Primary Site >> Stomach Cancer

Gene >> ANPEP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89806001:89806001(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201704361
CDS Mutation c.583C>T
AA Mutation p.Arg195Cys(p.R195C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89806166:89806166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776965284
CDS Mutation c.418C>T
AA Mutation p.Arg140Cys(p.R140C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89797604:89797604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2128G>T
AA Mutation p.Asp710Tyr(p.D710Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89801451:89801451(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746685166
CDS Mutation c.1726C>T
AA Mutation p.Arg576Cys(p.R576C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89805384:89805384(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375160446
CDS Mutation c.694G>A
AA Mutation p.Glu232Lys(p.E232K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89806321:89806321(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569385341
CDS Mutation c.263C>T
AA Mutation p.Thr88Met(p.T88M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89799276:89799276(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374140510
CDS Mutation c.1993G>A
AA Mutation p.Ala665Thr(p.A665T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000300060
Start 89804253:89804253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1179G>T
AA Mutation p.Gln393His(p.Q393H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000300060
Start 89805386:89805386(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.692C>T
AA Mutation p.Ala231Val(p.A231V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000300060
Start 89801563:89801563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1614C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000300060
Start 89803272:89803272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1536C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000300060
Start 89803728:89803728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1356C>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000300060
Start 89792180:89792181(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2507_2508delAA
AA Mutation p.Lys836ArgfsTer53(p.K836Rfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000300060
Start 89806406:89806407(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.177dupC
AA Mutation p.Ala60ArgfsTer10(p.A60Rfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript