Variant #0000805839 (NC_000012.11:g.53702994G>A, NM_015665.5:c.882C>T (AAAS))

Chromosome 12
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.53702994G>A
DNA change (hg38) -
Published as AAAS(NM_015665.5):c.882C>T (p.L294=)
ISCN -
DB-ID C12orf10_000008
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) 0.00028 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 2021-09-17 14:40:49 +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     
PFDN5 NM_002624.3 -?/. - c.*9865G>A r.(=) p.(=)
AAAS NM_015665.5 -?/. - c.882C>T r.(?) p.(Leu294=)
C12orf10 NM_021640.3 -?/. - c.*2061G>A r.(=) p.(=)


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