Variant #0000690831 (NC_000010.10:g.90985069_90985081del, NC_000010.10(NM_001127605.1):c.539-95_539-83del (LIPA))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90985069_90985081del
DNA change (hg38) -
Published as LIPA(NM_001127605.3):c.539-95_539-83delTCCGCGAGAGGGC
ISCN -
DB-ID LIPA_000084
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIPA NM_001127605.1 -/. - c.539-95_539-83del r.(=) p.(=)


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