Variant #0000866622 (NC_000021.8:g.34925225_34925278dup, NM_138927.2:c.3688_3741dup (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.34925225_34925278dup
DNA change (hg38) -
Published as SON(NM_032195.3):c.3688_3741dup (p.Y1230_T1247dup), SON(NM_138927.2):c.3688_3741dup (p.Y1230_T1247dup)
ISCN -
DB-ID SON_000039 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 16:01:56 +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.3688_3741dup r.(?) p.(Tyr1230_Thr1247dup)


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