Variant #0000997289 (NC_000008.10:g.6302633G>A, NM_001118887.1:c.*57989C>T (ANGPT2))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6302633G>A
DNA change (hg38) -
Published as MCPH1(NM_024596.3):c.1390G>A (p.(Val464Ile))
ISCN -
DB-ID ANGPT2_000047
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) 0.00031 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.*57989C>T r.(=) p.(=)
MCPH1 NM_024596.3 -?/. - c.1390G>A r.(?) p.(Val464Ile)


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