Variant #0001065170 (NC_000009.11:g.138710995G>A, NC_000009.11(NM_015447.3):c.3823-3C>T (CAMSAP1))

Chromosome 9
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.138710995G>A
DNA change (hg38) -
Published as CAMSAP1(NM_015447.4):c.3823-3C>T
ISCN -
DB-ID CAMSAP1_000023
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) 0.00155 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 2026-01-20 18:57:21 +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     
CAMSAP1 NM_015447.3 ?/. - c.3823-3C>T r.spl? p.?


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