Variant #0000853457 (NC_000012.11:g.53701436C>T, NM_015665.5:c.1478G>A (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.53701436C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID C12orf10_000009
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFDN5 NM_002624.3 ?/. - c.*8307C>T r.(=) p.(=)
AAAS NM_015665.5 ?/. - c.1478G>A r.(?) p.(Arg493His)
C12orf10 NM_021640.3 ?/. - c.*503C>T r.(=) p.(=)


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