Primary Site >> Stomach Cancer

Gene >> PLOD2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146070817:146070817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2114G>A
AA Mutation p.Gly705Asp(p.G705D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000360060
Start 146086906:146086906(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1008A>C
AA Mutation p.Glu336Asp(p.E336D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146106556:146106556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.591A>C
AA Mutation p.Lys197Asn(p.K197N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146071330:146071330(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368177696
CDS Mutation c.1879C>T
AA Mutation p.Arg627Trp(p.R627W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146072650:146072650(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1696T>G
AA Mutation p.Phe566Val(p.F566V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146081838:146081838(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142041189
CDS Mutation c.1258C>T
AA Mutation p.Arg420Cys(p.R420C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146104338:146104338(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.620C>A
AA Mutation p.Ala207Asp(p.A207D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146121200:146121200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.250A>T
AA Mutation p.Ile84Phe(p.I84F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146121166:146121166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.284A>G
AA Mutation p.Glu95Gly(p.E95G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360060
Start 146072631:146072631(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1715C>G
AA Mutation p.Ser572Cys(p.S572C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000360060
Start 146110403:146110403(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.384delA
AA Mutation p.Lys128AsnfsTer23(p.K128Nfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000360060
Start 146071138:146071138(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1962delA
AA Mutation p.Lys654AsnfsTer21(p.K654Nfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000360060
Start 146104288:146104288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.670G>T
AA Mutation p.Gly224Ter(p.G224*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript