832T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36299037:36299037(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2982G>T
AA Mutation p.Lys994Asn(p.K994N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36285290:36285290(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5314C>A
AA Mutation p.His1772Asn(p.H1772N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36285926:36285926(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372871106
CDS Mutation c.5089C>T
AA Mutation p.Arg1697Cys(p.R1697C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36292024:36292024(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373912645
CDS Mutation c.4306G>A
AA Mutation p.Ala1436Thr(p.A1436T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36296901:36296901(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532156048
CDS Mutation c.3214G>A
AA Mutation p.Ala1072Thr(p.A1072T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36282691:36282691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5860G>A
AA Mutation p.Ala1954Thr(p.A1954T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36288905:36288905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4592A>T
AA Mutation p.Glu1531Val(p.E1531V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36349061:36349061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176T>C
AA Mutation p.Val59Ala(p.V59A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36286804:36286804(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371410108
CDS Mutation c.4975G>A
AA Mutation p.Ala1659Thr(p.A1659T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36326596:36326596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.584C>T
AA Mutation p.Ala195Val(p.A195V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36284422:36284422(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5573C>T
AA Mutation p.Ala1858Val(p.A1858V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36284449:36284449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5546T>C
AA Mutation p.Leu1849Pro(p.L1849P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36293787:36293787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141904682
CDS Mutation c.3914C>T
AA Mutation p.Ala1305Val(p.A1305V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36314177:36314177(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1522C>A
AA Mutation p.Leu508Met(p.L508M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36320330:36320330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.902G>A
AA Mutation p.Arg301His(p.R301H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000216181
Start 36316518:36316518(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1379A>G
AA Mutation p.Asp460Gly(p.D460G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36293820:36293820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3881G>A
AA Mutation p.Ser1294Asn(p.S1294N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000216181
Start 36302568:36302568(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2499G>T
AA Mutation p.Lys833Asn(p.K833N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36349212:36349212(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.25T>C
AA Mutation p.Tyr9His(p.Y9H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36316617:36316617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760489771
CDS Mutation c.1280G>A
AA Mutation p.Arg427His(p.R427H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36318256:36318256(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202023656
CDS Mutation c.1178G>A
AA Mutation p.Arg393His(p.R393H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36348965:36348965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.272G>A
AA Mutation p.Cys91Tyr(p.C91Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36301009:36301009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2680G>A
AA Mutation p.Glu894Lys(p.E894K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36348927:36348927(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.310C>T
AA Mutation p.Arg104Cys(p.R104C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36294132:36294132(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375738970
CDS Mutation c.3797G>A
AA Mutation p.Arg1266His(p.R1266H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36320343:36320343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.889T>C
AA Mutation p.Tyr297His(p.Y297H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36300915:36300915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2774A>T
AA Mutation p.Glu925Val(p.E925V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36316595:36316595(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1302C>G
AA Mutation p.Asn434Lys(p.N434K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36285758:36285758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5174G>A
AA Mutation p.Arg1725Gln(p.R1725Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36297005:36297005(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3110G>A
AA Mutation p.Arg1037His(p.R1037H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36284436:36284436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775990931
CDS Mutation c.5559C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36288826:36288826(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4671G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36288820:36288820(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4677G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36293807:36293807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3894G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36288853:36288853(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765280741
CDS Mutation c.4644G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36341392:36341392(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs727503293
CDS Mutation c.468C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36319559:36319559(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768508765
CDS Mutation c.1089G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36326595:36326595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374395918
CDS Mutation c.585G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36305045:36305045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2217G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence frameshift_variant
Transcription ID ENST00000216181
Start 36304036:36304036(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2349delC
AA Mutation p.Ile784Ter(p.I784*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 47
Mutation Consequence stop_gained
Transcription ID ENST00000216181
Start 36294943:36294943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3619C>T
AA Mutation p.Gln1207Ter(p.Q1207*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 48
Mutation Consequence stop_gained
Transcription ID ENST00000216181
Start 36305973:36305973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2116C>T
AA Mutation p.Gln706Ter(p.Q706*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 49
Mutation Consequence splice_donor_variant
Transcription ID ENST00000216181
Start 36305928:36305928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2159+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 50
Mutation Consequence splice_donor_variant
Transcription ID ENST00000216181
Start 36322428:36322428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.705+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 51
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000216181
Start 36320364:36320364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 52
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000216181
Start 36294300:36294300(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3631-2A>G
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 53
Mutation Consequence inframe_insertion
Transcription ID ENST00000216181
Start 36316594:36316595(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1302_1303insGAT
AA Mutation p.Asn434_Lys435insAsp(p.N434_K435insD)
Mutation Classification In_Frame_Ins
Feature Type Transcript
Mutation ID 54
Mutation Consequence inframe_insertion
Transcription ID ENST00000216181
Start 36300867:36300868(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2819_2821dupAGA
AA Mutation p.Lys940dup(p.K940dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> MYH9

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36288281:36288281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4903G>A
AA Mutation p.Glu1635Lys(p.E1635K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36288332:36288332(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771657500
CDS Mutation c.4852G>T
AA Mutation p.Asp1618Tyr(p.D1618Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000216181
Start 36293464:36293464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3960G>T
AA Mutation p.Glu1320Asp(p.E1320D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36349065:36349065(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.172C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000216181
Start 36293789:36293789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3912C>T
Mutation Classification Silent
Feature Type Transcript