Primary Site >> Stomach Cancer

Gene >> LIFR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38505940:38505940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1256C>T
AA Mutation p.Ser419Leu(p.S419L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38499546:38499546(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1638T>G
AA Mutation p.Ser546Arg(p.S546R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481729:38481729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3160A>C
AA Mutation p.Ile1054Leu(p.I1054L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38506025:38506025(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373421600
CDS Mutation c.1171G>A
AA Mutation p.Glu391Lys(p.E391K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38523451:38523451(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.529C>A
AA Mutation p.Leu177Ile(p.L177I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38511859:38511859(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.667T>C
AA Mutation p.Tyr223His(p.Y223H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38503982:38503982(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1431A>C
AA Mutation p.Gln477His(p.Q477H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38527289:38527289(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs61751711
CDS Mutation c.263G>A
AA Mutation p.Arg88His(p.R88H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000263409
Start 38502798:38502798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781727104
CDS Mutation c.1439G>A
AA Mutation p.Arg480Gln(p.R480Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38506545:38506545(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1079C>T
AA Mutation p.Ala360Val(p.A360V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38482184:38482184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2705C>A
AA Mutation p.Pro902His(p.P902H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481821:38481821(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3068A>G
AA Mutation p.Asp1023Gly(p.D1023G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38496402:38496402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1865C>T
AA Mutation p.Ala622Val(p.A622V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38484843:38484843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2523C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38506050:38506050(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1146T>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38490226:38490226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2131T>C
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38506529:38506529(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1095T>C
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38484782:38484782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2584C>T
AA Mutation p.Arg862Ter(p.R862*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000263409
Start 38496564:38496565(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1702dupA
AA Mutation p.Ile568AsnfsTer12(p.I568Nfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript