Primary Site >> Stomach Cancer

Gene >> UBR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42617286:42617286(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1229G>A
AA Mutation p.Arg410Gln(p.R410Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42594271:42594271(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.498T>A
AA Mutation p.His166Gln(p.H166Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42652537:42652537(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2661C>G
AA Mutation p.Ser887Arg(p.S887R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42676072:42676072(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200468826
CDS Mutation c.4268C>T
AA Mutation p.Ala1423Val(p.A1423V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42665483:42665483(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3773A>G
AA Mutation p.Gln1258Arg(p.Q1258R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42658817:42658817(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3235G>C
AA Mutation p.Asp1079His(p.D1079H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42674138:42674138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4196A>C
AA Mutation p.Asn1399Thr(p.N1399T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42670127:42670127(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376138925
CDS Mutation c.3917C>T
AA Mutation p.Thr1306Met(p.T1306M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42644489:42644489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2237A>C
AA Mutation p.Asn746Thr(p.N746T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000372899
Start 42683066:42683066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4730A>G
AA Mutation p.Asn1577Ser(p.N1577S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000372899
Start 42573955:42573955(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.300T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000372899
Start 42635543:42635543(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1671A>G
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000372899
Start 42679770:42679770(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4656A>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000372899
Start 42658070:42658070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2919G>A
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000372899
Start 42645572:42645573(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2392_2393delAA
AA Mutation p.Lys798ValfsTer4(p.K798Vfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000372899
Start 42673873:42673873(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4169delG
AA Mutation p.Cys1390LeufsTer20(p.C1390Lfs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 17
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000372899
Start 42594302:42594302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.529G>T
AA Mutation p.Glu177Ter(p.E177*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000372899
Start 42658815:42658816(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3233_3234insCTTCCTC
AA Mutation p.Asp1079PhefsTer3(p.D1079Ffs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 19
Mutation Consequence splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000372899
Start 42594284:42594323(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.511_531+19delTCTGAAATTGAGGAAGAAGAGGTAAAAACATTTTCACAAA
Mutation Classification Splice_Site
Feature Type Transcript