Primary Site >> Stomach Cancer

Gene >> SNRPA

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000243563
Start 40765127:40765127(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750149923
CDS Mutation c.809C>T
AA Mutation p.Thr270Met(p.T270M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000243563
Start 40762928:40762928(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771537539
CDS Mutation c.454C>T
AA Mutation p.Arg152Cys(p.R152C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000243563
Start 40759501:40759501(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765984414
CDS Mutation c.317G>A
AA Mutation p.Arg106His(p.R106H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000243563
Start 40765046:40765046(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.728G>A
AA Mutation p.Arg243Gln(p.R243Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000243563
Start 40757333:40757333(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75G>C
AA Mutation p.Glu25Asp(p.E25D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000243563
Start 40757365:40757365(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.107A>G
AA Mutation p.Gln36Arg(p.Q36R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000243563
Start 40759609:40759609(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775580802
CDS Mutation c.425C>T
AA Mutation p.Pro142Leu(p.P142L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000243563
Start 40757363:40757363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.105C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000243563
Start 40759576:40759576(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.396delC
AA Mutation p.Val133TrpfsTer15(p.V133Wfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000243563
Start 40763674:40763674(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.688C>T
AA Mutation p.Gln230Ter(p.Q230*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript