Variant #0000503806 (NC_000001.10:g.156562143G>A, NC_000001.10(NM_144772.2):c.292-14G>A (APOA1BP))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156562143G>A
DNA change (hg38) g.156592351G>A
Published as -
ISCN -
DB-ID APOA1BP_000002
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) 0.95798 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC24 NM_001105669.2 -/. - c.*5801G>A r.(=) p.(=)
GPATCH4 NM_015590.3 -/. - c.*2862C>T r.(=) p.(=)
APOA1BP NM_144772.2 -/. - c.292-14G>A r.(=) p.(=)


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