Variant #0000924733 (NC_000007.13:g.45115581G>A, NM_031443.3:c.1260G>A (CCM2))

Chromosome 7
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.45115581G>A
DNA change (hg38) -
Published as CCM2(NM_001029835.2):c.1323G>A (p.(Glu441=)), CCM2(NM_001363458.2):c.1383G>A (p.E461=), CCM2(NM_031443.3):c.1260G>A (p.E420=)
ISCN -
DB-ID CCM2_000050 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) 0.00324 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NACAD NM_001146334.1 -/. - c.*4527C>T r.(=) p.(=)
CCM2 NM_031443.3 -/. - c.1260G>A r.(?) p.(Glu420=)


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