Variant #0001005702 (NC_000021.8:g.34957011G>A, NM_138927.2:c.*8281G>A (SON))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34957011G>A
DNA change (hg38) -
Published as DONSON(NM_017613.3):c.670C>T (p.(Pro224Ser))
ISCN -
DB-ID CRYZL1_000007
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 2024-08-28 13:16:32 +02:00 (CEST)
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.670C>T - r.(?) p.(Pro224Ser)
SON NM_138927.2 +/. - c.*8281G>A - r.(=) p.(=)
CRYZL1 NM_145858.2 +/. - c.*5117C>T - r.(=) p.(=)


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