Variant #0000577551 (NC_000023.10:g.77286962_77286966del, NM_000052.5:c.3176_3180del (ATP7A))

Chromosome X
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.77286962_77286966del
DNA change (hg38) g.78031464_78031468del
Published as ATP7A(NM_000052.6):c.3176_3180delTAAAG (p.V1059Gfs*4)
ISCN -
DB-ID PGAM4_000016
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 2020-10-01 19:36:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
ATP7A NM_000052.5 +/. - c.3176_3180del r.(?) p.(Val1059GlyfsTer4) -
PGAM4 NM_001029891.2 +/. - c.-61828_-61824del r.(?) p.(=) -


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