Primary Site >> Stomach Cancer

Gene >> SAMSN1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000400566
Start 14516978:14516978(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377428221
CDS Mutation c.193G>A
AA Mutation p.Gly65Ser(p.G65S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000400566
Start 14512456:14512456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.397C>A
AA Mutation p.Gln133Lys(p.Q133K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000400566
Start 14521188:14521188(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775995897
CDS Mutation c.91C>T
AA Mutation p.Arg31Trp(p.R31W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000400566
Start 14498442:14498442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.919A>C
AA Mutation p.Ile307Leu(p.I307L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000400566
Start 14510371:14510371(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746815653
CDS Mutation c.500G>A
AA Mutation p.Arg167His(p.R167H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000400566
Start 14521197:14521197(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769624629
CDS Mutation c.82G>A
AA Mutation p.Asp28Asn(p.D28N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000400566
Start 14521198:14521198(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192978628
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000400566
Start 14486089:14486089(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.945T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000400566
Start 14516963:14516963(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.208delA
AA Mutation p.Met70Ter(p.M70*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000400566
Start 14516984:14516984(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.187G>T
AA Mutation p.Gly63Ter(p.G63*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000400566
Start 14500591:14500591(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.706C>T
AA Mutation p.Arg236Ter(p.R236*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000400566
Start 14510463:14510463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.410-2A>G
Mutation Classification Splice_Site
Feature Type Transcript