Variant #0000951799 (NC_000023.10:g.77271282C>T, NM_000052.5:c.2530C>T (ATP7A))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.77271282C>T
DNA change (hg38) -
Published as ATP7A(NM_000052.6):c.2530C>T (p.R844C), ATP7A(NM_000052.7):c.2530C>T (p.R844C)
ISCN -
DB-ID PGAM4_000046 See all 2 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) 0.00013 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 2023-11-27 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     

P-domain     
ATP7A NM_000052.5 ?/. - c.2530C>T r.(?) p.(Arg844Cys) -
PGAM4 NM_001029891.2 ?/. - c.-46147G>A r.(?) p.(=) -


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