Variant #0000805646 (NC_000012.11:g.1988975C>T, NM_172364.4:c.1558G>A (CACNA2D4))

Chromosome 12
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.1988975C>T
DNA change (hg38) -
Published as CACNA2D4(NM_172364.4):c.1558G>A (p.E520K)
ISCN -
DB-ID CACNA2D4_000091
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) 5.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTM2 NM_001039029.2 ?/. - c.*45088C>T r.(=) p.(=)
CACNA2D4 NM_172364.4 ?/. - c.1558G>A r.(?) p.(Glu520Lys)


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