Variant #0001071222 (NC_000021.8:g.34924792_34924818del, NM_138927.2:c.3255_3281del (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.34924792_34924818del
DNA change (hg38) -
Published as -
ISCN -
DB-ID SON_000153
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs773188939
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-24 16:51:01 +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     
SON NM_138927.2 -?/. - c.3255_3281del r.(?) p.(Met1086_Ser1094del)


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