Variant #0000997294 (NC_000008.10:g.6479122C>T, NM_001118887.1:c.-58667G>A (ANGPT2))

Chromosome 8
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.6479122C>T
DNA change (hg38) -
Published as MCPH1(NM_024596.3):c.2362C>T (p.(Gln788*))
ISCN -
DB-ID ANGPT2_000051
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPT2 NM_001118887.1 +/. - c.-58667G>A r.(?) p.(=)
MCPH1 NM_024596.3 +/. - c.2362C>T r.(?) p.(Gln788*)


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