Primary Site >> Stomach Cancer

Gene >> CDH5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66387071:66387071(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150311666
CDS Mutation c.473C>T
AA Mutation p.Ala158Val(p.A158V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66403131:66403131(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2317C>G
AA Mutation p.Leu773Val(p.L773V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66402921:66402921(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777969255
CDS Mutation c.2107G>A
AA Mutation p.Gly703Arg(p.G703R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66400953:66400953(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183225007
CDS Mutation c.1774G>A
AA Mutation p.Ala592Thr(p.A592T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66392175:66392175(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147523967
CDS Mutation c.1009G>A
AA Mutation p.Val337Ile(p.V337I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66390516:66390516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.895C>T
AA Mutation p.Arg299Trp(p.R299W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66402898:66402898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768164275
CDS Mutation c.2084C>T
AA Mutation p.Ala695Val(p.A695V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66402835:66402835(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745701770
CDS Mutation c.2021C>T
AA Mutation p.Pro674Leu(p.P674L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66403044:66403044(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2230A>G
AA Mutation p.Ser744Gly(p.S744G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000341529
Start 66390549:66390549(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.928A>G
AA Mutation p.Thr310Ala(p.T310A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000341529
Start 66402818:66402818(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2004C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000341529
Start 66379409:66379409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.72A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000341529
Start 66403067:66403067(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2253C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000341529
Start 66396107:66396107(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1271delA
AA Mutation p.Lys424ArgfsTer20(p.K424Rfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000341529
Start 66389447:66389448(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.712dupG
AA Mutation p.Asp238GlyfsTer16(p.D238Gfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript