Primary Site >> Stomach Cancer

Gene >> CMIP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81660890:81660890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.688G>A
AA Mutation p.Ala230Thr(p.A230T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81607643:81607643(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.377C>T
AA Mutation p.Pro126Leu(p.P126L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81678595:81678595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369769411
CDS Mutation c.1355C>T
AA Mutation p.Thr452Met(p.T452M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81699773:81699773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1727C>T
AA Mutation p.Ala576Val(p.A576V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81696626:81696626(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1597G>T
AA Mutation p.Gly533Trp(p.G533W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000537098
Start 81699785:81699785(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1739A>G
AA Mutation p.Asn580Ser(p.N580S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000537098
Start 81652349:81652349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs562434205
CDS Mutation c.624G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000537098
Start 81705528:81705528(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376548023
CDS Mutation c.2121G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000537098
Start 81696658:81696658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369550544
CDS Mutation c.1629C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000537098
Start 81607683:81607683(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764628932
CDS Mutation c.417C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000537098
Start 81678548:81678548(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747368835
CDS Mutation c.1308C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000537098
Start 81671996:81671996(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.964delC
AA Mutation p.Arg322GlyfsTer31(p.R322Gfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000537098
Start 81707012:81707012(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2198-2A>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 14
Mutation Consequence splice_donor_variant
Transcription ID ENST00000537098
Start 81701802:81701802(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1896+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
ID 15
Mutation Consequence inframe_insertion
Transcription ID ENST00000537098
Start 81691829:81691830(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1445_1446insTTT
AA Mutation p.Phe482dup(p.F482dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript