Variant #0000573293 (NC_000023.10:g.119590616G>A, NM_001122606.1:c.73C>T (LAMP2))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.119590616G>A
DNA change (hg38) g.120456761G>A
Published as LAMP2(NM_002294.2):c.73C>T (p.R25W), LAMP2(NM_002294.3):c.73C>T (p.R25W)
ISCN -
DB-ID LAMP2_000142 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMP2 NM_001122606.1 ?/. - c.73C>T r.(?) p.(Arg25Trp)
LAMP2 NM_002294.2 ?/. - c.73C>T r.(?) p.(Arg25Trp)


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