Variant #0000624728 (NC_000023.10:g.77243763C>T, NM_000052.5:c.146C>T (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.77243763C>T
DNA change (hg38) g.77988267C>T
Published as ATP7A(NM_000052.7):c.146C>T (p.T49I)
ISCN -
DB-ID PGAM4_000022
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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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.146C>T r.(?) p.(Thr49Ile) -
PGAM4 NM_001029891.2 ?/. - c.-18628G>A r.(?) p.(=) -


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