Primary Site >> Stomach Cancer

Gene >> WEE2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141719150:141719150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369051862
CDS Mutation c.664G>A
AA Mutation p.Glu222Lys(p.E222K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141708868:141708868(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746485209
CDS Mutation c.110C>T
AA Mutation p.Ser37Leu(p.S37L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141725032:141725032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1228C>T
AA Mutation p.Arg410Trp(p.R410W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141727434:141727434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1523C>T
AA Mutation p.Ala508Val(p.A508V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141709042:141709042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755662789
CDS Mutation c.284C>A
AA Mutation p.Pro95Gln(p.P95Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141723176:141723176(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.923G>T
AA Mutation p.Gly308Val(p.G308V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000397541
Start 141716254:141716254(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.572G>T
AA Mutation p.Gly191Val(p.G191V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000397541
Start 141719131:141719131(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.645T>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000397541
Start 141724239:141724239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1185A>G
Mutation Classification Silent
Feature Type Transcript