TSC22D4
TSC22 domain family member 4
Summary
TSC22D4 is a member of the TSC22 domain family of leucine zipper transcriptional regulators (see TSC22D3; MIM 300506) (Kester et al., 1999 [PubMed 10488076]; Fiorenza et al., 2001 [PubMed 11707329]).[supplied by OMIM, Mar 2008]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375700826 | 7:100,064,598 | T/A | — | uncertain significance |
| rs781001373 | 7:100,064,619 | C/T | — | uncertain significance |
| rs746141146 | 7:100,064,631 | G/A | — | uncertain significance |
| rs1799291327 | 7:100,064,641 | G/T | — | uncertain significance |
| rs367574729 | 7:100,064,658 | G/A | — | uncertain significance |
| rs7811142 | 7:100,065,443 | A/T | upstream gene variant | — |
| rs111972532 | 7:100,069,088 | T/C | intron variant | — |
| rs2897360 | 7:100,071,391 | A/C | — | — |
| rs753187080 | 7:100,071,994 | T/G | — | uncertain significance |
| rs543620199 | 7:100,074,902 | G/T | — | uncertain significance |
| rs146306463 | 7:100,074,935 | G/A | — | uncertain significance |
| rs138670160 | 7:100,075,001 | C/T | — | uncertain significance |
| rs752742245 | 7:100,075,003 | G/A | — | likely benign |
| rs374915525 | 7:100,075,081 | C/T | — | uncertain significance |
| rs536240449 | 7:100,075,205 | G/C | — | uncertain significance |
| rs758778059 | 7:100,075,240 | G/A | — | uncertain significance |
| rs1423571548 | 7:100,075,343 | C/T | — | likely benign |
| rs754616032 | 7:100,075,346 | C/T | — | uncertain significance |
| rs751015786 | 7:100,075,406 | G/A | — | uncertain significance |
| rs777247706 | 7:100,075,459 | G/A | — | uncertain significance |
| rs2485743319 | 7:100,075,483 | T/C | — | uncertain significance |
| rs773455361 | 7:100,075,505 | C/G | — | uncertain significance |
| rs550042074 | 7:100,075,507 | G/A | — | uncertain significance |
| rs777368263 | 7:100,075,528 | T/C | — | likely benign |
| rs1270591994 | 7:100,075,600 | C/T | — | uncertain significance |
| rs1343534369 | 7:100,075,651 | C/T | — | uncertain significance |
| rs2406253 | 7:100,077,273 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.