| 15167582 | CV778398 | single nucleotide variant | NM_000915.4(OXT):c.323-5T>C | not provided [RCV000949086] | benign | 20 | 3072358 | 3072358 | Human | | name |
| 405738976 | CV3371195 | single nucleotide variant | NM_000915.4(OXT):c.26G>T (p.Cys9Phe) | not specified [RCV004497444] | uncertain significance | 20 | 3071681 | 3071681 | Human | | name |
| 597692754 | CV3578084 | single nucleotide variant | NM_000915.4(OXT):c.14G>A (p.Ser5Asn) | not specified [RCV004838843] | uncertain significance | 20 | 3071669 | 3071669 | Human | | name |
| 155977221 | CV2218700 | single nucleotide variant | NM_000915.4(OXT):c.143G>A (p.Gly48Asp) | not specified [RCV004084633] | uncertain significance | 20 | 3072099 | 3072099 | Human | | name |
| 156146468 | CV2265132 | single nucleotide variant | NM_000915.4(OXT):c.290G>A (p.Arg97His) | not specified [RCV004126264] | uncertain significance | 20 | 3072246 | 3072246 | Human | | name |
| 156209228 | CV2304442 | single nucleotide variant | NM_000915.4(OXT):c.323A>G (p.Asp108Gly) | not specified [RCV004164538] | uncertain significance | 20 | 3072363 | 3072363 | Human | | name |
| 405738983 | CV3371196 | single nucleotide variant | NM_000915.4(OXT):c.324C>G (p.Asp108Glu) | not specified [RCV004497445] | uncertain significance | 20 | 3072364 | 3072364 | Human | | name |
| 407517281 | CV3469948 | single nucleotide variant | NM_000915.4(OXT):c.305G>A (p.Gly102Asp) | not specified [RCV004650613] | uncertain significance | 20 | 3072261 | 3072261 | Human | | name |
| 40814598 | CV971141 | duplication | NM_000915.4(OXT):c.-3_9dup (p.Gly3_Pro4insThrMetAlaGly) | Neurodevelopmental disorder [RCV001262143] | uncertain significance | 20 | 3071650 | 3071651 | Human | 1 | name |
| 405262576 | CV3196674 | single nucleotide variant | NM_000916.4(OXTR):c.690C>T (p.Asn230=) | OXTR-related disorder [RCV003967353] | benign | 3 | 8767498 | 8767498 | Human | | name , trait , alternate_id |
| 405275679 | CV3199370 | single nucleotide variant | NM_000916.4(OXTR):c.712G>A (p.Ala238Thr) | OXTR-related disorder [RCV003916783] | benign | 3 | 8767476 | 8767476 | Human | | name , trait , alternate_id |
| 405275139 | CV3204659 | single nucleotide variant | NM_000916.4(OXTR):c.510G>T (p.Pro170=) | OXTR-related disorder [RCV003952061] | likely benign | 3 | 8767678 | 8767678 | Human | | name , trait , alternate_id |
| 405278933 | CV3220487 | single nucleotide variant | NM_000916.4(OXTR):c.159G>A (p.Ala53=) | OXTR-related disorder [RCV003976678] | likely benign | 3 | 8768029 | 8768029 | Human | | name , trait , alternate_id |
| 15172764 | CV698297 | single nucleotide variant | NM_000916.4(OXTR):c.1015G>A (p.Glu339Lys) | OXTR-related disorder [RCV003903200]|not provided [RCV000950098] | benign | 3 | 8753132 | 8753132 | Human | | name , trait , alternate_id |
| 15191898 | CV720646 | single nucleotide variant | NM_000916.4(OXTR):c.1068C>A (p.Arg356=) | OXTR-related disorder [RCV003948397]|not provided [RCV000888508] | benign | 3 | 8753079 | 8753079 | Human | | name , trait , alternate_id |
| 156126047 | CV2350251 | single nucleotide variant | NM_000916.4(OXTR):c.80G>C (p.Arg27Pro) | not specified [RCV004202207] | uncertain significance | 3 | 8768108 | 8768108 | Human | | name |
| 156136937 | CV2365076 | single nucleotide variant | NM_000916.4(OXTR):c.56C>T (p.Ala19Val) | not specified [RCV004224232] | uncertain significance | 3 | 8768132 | 8768132 | Human | | name |
| 15113129 | CV709055 | single nucleotide variant | NM_000916.4(OXTR):c.351C>T (p.Tyr117=) | not provided [RCV000961430] | benign | 3 | 8767837 | 8767837 | Human | | name |
| 15146397 | CV734308 | single nucleotide variant | NM_000916.4(OXTR):c.360G>T (p.Val120=) | not provided [RCV000900318] | likely benign | 3 | 8767828 | 8767828 | Human | | name |
| 15187053 | CV764183 | single nucleotide variant | NM_000916.4(OXTR):c.705C>A (p.Thr235=) | not provided [RCV000931542] | likely benign | 3 | 8767483 | 8767483 | Human | | name |
| 21068425 | CV795475 | single nucleotide variant | NM_000916.4(OXTR):c.65G>A (p.Gly22Glu) | not provided [RCV000997975] | uncertain significance | 3 | 8768123 | 8768123 | Human | | name |
| 401741110 | CV2713380 | single nucleotide variant | NM_000916.4(OXTR):c.172G>T (p.Ala58Ser) | not specified [RCV004319004] | uncertain significance | 3 | 8768016 | 8768016 | Human | | name |
| 405738997 | CV3371198 | single nucleotide variant | NM_000916.4(OXTR):c.202C>T (p.Arg68Cys) | not specified [RCV004497447] | uncertain significance | 3 | 8767986 | 8767986 | Human | | name |
| 407478654 | CV3469952 | single nucleotide variant | NM_000916.4(OXTR):c.202C>G (p.Arg68Gly) | not specified [RCV004663950] | uncertain significance | 3 | 8767986 | 8767986 | Human | | name |
| 598163181 | CV3995812 | single nucleotide variant | NM_000916.4(OXTR):c.263T>C (p.Val88Ala) | not specified [RCV005390943] | uncertain significance | 3 | 8767925 | 8767925 | Human | | name |
| 15125331 | CV734307 | single nucleotide variant | NM_000916.4(OXTR):c.1104G>A (p.Ser368=) | not provided [RCV000896744] | benign | 3 | 8753043 | 8753043 | Human | | name |
| 150510356 | CV1211598 | single nucleotide variant | NM_000916.4(OXTR):c.652G>A (p.Ala218Thr) | not provided [RCV001597390] | benign | 3 | 8767536 | 8767536 | Human | | name |
| 156049282 | CV2271787 | single nucleotide variant | NM_000916.4(OXTR):c.881T>A (p.Val294Glu) | not specified [RCV004130625] | uncertain significance | 3 | 8767307 | 8767307 | Human | | name |
| 156256658 | CV2368753 | single nucleotide variant | NM_000916.4(OXTR):c.538G>C (p.Val180Leu) | not specified [RCV004214635] | uncertain significance | 3 | 8767650 | 8767650 | Human | | name |
| 155908263 | CV2387268 | single nucleotide variant | NM_000916.4(OXTR):c.791A>G (p.Lys264Arg) | not specified [RCV004238360] | uncertain significance | 3 | 8767397 | 8767397 | Human | | name |
| 329401157 | CV2446201 | single nucleotide variant | NM_000916.4(OXTR):c.541G>T (p.Ala181Ser) | not specified [RCV004264604] | uncertain significance | 3 | 8767647 | 8767647 | Human | | name |
| 401775208 | CV2709862 | single nucleotide variant | NM_000916.4(OXTR):c.399G>A (p.Met133Ile) | not specified [RCV004321159] | uncertain significance | 3 | 8767789 | 8767789 | Human | | name |
| 401856537 | CV2764853 | single nucleotide variant | NM_000916.4(OXTR):c.643G>C (p.Val215Leu) | not specified [RCV004334948] | uncertain significance | 3 | 8767545 | 8767545 | Human | | name |
| 401883125 | CV2785544 | single nucleotide variant | NM_000916.4(OXTR):c.904G>A (p.Ala302Thr) | not specified [RCV004363064] | uncertain significance | 3 | 8767284 | 8767284 | Human | | name |
| 405739008 | CV3371199 | single nucleotide variant | NM_000916.4(OXTR):c.298G>A (p.Asp100Asn) | not specified [RCV004497448] | uncertain significance | 3 | 8767890 | 8767890 | Human | | name |
| 405739023 | CV3371201 | single nucleotide variant | NM_000916.4(OXTR):c.751G>A (p.Asp251Asn) | not specified [RCV004497450] | uncertain significance | 3 | 8767437 | 8767437 | Human | | name |
| 407427447 | CV3410682 | single nucleotide variant | NM_000916.4(OXTR):c.409C>A (p.Arg137Ser) | not specified [RCV004586329] | uncertain significance | 3 | 8767779 | 8767779 | Human | | name |
| 407478649 | CV3469951 | single nucleotide variant | NM_000916.4(OXTR):c.967T>G (p.Cys323Gly) | not specified [RCV004663949] | uncertain significance | 3 | 8753180 | 8753180 | Human | | name |
| 597692775 | CV3578086 | single nucleotide variant | NM_000916.4(OXTR):c.535G>A (p.Glu179Lys) | not specified [RCV004838845] | uncertain significance | 3 | 8767653 | 8767653 | Human | | name |
| 597692797 | CV3578088 | single nucleotide variant | NM_000916.4(OXTR):c.506C>T (p.Ala169Val) | not specified [RCV004838847] | likely benign | 3 | 8767682 | 8767682 | Human | | name |
| 597692809 | CV3578089 | single nucleotide variant | NM_000916.4(OXTR):c.706G>A (p.Ala236Thr) | not specified [RCV004838848] | uncertain significance | 3 | 8767482 | 8767482 | Human | | name |
| 597656771 | CV3578090 | single nucleotide variant | NM_000916.4(OXTR):c.707C>A (p.Ala236Asp) | not specified [RCV004827535] | uncertain significance | 3 | 8767481 | 8767481 | Human | | name |
| 597692820 | CV3578091 | single nucleotide variant | NM_000916.4(OXTR):c.713C>G (p.Ala238Gly) | not specified [RCV004838849] | uncertain significance | 3 | 8767475 | 8767475 | Human | | name |
| 15156510 | CV698298 | single nucleotide variant | NM_000916.4(OXTR):c.515T>C (p.Val172Ala) | not provided [RCV000946712] | benign | 3 | 8767673 | 8767673 | Human | | name |
| 15177029 | CV709054 | single nucleotide variant | NM_000916.4(OXTR):c.616C>G (p.Leu206Val) | not provided [RCV000973327] | benign | 3 | 8767572 | 8767572 | Human | | name |
| 155999756 | CV2396472 | single nucleotide variant | NM_000916.4(OXTR):c.1021G>A (p.Val341Met) | not specified [RCV004242182] | uncertain significance | 3 | 8753126 | 8753126 | Human | | name |
| 401864069 | CV2770902 | single nucleotide variant | NM_000916.4(OXTR):c.1051T>C (p.Tyr351His) | not specified [RCV004343574] | uncertain significance | 3 | 8753096 | 8753096 | Human | | name |
| 405738990 | CV3371197 | single nucleotide variant | NM_000916.4(OXTR):c.1066C>T (p.Arg356Cys) | not specified [RCV004497446] | uncertain significance | 3 | 8753081 | 8753081 | Human | | name |
| 407517284 | CV3469949 | single nucleotide variant | NM_000916.4(OXTR):c.1163C>T (p.Thr388Met) | not specified [RCV004650614] | likely benign | 3 | 8752984 | 8752984 | Human | | name |
| 407517286 | CV3469950 | single nucleotide variant | NM_000916.4(OXTR):c.1132T>C (p.Ser378Pro) | not specified [RCV004650615] | uncertain significance | 3 | 8753015 | 8753015 | Human | | name |
| 597692764 | CV3578085 | single nucleotide variant | NM_000916.4(OXTR):c.1067G>A (p.Arg356His) | not specified [RCV004838844] | uncertain significance | 3 | 8753080 | 8753080 | Human | | name |
| 597692787 | CV3578087 | single nucleotide variant | NM_000916.4(OXTR):c.1045G>A (p.Ala349Thr) | not specified [RCV004838846] | uncertain significance | 3 | 8753102 | 8753102 | Human | | name |
