| 329381810 | CV2467369 | single nucleotide variant | NM_017595.6(NKIRAS2):c.25G>A (p.Val9Met) | not specified [RCV004285157] | uncertain significance | 17 | 42021602 | 42021602 | Human | | name |
| 405706515 | CV3362213 | single nucleotide variant | NM_017595.6(NKIRAS2):c.168G>A (p.Gln56=) | not specified [RCV004493201] | likely benign | 17 | 42022472 | 42022472 | Human | | name |
| 597650799 | CV3556256 | single nucleotide variant | NM_017595.6(NKIRAS2):c.372A>G (p.Leu124=) | not specified [RCV004826815] | likely benign | 17 | 42023689 | 42023689 | Human | | name |
| 156330589 | CV2224288 | single nucleotide variant | NM_017595.6(NKIRAS2):c.286C>T (p.Arg96Cys) | not specified [RCV004096109] | uncertain significance | 17 | 42022590 | 42022590 | Human | | name |
| 156199530 | CV2365337 | single nucleotide variant | NM_017595.6(NKIRAS2):c.187C>T (p.Arg63Trp) | not specified [RCV004209422] | uncertain significance | 17 | 42022491 | 42022491 | Human | | name |
| 401766646 | CV2673444 | single nucleotide variant | NM_017595.6(NKIRAS2):c.107T>C (p.Ile36Thr) | not specified [RCV004288417] | uncertain significance | 17 | 42022411 | 42022411 | Human | | name |
| 405706508 | CV3362212 | single nucleotide variant | NM_017595.6(NKIRAS2):c.139A>G (p.Ile47Val) | not specified [RCV004493200] | uncertain significance | 17 | 42022443 | 42022443 | Human | | name |
| 405706523 | CV3362214 | single nucleotide variant | NM_017595.6(NKIRAS2):c.208G>A (p.Glu70Lys) | not specified [RCV004493202] | uncertain significance | 17 | 42022512 | 42022512 | Human | | name |
| 598193653 | CV3994599 | single nucleotide variant | NM_017595.6(NKIRAS2):c.289G>A (p.Val97Met) | not specified [RCV005374584] | uncertain significance | 17 | 42022593 | 42022593 | Human | | name |
| 598193660 | CV3994600 | single nucleotide variant | NM_017595.6(NKIRAS2):c.130G>A (p.Val44Met) | not specified [RCV005374585] | uncertain significance | 17 | 42022434 | 42022434 | Human | | name |
| 155950317 | CV2242879 | single nucleotide variant | NM_017595.6(NKIRAS2):c.526G>T (p.Ala176Ser) | not specified [RCV004107470] | uncertain significance | 17 | 42023843 | 42023843 | Human | | name |
| 329361647 | CV2455822 | single nucleotide variant | NM_017595.6(NKIRAS2):c.467C>T (p.Ser156Phe) | not specified [RCV004279110] | uncertain significance | 17 | 42023784 | 42023784 | Human | | name |
| 405706530 | CV3362215 | single nucleotide variant | NM_017595.6(NKIRAS2):c.317A>C (p.Lys106Thr) | not specified [RCV004493203] | uncertain significance | 17 | 42022621 | 42022621 | Human | | name |
| 597650782 | CV3556254 | single nucleotide variant | NM_017595.6(NKIRAS2):c.502A>G (p.Met168Val) | not specified [RCV004826813] | uncertain significance | 17 | 42023819 | 42023819 | Human | | name |
| 597650790 | CV3556255 | single nucleotide variant | NM_017595.6(NKIRAS2):c.382C>T (p.Arg128Trp) | not specified [RCV004826814] | uncertain significance | 17 | 42023699 | 42023699 | Human | | name |