Variant #0000925363 (NC_000011.9:g.20070668A>G, NM_145117.4:c.4297A>G (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.20070668A>G
DNA change (hg38) -
Published as NAV2(NM_001111018.1):c.4105A>G (p.(Ile1369Val)), NAV2(NM_001244963.1):c.4366A>G (p.I1456V)
ISCN -
DB-ID NAV2_000006 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) 0.01538 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAV2 NM_145117.4 -?/. - c.4297A>G r.(?) p.(Ile1433Val)


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