Variant #0000654994 (NC_000003.11:g.50385316C>T, NM_006030.2:c.*16781G>A (CACNA2D2))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.50385316C>T
DNA change (hg38) g.50347885C>T
Published as -
ISCN -
DB-ID CACNA2D2_000006
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA2D2 NM_006030.2 +?/. - c.*16781G>A r.(=) p.(=)
NPRL2 NM_006545.4 +?/. - c.949G>A r.(?) p.(Gly317Arg)
CYB561D2 NM_007022.3 +?/. - c.-3191C>T r.(?) p.(=)
TMEM115 NM_007024.4 +?/. - c.*7458G>A r.(=) p.(=)
ZMYND10 NM_015896.2 +?/. - c.-2306G>A r.(?) p.(=)


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