Variant #0000614956 (NC_000014.8:g.32257017T>C, NM_025152.2:c.545T>C (NUBPL))

Chromosome 14
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.32257017T>C
DNA change (hg38) g.31787811T>C
Published as NUBPL(NM_025152.2):c.545T>C (p.V182A), NUBPL(NM_025152.3):c.545T>C (p.(Val182Ala), p.V182A)
ISCN -
DB-ID NUBPL_000014 See all 3 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) 0.0025 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NUBPL NM_025152.2 -?/. - c.545T>C r.(?) p.(Val182Ala)


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