Variant #0001056997 (NC_000021.8:g.34960866T>G, NM_138927.2:c.*12136T>G (SON))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.34960866T>G
DNA change (hg38) -
Published as DONSON(NM_017613.4):c.82A>C (p.(Ser28Arg), p.S28R)
ISCN -
DB-ID CRYZL1_000006 See all 3 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) 0.00172 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
DONSON NM_017613.3 ?/. - c.82A>C - r.(?) p.(Ser28Arg)
SON NM_138927.2 ?/. - c.*12136T>G - r.(=) p.(=)
CRYZL1 NM_145858.2 ?/. - c.*1262A>C - r.(=) p.(=)


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