Variant #0001013247 (NC_000001.10:g.181765954G>A, NM_000721.3:c.6230G>A (CACNA1E))

Chromosome 1
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.181765954G>A
DNA change (hg38) -
Published as CACNA1E(NM_000721.3):c.6230G>A (p.(Arg2077Lys)), CACNA1E(NM_000721.4):c.6230G>A (p.R2077K)
ISCN -
DB-ID CACNA1E_000007 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) 0.00057 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 20:49:11 +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     
CACNA1E NM_000721.3 -?/. - c.6230G>A r.(?) p.(Arg2077Lys)
CACNA1E NM_001205293.1 -?/. - c.6359G>A r.(?) p.(Arg2120Lys)


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