Primary Site >> Esophagus Cancer

Gene >> NFE2L2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234247:177234247(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.70T>A
AA Mutation p.Trp24Arg(p.W24R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234217:177234217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.100C>G
AA Mutation p.Arg34Gly(p.R34G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234072:177234072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245A>C
AA Mutation p.Glu82Ala(p.E82A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234082:177234082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.235G>C
AA Mutation p.Glu79Gln(p.E79Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177231126:177231126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1477G>A
AA Mutation p.Ala493Thr(p.A493T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234232:177234232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85G>C
AA Mutation p.Asp29His(p.D29H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234076:177234076(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.241G>A
AA Mutation p.Gly81Ser(p.G81S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234072:177234072(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.245A>G
AA Mutation p.Glu82Gly(p.E82G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234075:177234075(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242G>T
AA Mutation p.Gly81Val(p.G81V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234225:177234225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.92G>C
AA Mutation p.Gly31Ala(p.G31A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234082:177234082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.235G>A
AA Mutation p.Glu79Lys(p.E79K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234225:177234225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.92G>A
AA Mutation p.Gly31Glu(p.G31E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000397062
Start 177234081:177234081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.236A>G
AA Mutation p.Glu79Gly(p.E79G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence inframe_deletion
Transcription ID ENST00000397062
Start 177234196:177234216(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.101_121delGAGAAGTATTTGACTTCAGTC
AA Mutation p.Arg34_Ser40del(p.R34_S40del)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 15
Mutation Consequence inframe_insertion
Transcription ID ENST00000397062
Start 177234232:177234233(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.82_84dupATA
AA Mutation p.Ile28dup(p.I28dup)
Mutation Classification In_Frame_Ins
Feature Type Transcript