Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC9A4

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000295269
Start 102508931:102508931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146323025
CDS Mutation c.1486C>T
AA Mutation p.Arg496Cys(p.R496C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102532504:102532504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2213G>A
AA Mutation p.Gly738Asp(p.G738D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102526278:102526278(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1970G>A
AA Mutation p.Arg657His(p.R657H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102503533:102503533(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768446992
CDS Mutation c.806G>A
AA Mutation p.Arg269Gln(p.R269Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102473948:102473948(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.189T>G
AA Mutation p.Asp63Glu(p.D63E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102479180:102479180(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770759366
CDS Mutation c.598G>A
AA Mutation p.Gly200Ser(p.G200S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102479238:102479238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.656G>A
AA Mutation p.Arg219His(p.R219H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102479225:102479225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.643T>C
AA Mutation p.Phe215Leu(p.F215L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102532518:102532518(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2227G>A
AA Mutation p.Val743Met(p.V743M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000295269
Start 102503657:102503657(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.930C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000295269
Start 102479236:102479236(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370371600
CDS Mutation c.654G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000295269
Start 102505332:102505332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1059C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000295269
Start 102508886:102508886(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1447delA
AA Mutation p.Thr483ProfsTer15(p.T483Pfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000295269
Start 102532678:102532678(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs766495973
CDS Mutation c.2394delA
AA Mutation p.Lys798AsnfsTer46(p.K798Nfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000295269
Start 102505332:102505332(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1059delC
AA Mutation p.Phe354SerfsTer2(p.F354Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000295269
Start 102532499:102532499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2208C>A
AA Mutation p.Tyr736Ter(p.Y736*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> SLC9A4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102519947:102519947(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761269889
CDS Mutation c.1810C>T
AA Mutation p.Arg604Trp(p.R604W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102505459:102505459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1186T>C
AA Mutation p.Trp396Arg(p.W396R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102525083:102525083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1878G>T
AA Mutation p.Glu626Asp(p.E626D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000295269
Start 102508280:102508280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1400A>C
AA Mutation p.Gln467Pro(p.Q467P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295269
Start 102514164:102514164(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1634C>A
AA Mutation p.Ser545Tyr(p.S545Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000295269
Start 102505332:102505332(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1059C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000295269
Start 102505331:102505332(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1058_1059insAGCATT
AA Mutation p.Tyr353delinsTer(p.Y353delins*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript