Variant #0001064881 (NC_000008.10:g.6357381G>A, NM_001118887.1:c.*3241C>T (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.6357381G>A
DNA change (hg38) -
Published as MCPH1(NM_001322042.1):c.2145G>A (p.W715*)
ISCN -
DB-ID ANGPT2_000017 See all 2 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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
ANGPT2 NM_001118887.1 +/. - c.*3241C>T r.(=) p.(=)
MCPH1 NM_024596.2 +/. - c.2145G>A r.(?) p.(Trp715Ter)
MCPH1 NM_024596.3 +/. - c.2145G>A r.(?) p.(Trp715Ter)


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