Variant #0000951273 (NC_000019.9:g.36042010A>T, NM_032635.3:c.*3661A>T (TMEM147))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36042010A>T
DNA change (hg38) -
Published as ATP4A(NM_000704.3):c.2889T>A (p.N963K)
ISCN -
DB-ID ATP4A_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     
ATP4A NM_000704.2 +?/. - c.2889T>A r.(?) p.(Asn963Lys)
TMEM147 NM_032635.3 +?/. - c.*3661A>T r.(=) p.(=)


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