Variant #0001039464 (NC_000012.11:g.75710214A>G, NM_032606.3:c.526T>C (CAPS2))

Chromosome 12
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.75710214A>G
DNA change (hg38) -
Published as CAPS2(NM_001355024.2):c.376T>C (p.(Cys126Arg))
ISCN -
DB-ID CAPS2_000003
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) 0.00152 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPS2 NM_032606.3 -?/. - c.526T>C r.(?) p.(Cys176Arg)
GLIPR1L1 NM_152779.2 -?/. - c.-18295A>G r.(?) p.(=)


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