VSTM1
V-set and transmembrane domain containing 1
Summary
Predicted to enable cytokine activity. Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in extracellular space and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142390977 | 19:54,543,747 | C/T | downstream gene variant | — |
| rs746783531 | 19:54,544,219 | A/T | — | uncertain significance |
| rs146430350 | 19:54,544,231 | G/A | — | uncertain significance |
| rs908103813 | 19:54,544,232 | C/T | — | uncertain significance |
| rs752197748 | 19:54,544,289 | C/T | — | uncertain significance |
| rs763830965 | 19:54,544,292 | T/C | — | uncertain significance |
| rs773562512 | 19:54,544,333 | G/A | — | uncertain significance |
| rs192971465 | 19:54,544,549 | A/T | intron variant | — |
| rs139461742 | 19:54,545,068 | C/T | — | uncertain significance |
| rs2514811159 | 19:54,545,552 | T/C | — | uncertain significance |
| rs76638738 | 19:54,545,779 | T/G | intron variant | — |
| rs148995267 | 19:54,545,893 | C/T | intron variant | — |
| rs147659047 | 19:54,546,705 | G/A | intron variant | — |
| rs73058801 | 19:54,548,856 | C/T | intron variant | — |
| rs11665958 | 19:54,549,557 | T/C | intron variant | — |
| rs117349374 | 19:54,549,671 | C/A | intron variant | — |
| rs10415777 | 19:54,551,115 | G/C | — | — |
| rs189966329 | 19:54,554,059 | C/A | intron variant | — |
| rs373982331 | 19:54,554,695 | G/C | — | uncertain significance |
| rs191684467 | 19:54,555,164 | G/A | intron variant | — |
| rs55917282 | 19:54,555,609 | G/A | intron variant | — |
| rs77931596 | 19:54,556,228 | C/T | — | — |
| rs746417147 | 19:54,560,174 | T/G | — | — |
| rs140416587 | 19:54,561,285 | G/C | intron variant | — |
| rs550711628 | 19:54,561,590 | T/C | — | uncertain significance |
| rs529993082 | 19:54,561,683 | C/T | — | uncertain significance |
| rs866861625 | 19:54,561,704 | C/T | — | uncertain significance |
| rs2515440090 | 19:54,561,706 | T/C | — | uncertain significance |
| rs144159930 | 19:54,561,722 | C/A | — | uncertain significance |
| rs199752981 | 19:54,561,740 | C/T | — | likely benign |
| rs201340122 | 19:54,561,776 | G/C | — | uncertain significance |
| rs760528949 | 19:54,561,789 | C/G | — | uncertain significance |
| rs200132130 | 19:54,561,818 | C/A | — | uncertain significance |
| rs183008688 | 19:54,562,624 | T/C | intron variant | — |
| rs144153193 | 19:54,564,144 | G/A | intron variant | — |
| rs568231259 | 19:54,565,043 | G/A | — | — |
| rs578177618 | 19:54,565,285 | T/G | — | — |
| rs199504672 | 19:54,567,012 | G/A | — | uncertain significance |
| rs612529 | 19:54,567,253 | A/G | upstream gene variant | — |
| rs148313235 | 19:54,568,665 | T/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.