Variant #0000677061 (NC_000003.11:g.50385235G>T, NM_006030.2:c.*16862C>A (CACNA2D2))

Chromosome 3
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.50385235G>T
DNA change (hg38) -
Published as NPRL2(NM_006545.4):c.1030C>A (p.L344I)
ISCN -
DB-ID CACNA2D2_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA2D2 NM_006030.2 ?/. - c.*16862C>A r.(=) p.(=)
NPRL2 NM_006545.4 ?/. - c.1030C>A r.(?) p.(Leu344Ile)
CYB561D2 NM_007022.3 ?/. - c.-3272G>T r.(?) p.(=)
TMEM115 NM_007024.4 ?/. - c.*7539C>A r.(=) p.(=)
ZMYND10 NM_015896.2 ?/. - c.-2225C>A r.(?) p.(=)


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