Primary Site >> Stomach Cancer

Gene >> STK31

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23772192:23772192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1879G>A
AA Mutation p.Asp627Asn(p.D627N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23772183:23772183(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202049703
CDS Mutation c.1870C>T
AA Mutation p.Pro624Ser(p.P624S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23769031:23769031(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1453G>A
AA Mutation p.Ala485Thr(p.A485T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23712109:23712109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61A>T
AA Mutation p.Ile21Phe(p.I21F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23781482:23781482(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2029A>G
AA Mutation p.Asn677Asp(p.N677D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000355870
Start 23832181:23832181(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2875A>C
AA Mutation p.Ser959Arg(p.S959R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000355870
Start 23735600:23735600(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000355870
Start 23769681:23769681(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768592589
CDS Mutation c.1638C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000355870
Start 23710318:23710318(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.33C>G
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000355870
Start 23788027:23788027(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2535G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000355870
Start 23783592:23783602(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2079_2089delTAGTTTGGCAC
AA Mutation p.Ser694GlufsTer5(p.S694Efs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000355870
Start 23710325:23710325(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.40G>T
AA Mutation p.Glu14Ter(p.E14*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000355870
Start 23754341:23754342(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1164dupA
AA Mutation p.Asp389ArgfsTer11(p.D389Rfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript