BCL2L13
BCL2 like 13
Summary
This gene encodes a mitochondrially-localized protein with conserved B-cell lymphoma 2 homology motifs. Overexpression of the encoded protein results in apoptosis. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2012]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs5746451 | 22:18,126,020 | T/C | upstream gene variant | — |
| rs5747308 | 22:18,133,500 | A/G | — | — |
| rs749197208 | 22:18,138,579 | A/C | — | uncertain significance |
| rs13054674 | 22:18,140,771 | A/T | — | — |
| rs5747315 | 22:18,147,423 | C/G | — | — |
| rs34891900 | 22:18,163,158 | C/A | — | — |
| rs2587070 | 22:18,165,995 | T/G | — | benign |
| rs904669706 | 22:18,166,023 | T/G | — | uncertain significance |
| rs5747327 | 22:18,169,212 | T/C | — | — |
| rs5013026 | 22:18,171,650 | C/T | intron variant | — |
| rs138294984 | 22:18,171,779 | A/G | — | uncertain significance |
| rs147280257 | 22:18,171,842 | T/G | — | uncertain significance |
| rs202002609 | 22:18,171,865 | C/G | — | uncertain significance |
| rs2535702 | 22:18,173,104 | T/A | — | — |
| rs773293223 | 22:18,178,923 | G/C | — | uncertain significance |
| rs766203253 | 22:18,178,929 | C/G | — | uncertain significance |
| rs754244583 | 22:18,178,930 | G/A | — | uncertain significance |
| rs144632534 | 22:18,185,060 | C/T | — | uncertain significance |
| rs201253896 | 22:18,185,118 | A/G | — | uncertain significance |
| rs78160286 | 22:18,185,123 | G/T | — | benign |
| rs559426158 | 22:18,197,015 | C/T | — | — |
| rs777222596 | 22:18,209,518 | A/G | — | uncertain significance |
| rs199666992 | 22:18,209,524 | C/A | — | uncertain significance |
| rs201411768 | 22:18,209,599 | C/T | — | uncertain significance |
| rs146700535 | 22:18,209,635 | G/C | — | uncertain significance |
| rs1400143447 | 22:18,209,674 | C/G | — | uncertain significance |
| rs759443880 | 22:18,209,711 | A/G | — | uncertain significance |
| rs2518636111 | 22:18,209,857 | C/G | — | uncertain significance |
| rs769440316 | 22:18,209,864 | C/A | — | uncertain significance |
| rs1296114946 | 22:18,209,882 | C/T | — | uncertain significance |
| rs777866528 | 22:18,209,948 | A/G | — | uncertain significance |
| rs201972889 | 22:18,209,962 | A/G | — | uncertain significance |
| rs1399537655 | 22:18,210,019 | A/G | — | uncertain significance |
| rs139164101 | 22:18,210,043 | G/A | — | likely benign |
| rs1010026322 | 22:18,210,062 | C/T | — | likely benign |
| rs1034245755 | 22:18,210,088 | G/C | — | uncertain significance |
| rs144977669 | 22:18,210,130 | G/A | — | uncertain significance |
| rs61740640 | 22:18,210,142 | G/A | — | uncertain significance |
| rs1048649467 | 22:18,210,149 | C/A | — | uncertain significance |
| rs770347827 | 22:18,210,176 | C/G | — | uncertain significance |
| rs2061328546 | 22:18,210,184 | G/A | — | uncertain significance |
| rs1388721797 | 22:18,210,196 | A/G | — | uncertain significance |
| rs200014585 | 22:18,210,200 | C/T | — | uncertain significance |
| rs752597147 | 22:18,210,222 | A/G | — | uncertain significance |
| rs764780025 | 22:18,210,241 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.