Variant #0000255893 (NC_000008.10:g.6272353A>G, NM_001118887.1:c.*88269T>C (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.6272353A>G
DNA change (hg38) g.6414832A>G
Published as MCPH1(NM_024596.4):c.182A>G (p.D61G)
ISCN -
DB-ID MCPH1_000058
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) 0.00206 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 2024-08-28 13:16:32 +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.*88269T>C r.(=) p.(=)
MCPH1 NM_024596.2 ?/. - c.182A>G r.(?) p.(Asp61Gly)
MCPH1 NM_024596.3 ?/. - c.182A>G r.(?) p.(Asp61Gly)


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