Primary Site >> Stomach Cancer

Gene >> LTK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41512866:41512866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.200C>A
AA Mutation p.Ser67Tyr(p.S67Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41505054:41505054(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145997165
CDS Mutation c.1936G>A
AA Mutation p.Ala646Thr(p.A646T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41504362:41504362(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150790185
CDS Mutation c.2326C>T
AA Mutation p.Arg776Cys(p.R776C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41508108:41508108(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1210G>A
AA Mutation p.Glu404Lys(p.E404K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41513001:41513001(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.163C>T
AA Mutation p.Pro55Ser(p.P55S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41504157:41504157(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2434T>G
AA Mutation p.Leu812Val(p.L812V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263800
Start 41505274:41505274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1859T>C
AA Mutation p.Leu620Pro(p.L620P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000263800
Start 41512751:41512751(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767961282
CDS Mutation c.315G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263800
Start 41512799:41512799(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.267G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000263800
Start 41504158:41504158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2433T>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000263800
Start 41507177:41507177(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1459delC
AA Mutation p.Gln487ArgfsTer43(p.Q487Rfs*43)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000263800
Start 41508207:41508207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1111G>T
AA Mutation p.Gly371Ter(p.G371*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript