Variant #0000279631 (NC_000008.10:g.6378784C>A, NM_001118887.1:c.714G>T (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.6378784C>A
DNA change (hg38) g.6521263C>A
Published as ANGPT2(NM_001147.3):c.714G>T (p.T238=), MCPH1(NM_024596.5):c.2214+21334C>A
ISCN -
DB-ID MCPH1_000041
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) 0.06439 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.714G>T r.(?) p.(Thr238=)
MCPH1 NM_024596.2 -/. - c.2214+21334C>A r.(=) p.(=)
MCPH1 NM_024596.3 -/. - c.2214+21334C>A r.(=) p.(=)


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