Primary Site >> Stomach Cancer

Gene >> MCPH1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6436084:6436084(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.358A>C
AA Mutation p.Thr120Pro(p.T120P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6442139:6442139(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.653G>A
AA Mutation p.Arg218His(p.R218H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6444822:6444822(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs190026099
CDS Mutation c.1100C>T
AA Mutation p.Pro367Leu(p.P367L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6442082:6442082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.596A>G
AA Mutation p.Gln199Arg(p.Q199R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6455228:6455228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1911G>T
AA Mutation p.Leu637Phe(p.L637F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6480818:6480818(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370011131
CDS Mutation c.2078G>A
AA Mutation p.Arg693His(p.R693H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6621499:6621499(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2260A>G
AA Mutation p.Thr754Ala(p.T754A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000344683
Start 6480722:6480722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1982A>G
AA Mutation p.Asn661Ser(p.N661S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6444902:6444902(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1180C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6445066:6445066(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201825242
CDS Mutation c.1344T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6621688:6621688(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2449T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6444484:6444484(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752061477
CDS Mutation c.762C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6499878:6499878(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2163C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6445111:6445111(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371566184
CDS Mutation c.1389C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000344683
Start 6444799:6444799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1077A>G
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000344683
Start 6445118:6445118(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1402delA
AA Mutation p.Thr468ProfsTer32(p.T468Pfs*32)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000344683
Start 6406675:6406675(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.12delC
AA Mutation p.Ile5SerfsTer2(p.I5Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000344683
Start 6621545:6621546(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2312dupC
AA Mutation p.Val772SerfsTer6(p.V772Sfs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript