Variant #0000322895 (NC_000012.11:g.53702572G>A, NM_015665.5:c.1024C>T (AAAS))

Chromosome 12
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.53702572G>A
DNA change (hg38) g.53308788G>A
Published as AAAS(NM_001173466.1):c.925C>T (p.(Arg309Ter)), AAAS(NM_015665.5):c.1024C>T (p.R342*)
ISCN -
DB-ID AAAS_000004 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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-02 16:03:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFDN5 NM_002624.3 ?/. - c.*9443G>A r.(=) p.(=)
AAAS NM_015665.5 ?/. - c.1024C>T r.(?) p.(Arg342Ter)
C12orf10 NM_021640.3 ?/. - c.*1639G>A r.(=) p.(=)


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