Variant #0000291618 (NC_000008.10:g.6302594G>A, NM_001118887.1:c.*58028C>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.6302594G>A
DNA change (hg38) g.6445073G>A
Published as MCPH1(NM_024596.4):c.1351G>A (p.E451K)
ISCN -
DB-ID MCPH1_000025
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) 0.00125 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPT2 NM_001118887.1 -?/. - c.*58028C>T r.(=) p.(=)
MCPH1 NM_024596.2 -?/. - c.1351G>A r.(?) p.(Glu451Lys)
MCPH1 NM_024596.3 -?/. - c.1351G>A r.(?) p.(Glu451Lys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.