Primary Site >> Stomach Cancer

Gene >> LDHA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18402890:18402890(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.469C>T
AA Mutation p.Arg157Cys(p.R157C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18400950:18400950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.358A>C
AA Mutation p.Ile120Leu(p.I120L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18399467:18399467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144856598
CDS Mutation c.163G>A
AA Mutation p.Glu55Lys(p.E55K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18399494:18399494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.190G>A
AA Mutation p.Asp64Asn(p.D64N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18402995:18402995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.574G>A
AA Mutation p.Glu192Lys(p.E192K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000379412
Start 18399546:18399546(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.242A>G
AA Mutation p.Lys81Arg(p.K81R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000379412
Start 18402933:18402933(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760172008
CDS Mutation c.512G>A
AA Mutation p.Arg171His(p.R171H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000379412
Start 18407173:18407173(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.891G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000379412
Start 18407200:18407200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.918G>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000379412
Start 18405503:18405504(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.766_767delGT
AA Mutation p.Val256SerfsTer12(p.V256Sfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000379412
Start 18396895:18396895(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.58delC
AA Mutation p.Gln20ArgfsTer21(p.Q20Rfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript