Variant #0000682352 (NC_000023.10:g.23898976C>T, APOO(NM_024122.4):c.103G>A)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23898976C>T
DNA change (hg38) -
Published as APOO(NM_024122.4):c.103G>A (p.(Val35Met))
ISCN -
DB-ID APOO_000010
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) 0.0001 View details
Owner VKGL-NL_Leiden
Database submission license No license selected
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOO NM_024122.4 -?/. - c.103G>A r.(?) p.(Val35Met)