Variant #0000885913 (NC_000003.11:g.50405242C>T, NC_000003.11(NM_006030.2):c.2234+1G>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.50405242C>T
DNA change (hg38) -
Published as CACNA2D2(NM_001005505.3):c.2234+1G>A
ISCN -
DB-ID CACNA2D2_000018
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +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.2234+1G>A r.spl? p.?
NPRL2 NM_006545.4 +?/. - c.-17159G>A r.(?) p.(=)
CYB561D2 NM_007022.3 +?/. - c.*14067C>T r.(=) p.(=)
TMEM115 NM_007024.4 +?/. - c.-8748G>A r.(?) p.(=)


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