Variant #0000695775 (NC_000012.11:g.40626176G>T, NM_198578.3:c.338G>T (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.40626176G>T
DNA change (hg38) g.40232374G>T
Published as -
ISCN -
DB-ID LRRK2_000055
Variant remarks -
Reference PubMed: Rubio 2012
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/27770
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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.338G>T r.(?) p.(Gly113Val)



Screenings

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