SAMD5

sterile alpha motif domain containing 5

Summary

Predicted to be involved in regulation of intracellular signal transduction. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants25 total

rsidPosition (GRCh37)AllelesClassClinVar
rs25347430136:147,830,276G/Tuncertain significance
rs25347430606:147,830,284T/Cuncertain significance
rs25347431026:147,830,296C/Auncertain significance
rs13656732966:147,830,297C/Tuncertain significance
rs21284385876:147,830,333T/Guncertain significance
rs25347433096:147,830,344C/Tuncertain significance
rs25347433116:147,830,345G/Tuncertain significance
rs5483491316:147,830,366G/Auncertain significance
rs3760418946:147,830,444A/Guncertain significance
rs1405264146:147,830,457G/Tuncertain significance
rs25347438356:147,830,469G/Tuncertain significance
rs7746499976:147,830,506C/Guncertain significance
rs25347439486:147,830,507C/Tuncertain significance
rs1454028646:147,830,509C/Tuncertain significance
rs7612420376:147,830,510C/Guncertain significance
rs1406432526:147,885,588G/Auncertain significance
rs93770636:147,934,947G/Aintron variant
rs111555096:147,942,236G/Aintron variant
rs13020196:147,971,574C/Tintron variant
rs48957186:147,973,296C/Tintron variant
rs11478526:147,980,909G/Aupstream gene variant
rs585212246:148,024,930G/A
rs12347476:148,117,036C/T
rs4742106:148,244,701A/T
rs117591906:148,266,419C/Aintron variant

Gene information from NCBI Gene. Variant classifications from ClinVar.