Primary Site >> Stomach Cancer

Gene >> CHEK1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000428830
Start 125653836:125653836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1324C>T
AA Mutation p.Arg442Trp(p.R442W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000428830
Start 125627818:125627818(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277T>G
AA Mutation p.Phe93Val(p.F93V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000428830
Start 125644546:125644546(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1136G>A
AA Mutation p.Arg379Gln(p.R379Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000428830
Start 125635483:125635483(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.668A>G
AA Mutation p.Glu223Gly(p.E223G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000428830
Start 125644173:125644173(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1006G>A
AA Mutation p.Asp336Asn(p.D336N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000428830
Start 125635517:125635517(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.702C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000428830
Start 125629293:125629293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.351G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_donor_variant
Transcription ID ENST00000428830
Start 125644645:125644645(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1233+2T>C
Mutation Classification Splice_Site
Feature Type Transcript