Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRAK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42202553:42202553(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1545C>A
AA Mutation p.Phe515Leu(p.F515L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42184718:42184718(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.397G>A
AA Mutation p.Gly133Ser(p.G133S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42125600:42125600(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774718665
CDS Mutation c.272C>T
AA Mutation p.Thr91Met(p.T91M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42223118:42223118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2243G>A
AA Mutation p.Gly748Asp(p.G748D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42188105:42188105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756252715
CDS Mutation c.541G>A
AA Mutation p.Ala181Thr(p.A181T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42223183:42223183(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2308T>G
AA Mutation p.Ser770Ala(p.S770A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42223114:42223114(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376571547
CDS Mutation c.2239C>T
AA Mutation p.Arg747Trp(p.R747W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42125452:42125452(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777442675
CDS Mutation c.124G>A
AA Mutation p.Glu42Lys(p.E42K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42202488:42202488(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780113075
CDS Mutation c.1480G>A
AA Mutation p.Asp494Asn(p.D494N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42125437:42125437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766699958
CDS Mutation c.109G>A
AA Mutation p.Asp37Asn(p.D37N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42222995:42222995(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367557305
CDS Mutation c.2120C>T
AA Mutation p.Thr707Met(p.T707M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42202608:42202608(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372408014
CDS Mutation c.1600C>T
AA Mutation p.Arg534Cys(p.R534C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000327628
Start 42222969:42222969(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2094T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000327628
Start 42188084:42188084(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.520C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000327628
Start 42223365:42223365(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2490C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000327628
Start 42209864:42209864(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748144263
CDS Mutation c.1842G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000327628
Start 42200958:42200958(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1336delC
AA Mutation p.Arg446GlyfsTer9(p.R446Gfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000327628
Start 42201052:42201052(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1427+1delG
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000327628
Start 42193199:42193200(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.894_895insTC
AA Mutation p.Lys299SerfsTer50(p.K299Sfs*50)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 20
Mutation Consequence start_lost
Transcription ID ENST00000327628
Start 42091470:42091470(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754091914
CDS Mutation c.1A>G
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript

Rectum Cancer: Gene >> TRAK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42200874:42200874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1247G>T
AA Mutation p.Arg416Ile(p.R416I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000327628
Start 42209901:42209901(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760093287
CDS Mutation c.1879G>A
AA Mutation p.Asp627Asn(p.D627N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000327628
Start 42223293:42223293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772671598
CDS Mutation c.2418C>T
Mutation Classification Silent
Feature Type Transcript