Variant #0000548028 (NC_000012.11:g.40629436T>C, NM_198578.3:c.356T>C (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.40629436T>C
DNA change (hg38) g.40235634T>C
Published as LRRK2(NM_198578.3):c.356T>C (p.L119P), LRRK2(NM_198578.4):c.356T>C (p.L119P)
ISCN -
DB-ID LRRK2_000062 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00124 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRK2 NM_198578.3 ?/. - c.356T>C r.(?) p.(Leu119Pro)


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