Primary Site >> Stomach Cancer

Gene >> KLK15

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50826971:50826971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.388C>A
AA Mutation p.Arg130Ser(p.R130S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50826973:50826973(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139927076
CDS Mutation c.386C>T
AA Mutation p.Thr129Met(p.T129M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50826985:50826985(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.374C>T
AA Mutation p.Ala125Val(p.A125V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50827048:50827048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.311G>A
AA Mutation p.Arg104His(p.R104H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50827126:50827126(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762905858
CDS Mutation c.233G>A
AA Mutation p.Arg78His(p.R78H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50826635:50826635(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.604G>A
AA Mutation p.Ala202Thr(p.A202T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50827127:50827127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.232C>T
AA Mutation p.Arg78Cys(p.R78C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000598239
Start 50826899:50826899(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.460G>A
AA Mutation p.Ala154Thr(p.A154T)
Mutation Classification Missense_Mutation
Feature Type Transcript