Primary Site >> Stomach Cancer

Gene >> RGMA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329082
Start 93045051:93045051(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1300C>G
AA Mutation p.Pro434Ala(p.P434A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000329082
Start 93045449:93045449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.902T>C
AA Mutation p.Val301Ala(p.V301A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000329082
Start 93045172:93045172(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370807777
CDS Mutation c.1179C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000329082
Start 93052272:93052272(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373906110
CDS Mutation c.366G>A
Mutation Classification Silent
Feature Type Transcript