Variant #0000612785 (NC_000010.10:g.90984991A>G, NC_000010.10(NM_001127605.1):c.539-6T>C (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.90984991A>G
DNA change (hg38) g.89225234A>G
Published as LIPA(NM_000235.3):c.539-6T>C, LIPA(NM_001127605.3):c.539-6T>C
ISCN -
DB-ID LIPA_000059 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) 0.00035 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIPA NM_001127605.1 -?/. - c.539-6T>C r.(=) p.(=)


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