Primary Site >> Stomach Cancer

Gene >> KIF18A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28069303:28069303(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374462377
CDS Mutation c.1546G>A
AA Mutation p.Glu516Lys(p.E516K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28023833:28023833(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369809315
CDS Mutation c.2522C>T
AA Mutation p.Ser841Leu(p.S841L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28090627:28090627(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.689C>A
AA Mutation p.Ala230Asp(p.A230D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28077012:28077012(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1420G>C
AA Mutation p.Glu474Gln(p.E474Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28097772:28097772(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.176C>T
AA Mutation p.Thr59Ile(p.T59I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28069279:28069279(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1570C>G
AA Mutation p.Gln524Glu(p.Q524E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263181
Start 28082914:28082914(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1204A>G
AA Mutation p.Asn402Asp(p.N402D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000263181
Start 28082900:28082900(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1218A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263181
Start 28097894:28097894(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.54A>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000263181
Start 28036616:28036617(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1996dupA
AA Mutation p.Arg666LysfsTer29(p.R666Kfs*29)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript