AHCYL2
adenosylhomocysteinase like 2
Summary
The protein encoded by this gene acts as a homotetramer and may be involved in the conversion of S-adenosyl-L-homocysteine to L-homocysteine and adenosine. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2011]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759520658 | 7:128,864,940 | C/G | — | uncertain significance |
| rs2546728636 | 7:128,865,038 | A/T | — | uncertain significance |
| rs763503462 | 7:128,865,086 | G/T | — | uncertain significance |
| rs2150666191 | 7:128,865,090 | A/C | — | uncertain significance |
| rs573313049 | 7:128,865,095 | C/T | — | uncertain significance |
| rs962318311 | 7:128,865,102 | T/G | — | uncertain significance |
| rs766068473 | 7:128,865,110 | C/T | — | uncertain significance |
| rs758474402 | 7:128,865,147 | C/T | — | uncertain significance |
| rs960912712 | 7:128,865,212 | C/T | — | uncertain significance |
| rs112189569 | 7:128,932,496 | T/C | intron variant | — |
| rs11979476 | 7:128,993,756 | T/G | intron variant | — |
| rs891954249 | 7:128,998,089 | C/T | — | — |
| rs11766298 | 7:129,004,847 | C/T | intron variant | — |
| rs774000794 | 7:129,019,496 | C/G | — | uncertain significance |
| rs143305987 | 7:129,019,530 | A/G | — | uncertain significance |
| rs7787531 | 7:129,023,597 | C/T | intron variant | — |
| rs1022825206 | 7:129,028,897 | C/T | — | uncertain significance |
| rs759563174 | 7:129,028,947 | C/G | — | uncertain significance |
| rs148295579 | 7:129,028,963 | A/G | — | uncertain significance |
| rs1795787388 | 7:129,037,073 | A/G | — | uncertain significance |
| rs2546975532 | 7:129,037,162 | A/C | — | uncertain significance |
| rs781422539 | 7:129,043,254 | T/C | — | uncertain significance |
| rs2546987310 | 7:129,043,307 | A/G | — | uncertain significance |
| rs752787133 | 7:129,044,967 | T/A | — | uncertain significance |
| rs9690544 | 7:129,048,940 | A/C | downstream gene variant | — |
| rs763002720 | 7:129,049,334 | T/C | — | uncertain significance |
| rs2547035016 | 7:129,062,706 | C/T | — | uncertain significance |
| rs1324874538 | 7:129,062,760 | G/A | — | uncertain significance |
| rs753369603 | 7:129,064,730 | C/T | — | uncertain significance |
| rs758168218 | 7:129,064,766 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.