Full data view for gene SPG11

Information The variants shown are described using the NM_025137.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     
+/. 36 c.6709del r.(?) p.(Ala2237Glnfs*7) Both (homozygous) - pathogenic g.44859668del g.44567470del - - SPG11_000008 variant absent in one patient with different phenotype (mental impairment, no spasticity) - - - Germline yes - - - - DNA micro, SEQ - - SPG11 - - family, 5 affecteds and several unaffected heterozygous carriers F yes (France);Sudan - - - yes - 5 Mahmoud Koko
+/. 36 c.6709del r.(?) p.(Ala2237Glnfs*7) Unknown - pathogenic (recessive) g.44859668del g.44567470del 6709delG - SPG11_000008 - - - - Germline yes - - - - DNA SEQ blood - SPG11 - - - M yes Egypt - - - - - 1 Sherifa Ahmed Hamed
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