Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPARGC1A

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23828493:23828493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664C>A
AA Mutation p.His222Asn(p.H222N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23831618:23831618(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.368C>T
AA Mutation p.Ala123Val(p.A123V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23795865:23795865(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2354T>C
AA Mutation p.Phe785Ser(p.F785S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23829534:23829534(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481T>C
AA Mutation p.Cys161Arg(p.C161R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23802234:23802234(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753923087
CDS Mutation c.2131C>T
AA Mutation p.Arg711Trp(p.R711W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23831654:23831654(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779660669
CDS Mutation c.332C>T
AA Mutation p.Ala111Val(p.A111V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23813031:23813031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1888C>T
AA Mutation p.Arg630Cys(p.R630C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23814360:23814360(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199772441
CDS Mutation c.1123C>T
AA Mutation p.Arg375Trp(p.R375W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23812796:23812796(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1970G>A
AA Mutation p.Arg657Gln(p.R657Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23814456:23814456(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1027A>G
AA Mutation p.Asn343Asp(p.N343D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23795830:23795830(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs34129331
CDS Mutation c.2389C>T
AA Mutation p.Arg797Cys(p.R797C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23831637:23831637(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.349G>A
AA Mutation p.Val117Met(p.V117M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23814370:23814370(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1113G>T
AA Mutation p.Arg371Ser(p.R371S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23814209:23814209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1274C>A
AA Mutation p.Ser425Tyr(p.S425Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23814033:23814033(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1450C>G
AA Mutation p.Leu484Val(p.L484V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23801826:23801826(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2197G>A
AA Mutation p.Glu733Lys(p.E733K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23795905:23795905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2314G>T
AA Mutation p.Asp772Tyr(p.D772Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264867
Start 23824312:23824312(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139281425
CDS Mutation c.845G>A
AA Mutation p.Arg282His(p.R282H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000264867
Start 23828506:23828506(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753811432
CDS Mutation c.651C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000264867
Start 23814526:23814526(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.957T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000264867
Start 23831599:23831599(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.387T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000264867
Start 23831563:23831563(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369519960
CDS Mutation c.423G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence stop_gained
Transcription ID ENST00000264867
Start 23814114:23814114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1369G>T
AA Mutation p.Glu457Ter(p.E457*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence stop_gained
Transcription ID ENST00000264867
Start 23814369:23814369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1114A>T
AA Mutation p.Lys372Ter(p.K372*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> PPARGC1A

No Mutation Annotation!