Primary Site >> Stomach Cancer

Gene >> TNFRSF11A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000586569
Start 62361778:62361778(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.715G>A
AA Mutation p.Gly239Arg(p.G239R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000586569
Start 62368728:62368728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.811A>G
AA Mutation p.Thr271Ala(p.T271A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000586569
Start 62369047:62369047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1130C>T
AA Mutation p.Pro377Leu(p.P377L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000586569
Start 62349934:62349934(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767154587
CDS Mutation c.280A>G
AA Mutation p.Thr94Ala(p.T94A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000586569
Start 62354506:62354506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.399C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000586569
Start 62369204:62369204(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1287C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000586569
Start 62369057:62369057(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1144delG
AA Mutation p.Glu382ArgfsTer5(p.E382Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000586569
Start 62361772:62361772(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.714delA
AA Mutation p.Ala241HisfsTer17(p.A241Hfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000586569
Start 62369304:62369305(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1391dupC
AA Mutation p.Arg466ThrfsTer16(p.R466Tfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript