Variant #0000322893 (NC_000012.11:g.53700866G>A, NM_015665.5:c.*407C>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.53700866G>A
DNA change (hg38) g.53307082G>A
Published as C12orf10(NM_021640.3):c.1064G>A (p.(Arg355Gln))
ISCN -
DB-ID C12orf10_000001
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) 3.0E-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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFDN5 NM_002624.3 ?/. - c.*7737G>A r.(=) p.(=)
AAAS NM_015665.5 ?/. - c.*407C>T r.(=) p.(=)
C12orf10 NM_021640.3 ?/. - c.1064G>A r.(?) p.(Arg355Gln)


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