Primary Site >> Stomach Cancer

Gene >> MORC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000397641
Start 30937622:30937622(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780264849
CDS Mutation c.1459C>T
AA Mutation p.Arg487Cys(p.R487C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000397641
Start 30937874:30937874(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1310G>A
AA Mutation p.Arg437Gln(p.R437Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000397641
Start 30932567:30932567(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770586964
CDS Mutation c.2725G>A
AA Mutation p.Asp909Asn(p.D909N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000397641
Start 30934998:30934998(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769791429
CDS Mutation c.1976G>A
AA Mutation p.Arg659Gln(p.R659Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000397641
Start 30928145:30928145(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2904T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000397641
Start 30949760:30949760(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.309G>T
Mutation Classification Silent
Feature Type Transcript