Variant #0001065502 (NC_000011.9:g.64813994T>C, NM_005468.2:c.1604A>G (NAALADL1))

Chromosome 11
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.64813994T>C
DNA change (hg38) -
Published as NAALADL1(NM_005468.3):c.1604A>G (p.(Lys535Arg))
ISCN -
DB-ID NAALADL1_000010
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) 0.00035 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAALADL1 NM_005468.2 ?/. - c.1604A>G r.(?) p.(Lys535Arg)
SAC3D1 NM_013299.3 ?/. - c.*1795T>C r.(=) p.(=)


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