Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MFGE8

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88906658:88906658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780674687
CDS Mutation c.508G>A
AA Mutation p.Asp170Asn(p.D170N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88906664:88906664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769108892
CDS Mutation c.502G>A
AA Mutation p.Glu168Lys(p.E168K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88907351:88907351(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs55959974
CDS Mutation c.231G>T
AA Mutation p.Glu77Asp(p.E77D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88906738:88906738(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772280903
CDS Mutation c.428C>T
AA Mutation p.Thr143Met(p.T143M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88901730:88901730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375727875
CDS Mutation c.691G>A
AA Mutation p.Ala231Thr(p.A231T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88901582:88901582(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369715289
CDS Mutation c.839C>T
AA Mutation p.Ala280Val(p.A280V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88909902:88909902(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.95G>A
AA Mutation p.Cys32Tyr(p.C32Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88907253:88907253(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140046500
CDS Mutation c.329G>A
AA Mutation p.Arg110His(p.R110H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88905837:88905837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.605C>T
AA Mutation p.Ala202Val(p.A202V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88899699:88899699(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.983C>T
AA Mutation p.Ala328Val(p.A328V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88899497:88899497(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751746916
CDS Mutation c.1062G>T
AA Mutation p.Lys354Asn(p.K354N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88899494:88899494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1065G>T
AA Mutation p.Lys355Asn(p.K355N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000268150
Start 88901581:88901581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202157001
CDS Mutation c.840G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000268150
Start 88899763:88899763(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.919delG
AA Mutation p.Ala307ProfsTer66(p.A307Pfs*66)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> MFGE8

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88906658:88906658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780674687
CDS Mutation c.508G>A
AA Mutation p.Asp170Asn(p.D170N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000268150
Start 88906664:88906664(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769108892
CDS Mutation c.502G>A
AA Mutation p.Glu168Lys(p.E168K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000268150
Start 88899698:88899698(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369704324
CDS Mutation c.984G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000268150
Start 88905757:88905757(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.685G>T
AA Mutation p.Gly229Ter(p.G229*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript