Primary Site >> Stomach Cancer

Gene >> WWP2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69930215:69930215(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777143460
CDS Mutation c.1402C>T
AA Mutation p.Arg468Cys(p.R468C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69798696:69798696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85C>T
AA Mutation p.Pro29Ser(p.P29S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69929480:69929480(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773617409
CDS Mutation c.1267G>A
AA Mutation p.Val423Met(p.V423M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69908789:69908789(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377619443
CDS Mutation c.943C>T
AA Mutation p.Arg315Cys(p.R315C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69931835:69931835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1627C>T
AA Mutation p.Arg543Trp(p.R543W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69934118:69934118(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1831T>C
AA Mutation p.Phe611Leu(p.F611L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69888195:69888195(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751715302
CDS Mutation c.860C>T
AA Mutation p.Ser287Leu(p.S287L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69931168:69931168(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1462C>A
AA Mutation p.Pro488Thr(p.P488T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69937636:69937636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2327T>A
AA Mutation p.Ile776Asn(p.I776N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69908807:69908807(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.961C>T
AA Mutation p.His321Tyr(p.H321Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000359154
Start 69840228:69840228(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.443T>G
AA Mutation p.Leu148Arg(p.L148R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359154
Start 69842040:69842040(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200091634
CDS Mutation c.495G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000359154
Start 69871807:69871807(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369827464
CDS Mutation c.579G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000359154
Start 69939345:69939345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2445C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000359154
Start 69842079:69842079(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.534G>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000359154
Start 69925465:69925465(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1219delC
AA Mutation p.Leu407SerfsTer17(p.L407Sfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000359154
Start 69930191:69930191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1378C>T
AA Mutation p.Arg460Ter(p.R460*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000359154
Start 69929465:69929465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1252G>T
AA Mutation p.Gly418Ter(p.G418*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript