Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOLH1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49157961:49157961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1523G>A
AA Mutation p.Gly508Asp(p.G508D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49206121:49206121(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.170A>C
AA Mutation p.Asn57Thr(p.N57T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000256999
Start 49171195:49171195(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1308G>T
AA Mutation p.Glu436Asp(p.E436D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49208366:49208366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.44C>T
AA Mutation p.Ala15Val(p.A15V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49154350:49154350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1766A>G
AA Mutation p.Asn589Ser(p.N589S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49208360:49208360(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.50G>A
AA Mutation p.Arg17His(p.R17H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49186745:49186745(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.538G>A
AA Mutation p.Ala180Thr(p.A180T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49164748:49164748(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1397G>A
AA Mutation p.Cys466Tyr(p.C466Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000256999
Start 49169256:49169256(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1311G>T
AA Mutation p.Glu437Asp(p.E437D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49154293:49154293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1823C>T
AA Mutation p.Ala608Val(p.A608V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49154426:49154426(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1690A>C
AA Mutation p.Lys564Gln(p.K564Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000256999
Start 49208328:49208328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.82C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000256999
Start 49185766:49185766(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.729A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000256999
Start 49185848:49185848(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.647delA
AA Mutation p.Asn216MetfsTer24(p.N216Mfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000256999
Start 49157983:49157983(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs764290022
CDS Mutation c.1501delA
AA Mutation p.Ser501ValfsTer12(p.S501Vfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000256999
Start 49175866:49175867(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1011_1012delTT
AA Mutation p.Ser338TyrfsTer13(p.S338Yfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000256999
Start 49169220:49169220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1347T>A
AA Mutation p.Tyr449Ter(p.Y449*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000256999
Start 49175922:49175922(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.956G>A
AA Mutation p.Trp319Ter(p.W319*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence stop_gained
Transcription ID ENST00000256999
Start 49185852:49185852(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.643A>T
AA Mutation p.Lys215Ter(p.K215*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000256999
Start 49157982:49157983(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1501dupA
AA Mutation p.Ser501LysfsTer20(p.S501Kfs*20)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000256999
Start 49157988:49157989(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1495_1496insTTTTC
AA Mutation p.Lys499IlefsTer16(p.K499Ifs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 22
Mutation Consequence splice_donor_variant
Transcription ID ENST00000256999
Start 49169194:49169194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1372+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 23
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000256999
Start 49169259:49169259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1309-1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 24
Mutation Consequence inframe_insertion
Transcription ID ENST00000256999
Start 49157989:49157990(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1494_1495insTTT
AA Mutation p.Thr498_Lys499insPhe(p.T498_K499insF)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FOLH1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49154404:49154404(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1712A>C
AA Mutation p.Lys571Thr(p.K571T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49200326:49200326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.340G>T
AA Mutation p.Asp114Tyr(p.D114Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000256999
Start 49200346:49200346(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320C>A
AA Mutation p.Ser107Tyr(p.S107Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence splice_donor_variant
Transcription ID ENST00000256999
Start 49148638:49148638(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2063+1G>A
Mutation Classification Splice_Site
Feature Type Transcript