Variant #0000266455 (NC_000012.11:g.1995403T>C, NM_172364.4:c.979A>G (CACNA2D4))

Chromosome 12
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.1995403T>C
DNA change (hg38) g.1886237T>C
Published as CACNA2D4(NM_172364.5):c.979A>G (p.I327V)
ISCN -
DB-ID CACNA2D4_000034
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) 0.90313 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTM2 NM_001039029.2 -/. - c.*51516T>C r.(=) p.(=)
CACNA2D4 NM_172364.4 -/. - c.979A>G r.(?) p.(Ile327Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.