Variant #0000264028 (NC_000003.11:g.53757924G>A, NM_000720.3:c.2058G>A (CACNA1D))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53757924G>A
DNA change (hg38) g.53723897G>A
Published as CACNA1D(NM_000720.3):c.2058G>A (p.L686=), CACNA1D(NM_000720.4):c.2058G>A (p.L686=)
ISCN -
DB-ID CACNA1D_000042 See all 3 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) 0.00199 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 -/. - c.2058G>A r.(?) p.(Leu686=)
CACNA1D NM_001128840.2 -/. - c.1998G>A r.(?) p.(Leu666=)


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