Variant #0000291631 (NC_000008.10:g.6479042C>T, NM_001118887.1:c.-58587G>A (ANGPT2))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6479042C>T
DNA change (hg38) g.6621521C>T
Published as MCPH1(NM_024596.4):c.2282C>T (p.A761V), MCPH1(NM_024596.5):c.2282C>T (p.A761V)
ISCN -
DB-ID MCPH1_000046 See all 3 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) 0.43306 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.-58587G>A r.(?) p.(=)
MCPH1 NM_024596.2 -/. - c.2282C>T r.(?) p.(Ala761Val)
MCPH1 NM_024596.3 -/. - c.2282C>T r.(?) p.(Ala761Val)


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