Full data view for gene ATP7A

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

7 entries on 1 page. Showing entries 1 - 7.
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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.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) - ATP7A_000289 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) - ATP7A_000289 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) - ATP7A_000289 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) - ATP7A_000289 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C ATP7A(NM_000052.6):c.2299G>C (p.V767L), ATP7A(NM_000052.7):c.2299G>C (p.V767L) - ATP7A_000289 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/-? 10 c.2299G>C r.(?) p.(Val767Leu) - Unknown - benign g.77268502G>C g.78013005G>C 2444G>C (V767L) - ATP7A_000289 - PubMed: Das 1994, PubMed: Tümer 1997, PubMed: Ogawa 2000, PubMed: Gu 2001, PubMed: Zhang 2008 - - Germline - - - - - DNA SEQ - - Healthy/Control - PubMed: Das 1994, PubMed: Tümer 1997, PubMed: Ogawa 2000, PubMed: Gu 2001, PubMed: Zhang 2008 - - - - - - - - - 1 Zeynep Tümer
?/? 10 c.2299G>C r.(?) p.(Val767Leu) - Unknown - VUS g.77268502G>C g.78013005G>C V767L - ATP7A_000289 recurrent, found 30 times; for privacy reasons only summary data are given - for details contact Lucy Raymond (flr24 @ cam.ac.uk) PubMed: Tarpey 2009 - - Germline - - - - - DNA SEQ - - ID - PubMed: Tarpey 2009 - - - - - - - - - 1 Zeynep Tümer
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