Primary Site >> Stomach Cancer

Gene >> MMP9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46010511:46010511(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200637345
CDS Mutation c.400C>T
AA Mutation p.Arg134Trp(p.R134W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012463:46012463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1211G>A
AA Mutation p.Gly404Asp(p.G404D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46011235:46011235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.742G>A
AA Mutation p.Gly248Ser(p.G248S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46013497:46013497(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1573G>A
AA Mutation p.Ala525Thr(p.A525T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012259:46012259(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755934245
CDS Mutation c.1120G>A
AA Mutation p.Ala374Thr(p.A374T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46010601:46010601(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.490G>A
AA Mutation p.Ala164Thr(p.A164T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012468:46012468(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373663809
CDS Mutation c.1216G>A
AA Mutation p.Ala406Thr(p.A406T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46011651:46011651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.901G>A
AA Mutation p.Ala301Thr(p.A301T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012247:46012247(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1108C>T
AA Mutation p.Arg370Cys(p.R370C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46011702:46011702(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776052269
CDS Mutation c.952G>A
AA Mutation p.Ala318Thr(p.A318T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46010526:46010526(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.415G>A
AA Mutation p.Asp139Asn(p.D139N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46010512:46010512(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.401G>A
AA Mutation p.Arg134Gln(p.R134Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46013362:46013362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1438C>T
AA Mutation p.Arg480Cys(p.R480C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000372330
Start 46012188:46012188(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1049C>A
AA Mutation p.Pro350His(p.P350H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46010570:46010570(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.459G>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46013310:46013310(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1386G>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46011159:46011159(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.666T>C
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46012536:46012536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1284G>C
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46013729:46013729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1683C>T
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000372330
Start 46013768:46013768(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1722G>A
Mutation Classification Silent
Feature Type Transcript
ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000372330
Start 46012537:46012537(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1290delC
AA Mutation p.Leu431CysfsTer6(p.L431Cfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000372330
Start 46013314:46013314(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1394delC
AA Mutation p.Pro465ArgfsTer45(p.P465Rfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000372330
Start 46012533:46012533(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1284delG
AA Mutation p.Leu431CysfsTer6(p.L431Cfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 24
Mutation Consequence stop_gained
Transcription ID ENST00000372330
Start 46016284:46016284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2040G>A
AA Mutation p.Trp680Ter(p.W680*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence splice_donor_variant
Transcription ID ENST00000372330
Start 46011317:46011317(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.823+1G>A
Mutation Classification Splice_Site
Feature Type Transcript