ST7L
suppression of tumorigenicity 7 like
Summary
This gene was identified by its similarity to the ST7 tumor suppressor gene found in the chromosome 7q31 region. This gene is clustered in a tail-to-tail manner with the WNT2B gene in a chromosomal region known to be deleted and rearranged in a variety of cancers. Several transcript variants encoding many different isoforms have been described, but some have not been fully characterized. [provided by RefSeq, Feb 2011]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12069022 | 1:113,068,651 | C/T | — | benign |
| rs12117479 | 1:113,076,819 | T/C | — | — |
| rs75322672 | 1:113,078,101 | C/T | intron variant | — |
| rs10857961 | 1:113,082,153 | C/T | — | — |
| rs1277862906 | 1:113,084,596 | T/C | — | uncertain significance |
| rs1355765113 | 1:113,084,641 | A/G | — | uncertain significance |
| rs142542242 | 1:113,093,246 | G/A | — | likely benign |
| rs6679414 | 1:113,098,006 | G/T | intron variant | — |
| rs760596487 | 1:113,098,564 | T/C | — | uncertain significance |
| rs370350367 | 1:113,117,098 | T/C | — | — |
| rs10776757 | 1:113,121,673 | G/C | intron variant | — |
| rs145597302 | 1:113,124,653 | C/T | — | uncertain significance |
| rs893517791 | 1:113,124,700 | A/G | — | uncertain significance |
| rs752741137 | 1:113,125,050 | T/C | — | uncertain significance |
| rs1283461769 | 1:113,125,079 | A/T | — | uncertain significance |
| rs144485512 | 1:113,126,605 | T/C | — | uncertain significance |
| rs2527733889 | 1:113,126,608 | T/C | — | uncertain significance |
| rs761722695 | 1:113,126,702 | T/C | — | uncertain significance |
| rs12045227 | 1:113,128,212 | G/A | intron variant | — |
| rs371440073 | 1:113,134,211 | A/G | — | uncertain significance |
| rs6691917 | 1:113,137,043 | G/A | — | — |
| rs6691932 | 1:113,144,263 | T/C | intron variant | — |
| rs55652172 | 1:113,147,607 | G/C | — | — |
| rs778283228 | 1:113,153,514 | C/G | — | uncertain significance |
| rs771641500 | 1:113,153,527 | G/T | — | uncertain significance |
| rs1668985279 | 1:113,153,594 | C/G | — | uncertain significance |
| rs760597401 | 1:113,153,603 | T/C | — | uncertain significance |
| rs2528225819 | 1:113,153,622 | A/G | — | uncertain significance |
| rs7546094 | 1:113,154,400 | C/G | — | — |
| rs114199731 | 1:113,159,464 | T/A | — | benign |
| rs374679582 | 1:113,161,573 | C/T | — | uncertain significance |
| rs1206133035 | 1:113,161,590 | C/G | — | uncertain significance |
| rs375549110 | 1:113,161,612 | C/T | — | uncertain significance |
| rs774231203 | 1:113,161,614 | C/T | — | uncertain significance |
| rs186026192 | 1:113,161,692 | G/A | — | uncertain significance |
| rs1370957415 | 1:113,161,711 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.