Primary Site >> Stomach Cancer

Gene >> NOV

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000259526
Start 119419293:119419293(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773316453
CDS Mutation c.725G>A
AA Mutation p.Arg242Gln(p.R242Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000259526
Start 119419131:119419131(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758892100
CDS Mutation c.563C>T
AA Mutation p.Ala188Val(p.A188V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000259526
Start 119422953:119422953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.895C>T
AA Mutation p.Arg299Cys(p.R299C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000259526
Start 119416796:119416796(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.137C>A
AA Mutation p.Thr46Lys(p.T46K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000259526
Start 119418198:119418198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.451C>T
AA Mutation p.Pro151Ser(p.P151S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000259526
Start 119416567:119416567(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.35G>T
AA Mutation p.Arg12Leu(p.R12L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000259526
Start 119418083:119418083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201508830
CDS Mutation c.336C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000259526
Start 119419255:119419255(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.687C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000259526
Start 119416891:119416891(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.232C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000259526
Start 119423063:119423063(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1005C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000259526
Start 119418200:119418200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.453T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000259526
Start 119423082:119423082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1024G>T
AA Mutation p.Glu342Ter(p.E342*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript