Variant #0000691379 (NC_000012.11:g.53701471G>A, NM_015665.5:c.1443C>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.53701471G>A
DNA change (hg38) -
Published as AAAS(NM_015665.5):c.1443C>T (p.H481=)
ISCN -
DB-ID C12orf10_000005
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.*8342G>A r.(=) p.(=)
AAAS NM_015665.5 -?/. - c.1443C>T r.(?) p.(His481=)
C12orf10 NM_021640.3 -?/. - c.*538G>A r.(=) p.(=)


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