All individuals with variants in gene SMS

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00172542 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 3 Lucy Raymond
00172543 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00177014 72555 PubMed: Abela 2016 3-generation family, affected twin brothers, unaffected heterozygous carrier mother M no Italy - - - - - EE HP:0001252 HP:0002509 HP:0001266 HP:0000219 HP:0002705 HP:000319 HP:0000286 HP:0000494 HP:0000508 HP:0011359 HP:0100798 1 2 Anaïs Begemann
00295014 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00307817 UK10K_FINDWGA5410846 PubMed: Grozeva 2015, Journal: Grozeva 2015 - M - - - - - - - ID - 1 1 Johan den Dunnen
00391600 094P - - M no Sri Lanka - - - - - ? - 1 1 Alejandro Brea-Fernández
00434635 CMC27 PubMed: Deshwar 2023 2-generation family, 1 affected, unaffected heterozygous parents M - - - - - - - NDD global developmental delay, intellectual disability,, seizures 1 1 Johan den Dunnen
00453451 - - - M no France - - - - - ? - 1 1 Marie-Laure Vuillaume
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