Primary Site >> Stomach Cancer

Gene >> AIFM3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20967952:20967952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8G>A
AA Mutation p.Gly3Asp(p.G3D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20977077:20977077(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774742086
CDS Mutation c.1264G>A
AA Mutation p.Val422Ile(p.V422I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20973310:20973310(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.35A>C
AA Mutation p.Glu12Ala(p.E12A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20977052:20977052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1239G>T
AA Mutation p.Lys413Asn(p.K413N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20976248:20976248(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201100852
CDS Mutation c.841G>A
AA Mutation p.Val281Met(p.V281M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20980115:20980115(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1748G>A
AA Mutation p.Arg583Gln(p.R583Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000399167
Start 20967973:20967973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.29C>T
AA Mutation p.Pro10Leu(p.P10L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20973409:20973409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767173371
CDS Mutation c.134C>T
AA Mutation p.Thr45Met(p.T45M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000399167
Start 20979650:20979650(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1600G>A
AA Mutation p.Val534Ile(p.V534I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000399167
Start 20974816:20974816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.720G>T
AA Mutation p.Lys240Asn(p.K240N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence inframe_deletion
Transcription ID ENST00000399167
Start 20974119:20974133(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.412_426delAGCACTGGGGACCTG
AA Mutation p.Ser138_Leu142del(p.S138_L142del)
Mutation Classification In_Frame_Del
Feature Type Transcript