Variant #0001000331 (NC_000012.11:g.75683555T>C, NM_032606.3:c.1298A>G (CAPS2))

Chromosome 12
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.75683555T>C
DNA change (hg38) -
Published as CAPS2(NM_032606.3):c.1298A>G (p.(Asp433Gly))
ISCN -
DB-ID CAPS2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAPS2 NM_032606.3 ?/. - c.1298A>G r.(?) p.(Asp433Gly)
GLIPR1L1 NM_152779.2 ?/. - c.-44954T>C r.(?) p.(=)


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