Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FXR1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180962896:180962896(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1091T>C
AA Mutation p.Leu364Pro(p.L364P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180975330:180975330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1621A>G
AA Mutation p.Ile541Val(p.I541V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180976171:180976171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1745G>A
AA Mutation p.Gly582Asp(p.G582D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180963045:180963045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153G>A
AA Mutation p.Gly385Arg(p.G385R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180963060:180963060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1168C>T
AA Mutation p.Arg390Cys(p.R390C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180961499:180961499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1022A>C
AA Mutation p.Lys341Thr(p.K341T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000357559
Start 180976275:180976275(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1849C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000357559
Start 180948777:180948777(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.481delT
AA Mutation p.Tyr161ThrfsTer8(p.Y161Tfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000357559
Start 180957832:180957832(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.899delA
AA Mutation p.Asn300MetfsTer8(p.N300Mfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000357559
Start 180953776:180953776(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.821delA
AA Mutation p.Lys274ArgfsTer23(p.K274Rfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000357559
Start 180949236:180949236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.523G>T
AA Mutation p.Glu175Ter(p.E175*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000357559
Start 180963040:180963041(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1148_1149insGCTGTTC
AA Mutation p.Tyr383Ter(p.Y383*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000357559
Start 180962931:180962931(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1126C>T
AA Mutation p.Arg376Ter(p.R376*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000357559
Start 180948439:180948440(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.371dupA
AA Mutation p.Asn124LysfsTer5(p.N124Kfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000357559
Start 180970330:180970331(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1575_1576insTCTGTATTATC
AA Mutation p.Thr526SerfsTer13(p.T526Sfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FXR1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180970295:180970295(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1540G>A
AA Mutation p.Asp514Asn(p.D514N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180968215:180968215(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762872016
CDS Mutation c.1363C>T
AA Mutation p.Arg455Cys(p.R455C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180948456:180948456(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.380T>C
AA Mutation p.Phe127Ser(p.F127S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180951352:180951352(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.685T>G
AA Mutation p.Leu229Val(p.L229V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357559
Start 180963042:180963042(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1150A>G
AA Mutation p.Ser384Gly(p.S384G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000357559
Start 180957823:180957823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.885A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000357559
Start 180975375:180975375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1666G>T
AA Mutation p.Glu556Ter(p.E556*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript