Variant #0000983961 (NC_000021.8:g.34923703_34923705dup, NM_138927.2:c.2166_2168dup (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.34923703_34923705dup
DNA change (hg38) -
Published as SON(NM_032195.3):c.2166_2168dupGAC (p.T723dup), SON(NM_138927.4):c.2166_2168dup (p.(Thr723dup))
ISCN -
DB-ID SON_000098 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
SON NM_138927.2 -?/. - c.2166_2168dup r.(?) p.(Thr723dup)


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