Variant #0000322459 (NC_000011.9:g.96124465A>T, NM_024725.3:c.-1596T>A (CCDC82))

Chromosome 11
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.96124465A>T
DNA change (hg38) g.96391301A>T
Published as JRKL(NM_003772.3):c.652A>T (p.(Thr218Ser))
ISCN -
DB-ID JRKL_000001
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 2018-01-15 20:58:59 +01:00 (CET)
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)     

RNA change     

Protein     
JRKL NM_003772.3 ?/. - c.652A>T r.(?) p.(Thr218Ser)
CCDC82 NM_024725.3 ?/. - c.-1596T>A r.(?) p.(=)


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