Variant #0000250570 (NC_000001.10:g.38056362A>T, NM_003462.3:c.*25700A>T (DNALI1))

Chromosome 1
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.38056362A>T
DNA change (hg38) g.37590761A>T
Published as GNL2(NM_013285.3):c.329T>A (p.V110D)
ISCN -
DB-ID GNL2_000004
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNALI1 NM_003462.3 ?/. - c.*25700A>T r.(=) p.(=)
GNL2 NM_013285.2 ?/. - c.329T>A r.(?) p.(Val110Asp)


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