Variant #0000282107 (NC_000023.10:g.119589400C>A, NM_001122606.1:c.209G>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.119589400C>A
DNA change (hg38) g.120455545C>A
Published as LAMP2(NM_002294.3):c.209G>T (p.G70V)
ISCN -
DB-ID LAMP2_000111
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.209G>T r.(?) p.(Gly70Val)
LAMP2 NM_002294.2 -?/. - c.209G>T r.(?) p.(Gly70Val)


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