Variant #0000894038 (NC_000017.10:g.48646274G>A, NM_018896.4:c.286G>A (CACNA1G))

Chromosome 17
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.48646274G>A
DNA change (hg38) -
Published as CACNA1G(NM_018896.4):c.286G>A (p.V96M), CACNA1G(NM_018896.5):c.286G>A (p.V96M)
ISCN -
DB-ID CACNA1G_000018 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) 0.0004 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 2022-11-01 13:41:49 +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     
CACNA1G NM_018896.4 -?/. - c.286G>A r.(?) p.(Val96Met)


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