Variant #0000804628 (NC_000010.10:g.91007160_91007168del, NC_000010.10(NM_001127605.1):c.111+150_111+158del (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.91007160_91007168del
DNA change (hg38) -
Published as LIPA(NM_000235.4):c.111+150_111+158delTTTTTTTTT, LIPA(NM_001127605.3):c.111+150_111+158delTTTTTTTTT
ISCN -
DB-ID LIPA_000107
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIPA NM_000235.3 -?/. - c.111+150_111+158del r.(=) p.(=)
LIPA NM_001127605.1 -?/. - c.111+150_111+158del r.(=) p.(=)


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