Primary Site >> Stomach Cancer

Gene >> GRAMD1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123612777:123612777(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1507C>T
AA Mutation p.Arg503Cys(p.R503C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123606745:123606745(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1031A>G
AA Mutation p.Asp344Gly(p.D344G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123613614:123613614(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757313912
CDS Mutation c.1754C>T
AA Mutation p.Thr585Met(p.T585M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123606738:123606738(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1024T>G
AA Mutation p.Phe342Val(p.F342V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123577492:123577492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.149C>T
AA Mutation p.Ser50Leu(p.S50L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000529750
Start 123613602:123613602(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1742G>A
AA Mutation p.Ser581Asn(p.S581N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000529750
Start 123610309:123610309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1461C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000529750
Start 123613615:123613615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1755G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000529750
Start 123608726:123608726(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780116124
CDS Mutation c.1152C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000529750
Start 123613653:123613653(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1793delT
AA Mutation p.Val598GlyfsTer33(p.V598Gfs*33)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000529750
Start 123595964:123595970(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.467_473delTCTGTTC
AA Mutation p.Ile156ThrfsTer2(p.I156Tfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000529750
Start 123610331:123610331(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1483C>T
AA Mutation p.Arg495Ter(p.R495*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000529750
Start 123619177:123619178(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2085dupA
AA Mutation p.Trp696MetfsTer13(p.W696Mfs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript