Variant #0001037024 (NC_000008.10:g.6357416C>T, NM_001118887.1:c.*3206G>A (ANGPT2))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.6357416C>T
DNA change (hg38) -
Published as MCPH1(NM_024596.4):c.2180C>T (p.P727L), MCPH1(NM_024596.5):c.2180C>T (p.(Pro727Leu), p.P727L)
ISCN -
DB-ID ANGPT2_000018 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) 0.00098 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPT2 NM_001118887.1 ?/. - c.*3206G>A r.(=) p.(=)
MCPH1 NM_024596.2 ?/. - c.2180C>T r.(?) p.(Pro727Leu)
MCPH1 NM_024596.3 ?/. - c.2180C>T r.(?) p.(Pro727Leu)


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