Primary Site >> Stomach Cancer

Gene >> DROSHA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31406913:31406913(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3887G>A
AA Mutation p.Arg1296Gln(p.R1296Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31421343:31421343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3454T>G
AA Mutation p.Ser1152Ala(p.S1152A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31504592:31504592(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1631G>A
AA Mutation p.Arg544His(p.R544H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31526667:31526667(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200906186
CDS Mutation c.266C>T
AA Mutation p.Ala89Val(p.A89V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31449320:31449320(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2782G>A
AA Mutation p.Gly928Arg(p.G928R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31508679:31508679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1529G>A
AA Mutation p.Arg510His(p.R510H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31526235:31526235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.698A>T
AA Mutation p.His233Leu(p.H233L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31526709:31526709(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs546365755
CDS Mutation c.224G>A
AA Mutation p.Arg75Gln(p.R75Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31511112:31511112(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1355T>C
AA Mutation p.Leu452Ser(p.L452S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31401520:31401520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4037G>A
AA Mutation p.Arg1346Gln(p.R1346Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000344624
Start 31508658:31508658(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1550G>A
AA Mutation p.Arg517Gln(p.R517Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000344624
Start 31515072:31515072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1206G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000344624
Start 31521134:31521134(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.936G>A
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000344624
Start 31526387:31526387(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546T>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000344624
Start 31449369:31449369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2733T>C
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000344624
Start 31526685:31526685(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.248delC
AA Mutation p.Pro83HisfsTer25(p.P83Hfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000344624
Start 31526779:31526779(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.154C>T
AA Mutation p.Gln52Ter(p.Q52*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000344624
Start 31401461:31401462(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4094_4095dupAG
AA Mutation p.Pro1366SerfsTer24(p.P1366Sfs*24)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript