Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MMP19

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55837869:55837869(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1034G>A
AA Mutation p.Arg345Gln(p.R345Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000322569
Start 55841234:55841234(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176C>A
AA Mutation p.Ala59Asp(p.A59D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55840829:55840829(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.358C>T
AA Mutation p.Leu120Phe(p.L120F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55839547:55839547(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.715C>T
AA Mutation p.Pro239Ser(p.P239S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55839643:55839643(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs567533354
CDS Mutation c.619C>T
AA Mutation p.Arg207Cys(p.R207C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55838001:55838001(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749262995
CDS Mutation c.902G>A
AA Mutation p.Arg301His(p.R301H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55840811:55840811(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201894718
CDS Mutation c.376C>T
AA Mutation p.Arg126Trp(p.R126W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55837340:55837340(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764541674
CDS Mutation c.1223G>A
AA Mutation p.Arg408Gln(p.R408Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55839534:55839534(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.728T>C
AA Mutation p.Leu243Pro(p.L243P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000322569
Start 55839566:55839566(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.696A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000322569
Start 55837605:55837605(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1138C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000322569
Start 55837201:55837201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1362G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000322569
Start 55837850:55837850(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053C>T
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> MMP19

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55837869:55837869(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1034G>A
AA Mutation p.Arg345Gln(p.R345Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55840810:55840810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs151295753
CDS Mutation c.377G>A
AA Mutation p.Arg126Gln(p.R126Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55839682:55839682(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs536616162
CDS Mutation c.580G>A
AA Mutation p.Glu194Lys(p.E194K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000322569
Start 55837651:55837651(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1092G>T
AA Mutation p.Lys364Asn(p.K364N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000322569
Start 55842439:55842440(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.88-2_88-1delAG
Mutation Classification Splice_Site
Feature Type Transcript