Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NOX4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89337455:89337455(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1507G>C
AA Mutation p.Gly503Arg(p.G503R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89337457:89337457(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1505A>T
AA Mutation p.Asp502Val(p.D502V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89402378:89402378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.794A>T
AA Mutation p.Lys265Ile(p.K265I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000263317
Start 89444230:89444230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768559870
CDS Mutation c.352G>A
AA Mutation p.Val118Met(p.V118M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89451843:89451843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.206G>T
AA Mutation p.Ser69Ile(p.S69I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89340068:89340068(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1441A>G
AA Mutation p.Asn481Asp(p.N481D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89342152:89342152(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1259C>T
AA Mutation p.Ser420Leu(p.S420L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89421940:89421940(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.591C>A
AA Mutation p.Phe197Leu(p.F197L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89400230:89400230(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996A>T
AA Mutation p.Lys332Asn(p.K332N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89444142:89444142(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147350656
CDS Mutation c.440G>A
AA Mutation p.Arg147Gln(p.R147Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89400066:89400066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1025A>G
AA Mutation p.His342Arg(p.H342R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000263317
Start 89400369:89400370(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.856_857insAAAATTTTCTTTGACCATTC
AA Mutation p.Trp286Ter(p.W286*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000263317
Start 89373415:89373434(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1133_1135+17delCAGGTATGTAGAACATACAG
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000263317
Start 89421901:89421901(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.629+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 15
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000263317
Start 89342195:89342195(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1218-2A>G
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> NOX4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89449489:89449489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.300A>C
AA Mutation p.Lys100Asn(p.K100N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89402376:89402376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.796T>G
AA Mutation p.Phe266Val(p.F266V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263317
Start 89440708:89440708(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455G>T
AA Mutation p.Arg152Ile(p.R152I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000263317
Start 89373454:89373454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1113T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000263317
Start 89402439:89402439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733G>T
AA Mutation p.Glu245Ter(p.E245*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript