Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH13

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83217486:83217486(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766066852
CDS Mutation c.625G>A
AA Mutation p.Ala209Thr(p.A209T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83486599:83486599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904G>A
AA Mutation p.Asp302Asn(p.D302N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83032160:83032160(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199539898
CDS Mutation c.308C>T
AA Mutation p.Ala103Val(p.A103V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83486639:83486639(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775593596
CDS Mutation c.944C>T
AA Mutation p.Ala315Val(p.A315V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83486492:83486492(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575136203
CDS Mutation c.797G>A
AA Mutation p.Arg266Gln(p.R266Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 82627127:82627127(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.35T>C
AA Mutation p.Leu12Pro(p.L12P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83602460:83602460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.967G>A
AA Mutation p.Glu323Lys(p.E323K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83344950:83344950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.725G>T
AA Mutation p.Arg242Leu(p.R242L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83032148:83032148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369916041
CDS Mutation c.296G>A
AA Mutation p.Arg99Gln(p.R99Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83486543:83486543(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760476515
CDS Mutation c.848G>A
AA Mutation p.Arg283Gln(p.R283Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83125461:83125461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.443C>A
AA Mutation p.Pro148Gln(p.P148Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83217408:83217408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.547G>A
AA Mutation p.Glu183Lys(p.E183K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 82627103:82627103(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11G>T
AA Mutation p.Arg4Ile(p.R4I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000567109
Start 83217449:83217449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs564006725
CDS Mutation c.588C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000567109
Start 83678429:83678429(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs184869802
CDS Mutation c.1506G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000567109
Start 83344912:83344912(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.687G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000567109
Start 83032155:83032155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.303C>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000567109
Start 83032195:83032195(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.345delA
AA Mutation p.Asp116ThrfsTer31(p.D116Tfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000567109
Start 83032189:83032189(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.342delG
AA Mutation p.Asp116ThrfsTer31(p.D116Tfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> CDH13

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83032045:83032045(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368685803
CDS Mutation c.193C>T
AA Mutation p.Arg65Cys(p.R65C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83344908:83344908(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773529566
CDS Mutation c.683C>T
AA Mutation p.Pro228Leu(p.P228L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83780163:83780163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1877C>A
AA Mutation p.Ala626Asp(p.A626D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83780116:83780116(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1830T>G
AA Mutation p.Asp610Glu(p.D610E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000567109
Start 83678313:83678313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200591230
CDS Mutation c.1390G>A
AA Mutation p.Val464Ile(p.V464I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000567109
Start 83783408:83783408(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374049780
CDS Mutation c.2070C>T
Mutation Classification Silent
Feature Type Transcript