Primary Site >> Stomach Cancer

Gene >> ERCC4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13922149:13922149(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767586458
CDS Mutation c.326C>T
AA Mutation p.Ala109Val(p.A109V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13935361:13935361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs41557814
CDS Mutation c.1429C>T
AA Mutation p.Arg477Trp(p.R477W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000311895
Start 13926561:13926561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.389G>A
AA Mutation p.Gly130Asp(p.G130D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13947661:13947661(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149364215
CDS Mutation c.2065C>T
AA Mutation p.Arg689Cys(p.R689C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13935362:13935362(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775398434
CDS Mutation c.1430G>A
AA Mutation p.Arg477Gln(p.R477Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13948144:13948144(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2548G>C
AA Mutation p.Asp850His(p.D850H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13932268:13932268(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1085A>G
AA Mutation p.Glu362Gly(p.E362G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000311895
Start 13926620:13926620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145402255
CDS Mutation c.448C>T
AA Mutation p.Arg150Cys(p.R150C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000311895
Start 13948339:13948339(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2747delA
AA Mutation p.Lys916SerfsTer4(p.K916Sfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000311895
Start 13935429:13935429(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1500delA
AA Mutation p.Lys500AsnfsTer19(p.K500Nfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000311895
Start 13935478:13935478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1546C>T
AA Mutation p.Arg516Ter(p.R516*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence splice_donor_variant
Transcription ID ENST00000311895
Start 13944837:13944837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2017+2T>C
Mutation Classification Splice_Site
Feature Type Transcript