Variant #0000570580 (NC_000021.8:g.34960634G>C, NM_138927.2:c.*11904G>C (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.34960634G>C
DNA change (hg38) g.33588328G>C
Published as DONSON(NM_017613.3):c.314C>G (p.(Pro105Arg))
ISCN -
DB-ID CRYZL1_000002
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) 0.02301 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
DONSON NM_017613.3 -?/. - c.314C>G - r.(?) p.(Pro105Arg)
SON NM_138927.2 -?/. - c.*11904G>C - r.(=) p.(=)
CRYZL1 NM_145858.2 -?/. - c.*1494C>G - r.(=) p.(=)


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