Variant #0000334745 (NC_000023.10:g.77244235G>A, ATP7A(NM_000052.5):c.610+8G>A)

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.77244235G>A
DNA change (hg38) g.77988739G>A
Published as ATP7A(NM_000052.5):c.610+8G>A (p.(=)), ATP7A(NM_000052.7):c.610+8G>A
ISCN -
DB-ID ATP7A_000371 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) 0.00125 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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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.610+8G>A r.(=) p.(=) -
PGAM4 NM_001029891.2 -?/. - c.-19100C>T r.(?) p.(=) -