Variant #0000272519 (NC_000001.10:g.201060837T>C, NM_000069.2:c.625A>G (CACNA1S))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.201060837T>C
DNA change (hg38) g.201091709T>C
Published as CACNA1S(NM_000069.2):c.625A>G (p.I209V), CACNA1S(NM_000069.3):c.625A>G (p.(Ile209Val))
ISCN -
DB-ID CACNA1S_000069 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) Retrieve
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 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1S NM_000069.2 ?/. - c.625A>G r.(?) p.(Ile209Val)


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