Primary Site >> Liver Cancer

Gene >> RELN

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103636397:103636397(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2141G>A
AA Mutation p.Ser714Asn(p.S714N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103610720:103610720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2983A>G
AA Mutation p.Ile995Val(p.I995V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103519429:103519429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7756A>T
AA Mutation p.Thr2586Ser(p.T2586S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103574129:103574129(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4474G>A
AA Mutation p.Glu1492Lys(p.E1492K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103539116:103539116(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7142A>G
AA Mutation p.Asp2381Gly(p.D2381G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103723185:103723185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.760A>G
AA Mutation p.Thr254Ala(p.T254A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103515428:103515428(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7876C>G
AA Mutation p.Leu2626Val(p.L2626V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103551200:103551200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6169C>A
AA Mutation p.Leu2057Ile(p.L2057I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000428762
Start 103486284:103486284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.9896C>T
AA Mutation p.Ala3299Val(p.A3299V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000428762
Start 103561619:103561619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5442T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000428762
Start 103651717:103651717(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1836C>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000428762
Start 103557143:103557143(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5631T>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000428762
Start 103539265:103539265(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6993T>C
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000428762
Start 103558049:103558049(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5530delG
AA Mutation p.Glu1844LysfsTer3(p.E1844Kfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript