Variant #0000573289 (NC_000023.10:g.119589270G>A, NM_001122606.1:c.339C>T (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.119589270G>A
DNA change (hg38) g.120455415G>A
Published as LAMP2(NM_002294.2):c.339C>T (p.S113=), LAMP2(NM_002294.3):c.339C>T (p.S113=)
ISCN -
DB-ID LAMP2_000109 See all 5 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) 0.00074 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.339C>T r.(?) p.(Ser113=)
LAMP2 NM_002294.2 -?/. - c.339C>T r.(?) p.(Ser113=)


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