Variant #0000290850 (NC_000023.10:g.119590533T>A, NM_001122606.1:c.156A>T (LAMP2))

Chromosome X
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.119590533T>A
DNA change (hg38) g.120456678T>A
Published as LAMP2(NM_002294.2):c.156A>T (p.V52=), LAMP2(NM_002294.3):c.156A>T (p.V52=)
ISCN -
DB-ID LAMP2_000001 See all 8 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) 0.38951 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 2018-01-15 20:58:59 +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     
LAMP2 NM_001122606.1 -/. - c.156A>T r.(?) p.(Val52=)
LAMP2 NM_002294.2 -/. - c.156A>T r.(?) p.(Val52=)


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