Variant #0000925365 (NC_000011.9:g.20129244G>A, NM_145117.4:c.6876G>A (NAV2))

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.20129244G>A
DNA change (hg38) -
Published as NAV2(NM_001111018.1):c.6684G>A (p.(Val2228=))
ISCN -
DB-ID NAV2_000024
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) 0.00016 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAV2 NM_145117.4 -?/. - c.6876G>A r.(?) p.(Val2292=)


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