Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNRC6A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24793576:24793576(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3279A>C
AA Mutation p.Glu1093Asp(p.E1093D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24822892:24822892(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5392C>T
AA Mutation p.Arg1798Cys(p.R1798C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790144:24790144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1502G>T
AA Mutation p.Gly501Val(p.G501V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24804733:24804733(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3866A>G
AA Mutation p.Asn1289Ser(p.N1289S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791632:24791632(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368712374
CDS Mutation c.2990G>A
AA Mutation p.Arg997His(p.R997H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777269:24777269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.500A>C
AA Mutation p.Lys167Thr(p.K167T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24789668:24789668(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1026G>A
AA Mutation p.Met342Ile(p.M342I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791298:24791298(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767104641
CDS Mutation c.2656G>A
AA Mutation p.Gly886Ser(p.G886S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791353:24791353(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2711C>T
AA Mutation p.Pro904Leu(p.P904L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24823634:24823634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5716T>C
AA Mutation p.Ser1906Pro(p.S1906P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790951:24790951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2309C>T
AA Mutation p.Thr770Ile(p.T770I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790992:24790992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2350G>T
AA Mutation p.Gly784Cys(p.G784C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791646:24791646(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3004G>A
AA Mutation p.Asp1002Asn(p.D1002N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24823458:24823458(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5540T>A
AA Mutation p.Leu1847His(p.L1847H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24750781:24750781(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758665959
CDS Mutation c.109G>A
AA Mutation p.Asp37Asn(p.D37N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24789537:24789537(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.895A>G
AA Mutation p.Ser299Gly(p.S299G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777185:24777185(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs563907833
CDS Mutation c.416G>A
AA Mutation p.Arg139Gln(p.R139Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24823766:24823766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5848C>A
AA Mutation p.Leu1950Ile(p.L1950I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24818649:24818649(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5029C>T
AA Mutation p.Arg1677Cys(p.R1677C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777281:24777281(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.512G>T
AA Mutation p.Ser171Ile(p.S171I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24816855:24816855(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4871T>C
AA Mutation p.Ile1624Thr(p.I1624T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24789691:24789691(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1049C>A
AA Mutation p.Ser350Tyr(p.S350Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791326:24791326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2684C>T
AA Mutation p.Ser895Phe(p.S895F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791086:24791086(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768793572
CDS Mutation c.2444A>G
AA Mutation p.Lys815Arg(p.K815R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790811:24790811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2169G>T
AA Mutation p.Trp723Cys(p.W723C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24793588:24793588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3291G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24820344:24820344(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778604090
CDS Mutation c.5286C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24793606:24793606(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768040697
CDS Mutation c.3309G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000395799
Start 24777339:24777339(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749183774
CDS Mutation c.570G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24789434:24789435(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.797_798delGA
AA Mutation p.Arg266LysfsTer13(p.R266Kfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000395799
Start 24793488:24793488(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3196delG
AA Mutation p.Glu1066SerfsTer20(p.E1066Sfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000395799
Start 24805071:24805071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4042C>T
AA Mutation p.Gln1348Ter(p.Q1348*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence inframe_deletion
Transcription ID ENST00000395799
Start 24790570:24790572(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1930_1932delACT
AA Mutation p.Thr644del(p.T644del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> TNRC6A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777190:24777190(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758756773
CDS Mutation c.421C>T
AA Mutation p.Arg141Cys(p.R141C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24804795:24804795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3928C>G
AA Mutation p.Gln1310Glu(p.Q1310E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24790354:24790354(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370193931
CDS Mutation c.1712G>A
AA Mutation p.Gly571Asp(p.G571D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777207:24777207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438A>C
AA Mutation p.Lys146Asn(p.K146N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791292:24791292(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139177520
CDS Mutation c.2650G>A
AA Mutation p.Val884Ile(p.V884I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24789673:24789673(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1031C>A
AA Mutation p.Ala344Asp(p.A344D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24750810:24750810(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.138G>T
AA Mutation p.Lys46Asn(p.K46N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24777067:24777067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.298C>A
AA Mutation p.Gln100Lys(p.Q100K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24809455:24809455(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4646C>A
AA Mutation p.Ser1549Tyr(p.S1549Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24820169:24820169(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5111C>T
AA Mutation p.Ser1704Phe(p.S1704F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24823680:24823680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5762C>T
AA Mutation p.Thr1921Ile(p.T1921I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24791413:24791413(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2771A>G
AA Mutation p.Asp924Gly(p.D924G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000395799
Start 24815270:24815270(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4796C>T
AA Mutation p.Ser1599Leu(p.S1599L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000395799
Start 24777184:24777184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.415C>T
AA Mutation p.Arg139Ter(p.R139*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000395799
Start 24790434:24790434(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1792C>T
AA Mutation p.Arg598Ter(p.R598*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript