Variant #0000997293 (NC_000008.10:g.6420445A>G, NM_001118887.1:c.11T>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.6420445A>G
DNA change (hg38) -
Published as ANGPT2(NM_001147.2):c.11T>C (p.(Ile4Thr))
ISCN -
DB-ID ANGPT2_000050
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANGPT2 NM_001118887.1 ?/. - c.11T>C r.(?) p.(Ile4Thr)
MCPH1 NM_024596.3 ?/. - c.2215-58530A>G r.(=) p.(=)


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