Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916696:47916696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1131G>T
AA Mutation p.Lys377Asn(p.K377N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47875744:47875744(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368502026
CDS Mutation c.2263C>T
AA Mutation p.Arg755Cys(p.R755C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47914868:47914868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1948G>A
AA Mutation p.Glu650Lys(p.E650K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47921813:47921813(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.481G>A
AA Mutation p.Asp161Asn(p.D161N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916976:47916976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.851T>C
AA Mutation p.Leu284Ser(p.L284S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916410:47916410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1417G>A
AA Mutation p.Ala473Thr(p.A473T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47918746:47918746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.625G>A
AA Mutation p.Val209Ile(p.V209I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47871951:47871951(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2472G>T
AA Mutation p.Arg824Ser(p.R824S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47921816:47921816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.478G>T
AA Mutation p.Ala160Ser(p.A160S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916056:47916056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1771G>T
AA Mutation p.Asp591Tyr(p.D591Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916325:47916325(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1502G>A
AA Mutation p.Gly501Asp(p.G501D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47872070:47872070(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2353C>T
AA Mutation p.Arg785Trp(p.R785W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47914915:47914915(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1901A>G
AA Mutation p.Lys634Arg(p.K634R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47921811:47921811(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.483T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47869220:47869220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200032630
CDS Mutation c.2967G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000360240
Start 47869309:47869309(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2878delA
AA Mutation p.Thr960GlnfsTer35(p.T960Qfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000360240
Start 47867318:47867318(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2994delA
AA Mutation p.Val999Ter(p.V999*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000360240
Start 47870917:47870917(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2755delC
AA Mutation p.Arg919GlyfsTer14(p.R919Gfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> MAP4

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360240
Start 47917174:47917174(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.653T>G
AA Mutation p.Val218Gly(p.V218G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47916292:47916292(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1535C>T
AA Mutation p.Thr512Ile(p.T512I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360240
Start 47914824:47914824(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1992G>T
AA Mutation p.Glu664Asp(p.E664D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47916432:47916432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1395A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47916726:47916726(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1101C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000360240
Start 47916450:47916450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1377C>A
Mutation Classification Silent
Feature Type Transcript