Variant #0000334737 (NC_000023.10:g.77224487C>T, NC_000023.10(NM_000052.5):c.-21-2631C>T (ATP7A))

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.77224487C>T
DNA change (hg38) g.77968990C>T
Published as PGAM4(NM_001029891.2):c.649G>A (p.(Val217Ile))
ISCN -
DB-ID ATP7A_000359
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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-10-01 19:36:39 +02:00 (CEST)
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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.-21-2631C>T r.(=) p.(=) -
PGAM4 NM_001029891.2 -?/. - c.649G>A r.(?) p.(Val217Ile) -


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