Variant #0000577553 (NC_000023.10:g.77298875C>T, NM_000052.5:c.4066C>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.77298875C>T
DNA change (hg38) g.78043377C>T
Published as ATP7A(NM_000052.5):c.4066C>T (p.(Arg1356Trp)), ATP7A(NM_000052.6):c.4066C>T (p.R1356W)
ISCN -
DB-ID PGAM4_000018 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) 0.0006 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 2019-07-18 18:22:55 +02:00 (CEST)
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.4066C>T r.(?) p.(Arg1356Trp) -
PGAM4 NM_001029891.2 -?/. - c.-73740G>A r.(?) p.(=) -


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