Variant #0000927422 (NC_000023.10:g.77268390G>C, NM_000052.5:c.2187G>C (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.77268390G>C
DNA change (hg38) -
Published as ATP7A(NM_000052.6):c.2187G>C (p.W729C), ATP7A(NM_000052.7):c.2187G>C (p.W729C)
ISCN -
DB-ID PGAM4_000037 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +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.2187G>C r.(?) p.(Trp729Cys) -
PGAM4 NM_001029891.2 ?/. - c.-43255C>G r.(?) p.(=) -


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