MAP3K7CL
MAP3K7 C-terminal like
Summary
Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9977696 | 21:30,453,645 | T/A | — | — |
| rs2085916389 | 21:30,458,189 | A/C | — | uncertain significance |
| rs751144191 | 21:30,458,208 | A/C | — | uncertain significance |
| rs140644118 | 21:30,458,221 | G/A | — | uncertain significance |
| rs2516990666 | 21:30,458,222 | A/C | — | uncertain significance |
| rs550445355 | 21:30,458,225 | C/A | — | uncertain significance |
| rs778968904 | 21:30,464,782 | A/G | — | uncertain significance |
| rs142227725 | 21:30,464,794 | A/C | — | uncertain significance |
| rs776413595 | 21:30,464,830 | A/G | — | likely benign |
| rs766680699 | 21:30,464,836 | G/A | — | uncertain significance |
| rs2146503768 | 21:30,464,861 | A/G | — | uncertain significance |
| rs757578574 | 21:30,464,890 | A/G | — | uncertain significance |
| rs2832171 | 21:30,465,586 | C/T | intron variant | — |
| rs9975695 | 21:30,487,127 | A/T | — | — |
| rs2832191 | 21:30,489,300 | A/G | — | — |
| rs68046920 | 21:30,492,837 | A/G | intron variant | — |
| rs11330686 | 21:30,513,854 | G/T | — | — |
| rs4817273 | 21:30,514,575 | A/G | upstream gene variant | — |
| rs752198255 | 21:30,521,518 | C/G | — | uncertain significance |
| rs1205598066 | 21:30,521,521 | C/G | — | uncertain significance |
| rs780402725 | 21:30,521,559 | C/A | — | uncertain significance |
| rs2832223 | 21:30,529,142 | G/T | intron variant | — |
| rs1999323 | 21:30,534,128 | C/T | intron variant | — |
| rs2832229 | 21:30,535,087 | A/G | regulatory region variant | — |
| rs73193808 | 21:30,535,302 | C/A | regulatory region variant | — |
| rs2471949 | 21:30,537,836 | A/T | — | — |
| rs56968346 | 21:30,540,165 | C/T | intron variant | — |
| rs28462110 | 21:30,544,318 | C/T | intron variant | — |
| rs73193819 | 21:30,544,657 | T/G | — | — |
| rs73193820 | 21:30,544,669 | T/C | regulatory region variant | — |
| rs768389557 | 21:30,547,090 | G/C | — | uncertain significance |
| rs200856600 | 21:30,547,097 | C/T | — | uncertain significance |
| rs376957652 | 21:30,547,098 | G/A | — | uncertain significance |
| rs529502618 | 21:30,547,116 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.