Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> POLD3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74636225:74636225(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150870592
CDS Mutation c.1148G>A
AA Mutation p.Arg383Gln(p.R383Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74625476:74625476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.802G>A
AA Mutation p.Val268Met(p.V268M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74620030:74620030(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762619624
CDS Mutation c.674G>A
AA Mutation p.Gly225Asp(p.G225D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74611531:74611531(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252A>C
AA Mutation p.Lys84Asn(p.K84N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74604721:74604721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.146G>A
AA Mutation p.Arg49Gln(p.R49Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000263681
Start 74618777:74618777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370291355
CDS Mutation c.633G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000263681
Start 74625564:74625565(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.897_898delAA
AA Mutation p.Arg300GlyfsTer8(p.R300Gfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000263681
Start 74625453:74625453(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.784delA
AA Mutation p.Ile262Ter(p.I262*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000263681
Start 74618715:74618715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571G>T
AA Mutation p.Gly191Ter(p.G191*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> POLD3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263681
Start 74629285:74629285(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.968G>T
AA Mutation p.Arg323Ile(p.R323I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000263681
Start 74618777:74618777(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370291355
CDS Mutation c.633G>A
Mutation Classification Silent
Feature Type Transcript