Primary Site >> Stomach Cancer

Gene >> INPP4B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142086175:142086175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2456A>T
AA Mutation p.Lys819Met(p.K819M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142270730:142270730(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762779783
CDS Mutation c.548T>C
AA Mutation p.Val183Ala(p.V183A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142028816:142028816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2741C>A
AA Mutation p.Pro914His(p.P914H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142145990:142145990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1570G>A
AA Mutation p.Val524Met(p.V524M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142193111:142193111(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753545130
CDS Mutation c.1157A>G
AA Mutation p.His386Arg(p.H386R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142402963:142402963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.347A>G
AA Mutation p.Asp116Gly(p.D116G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142145861:142145861(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1699G>T
AA Mutation p.Ala567Ser(p.A567S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142082052:142082052(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2621G>T
AA Mutation p.Arg874Leu(p.R874L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262992
Start 142028903:142028903(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs568595082
CDS Mutation c.2654G>A
AA Mutation p.Arg885His(p.R885H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000262992
Start 142260520:142260520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.660A>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000262992
Start 142124648:142124648(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758131494
CDS Mutation c.1833G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000262992
Start 142173689:142173689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1302T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000262992
Start 142086179:142086179(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2452delA
AA Mutation p.Arg818GlufsTer4(p.R818Efs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence inframe_insertion
Transcription ID ENST00000262992
Start 142028842:142028843(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2709_2714dupACAGCT
AA Mutation p.Gln904_Leu905dup(p.Q904_L905dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript