Variant #0000910822 (NC_000001.10:g.160160756A>G, NM_001231.4:c.215A>G (CASQ1))

Chromosome 1
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.160160756A>G
DNA change (hg38) -
Published as CASQ1(NM_001231.5):c.215A>G (p.H72R)
ISCN -
DB-ID ATP1A4_000008
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) 0.00327 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 2023-01-11 15:44:22 +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     
CASQ1 NM_001231.4 -/. - c.215A>G r.(?) p.(His72Arg)
ATP1A4 NM_144699.3 -/. - c.*4267A>G r.(=) p.(=)


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