Variant #0000719529 (NC_000003.11:g.50385077C>T, NM_006030.2:c.*17020G>A (CACNA2D2))

Chromosome 3
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.50385077C>T
DNA change (hg38) -
Published as NPRL2(NM_006545.4):c.1103G>A (p.R368Q)
ISCN -
DB-ID CACNA2D2_000008
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA2D2 NM_006030.2 -?/. - c.*17020G>A r.(=) p.(=)
NPRL2 NM_006545.4 -?/. - c.1103G>A r.(?) p.(Arg368Gln)
CYB561D2 NM_007022.3 -?/. - c.-3430C>T r.(?) p.(=)
TMEM115 NM_007024.4 -?/. - c.*7697G>A r.(=) p.(=)
ZMYND10 NM_015896.2 -?/. - c.-2067G>A r.(?) p.(=)


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