Primary Site >> Stomach Cancer

Gene >> HHIPL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222538690:222538690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1535C>T
AA Mutation p.Pro512Leu(p.P512L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222543651:222543651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.860G>A
AA Mutation p.Arg287His(p.R287H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222540192:222540192(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149049815
CDS Mutation c.1268G>A
AA Mutation p.Arg423His(p.R423H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222522630:222522630(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2146C>A
AA Mutation p.Gln716Lys(p.Q716K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222547819:222547819(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375371391
CDS Mutation c.226C>T
AA Mutation p.Arg76Cys(p.R76C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222540280:222540280(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548883263
CDS Mutation c.1180C>T
AA Mutation p.Arg394Trp(p.R394W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222544159:222544159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776221156
CDS Mutation c.352G>A
AA Mutation p.Asp118Asn(p.D118N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222522693:222522693(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144597197
CDS Mutation c.2083C>T
AA Mutation p.Arg695Cys(p.R695C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222540204:222540204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1256G>A
AA Mutation p.Arg419Lys(p.R419K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000343410
Start 222543751:222543751(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.760C>T
AA Mutation p.Pro254Ser(p.P254S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000343410
Start 222540014:222540014(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1446T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000343410
Start 222522736:222522736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2040A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000343410
Start 222543902:222543902(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.609C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000343410
Start 222540128:222540128(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767728663
CDS Mutation c.1332C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000343410
Start 222543869:222543869(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747441729
CDS Mutation c.642C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000343410
Start 222540167:222540167(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1293delC
AA Mutation p.Ile432SerfsTer26(p.I432Sfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000343410
Start 222547915:222547915(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.130delC
AA Mutation p.Gln44SerfsTer48(p.Q44Sfs*48)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000343410
Start 222543607:222543607(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904G>T
AA Mutation p.Glu302Ter(p.E302*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript