Primary Site >> Stomach Cancer

Gene >> MAPK9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000452135
Start 180261787:180261787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.347G>A
AA Mutation p.Cys116Tyr(p.C116Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000452135
Start 180236398:180236398(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1261G>A
AA Mutation p.Glu421Lys(p.E421K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000452135
Start 180249123:180249123(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.466A>G
AA Mutation p.Asn156Asp(p.N156D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000452135
Start 180249011:180249011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.578C>T
AA Mutation p.Ala193Val(p.A193V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000452135
Start 180241088:180241088(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs116346965
CDS Mutation c.939C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000452135
Start 180236507:180236507(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1152C>T
Mutation Classification Silent
Feature Type Transcript