Variant #0000888431 (NC_000008.10:g.6357438C>A, NM_001118887.1:c.*3184G>T (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.6357438C>A
DNA change (hg38) -
Published as MCPH1(NM_024596.5):c.2202C>A (p.F734L)
ISCN -
DB-ID ANGPT2_000040
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) 0.00056 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.*3184G>T r.(=) p.(=)
MCPH1 NM_024596.3 ?/. - c.2202C>A r.(?) p.(Phe734Leu)


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