Full data view for gene ATP7A

Information The variants shown are described using the NM_000052.5 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
./. - c.499C>T r.(?) p.(Gln167*) - Both (homozygous) - VUS g.77244116C>T g.77988620C>T - - ATP7A_000055 - - - - Germline - - - - - DNA SEQ-NG - - - - PubMed: Bell 2011 - - - - - - - - - 1 Gerard C.P. Schaafsma
+/+? 3 c.499C>T r.(?) p.(Gln167*) - Unknown - pathogenic (recessive) g.77244116C>T g.77988620C>T C644>T - ATP7A_000055 Decreased level with NB PubMed: Das 1994 PubMed: Bell 2011 - - Germline - - - - - DNA, RNA SEQ - - MNK - PubMed: Das 1994 PubMed: Bell 2011 single case - - - - - - - - 1 Zeynep Tümer
+/+? 3 c.499C>T r.(?) p.(Gln167*) - Unknown - pathogenic (recessive) g.77244116C>T g.77988620C>T 644C>T (Q167X) - ATP7A_000055 - PubMed: Gu 2001 - - Germline - - - - - DNA SEQ - - MNK - PubMed: Gu 2001 - - - - - - - - - 1 Zeynep Tümer
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