Primary Site >> Stomach Cancer

Gene >> EGR3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000317216
Start 22690702:22690702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.935G>A
AA Mutation p.Arg312Gln(p.R312Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000317216
Start 22692808:22692808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.137A>G
AA Mutation p.Tyr46Cys(p.Y46C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000317216
Start 22690786:22690786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.851G>A
AA Mutation p.Arg284His(p.R284H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000317216
Start 22691235:22691235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.402G>T
AA Mutation p.Gln134His(p.Q134H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000317216
Start 22690609:22690609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1028C>T
AA Mutation p.Ala343Val(p.A343V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000317216
Start 22690608:22690608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1029G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000317216
Start 22692849:22692849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.96G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000317216
Start 22690962:22690962(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.675T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000317216
Start 22690515:22690515(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1122G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000317216
Start 22691280:22691280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000317216
Start 22691199:22691199(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.438delC
AA Mutation p.Tyr147ThrfsTer44(p.Y147Tfs*44)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000317216
Start 22691036:22691037(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.600dupC
AA Mutation p.Asn201GlnfsTer66(p.N201Qfs*66)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript