Variant #0000927248 (NC_000023.10:g.119590604A>G, NM_001122606.1:c.85T>C (LAMP2))

Chromosome X
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.119590604A>G
DNA change (hg38) -
Published as LAMP2(NM_002294.2):c.85T>C (p.L29=), LAMP2(NM_002294.3):c.85T>C (p.L29=)
ISCN -
DB-ID LAMP2_000116 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) 3.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMP2 NM_001122606.1 -?/. - c.85T>C r.(?) p.(Leu29=)
LAMP2 NM_002294.2 -?/. - c.85T>C r.(?) p.(Leu29=)


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