Variant #0000541510 (NC_000010.10:g.90983509T>A, NM_001127605.1:c.754A>T (LIPA))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90983509T>A
DNA change (hg38) g.89223752T>A
Published as LIPA(NM_000235.3):c.754A>T (p.I252L), LIPA(NM_000235.4):c.754A>T (p.I252L)
ISCN -
DB-ID LIPA_000009 See all 2 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) 0.00139 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 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIPA NM_000235.3 -?/. - c.754A>T r.(?) p.(Ile252Leu)
LIPA NM_001127605.1 -?/. - c.754A>T r.(?) p.(Ile252Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.