Variant #0000544952 (NC_000011.9:g.64821742G>A, NM_005468.2:c.972C>T (NAALADL1))

Chromosome 11
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.64821742G>A
DNA change (hg38) g.65054270G>A
Published as NAALADL1(NM_005468.3):c.972C>T (p.D324=)
ISCN -
DB-ID NAALADL1_000006
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 18:01:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAALADL1 NM_005468.2 -?/. - c.972C>T r.(?) p.(Asp324=)
SAC3D1 NM_013299.3 -?/. - c.*9543G>A r.(=) p.(=)


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