Variant #0000905500 (NC_000001.10:g.21887145C>T, NM_000478.4:c.88C>T (ALPL))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.21887145C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ALPL_000063 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1057516334
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-01 17:10:01 +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 +/. - c.88C>T r.(?) p.(Arg30Ter) -


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