Variant #0000809831 (NC_000023.10:g.119603028C>G, NM_001122606.1:c.-4G>C (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.119603028C>G
DNA change (hg38) -
Published as LAMP2(NM_002294.3):c.-4G>C
ISCN -
DB-ID LAMP2_000145 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) 0.00021 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +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.-4G>C r.(?) p.(=)
LAMP2 NM_002294.2 -/. - c.-4G>C r.(?) p.(=)


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