Primary Site >> Stomach Cancer

Gene >> ARHGAP9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57474473:57474473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376421872
CDS Mutation c.1733G>A
AA Mutation p.Arg578His(p.R578H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57473639:57473639(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs577648313
CDS Mutation c.1988A>G
AA Mutation p.His663Arg(p.H663R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57477508:57477508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.707T>C
AA Mutation p.Leu236Pro(p.L236P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000393791
Start 57475396:57475396(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1447C>T
AA Mutation p.Arg483Trp(p.R483W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57479403:57479403(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4C>A
AA Mutation p.Leu2Ile(p.L2I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57474170:57474170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368092491
CDS Mutation c.1790G>A
AA Mutation p.Arg597Gln(p.R597Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57478622:57478622(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.452G>A
AA Mutation p.Ser151Asn(p.S151N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57475546:57475546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1381G>A
AA Mutation p.Glu461Lys(p.E461K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57477173:57477173(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775171275
CDS Mutation c.853G>A
AA Mutation p.Glu285Lys(p.E285K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57479382:57479382(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.25A>G
AA Mutation p.Ser9Gly(p.S9G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000393791
Start 57475516:57475516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1411C>T
AA Mutation p.Pro471Ser(p.P471S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000393791
Start 57477598:57477598(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.617delC
AA Mutation p.Pro206GlnfsTer28(p.P206Qfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000393791
Start 57472564:57472564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2149C>T
AA Mutation p.Gln717Ter(p.Q717*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript