Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NRCAM

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108160444:108160444(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3515G>A
AA Mutation p.Gly1172Asp(p.G1172D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108149927:108149927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3898A>C
AA Mutation p.Met1300Leu(p.M1300L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108226289:108226289(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752888953
CDS Mutation c.640G>A
AA Mutation p.Glu214Lys(p.E214K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108231078:108231078(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.503G>A
AA Mutation p.Arg168Lys(p.R168K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108180258:108180258(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2816C>T
AA Mutation p.Ala939Val(p.A939V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108182905:108182905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774089913
CDS Mutation c.2320G>A
AA Mutation p.Glu774Lys(p.E774K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108180276:108180276(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2798G>T
AA Mutation p.Gly933Val(p.G933V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108184452:108184452(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2198G>T
AA Mutation p.Ser733Ile(p.S733I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108232445:108232445(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749483134
CDS Mutation c.308C>T
AA Mutation p.Thr103Met(p.T103M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108209465:108209465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031A>T
AA Mutation p.Asn344Ile(p.N344I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108194388:108194388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1504T>C
AA Mutation p.Tyr502His(p.Y502H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108182793:108182793(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766439513
CDS Mutation c.2432C>T
AA Mutation p.Thr811Met(p.T811M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108167037:108167037(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3350C>A
AA Mutation p.Ser1117Tyr(p.S1117Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108209590:108209590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.906T>G
AA Mutation p.Ile302Met(p.I302M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108197979:108197979(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1328C>T
AA Mutation p.Ala443Val(p.A443V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108166941:108166941(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3446A>T
AA Mutation p.Asp1149Val(p.D1149V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000379028
Start 108197975:108197975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1332C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000379028
Start 108191763:108191763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1869C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000379028
Start 108189730:108189730(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1950delC
AA Mutation p.Phe651LeufsTer3(p.F651Lfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000379028
Start 108209464:108209464(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1032delC
AA Mutation p.Asn344LysfsTer3(p.N344Kfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 21
Mutation Consequence stop_gained
Transcription ID ENST00000379028
Start 108166984:108166984(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201318713
CDS Mutation c.3403C>T
AA Mutation p.Arg1135Ter(p.R1135*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000379028
Start 108209463:108209464(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1032_1033insT
AA Mutation p.Ala345CysfsTer12(p.A345Cfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000379028
Start 108180368:108180369(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2705dupA
AA Mutation p.Ile903AspfsTer20(p.I903Dfs*20)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 24
Mutation Consequence inframe_insertion
Transcription ID ENST00000379028
Start 108176505:108176506(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3075_3076insCATAAACTTAAAGAT
AA Mutation p.Lys1025_Phe1026insHisLysLeuLysAsp(p.K1025_F1026insHKLKD)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> NRCAM

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108182905:108182905(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774089913
CDS Mutation c.2320G>A
AA Mutation p.Glu774Lys(p.E774K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108176522:108176522(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3059T>C
AA Mutation p.Phe1020Ser(p.F1020S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108240025:108240025(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.40G>A
AA Mutation p.Ala14Thr(p.A14T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379028
Start 108176497:108176497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3084C>A
AA Mutation p.Phe1028Leu(p.F1028L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000379028
Start 108226290:108226290(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758654630
CDS Mutation c.639C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000379028
Start 108167053:108167053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3334G>T
AA Mutation p.Glu1112Ter(p.E1112*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript