Variant #0000710080 (NC_000001.10:g.21880603T>C, NM_000478.4:c.29T>C (ALPL))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.21880603T>C
DNA change (hg38) g.21554110T>C
Published as -
ISCN -
DB-ID ALPL_000052 See all 3 reported entries
Variant remarks cDNA expression cloning varriant and variant+WT in MDCKII cells
Reference PubMed: del Angel 2020
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-12-30 15:27:54 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
ALPL NM_000478.4 +/. 2 c.29T>C - p.Ile10Thr 0.29 relative activity, 0.65 WT/combined activity


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