Variant #0000695747 (NC_000012.11:g.40618777A>G, NM_198578.3:c.-157A>G (LRRK2))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40618777A>G
DNA change (hg38) -
Published as c.-121-u36A>G
ISCN -
DB-ID LRRK2_000024
Variant remarks -
Reference PubMed: Rubio 2012
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/2882
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Justin Rubio
Database submission license No license selected
Created by Justin Rubio
Date created 2012-04-27 21:16:32 +02:00 (CEST)
Date last edited 2020-10-03 11:32:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRK2 NM_198578.3 ?/. ? c.-157A>G r.(?) p.(=)



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