Primary Site >> Stomach Cancer

Gene >> DIAPH3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59666663:59666663(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772731233
CDS Mutation c.3503C>T
AA Mutation p.Thr1168Met(p.T1168M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59833220:59833220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781747042
CDS Mutation c.2914G>A
AA Mutation p.Glu972Lys(p.E972K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59879337:59879337(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2499C>A
AA Mutation p.Ser833Arg(p.S833R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59924834:59924834(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762124184
CDS Mutation c.2111C>T
AA Mutation p.Ser704Leu(p.S704L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59970905:59970905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1906C>G
AA Mutation p.Pro636Ala(p.P636A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59916228:59916228(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2192G>A
AA Mutation p.Arg731Gln(p.R731Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59991197:59991197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1322T>G
AA Mutation p.Leu441Arg(p.L441R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59991242:59991242(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1277G>T
AA Mutation p.Ser426Ile(p.S426I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000400324
Start 59970863:59970863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1948A>C
AA Mutation p.Asn650His(p.N650H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000400324
Start 60132971:60132971(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373421558
CDS Mutation c.199C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000400324
Start 60015940:60015940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.744G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000400324
Start 60008585:60008585(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.973delT
AA Mutation p.Cys325ValfsTer15(p.C325Vfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000400324
Start 59810896:59810896(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3055delA
AA Mutation p.Arg1019GlufsTer12(p.R1019Efs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000400324
Start 59924820:59924820(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs777749882
CDS Mutation c.2125delA
AA Mutation p.Ile709LeufsTer7(p.I709Lfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000400324
Start 59991231:59991231(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1288G>T
AA Mutation p.Glu430Ter(p.E430*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000400324
Start 59666823:59666823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3343G>T
AA Mutation p.Glu1115Ter(p.E1115*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000400324
Start 59839416:59839416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2770C>T
AA Mutation p.Gln924Ter(p.Q924*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000400324
Start 59774249:59774249(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3260-1G>T
Mutation Classification Splice_Site
Feature Type Transcript