Primary Site >> Stomach Cancer

Gene >> LYN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 55952071:55952071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.593G>A
AA Mutation p.Arg198Gln(p.R198Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 56010057:56010057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527508795
CDS Mutation c.1486G>A
AA Mutation p.Val496Ile(p.V496I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 55966794:55966794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.870A>C
AA Mutation p.Glu290Asp(p.E290D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 55998400:55998400(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1105C>G
AA Mutation p.Arg369Gly(p.R369G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 55999442:55999442(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1229C>T
AA Mutation p.Thr410Met(p.T410M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000519728
Start 55953856:55953856(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.662G>A
AA Mutation p.Arg221Lys(p.R221K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000519728
Start 55950747:55950747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.450T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000519728
Start 55998363:55998363(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1068A>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000519728
Start 55950495:55950495(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.327delA
AA Mutation p.Glu110LysfsTer15(p.E110Kfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript