Variant #0000577558 (NC_000023.10:g.77301954A>G, NM_000052.5:c.4390A>G (ATP7A))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77301954A>G
DNA change (hg38) g.78046457A>G
Published as ATP7A(NM_000052.5):c.4390A>G (p.(Ile1464Val)), ATP7A(NM_000052.6):c.4390A>G (p.I1464V), ATP7A(NM_000052.7):c.4390A>G (p.I1464V)
ISCN -
DB-ID ATP7A_000296 See all 4 reported entries
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) 0.0013 View details
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 2023-01-11 15:44:22 +01:00 (CET)
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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.4390A>G r.(?) p.(Ile1464Val) -
PGAM4 NM_001029891.2 -/. - c.-76819T>C r.(?) p.(=) -


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