Variant #0000966993 (NC_000012.11:g.53701482G>A, NM_015665.5:c.1432C>T (AAAS))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.53701482G>A
DNA change (hg38) -
Published as AAAS(NM_015665.6):c.1432C>T (p.R478*)
ISCN -
DB-ID AAAS_000019 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) 4.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFDN5 NM_002624.3 +/. - c.*8353G>A r.(=) p.(=)
AAAS NM_015665.5 +/. - c.1432C>T r.(?) p.(Arg478*)
C12orf10 NM_021640.3 +/. - c.*549G>A r.(=) p.(=)


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