Variant #0000867579 (NC_000023.10:g.77294378G>A, NM_000052.5:c.3556G>A (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.77294378G>A
DNA change (hg38) -
Published as ATP7A(NM_000052.7):c.3556G>A (p.E1186K)
ISCN -
DB-ID PGAM4_000063
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
ATP7A NM_000052.5 ?/. - c.3556G>A r.(?) p.(Glu1186Lys) -
PGAM4 NM_001029891.2 ?/. - c.-69243C>T r.(?) p.(=) -


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