Variant #0000931467 (NC_000023.10:g.77224504G>A, NC_000023.10(NM_000052.5):c.-21-2614G>A (ATP7A))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77224504G>A
DNA change (hg38) -
Published as ATP7A(NM_000052.7):c.-21-2614G>A
ISCN -
DB-ID PGAM4_000070
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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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.-21-2614G>A r.(=) p.(=) -
PGAM4 NM_001029891.2 -?/. - c.632C>T r.(?) p.(Pro211Leu) -


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