Variant #0000260088 (NC_000001.10:g.21889760G>A, ALPL(NM_000478.4):c.455G>A)

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.21889760G>A
DNA change (hg38) g.21563267G>A
Published as ALPL(NM_000478.4):c.455G>A (p.(Arg152His)), ALPL(NM_000478.5):c.455G>A (p.R152H)
ISCN -
DB-ID ALPL_000002 See all 7 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01157 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
ALPL NM_000478.4 -/. - c.455G>A r.(?) p.(Arg152His) -