Primary Site >> Liver Cancer

Gene >> TLN2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306829
Start 62797362:62797362(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6194T>A
AA Mutation p.Leu2065Gln(p.L2065Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306829
Start 62717621:62717621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2809G>A
AA Mutation p.Ala937Thr(p.A937T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306829
Start 62656049:62656049(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776986439
CDS Mutation c.623C>T
AA Mutation p.Ser208Leu(p.S208L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000306829
Start 62809926:62809926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6665A>C
AA Mutation p.Gln2222Pro(p.Q2222P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306829
Start 62776831:62776831(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5435T>C
AA Mutation p.Met1812Thr(p.M1812T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000306829
Start 62739356:62739356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3696A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000306829
Start 62697838:62697838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1443G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000306829
Start 62707161:62707161(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2080C>T
AA Mutation p.Gln694Ter(p.Q694*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript