Variant #0001025403 (NC_000007.13:g.45113054C>T, NC_000007.13(NM_031443.3):c.804-5C>T (CCM2))

Chromosome 7
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.45113054C>T
DNA change (hg38) -
Published as CCM2(NM_001029835.2):c.867-5C>T (p.?), CCM2(NM_031443.3):c.804-5C>T, CCM2(NM_031443.4):c.804-5C>T
ISCN -
DB-ID CCM2_000026 See all 3 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) 0.00236 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 2025-02-07 18:57:27 +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     
CCM2 NM_031443.3 -?/. - c.804-5C>T r.spl? p.?


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