Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MMP21

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125770357:125770357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1214G>T
AA Mutation p.Arg405Ile(p.R405I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125772278:125772278(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.919C>T
AA Mutation p.Pro307Ser(p.P307S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125775725:125775725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.97C>T
AA Mutation p.Arg33Cys(p.R33C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125766847:125766847(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145727162
CDS Mutation c.1525G>A
AA Mutation p.Ala509Thr(p.A509T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125767677:125767677(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1265A>G
AA Mutation p.Asp422Gly(p.D422G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125775815:125775815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7G>A
AA Mutation p.Ala3Thr(p.A3T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000368808
Start 125767596:125767597(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1345dupA
AA Mutation p.Ser449LysfsTer9(p.S449Kfs*9)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> MMP21

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125766849:125766849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1523C>T
AA Mutation p.Ser508Phe(p.S508F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125770480:125770480(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1091A>G
AA Mutation p.Tyr364Cys(p.Y364C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368808
Start 125770540:125770540(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031G>T
AA Mutation p.Arg344Ile(p.R344I)
Mutation Classification Missense_Mutation
Feature Type Transcript