Variant #0000535230 (NC_000008.10:g.6478981C>T, NM_001118887.1:c.-58526G>A (ANGPT2))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6478981C>T
DNA change (hg38) g.6621460C>T
Published as MCPH1(NM_024596.4):c.2221C>T (p.R741*)
ISCN -
DB-ID ANGPT2_000020 See all 4 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) 5.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-58526G>A r.(?) p.(=)
MCPH1 NM_024596.2 +/. - c.2221C>T r.(?) p.(Arg741Ter)
MCPH1 NM_024596.3 +/. - c.2221C>T r.(?) p.(Arg741Ter)


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