Primary Site >> Stomach Cancer

Gene >> DHX15

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24540153:24540153(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1741T>C
AA Mutation p.Tyr581His(p.Y581H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24549000:24549000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1103G>T
AA Mutation p.Arg368Ile(p.R368I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24548907:24548907(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754378482
CDS Mutation c.1196G>A
AA Mutation p.Arg399His(p.R399H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24554849:24554849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.956T>C
AA Mutation p.Val319Ala(p.V319A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000336812
Start 24554725:24554725(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1080G>T
AA Mutation p.Glu360Asp(p.E360D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24540941:24540941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1493C>T
AA Mutation p.Thr498Ile(p.T498I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24570819:24570819(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.536G>A
AA Mutation p.Arg179Gln(p.R179Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24576562:24576562(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188C>T
AA Mutation p.Ala63Val(p.A63V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24556394:24556394(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.718A>G
AA Mutation p.Met240Val(p.M240V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000336812
Start 24533045:24533045(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1919C>T
AA Mutation p.Ser640Leu(p.S640L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000336812
Start 24540238:24540238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1656T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000336812
Start 24548878:24548879(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1224dupA
AA Mutation p.Gln409ThrfsTer14(p.Q409Tfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000336812
Start 24527940:24527941(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2370_2371dupGG
AA Mutation p.Glu791GlyfsTer11(p.E791Gfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript