Variant #0000690314 (NC_000008.10:g.6335137C>G, NM_001118887.1:c.*25485G>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.6335137C>G
DNA change (hg38) -
Published as MCPH1(NM_024596.5):c.1958C>G (p.T653R)
ISCN -
DB-ID ANGPT2_000030
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) 1.0E-5 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 2020-09-15 15:50:26 +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.*25485G>C r.(=) p.(=)
MCPH1 NM_024596.2 ?/. - c.1958C>G r.(?) p.(Thr653Arg)
MCPH1 NM_024596.3 ?/. - c.1958C>G r.(?) p.(Thr653Arg)


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