Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PPP1R13B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103754100:103754100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.601G>A
AA Mutation p.Asp201Asn(p.D201N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103749908:103749908(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.855A>C
AA Mutation p.Gln285His(p.Q285H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103778797:103778797(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.302G>A
AA Mutation p.Arg101Gln(p.R101Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103740279:103740279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2137G>A
AA Mutation p.Glu713Lys(p.E713K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103742758:103742758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1216G>A
AA Mutation p.Ala406Thr(p.A406T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103738992:103738992(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2624C>T
AA Mutation p.Ser875Leu(p.S875L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103742792:103742792(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1182G>T
AA Mutation p.Gln394His(p.Q394H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103739878:103739878(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2538G>T
AA Mutation p.Glu846Asp(p.E846D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103784830:103784830(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.242G>A
AA Mutation p.Arg81Gln(p.R81Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103797501:103797501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.27C>A
AA Mutation p.Phe9Leu(p.F9L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103749867:103749867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759776212
CDS Mutation c.896G>A
AA Mutation p.Arg299His(p.R299H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000202556
Start 103736102:103736102(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371359449
CDS Mutation c.3132C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000202556
Start 103735175:103735175(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3252C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000202556
Start 103740095:103740095(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2321delC
AA Mutation p.Pro774LeufsTer97(p.P774Lfs*97)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000202556
Start 103778798:103778798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.301C>T
AA Mutation p.Arg101Ter(p.R101*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000202556
Start 103753129:103753130(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.698dupT
AA Mutation p.Leu233PhefsTer4(p.L233Ffs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> PPP1R13B

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103746457:103746457(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs530083884
CDS Mutation c.1066G>A
AA Mutation p.Gly356Arg(p.G356R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103754121:103754121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.580C>T
AA Mutation p.Arg194Cys(p.R194C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103778788:103778788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311G>T
AA Mutation p.Arg104Ile(p.R104I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103742020:103742020(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1592C>T
AA Mutation p.Pro531Leu(p.P531L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103737809:103737809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2916G>T
AA Mutation p.Gln972His(p.Q972H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000202556
Start 103741934:103741934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1678A>G
AA Mutation p.Lys560Glu(p.K560E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000202556
Start 103740517:103740517(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs3742368
CDS Mutation c.1899G>A
Mutation Classification Silent
Feature Type Transcript