Variant #0000535232 (NC_000008.10:g.6479054C>G, NM_001118887.1:c.-58599G>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.6479054C>G
DNA change (hg38) g.6621533C>G
Published as MCPH1(NM_024596.4):c.2294C>G (p.S765W)
ISCN -
DB-ID ANGPT2_000022
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) 0.00028 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 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.-58599G>C r.(?) p.(=)
MCPH1 NM_024596.2 ?/. - c.2294C>G r.(?) p.(Ser765Trp)
MCPH1 NM_024596.3 ?/. - c.2294C>G r.(?) p.(Ser765Trp)


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