All individuals with variants in gene SPTB

12 entries on 1 page. Showing entries 1 - 12.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00291086 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291087 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291088 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 170 Mohammed Faruq
00291089 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00291090 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00291091 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00291092 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00303369 - - child of heterozygous mother with a history of neonatal hemolytic anemia M - United States Mexico;Ecuador 00y03m - no phototherapy HAG Decreased glucose-6-phosphate dehydrogenase level in red blood cells; Neonatal hemolytic anemia; Hb10.5g/dL; HCT 29.7%; RET 2.54% (89.9x10^3/uL); G6PD activity 2.9U/gHb (ref 9.9-16.6 U/gHb) 1 1 Scott Reading
00304439 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00308744 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00310615 family PubMed: Nieminen 2021 5-generation family, 22 affected (8F, 14M) F;M ? United States - - - Yes - SPH - 1 22 Taina Nieminen
00386827 OGI629_001292 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.