Variant #0000272528 (NC_000012.11:g.1963173C>T, NM_172364.4:c.2190G>A (CACNA2D4))

Chromosome 12
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.1963173C>T
DNA change (hg38) g.1854007C>T
Published as CACNA2D4(NM_172364.4):c.2190G>A (p.A730=), CACNA2D4(NM_172364.5):c.2190G>A (p.A730=)
ISCN -
DB-ID CACNA2D4_000021 See all 2 reported entries
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) 0.00054 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTM2 NM_001039029.2 -?/. - c.*19286C>T r.(=) p.(=)
CACNA2D4 NM_172364.4 -?/. - c.2190G>A r.(?) p.(Ala730=)


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