SHCBP1L
SHC binding and spindle associated 1 like
Summary
This gene encodes a Src homology 2 domain-binding protein 1-like protein. The encoded protein interacts with heat shock 70 kDa protein 2 and may be involved in maintaining spindle integrity during meiosis. This gene is located in region of chromoso0me 1 encompassing a prostate cancer susceptibility locus. [provided by RefSeq, Sep 2016]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368375651 | 1:182,869,182 | A/G | — | uncertain significance |
| rs765453440 | 1:182,869,252 | T/C | — | uncertain significance |
| rs757649009 | 1:182,869,270 | C/T | — | likely benign |
| rs141404677 | 1:182,869,312 | A/G | — | uncertain significance |
| rs377506931 | 1:182,869,323 | C/T | — | likely benign |
| rs775788864 | 1:182,872,199 | C/T | — | uncertain significance |
| rs370479425 | 1:182,872,229 | T/C | — | uncertain significance |
| rs372931332 | 1:182,873,320 | C/T | — | uncertain significance |
| rs200202390 | 1:182,873,340 | G/A | — | uncertain significance |
| rs1296371010 | 1:182,873,398 | T/C | — | likely benign |
| rs369569661 | 1:182,873,437 | C/T | — | uncertain significance |
| rs765580510 | 1:182,873,475 | T/C | — | uncertain significance |
| rs201932234 | 1:182,873,490 | T/C | — | uncertain significance |
| rs143434276 | 1:182,873,562 | A/G | — | likely benign |
| rs144570390 | 1:182,874,667 | T/G | — | uncertain significance |
| rs769949459 | 1:182,874,684 | C/T | — | uncertain significance |
| rs760282980 | 1:182,874,718 | A/T | — | uncertain significance |
| rs186768855 | 1:182,880,016 | A/G | intron variant | — |
| rs1431652081 | 1:182,898,885 | A/G | — | uncertain significance |
| rs752005780 | 1:182,908,332 | A/G | — | uncertain significance |
| rs932846889 | 1:182,908,369 | A/G | — | uncertain significance |
| rs143457159 | 1:182,908,434 | A/G | — | uncertain significance |
| rs200451412 | 1:182,908,446 | C/T | — | uncertain significance |
| rs764095688 | 1:182,908,453 | T/C | — | uncertain significance |
| rs1651278659 | 1:182,908,468 | A/C | — | uncertain significance |
| rs193921086 | 1:182,908,506 | G/T | — | uncertain significance |
| rs201970145 | 1:182,908,512 | T/G | — | uncertain significance |
| rs143546680 | 1:182,908,516 | G/T | — | uncertain significance |
| rs2526603750 | 1:182,908,627 | C/T | — | uncertain significance |
| rs2526603775 | 1:182,908,633 | A/G | — | uncertain significance |
| rs988999207 | 1:182,908,663 | C/G | — | uncertain significance |
| rs1651315824 | 1:182,909,486 | C/G | — | uncertain significance |
| rs374803869 | 1:182,909,644 | C/T | — | uncertain significance |
| rs781765952 | 1:182,909,647 | G/A | — | uncertain significance |
| rs374471051 | 1:182,920,473 | A/G | — | uncertain significance |
| rs2526638907 | 1:182,920,552 | C/A | — | uncertain significance |
| rs372362749 | 1:182,921,920 | T/A | — | uncertain significance |
| rs149567583 | 1:182,921,925 | C/T | — | uncertain significance |
| rs761718095 | 1:182,921,932 | G/T | — | uncertain significance |
| rs748096896 | 1:182,922,012 | G/A | — | uncertain significance |
| rs1457657178 | 1:182,922,027 | G/T | — | uncertain significance |
| rs898417828 | 1:182,922,039 | T/C | — | uncertain significance |
| rs1018935200 | 1:182,922,076 | T/C | — | likely benign |
| rs1467438689 | 1:182,922,081 | C/T | — | uncertain significance |
| rs566853974 | 1:182,922,100 | C/G | — | uncertain significance |
| rs2526648281 | 1:182,922,117 | A/T | — | uncertain significance |
| rs1297094250 | 1:182,922,123 | G/A | — | uncertain significance |
| rs2526648387 | 1:182,922,130 | C/T | — | uncertain significance |
| rs1558008110 | 1:182,922,138 | G/T | — | uncertain significance |
| rs911892646 | 1:182,922,141 | G/A | — | uncertain significance |
| rs943402537 | 1:182,922,144 | C/A | — | uncertain significance |
| rs1276635544 | 1:182,922,225 | C/T | — | uncertain significance |
| rs1210844837 | 1:182,922,231 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.