Variant #0000612795 (NC_000010.10:g.91007629_91007640del, NC_000010.10(NM_001127605.1):c.-1-209_-1-198del (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.91007629_91007640del
DNA change (hg38) g.89247872_89247883del
Published as LIPA(NM_000235.4):c.-1-209_-1-198delTAAATAAATAAA
ISCN -
DB-ID LIPA_000073
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 2019-12-04 15:24:38 +01:00 (CET)
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     
LIPA NM_001127605.1 -/. - c.-1-209_-1-198del r.(=) p.(=)


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