Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PROM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15992324:15992324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1835C>T
AA Mutation p.Ala612Val(p.A612V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16025217:16025217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200352674
CDS Mutation c.605G>A
AA Mutation p.Arg202Gln(p.R202Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16024343:16024343(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.646T>G
AA Mutation p.Leu216Val(p.L216V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16006673:16006673(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1319T>G
AA Mutation p.Val440Gly(p.V440G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16018430:16018430(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200809630
CDS Mutation c.895C>T
AA Mutation p.Arg299Trp(p.R299W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15985992:15985992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2176T>A
AA Mutation p.Phe726Ile(p.F726I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16009005:16009005(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1245C>A
AA Mutation p.Asn415Lys(p.N415K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16008958:16008958(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1292A>G
AA Mutation p.Asp431Gly(p.D431G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16006584:16006584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1408A>T
AA Mutation p.Thr470Ser(p.T470S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15980429:15980429(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2482T>C
AA Mutation p.Tyr828His(p.Y828H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15980449:15980449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370736469
CDS Mutation c.2462G>A
AA Mutation p.Arg821Gln(p.R821Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16013299:16013299(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137853006
CDS Mutation c.1117C>T
AA Mutation p.Arg373Cys(p.R373C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15980458:15980458(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2453A>G
AA Mutation p.Tyr818Cys(p.Y818C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000447510
Start 16033375:16033375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000447510
Start 15993990:15993990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1764T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000447510
Start 15984335:15984335(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376589328
CDS Mutation c.2301G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000447510
Start 15994057:15994057(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs762078182
CDS Mutation c.1697delA
AA Mutation p.Asn566IlefsTer29(p.N566Ifs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> PROM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15992363:15992363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1796A>G
AA Mutation p.Glu599Gly(p.E599G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 15984306:15984306(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2330C>A
AA Mutation p.Thr777Asn(p.T777N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000447510
Start 16025217:16025217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200352674
CDS Mutation c.605G>A
AA Mutation p.Arg202Gln(p.R202Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000447510
Start 15998444:15998444(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1623T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000447510
Start 16035747:16035747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747241561
CDS Mutation c.291C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000447510
Start 16018372:16018400(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.925_953delGTGCATCCATCAAGTGAAACCTGCAACAG
AA Mutation p.Val309HisfsTer10(p.V309Hfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000447510
Start 16000620:16000620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1455-1G>T
Mutation Classification Splice_Site
Feature Type Transcript