Variant #0000272834 (NC_000007.13:g.45115396G>T, NM_031443.3:c.1075G>T (CCM2))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45115396G>T
DNA change (hg38) g.45075797G>T
Published as CCM2(NM_031443.3):c.1075G>T (p.E359*)
ISCN -
DB-ID CCM2_000031
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 15:55:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NACAD NM_001146334.1 +/. - c.*4712C>A r.(=) p.(=)
CCM2 NM_031443.3 +/. - c.1075G>T r.(?) p.(Glu359Ter)


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