GRIN3A
glutamate ionotropic receptor NMDA type subunit 3A
Summary
This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptors, which belong to the superfamily of glutamate-regulated ion channels, and function in physiological and pathological processes in the central nervous system. This subunit shows greater than 90% identity to the corresponding subunit in rat. Studies in the knockout mouse deficient in this subunit suggest that this gene may be involved in the development of synaptic elements by modulating NMDA receptor activity. [provided by RefSeq, Jul 2008]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs762678837 | 9:104,335,502 | G/A | — | uncertain significance |
| rs777496448 | 9:104,335,589 | C/T | — | uncertain significance |
| rs139990682 | 9:104,335,596 | C/T | — | uncertain significance |
| rs71509734 | 9:104,335,619 | C/T | — | benign |
| rs199945164 | 9:104,335,628 | C/T | — | uncertain significance |
| rs367772655 | 9:104,335,683 | G/A | — | uncertain significance |
| rs2490319116 | 9:104,335,703 | C/A | — | uncertain significance |
| rs75201933 | 9:104,335,719 | A/G | — | likely benign |
| rs1194653835 | 9:104,335,736 | T/A | — | uncertain significance |
| rs80306210 | 9:104,335,767 | C/T | — | uncertain significance |
| rs141253502 | 9:104,341,543 | A/G | — | uncertain significance |
| rs143034818 | 9:104,341,634 | T/A | — | uncertain significance |
| rs11788456 | 9:104,348,150 | G/A | intron variant | — |
| rs17189632 | 9:104,368,002 | T/A | intron variant | — |
| rs200636529 | 9:104,375,693 | C/G | — | uncertain significance |
| rs79404655 | 9:104,375,801 | T/C | — | uncertain significance |
| rs10121600 | 9:104,378,003 | C/T | intron variant | — |
| rs1176709920 | 9:104,385,642 | C/T | — | uncertain significance |
| rs780438004 | 9:104,385,650 | A/G | — | uncertain significance |
| rs960894555 | 9:104,390,548 | C/T | — | uncertain significance |
| rs778415229 | 9:104,390,606 | G/T | — | uncertain significance |
| rs144770241 | 9:104,390,659 | G/T | — | uncertain significance |
| rs10989568 | 9:104,396,304 | A/T | — | — |
| rs12380816 | 9:104,413,670 | T/C | intron variant | — |
| rs10819974 | 9:104,422,344 | C/T | intron variant | — |
| rs750954593 | 9:104,432,513 | C/A | — | uncertain significance |
| rs758784929 | 9:104,432,532 | T/C | — | uncertain significance |
| rs2490418419 | 9:104,432,596 | G/A | — | uncertain significance |
| rs866327735 | 9:104,432,674 | G/A | — | uncertain significance |
| rs757280646 | 9:104,432,691 | G/C | — | uncertain significance |
| rs143140184 | 9:104,432,715 | C/T | — | uncertain significance |
| rs1360008284 | 9:104,432,773 | C/A | — | uncertain significance |
| rs778793239 | 9:104,432,794 | T/C | — | uncertain significance |
| rs2490419247 | 9:104,432,950 | C/A | — | uncertain significance |
| rs371244839 | 9:104,433,000 | T/C | — | uncertain significance |
| rs757531020 | 9:104,433,051 | G/A | — | uncertain significance |
| rs746023967 | 9:104,433,055 | T/C | — | uncertain significance |
| rs758777062 | 9:104,433,057 | G/T | — | uncertain significance |
| rs2490419707 | 9:104,433,132 | A/C | — | uncertain significance |
| rs889324788 | 9:104,433,178 | G/T | — | uncertain significance |
| rs773322226 | 9:104,433,216 | T/A | — | uncertain significance |
| rs80097802 | 9:104,433,265 | T/C | — | uncertain significance |
| rs201880306 | 9:104,433,275 | C/T | — | uncertain significance |
| rs777473704 | 9:104,433,325 | C/T | — | likely benign |
| rs373415839 | 9:104,433,336 | C/T | — | uncertain significance |
| rs370525524 | 9:104,433,382 | C/T | — | uncertain significance |
| rs1377592486 | 9:104,433,389 | C/A | — | uncertain significance |
| rs2490063634 | 9:104,448,945 | T/A | — | uncertain significance |
| rs779679486 | 9:104,448,983 | A/G | — | uncertain significance |
| rs746600726 | 9:104,448,984 | C/T | — | uncertain significance |
| rs573954685 | 9:104,448,993 | C/T | — | uncertain significance |
| rs757911224 | 9:104,449,020 | A/T | — | uncertain significance |
| rs1350924409 | 9:104,449,021 | G/C | — | uncertain significance |
| rs10989591 | 9:104,449,098 | C/A | missense variant | — |
| rs777573584 | 9:104,449,136 | G/A | — | uncertain significance |
| rs564083866 | 9:104,449,172 | C/A | — | uncertain significance |
| rs763495503 | 9:104,449,175 | C/T | — | uncertain significance |
| rs1290766724 | 9:104,449,265 | T/G | — | uncertain significance |
| rs775036167 | 9:104,449,283 | T/C | — | uncertain significance |
| rs1247026427 | 9:104,449,299 | T/C | — | uncertain significance |
| rs2050641 | 9:104,489,367 | C/A | — | — |
| rs532234392 | 9:104,499,651 | C/T | — | uncertain significance |
| rs2490148947 | 9:104,499,823 | A/T | — | uncertain significance |
| rs139027120 | 9:104,499,850 | C/A | — | uncertain significance |
| rs113819148 | 9:104,499,883 | C/T | — | uncertain significance |
| rs1349133294 | 9:104,499,913 | C/T | — | likely benign |
| rs920921335 | 9:104,500,016 | C/G | — | uncertain significance |
| rs1353038870 | 9:104,500,062 | C/G | — | uncertain significance |
| rs1031315248 | 9:104,500,141 | G/T | — | uncertain significance |
| rs957551703 | 9:104,500,204 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.