Primary Site >> Stomach Cancer

Gene >> MTMR3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30012465:30012465(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752456939
CDS Mutation c.1219C>T
AA Mutation p.Arg407Trp(p.R407W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30019745:30019745(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2086G>A
AA Mutation p.Ala696Thr(p.A696T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30007143:30007143(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.701G>A
AA Mutation p.Arg234His(p.R234H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30020534:30020534(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755680177
CDS Mutation c.2875G>A
AA Mutation p.Ala959Thr(p.A959T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30017952:30017952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1700G>A
AA Mutation p.Arg567His(p.R567H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30020747:30020747(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs189578908
CDS Mutation c.3088C>T
AA Mutation p.Arg1030Cys(p.R1030C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30025761:30025761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3557A>G
AA Mutation p.Asp1186Gly(p.D1186G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30022078:30022078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3275G>A
AA Mutation p.Arg1092His(p.R1092H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000401950
Start 30020337:30020337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2678C>T
AA Mutation p.Pro893Leu(p.P893L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000401950
Start 30019624:30019624(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1965C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000401950
Start 30016626:30016626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1602T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000401950
Start 30009061:30009061(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1053C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000401950
Start 29978980:29978980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.138C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000401950
Start 30020749:30020749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3090C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000401950
Start 30018059:30018059(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1813delC
AA Mutation p.Leu605Ter(p.L605*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript