Variant #0000915447 (NC_000021.8:g.34918579G>A, NM_138927.2:c.138G>A (SON))

Chromosome 21
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.34918579G>A
DNA change (hg38) -
Published as SON(NM_138927.2):c.138G>A (p.A46=)
ISCN -
DB-ID GART_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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GART NM_000819.4 -?/. - c.-4250C>T r.(?) p.(=)
SON NM_138927.2 -?/. - c.138G>A r.(?) p.(Ala46=)


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