Variant #0000503805 (NC_000001.10:g.156561929T>A, NM_144772.2:c.219T>A (APOA1BP))

Chromosome 1
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.156561929T>A
DNA change (hg38) g.156592137T>A
Published as NAXE(NM_144772.2):c.219T>A (p.F73L)
ISCN -
DB-ID APOA1BP_000001
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) Retrieve
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 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.*5587T>A r.(=) p.(=)
GPATCH4 NM_015590.3 -?/. - c.*3076A>T r.(=) p.(=)
APOA1BP NM_144772.2 -?/. - c.219T>A r.(?) p.(Phe73Leu)


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