Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRKCB

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24191177:24191177(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1810G>T
AA Mutation p.Asp604Tyr(p.D604Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 23836296:23836296(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.121G>A
AA Mutation p.Ala41Thr(p.A41T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24094281:24094281(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756684442
CDS Mutation c.805G>A
AA Mutation p.Ala269Thr(p.A269T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24172317:24172317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1287G>T
AA Mutation p.Met429Ile(p.M429I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24185178:24185178(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1601T>A
AA Mutation p.Met534Lys(p.M534K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24035493:24035493(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754659392
CDS Mutation c.475C>T
AA Mutation p.Arg159Cys(p.R159C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24185464:24185464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1619C>A
AA Mutation p.Pro540His(p.P540H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24191196:24191196(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs563116744
CDS Mutation c.1829G>A
AA Mutation p.Arg610His(p.R610H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24185548:24185548(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1703C>A
AA Mutation p.Ala568Asp(p.A568D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24180920:24180920(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1525G>A
AA Mutation p.Ala509Thr(p.A509T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24094201:24094201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.725T>C
AA Mutation p.Val242Ala(p.V242A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24154820:24154820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1202C>A
AA Mutation p.Pro401His(p.P401H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24035500:24035500(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482G>A
AA Mutation p.Arg161His(p.R161H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000321728
Start 24032245:24032245(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.398A>C
AA Mutation p.Asp133Ala(p.D133A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24172309:24172309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1279G>A
AA Mutation p.Asp427Asn(p.D427N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24191138:24191138(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774746011
CDS Mutation c.1771G>A
AA Mutation p.Glu591Lys(p.E591K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24219988:24219988(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1891G>A
AA Mutation p.Asp631Asn(p.D631N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000321728
Start 24180919:24180919(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs17847876
CDS Mutation c.1524C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000321728
Start 24180793:24180793(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1398C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000321728
Start 24185516:24185516(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747289504
CDS Mutation c.1671C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000321728
Start 24185168:24185168(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1591C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000321728
Start 23988587:23988587(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371087215
CDS Mutation c.285C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000321728
Start 24032137:24032138(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.295dupC
AA Mutation p.Arg99ProfsTer7(p.R99Pfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> PRKCB

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24092868:24092868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.607G>A
AA Mutation p.Asp203Asn(p.D203N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 23836338:23836338(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.163G>A
AA Mutation p.Asp55Asn(p.D55N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24094232:24094232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.756G>T
AA Mutation p.Arg252Ser(p.R252S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24123923:24123923(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1007G>A
AA Mutation p.Arg336Gln(p.R336Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24092914:24092914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.653C>T
AA Mutation p.Ser218Phe(p.S218F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24123937:24123937(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1021G>A
AA Mutation p.Asp341Asn(p.D341N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000321728
Start 23988588:23988588(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751886977
CDS Mutation c.286G>A
AA Mutation p.Asp96Asn(p.D96N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000321728
Start 24172273:24172273(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1243C>T
AA Mutation p.Arg415Cys(p.R415C)
Mutation Classification Missense_Mutation
Feature Type Transcript