Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NCAM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113255922:113255922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1874G>T
AA Mutation p.Gly625Val(p.G625V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204360:113204360(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.202C>T
AA Mutation p.Arg68Trp(p.R68W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113232260:113232260(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1331C>T
AA Mutation p.Ala444Val(p.A444V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204486:113204486(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782700835
CDS Mutation c.328G>A
AA Mutation p.Val110Ile(p.V110I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113205544:113205544(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782167976
CDS Mutation c.368C>T
AA Mutation p.Ala123Val(p.A123V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235153:113235153(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782353037
CDS Mutation c.1814C>T
AA Mutation p.Thr605Met(p.T605M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204414:113204414(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782428703
CDS Mutation c.256G>A
AA Mutation p.Ala86Thr(p.A86T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204426:113204426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268G>A
AA Mutation p.Asp90Asn(p.D90N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113233217:113233217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1593A>C
AA Mutation p.Glu531Asp(p.E531D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113204303:113204303(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.145G>T
AA Mutation p.Asp49Tyr(p.D49Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000316851
Start 113232814:113232814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1522G>T
AA Mutation p.Asp508Tyr(p.D508Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113275350:113275350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2540A>G
AA Mutation p.Asp847Gly(p.D847G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235134:113235134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1795G>T
AA Mutation p.Ala599Ser(p.A599S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113271785:113271785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2365G>A
AA Mutation p.Val789Met(p.V789M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113207338:113207338(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782530698
CDS Mutation c.706G>A
AA Mutation p.Asp236Asn(p.D236N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113205564:113205564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.388C>T
AA Mutation p.Arg130Trp(p.R130W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113206138:113206138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.586C>T
AA Mutation p.Arg196Trp(p.R196W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113207979:113207979(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.893C>T
AA Mutation p.Ala298Val(p.A298V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113232277:113232277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781941272
CDS Mutation c.1348C>T
AA Mutation p.Arg450Trp(p.R450W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113275272:113275272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2462G>A
AA Mutation p.Gly821Asp(p.G821D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113232773:113232773(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367640227
CDS Mutation c.1481G>A
AA Mutation p.Arg494His(p.R494H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113235133:113235133(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199567425
CDS Mutation c.1794C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113255899:113255899(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782372161
CDS Mutation c.1851C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113255962:113255962(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370796324
CDS Mutation c.1914C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113235142:113235142(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536431053
CDS Mutation c.1803C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113270384:113270384(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2328G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113214481:113214481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1029T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113207926:113207926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.840C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113235154:113235154(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561652532
CDS Mutation c.1815G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 113260319:113260319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2127C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000316851
Start 113270352:113270352(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2299delG
AA Mutation p.Ala767ProfsTer49(p.A767Pfs*49)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> NCAM1

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000316851
Start 113221297:113221297(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1061C>T
AA Mutation p.Ala354Val(p.A354V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235129:113235129(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1790T>A
AA Mutation p.Ile597Asn(p.I597N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113205613:113205613(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437C>T
AA Mutation p.Pro146Leu(p.P146L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113214379:113214379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.927A>T
AA Mutation p.Lys309Asn(p.K309N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113235153:113235153(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs782353037
CDS Mutation c.1814C>T
AA Mutation p.Thr605Met(p.T605M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113231688:113231688(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1133C>T
AA Mutation p.Ser378Leu(p.S378L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113232277:113232277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781941272
CDS Mutation c.1348C>T
AA Mutation p.Arg450Trp(p.R450W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113270215:113270215(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2159G>A
AA Mutation p.Ser720Asn(p.S720N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000316851
Start 113255928:113255928(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1880C>A
AA Mutation p.Ser627Tyr(p.S627Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000316851
Start 112961618:112961618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6G>A
Mutation Classification Silent
Feature Type Transcript