Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EPHB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132916:135132916(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1164G>T
AA Mutation p.Glu388Asp(p.E388D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135249362:135249362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2717C>G
AA Mutation p.Ser906Cys(p.S906C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132951:135132951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1199C>T
AA Mutation p.Thr400Ile(p.T400I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134925861:134925861(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536029159
CDS Mutation c.104C>T
AA Mutation p.Thr35Met(p.T35M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134925824:134925824(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.67A>G
AA Mutation p.Met23Val(p.M23V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132731:135132731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.979C>T
AA Mutation p.Arg327Cys(p.R327C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135162090:135162090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1495G>A
AA Mutation p.Gly499Ser(p.G499S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951429:134951429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182G>A
AA Mutation p.Cys61Tyr(p.C61Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951498:134951498(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.251G>A
AA Mutation p.Arg84His(p.R84H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132972:135132972(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1220A>G
AA Mutation p.Gln407Arg(p.Q407R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135249359:135249359(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201702941
CDS Mutation c.2714G>A
AA Mutation p.Arg905His(p.R905H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135201590:135201590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2247C>A
AA Mutation p.Asn749Lys(p.N749K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135248505:135248505(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749600936
CDS Mutation c.2686G>A
AA Mutation p.Ala896Thr(p.A896T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135249409:135249409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373797543
CDS Mutation c.2764G>A
AA Mutation p.Ala922Thr(p.A922T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135249431:135249431(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2786G>T
AA Mutation p.Arg929Met(p.R929M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000398015
Start 135132716:135132716(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770155473
CDS Mutation c.964G>A
AA Mutation p.Val322Ile(p.V322I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135241217:135241217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416G>A
AA Mutation p.Asp806Asn(p.D806N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135192618:135192618(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768101201
CDS Mutation c.1925G>A
AA Mutation p.Gly642Asp(p.G642D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135248361:135248361(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2542G>A
AA Mutation p.Asp848Asn(p.D848N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135192789:135192789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2096T>C
AA Mutation p.Phe699Ser(p.F699S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951951:134951951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.704C>A
AA Mutation p.Pro235His(p.P235H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135192667:135192667(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs534215366
CDS Mutation c.1974G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135192682:135192682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1989G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135248435:135248435(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760099232
CDS Mutation c.2616G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 134925874:134925874(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762148161
CDS Mutation c.117G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135192586:135192586(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1893A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 134951604:134951604(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135179972:135179972(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370958852
CDS Mutation c.1872C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135132970:135132970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1218C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 134951439:134951439(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755589996
CDS Mutation c.192C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000398015
Start 135201509:135201509(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2168delG
AA Mutation p.Gly723ValfsTer10(p.G723Vfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000398015
Start 135248349:135248349(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs754939903
CDS Mutation c.2534delC
AA Mutation p.Pro845HisfsTer34(p.P845Hfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000398015
Start 135167003:135167003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1756C>T
AA Mutation p.Arg586Ter(p.R586*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> EPHB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132854:135132854(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs576710309
CDS Mutation c.1102C>T
AA Mutation p.Arg368Trp(p.R368W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135248467:135248467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs186851943
CDS Mutation c.2648G>A
AA Mutation p.Arg883Gln(p.R883Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135132815:135132815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1063A>G
AA Mutation p.Thr355Ala(p.T355A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135248505:135248505(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749600936
CDS Mutation c.2686G>A
AA Mutation p.Ala896Thr(p.A896T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951912:134951912(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752494038
CDS Mutation c.665G>A
AA Mutation p.Arg222Gln(p.R222Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135201570:135201570(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746798014
CDS Mutation c.2227C>T
AA Mutation p.Arg743Trp(p.R743W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 135192764:135192764(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767340477
CDS Mutation c.2071C>T
AA Mutation p.Arg691Trp(p.R691W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951619:134951619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.372G>T
AA Mutation p.Lys124Asn(p.K124N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000398015
Start 134951993:134951993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.746C>A
AA Mutation p.Pro249His(p.P249H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135192784:135192784(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2091A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000398015
Start 135166017:135166017(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375267802
CDS Mutation c.1635G>A
Mutation Classification Silent
Feature Type Transcript