Variant #0000535223 (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) g.6499860G>A
Published as MCPH1(NM_001322042.1):c.2145G>A (p.W715*)
ISCN -
DB-ID ANGPT2_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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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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