| 150337766 | CV1166573 | single nucleotide variant | NM_001085049.3(MRAS):c.-7G>A | MRAS-related disorder [RCV003956221]|not specified [RCV001532914] | likely benign|uncertain significance | 3 | 138372877 | 138372877 | Human | 1 | name , trait , alternate_id |
| 151663153 | CV1330961 | single nucleotide variant | NM_001085049.3(MRAS):c.*6C>G | not specified [RCV001825139] | uncertain significance | 3 | 138402275 | 138402275 | Human | | name |
| 126728756 | CV985602 | single nucleotide variant | NM_001085049.3(MRAS):c.*8G>C | not specified [RCV001293513] | benign|likely benign | 3 | 138402277 | 138402277 | Human | | name |
| 150492740 | CV1238535 | single nucleotide variant | NM_001085049.3(MRAS):c.*87C>T | not provided [RCV001655079] | benign | 3 | 138402356 | 138402356 | Human | | name |
| 153305651 | CV1688707 | single nucleotide variant | NM_001085049.3(MRAS):c.*11G>T | not specified [RCV002266446] | benign | 3 | 138402280 | 138402280 | Human | | name |
| 150510594 | CV1211784 | single nucleotide variant | NM_001085049.3(MRAS):c.-18-7G>T | not provided [RCV001597680] | benign | 3 | 138372859 | 138372859 | Human | | name |
| 151811292 | CV1448591 | single nucleotide variant | NM_001085049.3(MRAS):c.193+8C>G | not provided [RCV001974800] | likely benign|uncertain significance | 3 | 138373084 | 138373084 | Human | | name |
| 152037010 | CV1524811 | single nucleotide variant | NM_001085049.3(MRAS):c.347+6C>T | not provided [RCV002165116] | likely benign | 3 | 138397483 | 138397483 | Human | | name |
| 152077198 | CV1536354 | single nucleotide variant | NM_001085049.3(MRAS):c.*1011C>T | not provided [RCV002148842] | benign | 3 | 138403280 | 138403280 | Human | 7 | name |
| 152116457 | CV1553440 | single nucleotide variant | NM_001085049.3(MRAS):c.347+7A>G | not provided [RCV002080961] | likely benign | 3 | 138397484 | 138397484 | Human | | name |
| 152078417 | CV1557732 | single nucleotide variant | NM_001085049.3(MRAS):c.348-5C>T | not provided [RCV002170232] | likely benign | 3 | 138398464 | 138398464 | Human | | name |
| 152126864 | CV1571995 | single nucleotide variant | NM_001085049.3(MRAS):c.448-7C>T | not provided [RCV002217529] | likely benign | 3 | 138400527 | 138400527 | Human | | name |
| 152145591 | CV1582688 | single nucleotide variant | NM_001085049.3(MRAS):c.528-6C>A | not provided [RCV002201190] | likely benign | 3 | 138402164 | 138402164 | Human | | name |
| 152111669 | CV1618528 | single nucleotide variant | NM_001085049.3(MRAS):c.448-4C>T | not provided [RCV002080337] | likely benign | 3 | 138400530 | 138400530 | Human | | name |
| 156006979 | CV1981183 | single nucleotide variant | NM_001085049.3(MRAS):c.194-5C>T | not provided [RCV002618715] | likely benign | 3 | 138397319 | 138397319 | Human | | name |
| 155998490 | CV2057287 | single nucleotide variant | NM_001085049.3(MRAS):c.347+4A>G | not provided [RCV002819536] | uncertain significance | 3 | 138397481 | 138397481 | Human | | name |
| 405080644 | CV2854864 | single nucleotide variant | NM_001085049.3(MRAS):c.527+9T>C | not provided [RCV003549203] | likely benign | 3 | 138400622 | 138400622 | Human | | name |
| 405183510 | CV3057813 | single nucleotide variant | NM_001085049.3(MRAS):c.347+3G>A | not provided [RCV003729030] | uncertain significance | 3 | 138397480 | 138397480 | Human | | name |
| 405077215 | CV3156247 | single nucleotide variant | NM_001085049.3(MRAS):c.348-4C>T | not provided [RCV003851305] | likely benign | 3 | 138398465 | 138398465 | Human | | name |
| 597907103 | CV3738867 | single nucleotide variant | NM_001085049.3(MRAS):c.527+8C>T | not provided [RCV005073102] | likely benign | 3 | 138400621 | 138400621 | Human | | name |
| 597938434 | CV3788271 | single nucleotide variant | NM_001085049.3(MRAS):c.194-9C>A | not provided [RCV005132946] | uncertain significance | 3 | 138397315 | 138397315 | Human | | name |
| 13519997 | CV487053 | deletion | NM_001085049.3(MRAS):c.528-2del | MRAS-related disorder [RCV003915685]|RASopathy [RCV005252051]|not provided [RCV000586951] | benign|likely benign | 3 | 138402165 | 138402165 | Human | 2 | name , trait , alternate_id |
| 152140320 | CV1555773 | single nucleotide variant | NM_001085049.3(MRAS):c.347+18G>A | not provided [RCV002200488] | likely benign | 3 | 138397495 | 138397495 | Human | | name |
| 152094909 | CV1561858 | single nucleotide variant | NM_001085049.3(MRAS):c.528-18C>T | not provided [RCV002194788] | likely benign | 3 | 138402152 | 138402152 | Human | | name |
| 152159981 | CV1590079 | single nucleotide variant | NM_001085049.3(MRAS):c.527+15C>T | not provided [RCV002203260] | likely benign | 3 | 138400628 | 138400628 | Human | | name |
| 152170805 | CV1592589 | single nucleotide variant | NM_001085049.3(MRAS):c.194-16C>T | not provided [RCV002161892] | likely benign | 3 | 138397308 | 138397308 | Human | | name |
| 152152862 | CV1609963 | single nucleotide variant | NM_001085049.3(MRAS):c.347+11A>G | not provided [RCV002179723] | likely benign | 3 | 138397488 | 138397488 | Human | | name |
| 156414929 | CV1955240 | single nucleotide variant | NM_001085049.3(MRAS):c.447+13G>A | not provided [RCV002588883] | likely benign | 3 | 138398581 | 138398581 | Human | | name |
| 156153497 | CV1967540 | single nucleotide variant | NM_001085049.3(MRAS):c.447+15G>T | not provided [RCV002594222] | likely benign | 3 | 138398583 | 138398583 | Human | | name |
| 156125472 | CV1969395 | single nucleotide variant | NM_001085049.3(MRAS):c.348-15T>G | not provided [RCV002593292] | likely benign | 3 | 138398454 | 138398454 | Human | | name |
| 155910563 | CV1980122 | single nucleotide variant | NM_001085049.3(MRAS):c.527+13C>A | not provided [RCV002613958] | likely benign | 3 | 138400626 | 138400626 | Human | | name |
| 156055842 | CV2007958 | single nucleotide variant | NM_001085049.3(MRAS):c.347+10A>C | not provided [RCV002705219] | likely benign | 3 | 138397487 | 138397487 | Human | | name |
| 156183060 | CV2020564 | single nucleotide variant | NM_001085049.3(MRAS):c.194-10C>T | not provided [RCV002710843] | likely benign | 3 | 138397314 | 138397314 | Human | | name |
| 156050952 | CV2060047 | single nucleotide variant | NM_001085049.3(MRAS):c.348-10T>C | not provided [RCV002796766] | likely benign | 3 | 138398459 | 138398459 | Human | | name |
| 156282717 | CV2133912 | single nucleotide variant | NM_001085049.3(MRAS):c.447+19G>A | not provided [RCV003009657] | likely benign | 3 | 138398587 | 138398587 | Human | | name |
| 155971634 | CV2158213 | single nucleotide variant | NM_001085049.3(MRAS):c.347+13G>A | not provided [RCV003033463] | likely benign | 3 | 138397490 | 138397490 | Human | | name |
| 156322354 | CV2166700 | single nucleotide variant | NM_001085049.3(MRAS):c.348-19C>T | not provided [RCV003029259] | likely benign | 3 | 138398450 | 138398450 | Human | | name |
| 156337891 | CV2168591 | single nucleotide variant | NM_001085049.3(MRAS):c.528-13A>G | not provided [RCV003030120] | likely benign | 3 | 138402157 | 138402157 | Human | | name |
| 156117944 | CV2174115 | single nucleotide variant | NM_001085049.3(MRAS):c.527+17C>T | not provided [RCV003055352] | likely benign | 3 | 138400630 | 138400630 | Human | | name |
| 156067332 | CV2176161 | single nucleotide variant | NM_001085049.3(MRAS):c.527+14T>G | not provided [RCV003053608] | likely benign | 3 | 138400627 | 138400627 | Human | | name |
| 402514533 | CV2855575 | single nucleotide variant | NM_001085049.3(MRAS):c.348-17G>C | not provided [RCV003547293] | likely benign | 3 | 138398452 | 138398452 | Human | | name |
| 405202765 | CV2979095 | single nucleotide variant | NM_001085049.3(MRAS):c.527+10G>A | not provided [RCV003678225] | likely benign | 3 | 138400623 | 138400623 | Human | | name |
| 402486543 | CV2998924 | single nucleotide variant | NM_001085049.3(MRAS):c.527+18C>T | not provided [RCV003687051] | likely benign | 3 | 138400631 | 138400631 | Human | | name |
| 404978934 | CV3013218 | single nucleotide variant | NM_001085049.3(MRAS):c.348-13C>G | not provided [RCV003690880] | likely benign | 3 | 138398456 | 138398456 | Human | | name |
| 405214817 | CV3124426 | single nucleotide variant | NM_001085049.3(MRAS):c.447+12C>T | not provided [RCV003823788] | likely benign | 3 | 138398580 | 138398580 | Human | | name |
| 597973155 | CV3790975 | single nucleotide variant | NM_001085049.3(MRAS):c.448-19G>C | not provided [RCV005143190] | likely benign | 3 | 138400515 | 138400515 | Human | | name |
| 597973977 | CV3801667 | single nucleotide variant | NM_001085049.3(MRAS):c.528-11T>C | not provided [RCV005143656] | likely benign | 3 | 138402159 | 138402159 | Human | | name |
| 126728863 | CV985600 | single nucleotide variant | NM_001085049.3(MRAS):c.348-17G>A | not provided [RCV002070123]|not specified [RCV001293557] | likely benign|uncertain significance | 3 | 138398452 | 138398452 | Human | | name |
| 150464766 | CV1252763 | single nucleotide variant | NM_001085049.3(MRAS):c.348-162C>G | not provided [RCV001670087] | benign | 3 | 138398307 | 138398307 | Human | | name |
| 150463762 | CV1263853 | single nucleotide variant | NM_001085049.3(MRAS):c.193+110G>A | not provided [RCV001682554] | benign | 3 | 138373186 | 138373186 | Human | | name |
| 150458835 | CV1269700 | single nucleotide variant | NM_001085049.3(MRAS):c.447+154A>G | not provided [RCV001693240] | benign | 3 | 138398722 | 138398722 | Human | | name |
| 151800795 | CV1474950 | duplication | NM_001085049.3(MRAS):c.337_347+6dup | not provided [RCV001952904] | uncertain significance | 3 | 138397464 | 138397465 | Human | | name |
| 151768273 | CV1444569 | single nucleotide variant | NM_001085049.3(MRAS):c.12C>T (p.Ser4=) | Inborn genetic diseases [RCV002386749]|not provided [RCV001949907] | likely benign | 3 | 138372895 | 138372895 | Human | 1 | name |
| 151826467 | CV1447215 | duplication | NM_001085049.3(MRAS):c.347+6_347+22dup | not provided [RCV001870109] | uncertain significance | 3 | 138397467 | 138397468 | Human | | name |
| 151765595 | CV1495882 | deletion | NM_001085049.3(MRAS):c.347+6_347+22del | not provided [RCV001873940] | uncertain significance | 3 | 138397468 | 138397484 | Human | | name |
| 152124165 | CV1660490 | single nucleotide variant | NM_001085049.3(MRAS):c.15C>T (p.Ala5=) | Inborn genetic diseases [RCV003161347]|not provided [RCV002154645] | likely benign | 3 | 138372898 | 138372898 | Human | 1 | name |
| 152122335 | CV1541494 | single nucleotide variant | NM_001085049.3(MRAS):c.66G>T (p.Gly22=) | Inborn genetic diseases [RCV002363694]|not provided [RCV002175745] | benign|likely benign | 3 | 138372949 | 138372949 | Human | 1 | name |
| 152094757 | CV1603703 | single nucleotide variant | NM_001085049.3(MRAS):c.57G>A (p.Val19=) | not provided [RCV002213211] | likely benign | 3 | 138372940 | 138372940 | Human | | name |
| 155928630 | CV2067140 | single nucleotide variant | NM_001085049.3(MRAS):c.39A>G (p.Thr13=) | not provided [RCV002838650] | likely benign | 3 | 138372922 | 138372922 | Human | | name |
| 329365435 | CV2433476 | single nucleotide variant | NM_001085049.3(MRAS):c.45G>A (p.Lys15=) | Inborn genetic diseases [RCV003182233] | likely benign | 3 | 138372928 | 138372928 | Human | 1 | name |
| 405131801 | CV2905428 | single nucleotide variant | NM_001085049.3(MRAS):c.36C>T (p.Pro12=) | not provided [RCV003560102] | likely benign | 3 | 138372919 | 138372919 | Human | | name |
| 405111005 | CV2942050 | single nucleotide variant | NM_001085049.3(MRAS):c.30C>T (p.Asn10=) | not provided [RCV003666250] | likely benign | 3 | 138372913 | 138372913 | Human | | name |
| 405153016 | CV2950544 | single nucleotide variant | NM_001085049.3(MRAS):c.42C>T (p.Tyr14=) | Inborn genetic diseases [RCV004371578]|not provided [RCV003670162] | likely benign | 3 | 138372925 | 138372925 | Human | 1 | name |
| 405233147 | CV2985364 | single nucleotide variant | NM_001085049.3(MRAS):c.84C>A (p.Ala28=) | not provided [RCV003711762] | likely benign | 3 | 138372967 | 138372967 | Human | | name |
| 597701899 | CV3560768 | single nucleotide variant | NM_001085049.3(MRAS):c.81T>C (p.Ser27=) | Inborn genetic diseases [RCV004956613] | likely benign | 3 | 138372964 | 138372964 | Human | 1 | name |
| 597701894 | CV3560769 | single nucleotide variant | NM_001085049.3(MRAS):c.78A>G (p.Lys26=) | Inborn genetic diseases [RCV004956614] | likely benign | 3 | 138372961 | 138372961 | Human | 1 | name |
| 597938273 | CV3788237 | single nucleotide variant | NM_001085049.3(MRAS):c.54G>C (p.Val18=) | Inborn genetic diseases [RCV005365414]|not provided [RCV005132912] | likely benign | 3 | 138372937 | 138372937 | Human | 1 | name |
| 151863574 | CV1347956 | single nucleotide variant | NM_001085049.3(MRAS):c.162G>A (p.Thr54=) | Inborn genetic diseases [RCV002398026]|not provided [RCV001959543] | likely benign|uncertain significance | 3 | 138373045 | 138373045 | Human | 1 | name |
| 151744252 | CV1401534 | single nucleotide variant | NM_001085049.3(MRAS):c.13G>A (p.Ala5Thr) | Noonan syndrome 11 [RCV004785354]|not provided [RCV001947417] | uncertain significance | 3 | 138372896 | 138372896 | Human | 1 | name |
| 151875603 | CV1461273 | single nucleotide variant | NM_001085049.3(MRAS):c.16G>A (p.Val6Ile) | Inborn genetic diseases [RCV002407068]|not provided [RCV001925780]|not specified [RCV003479367] | uncertain significance | 3 | 138372899 | 138372899 | Human | 1 | name |
| 152106501 | CV1560092 | single nucleotide variant | NM_001085049.3(MRAS):c.138T>C (p.Ile46=) | Inborn genetic diseases [RCV004948631]|not provided [RCV002133918] | likely benign | 3 | 138373021 | 138373021 | Human | 1 | name |
| 152131597 | CV1568045 | single nucleotide variant | NM_001085049.3(MRAS):c.159T>C (p.His53=) | Inborn genetic diseases [RCV002398187]|not provided [RCV002218146] | likely benign | 3 | 138373042 | 138373042 | Human | 1 | name |
| 152031827 | CV1571950 | single nucleotide variant | NM_001085049.3(MRAS):c.225C>T (p.Ser75=) | Inborn genetic diseases [RCV002443108]|not provided [RCV002186779] | likely benign | 3 | 138397355 | 138397355 | Human | 1 | name |
| 152055506 | CV1610145 | single nucleotide variant | NM_001085049.3(MRAS):c.189G>A (p.Leu63=) | Inborn genetic diseases [RCV002407341]|not provided [RCV002167380] | likely benign | 3 | 138373072 | 138373072 | Human | 1 | name |
| 155679887 | CV1807083 | single nucleotide variant | NM_001085049.3(MRAS):c.120T>G (p.Pro40=) | Inborn genetic diseases [RCV002353372] | likely benign | 3 | 138373003 | 138373003 | Human | 1 | name |
| 155740172 | CV1846204 | single nucleotide variant | NM_001085049.3(MRAS):c.192C>T (p.Asp64=) | Inborn genetic diseases [RCV002410873]|MRAS-related disorder [RCV003943399]|not provided [RCV003108092] | likely benign|uncertain significance | 3 | 138373075 | 138373075 | Human | 2 | name , trait , alternate_id |
| 155726414 | CV1848595 | single nucleotide variant | NM_001085049.3(MRAS):c.255G>A (p.Gly85=) | Inborn genetic diseases [RCV002433375] | likely benign | 3 | 138397385 | 138397385 | Human | 1 | name |
| 155703797 | CV1852405 | single nucleotide variant | NM_001085049.3(MRAS):c.267C>T (p.Leu89=) | Inborn genetic diseases [RCV002428886]|not provided [RCV003720636] | likely benign | 3 | 138397397 | 138397397 | Human | 1 | name |
| 155666132 | CV1855521 | single nucleotide variant | NM_001085049.3(MRAS):c.285T>C (p.Thr95=) | Inborn genetic diseases [RCV002435477]|not provided [RCV003775401] | likely benign | 3 | 138397415 | 138397415 | Human | 1 | name |
| 156052097 | CV1867740 | single nucleotide variant | NM_001085049.3(MRAS):c.27C>A (p.Asp9Glu) | not provided [RCV002510213] | uncertain significance | 3 | 138372910 | 138372910 | Human | | name |
| 156278010 | CV1954772 | single nucleotide variant | NM_001085049.3(MRAS):c.261C>T (p.Gly87=) | not provided [RCV002577386]|not specified [RCV004700778] | likely benign | 3 | 138397391 | 138397391 | Human | | name |
| 156122818 | CV1982837 | single nucleotide variant | NM_001085049.3(MRAS):c.279C>T (p.Ser93=) | not provided [RCV002623010] | likely benign | 3 | 138397409 | 138397409 | Human | | name |
| 156131721 | CV1998487 | single nucleotide variant | NM_001085049.3(MRAS):c.270C>T (p.Ile90=) | Inborn genetic diseases [RCV004066786]|not provided [RCV002663245] | likely benign | 3 | 138397400 | 138397400 | Human | 1 | name |
| 156026283 | CV2020297 | single nucleotide variant | NM_001085049.3(MRAS):c.23G>C (p.Ser8Thr) | not provided [RCV002691242] | uncertain significance | 3 | 138372906 | 138372906 | Human | | name |
| 156288346 | CV2154993 | single nucleotide variant | NM_001085049.3(MRAS):c.282C>T (p.Val94=) | not provided [RCV003009865] | likely benign | 3 | 138397412 | 138397412 | Human | | name |
| 401784077 | CV2721018 | single nucleotide variant | NM_001085049.3(MRAS):c.196C>T (p.Leu66=) | Inborn genetic diseases [RCV003310225]|not provided [RCV003777128] | likely benign | 3 | 138397326 | 138397326 | Human | 1 | name |
| 405243949 | CV2971812 | single nucleotide variant | NM_001085049.3(MRAS):c.276C>T (p.Tyr92=) | not provided [RCV003684718] | likely benign | 3 | 138397406 | 138397406 | Human | | name |
| 402485191 | CV2998249 | single nucleotide variant | NM_001085049.3(MRAS):c.171C>T (p.Asp57=) | not provided [RCV003686906] | likely benign | 3 | 138373054 | 138373054 | Human | | name |
| 405075298 | CV3031593 | single nucleotide variant | NM_001085049.3(MRAS):c.114T>C (p.Phe38=) | Inborn genetic diseases [RCV004636812]|not provided [RCV003698561] | likely benign | 3 | 138372997 | 138372997 | Human | 1 | name |
| 597830519 | CV3743056 | single nucleotide variant | NM_001085049.3(MRAS):c.288C>T (p.Asp96=) | Inborn genetic diseases [RCV005377705]|not provided [RCV005062064] | likely benign | 3 | 138397418 | 138397418 | Human | 1 | name |
| 597857444 | CV3822254 | single nucleotide variant | NM_001085049.3(MRAS):c.132C>T (p.Pro44=) | not provided [RCV005174552] | likely benign | 3 | 138373015 | 138373015 | Human | | name |
| 597974437 | CV3831642 | single nucleotide variant | NM_001085049.3(MRAS):c.240A>G (p.Gln80=) | not provided [RCV005168581] | likely benign | 3 | 138397370 | 138397370 | Human | | name |
| 598168652 | CV3982593 | single nucleotide variant | NM_001085049.3(MRAS):c.273C>T (p.Val91=) | Inborn genetic diseases [RCV005369742] | likely benign | 3 | 138397403 | 138397403 | Human | 1 | name |
| 617153346 | CV4018572 | single nucleotide variant | NM_001085049.3(MRAS):c.204A>C (p.Thr68=) | not specified [RCV005418834] | likely benign | 3 | 138397334 | 138397334 | Human | | name |
| 13520043 | CV486962 | single nucleotide variant | NM_001085049.3(MRAS):c.22A>G (p.Ser8Gly) | Inborn genetic diseases [RCV002456290]|not provided [RCV000587030] | benign|likely benign|uncertain significance | 3 | 138372905 | 138372905 | Human | 1 | name |
| 13521724 | CV487038 | single nucleotide variant | NM_001085049.3(MRAS):c.177A>G (p.Gln59=) | MRAS-related disorder [RCV003980070]|RASopathy [RCV005252049]|not provided [RCV000590005] | benign | 3 | 138373060 | 138373060 | Human | 2 | name , trait , alternate_id |
| 34895960 | CV916894 | single nucleotide variant | NM_001085049.3(MRAS):c.252G>A (p.Thr84=) | Inborn genetic diseases [RCV002429850]|not provided [RCV002069216]|not specified [RCV001193226] | benign|likely benign | 3 | 138397382 | 138397382 | Human | 1 | name |
| 34896448 | CV916895 | single nucleotide variant | NM_001085049.3(MRAS):c.291G>A (p.Lys97=) | Inborn genetic diseases [RCV002436765]|not provided [RCV002069238]|not specified [RCV001193828] | benign|likely benign | 3 | 138397421 | 138397421 | Human | 1 | name |
| 150534879 | CV1311668 | single nucleotide variant | NM_001085049.3(MRAS):c.369C>T (p.Leu123=) | Inborn genetic diseases [RCV002343848]|not provided [RCV002074066]|not specified [RCV001779478] | benign|likely benign | 3 | 138398490 | 138398490 | Human | 1 | name |
| 151716858 | CV1465005 | single nucleotide variant | NM_001085049.3(MRAS):c.29A>G (p.Asn10Ser) | Inborn genetic diseases [RCV003303563]|not provided [RCV002003057] | uncertain significance | 3 | 138372912 | 138372912 | Human | 1 | name |
| 151874031 | CV1493456 | single nucleotide variant | NM_001085049.3(MRAS):c.498A>G (p.Lys166=) | not provided [RCV001906844] | likely benign|uncertain significance | 3 | 138400584 | 138400584 | Human | | name |
| 152052892 | CV1523650 | single nucleotide variant | NM_001085049.3(MRAS):c.330C>T (p.Ile110=) | Inborn genetic diseases [RCV002325635]|MRAS-related disorder [RCV003913745]|not provided [RCV002127449] | benign|likely benign | 3 | 138397460 | 138397460 | Human | 2 | name , trait , alternate_id |
| 152148759 | CV1528943 | single nucleotide variant | NM_001085049.3(MRAS):c.441A>G (p.Lys147=) | Inborn genetic diseases [RCV002331777]|not provided [RCV002101892] | likely benign | 3 | 138398562 | 138398562 | Human | 1 | name |
| 152077410 | CV1564676 | single nucleotide variant | NM_001085049.3(MRAS):c.471C>T (p.Ala157=) | not provided [RCV002192597] | likely benign | 3 | 138400557 | 138400557 | Human | | name |
| 152063851 | CV1575249 | single nucleotide variant | NM_001085049.3(MRAS):c.609G>A (p.Leu203=) | Inborn genetic diseases [RCV002352891]|not provided [RCV002110476] | likely benign | 3 | 138402251 | 138402251 | Human | 1 | name |
| 152096583 | CV1583610 | single nucleotide variant | NM_001085049.3(MRAS):c.489T>C (p.Asn163=) | not provided [RCV002132714] | likely benign | 3 | 138400575 | 138400575 | Human | | name |
| 152112895 | CV1586500 | single nucleotide variant | NM_001085049.3(MRAS):c.411C>G (p.Thr137=) | Inborn genetic diseases [RCV002324534]|not provided [RCV002197017] | likely benign | 3 | 138398532 | 138398532 | Human | 1 | name |
| 152096789 | CV1599793 | single nucleotide variant | NM_001085049.3(MRAS):c.435G>A (p.Ala145=) | not provided [RCV002151301] | likely benign | 3 | 138398556 | 138398556 | Human | | name |
| 152175082 | CV1637513 | single nucleotide variant | NM_001085049.3(MRAS):c.324G>A (p.Gln108=) | not provided [RCV002144661] | likely benign | 3 | 138397454 | 138397454 | Human | | name |
| 152167866 | CV1644890 | single nucleotide variant | NM_001085049.3(MRAS):c.540G>A (p.Pro180=) | Inborn genetic diseases [RCV002346451]|not provided [RCV002142267]|not specified [RCV004700635] | benign|likely benign | 3 | 138402182 | 138402182 | Human | 1 | name |
| 152121315 | CV1657637 | single nucleotide variant | NM_001085049.3(MRAS):c.360G>A (p.Pro120=) | Inborn genetic diseases [RCV003161416]|not provided [RCV002216815] | likely benign | 3 | 138398481 | 138398481 | Human | 1 | name |
| 153305652 | CV1688708 | single nucleotide variant | NM_001085049.3(MRAS):c.525T>C (p.Ile175=) | not provided [RCV005058199]|not specified [RCV002266447] | benign | 3 | 138400611 | 138400611 | Human | | name |
| 155732213 | CV1785686 | single nucleotide variant | NM_001085049.3(MRAS):c.336C>A (p.Arg112=) | Inborn genetic diseases [RCV002451706]|not provided [RCV003099430] | likely benign | 3 | 138397466 | 138397466 | Human | 1 | name |
| 155732263 | CV1785699 | single nucleotide variant | NM_001085049.3(MRAS):c.336C>T (p.Arg112=) | Inborn genetic diseases [RCV002451719]|not provided [RCV003099432] | likely benign | 3 | 138397466 | 138397466 | Human | 1 | name |
| 155697585 | CV1790388 | single nucleotide variant | NM_001085049.3(MRAS):c.402G>A (p.Arg134=) | Inborn genetic diseases [RCV002375750] | likely benign | 3 | 138398523 | 138398523 | Human | 1 | name |
| 155724422 | CV1790821 | single nucleotide variant | NM_001085049.3(MRAS):c.417G>A (p.Glu139=) | Inborn genetic diseases [RCV002327699] | likely benign | 3 | 138398538 | 138398538 | Human | 1 | name |
| 155680774 | CV1807288 | single nucleotide variant | NM_001085049.3(MRAS):c.588G>A (p.Arg196=) | Inborn genetic diseases [RCV002353577] | likely benign | 3 | 138402230 | 138402230 | Human | 1 | name |
| 155907609 | CV1983315 | single nucleotide variant | NM_001085049.3(MRAS):c.32T>C (p.Leu11Pro) | not provided [RCV002613765] | uncertain significance | 3 | 138372915 | 138372915 | Human | | name |
| 156246662 | CV1992791 | single nucleotide variant | NM_001085049.3(MRAS):c.612A>G (p.Gln204=) | not provided [RCV002627314] | likely benign | 3 | 138402254 | 138402254 | Human | | name |
| 156074976 | CV2011757 | single nucleotide variant | NM_001085049.3(MRAS):c.525T>A (p.Ile175=) | not provided [RCV002705803] | likely benign | 3 | 138400611 | 138400611 | Human | | name |
| 156288672 | CV2012974 | single nucleotide variant | NM_001085049.3(MRAS):c.384C>T (p.Val128=) | Inborn genetic diseases [RCV005375144]|not provided [RCV002715564] | likely benign | 3 | 138398505 | 138398505 | Human | 1 | name |
| 156042997 | CV2089742 | single nucleotide variant | NM_001085049.3(MRAS):c.372G>T (p.Val124=) | not provided [RCV002867516] | likely benign | 3 | 138398493 | 138398493 | Human | | name |
| 155940753 | CV2142915 | single nucleotide variant | NM_001085049.3(MRAS):c.621C>A (p.Ile207=) | not provided [RCV002994036] | likely benign | 3 | 138402263 | 138402263 | Human | | name |
| 156025577 | CV2145655 | single nucleotide variant | NM_001085049.3(MRAS):c.85C>T (p.Leu29Phe) | not provided [RCV003018440] | uncertain significance | 3 | 138372968 | 138372968 | Human | | name |
| 401744410 | CV2730729 | single nucleotide variant | NM_001085049.3(MRAS):c.456C>T (p.Tyr152=) | Inborn genetic diseases [RCV003293310]|not provided [RCV005102763] | likely benign | 3 | 138400542 | 138400542 | Human | 1 | name |
| 402482412 | CV2860622 | duplication | NM_001085049.3(MRAS):c.160dup (p.Thr54fs) | not provided [RCV003544159] | uncertain significance | 3 | 138373042 | 138373043 | Human | | name |
| 405055932 | CV3023313 | single nucleotide variant | NM_001085049.3(MRAS):c.38C>T (p.Thr13Ile) | not provided [RCV003697339] | uncertain significance | 3 | 138372921 | 138372921 | Human | | name |
| 405208721 | CV3162499 | single nucleotide variant | NM_001085049.3(MRAS):c.331C>T (p.Leu111=) | not provided [RCV003861798] | likely benign | 3 | 138397461 | 138397461 | Human | | name |
| 405692073 | CV3387283 | single nucleotide variant | NM_001085049.3(MRAS):c.429A>G (p.Glu143=) | Inborn genetic diseases [RCV004519455] | likely benign | 3 | 138398550 | 138398550 | Human | 1 | name |
| 405692079 | CV3387284 | single nucleotide variant | NM_001085049.3(MRAS):c.465C>T (p.Thr155=) | Inborn genetic diseases [RCV004519456] | likely benign | 3 | 138400551 | 138400551 | Human | 1 | name |
| 597701906 | CV3560766 | single nucleotide variant | NM_001085049.3(MRAS):c.600C>T (p.Thr200=) | Inborn genetic diseases [RCV004956612] | likely benign | 3 | 138402242 | 138402242 | Human | 1 | name |
| 597882770 | CV3764000 | single nucleotide variant | NM_001085049.3(MRAS):c.86T>G (p.Leu29Arg) | not provided [RCV005109401] | uncertain significance | 3 | 138372969 | 138372969 | Human | | name |
| 597891849 | CV3809739 | single nucleotide variant | NM_001085049.3(MRAS):c.315C>T (p.Arg105=) | not provided [RCV005151459] | likely benign | 3 | 138397445 | 138397445 | Human | | name |
| 597946375 | CV3841641 | single nucleotide variant | NM_001085049.3(MRAS):c.435G>C (p.Ala145=) | not provided [RCV005189074] | likely benign | 3 | 138398556 | 138398556 | Human | | name |
| 598201828 | CV3982594 | single nucleotide variant | NM_001085049.3(MRAS):c.34C>T (p.Pro12Ser) | Inborn genetic diseases [RCV005376115] | uncertain significance | 3 | 138372917 | 138372917 | Human | 1 | name |
| 13520480 | CV487046 | single nucleotide variant | NM_001085049.3(MRAS):c.306C>T (p.His102=) | Inborn genetic diseases [RCV002448827]|not provided [RCV000587833] | benign|likely benign | 3 | 138397436 | 138397436 | Human | 1 | name |
| 13521696 | CV487050 | single nucleotide variant | NM_001085049.3(MRAS):c.453G>A (p.Pro151=) | Inborn genetic diseases [RCV002341506]|MRAS-related disorder [RCV003935586]|RASopathy [RCV005252050]|not provided [RCV000589879] | benign|likely benign | 3 | 138400539 | 138400539 | Human | 3 | name , trait , alternate_id |
| 13796154 | CV551761 | single nucleotide variant | NM_001085049.3(MRAS):c.67G>C (p.Gly23Arg) | RASopathy [RCV000678907] | likely pathogenic | 3 | 138372950 | 138372950 | Human | 1 | name |
| 14698078 | CV623612 | single nucleotide variant | NM_001085049.3(MRAS):c.68G>T (p.Gly23Val) | Noonan syndrome 11 [RCV000787303]|RASopathy [RCV003155311]|not provided [RCV005092354] | pathogenic|likely pathogenic | 3 | 138372951 | 138372951 | Human | 2 | name |
| 40888047 | CV973339 | single nucleotide variant | NM_001085049.3(MRAS):c.80G>C (p.Ser27Thr) | Inborn genetic diseases [RCV001267574] | uncertain significance | 3 | 138372963 | 138372963 | Human | 1 | name |
| 151854033 | CV1455580 | single nucleotide variant | NM_001085049.3(MRAS):c.181G>A (p.Ala61Thr) | not provided [RCV002016955] | uncertain significance | 3 | 138373064 | 138373064 | Human | | name |
| 151887932 | CV1472121 | single nucleotide variant | NM_001085049.3(MRAS):c.208G>C (p.Gly70Arg) | not provided [RCV002000983] | uncertain significance | 3 | 138397338 | 138397338 | Human | | name |
| 155715291 | CV1849383 | single nucleotide variant | NM_001085049.3(MRAS):c.271G>A (p.Val91Ile) | Inborn genetic diseases [RCV002431273]|not provided [RCV003102144]|not specified [RCV002509842] | uncertain significance | 3 | 138397401 | 138397401 | Human | 1 | name |
| 156297023 | CV2065377 | single nucleotide variant | NM_001085049.3(MRAS):c.275A>C (p.Tyr92Ser) | not provided [RCV002856988] | uncertain significance | 3 | 138397405 | 138397405 | Human | | name |
| 156326878 | CV2068679 | single nucleotide variant | NM_001085049.3(MRAS):c.184A>G (p.Ile62Val) | not provided [RCV002835066] | uncertain significance | 3 | 138373067 | 138373067 | Human | | name |
| 156127733 | CV2185769 | single nucleotide variant | NM_001085049.3(MRAS):c.161C>T (p.Thr54Met) | not provided [RCV003055717] | uncertain significance | 3 | 138373044 | 138373044 | Human | | name |
| 156357808 | CV2187243 | single nucleotide variant | NM_001085049.3(MRAS):c.271G>C (p.Val91Leu) | not provided [RCV003048812] | uncertain significance | 3 | 138397401 | 138397401 | Human | | name |
| 329365431 | CV2433474 | single nucleotide variant | NM_001085049.3(MRAS):c.165G>C (p.Glu55Asp) | Inborn genetic diseases [RCV003182231] | uncertain significance | 3 | 138373048 | 138373048 | Human | 1 | name |
| 401913510 | CV2830426 | single nucleotide variant | NM_001085049.3(MRAS):c.196C>G (p.Leu66Val) | not provided [RCV003441641] | uncertain significance | 3 | 138397326 | 138397326 | Human | | name |
| 405174186 | CV2955519 | single nucleotide variant | NM_001085049.3(MRAS):c.173A>G (p.Asn58Ser) | not provided [RCV003675685] | uncertain significance | 3 | 138373056 | 138373056 | Human | | name |
| 402501371 | CV3010581 | single nucleotide variant | NM_001085049.3(MRAS):c.292G>A (p.Ala98Thr) | not provided [RCV003688528] | uncertain significance | 3 | 138397422 | 138397422 | Human | | name |
| 405231962 | CV3144603 | single nucleotide variant | NM_001085049.3(MRAS):c.293C>A (p.Ala98Asp) | not provided [RCV003853056] | uncertain significance | 3 | 138397423 | 138397423 | Human | | name |
| 405169897 | CV3151582 | single nucleotide variant | NM_001085049.3(MRAS):c.251C>T (p.Thr84Met) | Inborn genetic diseases [RCV004950733]|Noonan syndrome 11 [RCV004796855]|not provided [RCV003857733] | uncertain significance | 3 | 138397381 | 138397381 | Human | 2 | name |
| 405244658 | CV3161559 | single nucleotide variant | NM_001085049.3(MRAS):c.232C>T (p.Arg78Trp) | not provided [RCV003868272] | uncertain significance | 3 | 138397362 | 138397362 | Human | | name |
| 402487262 | CV3171394 | single nucleotide variant | NM_001085049.3(MRAS):c.248G>A (p.Arg83His) | not provided [RCV003876421] | uncertain significance | 3 | 138397378 | 138397378 | Human | | name |
| 405692062 | CV3387281 | single nucleotide variant | NM_001085049.3(MRAS):c.130C>T (p.Pro44Ser) | Inborn genetic diseases [RCV004519453] | uncertain significance | 3 | 138373013 | 138373013 | Human | 1 | name |
| 405692070 | CV3387282 | single nucleotide variant | NM_001085049.3(MRAS):c.182C>T (p.Ala61Val) | Inborn genetic diseases [RCV004519454] | uncertain significance | 3 | 138373065 | 138373065 | Human | 1 | name |
| 407519029 | CV3454069 | single nucleotide variant | NM_001085049.3(MRAS):c.254G>A (p.Gly85Glu) | Inborn genetic diseases [RCV004629102] | uncertain significance | 3 | 138397384 | 138397384 | Human | 1 | name |
| 597654467 | CV3551642 | single nucleotide variant | NM_001085049.3(MRAS):c.136A>T (p.Ile46Phe) | Noonan syndrome 11 [RCV004820355] | uncertain significance | 3 | 138373019 | 138373019 | Human | 1 | name |
| 597701884 | CV3560772 | single nucleotide variant | NM_001085049.3(MRAS):c.235G>C (p.Glu79Gln) | Inborn genetic diseases [RCV004956616] | uncertain significance | 3 | 138397365 | 138397365 | Human | 1 | name |
| 597949842 | CV3746034 | single nucleotide variant | NM_001085049.3(MRAS):c.280G>A (p.Val94Ile) | not provided [RCV005079218] | uncertain significance | 3 | 138397410 | 138397410 | Human | | name |
| 597940824 | CV3757288 | single nucleotide variant | NM_001085049.3(MRAS):c.134C>G (p.Thr45Ser) | not provided [RCV005077474] | uncertain significance | 3 | 138373017 | 138373017 | Human | | name |
| 597955474 | CV3809477 | single nucleotide variant | NM_001085049.3(MRAS):c.275A>G (p.Tyr92Cys) | not provided [RCV005162202] | uncertain significance | 3 | 138397405 | 138397405 | Human | | name |
| 597853411 | CV3825176 | single nucleotide variant | NM_001085049.3(MRAS):c.272T>C (p.Val91Ala) | not provided [RCV005174024] | uncertain significance | 3 | 138397402 | 138397402 | Human | | name |
| 597877524 | CV3860274 | duplication | NM_001085049.3(MRAS):c.547dup (p.Ser183fs) | not provided [RCV005198483] | uncertain significance | 3 | 138402183 | 138402184 | Human | | name |
| 616934377 | CV4012376 | single nucleotide variant | NM_001085049.3(MRAS):c.185T>C (p.Ile62Thr) | not specified [RCV005409412] | uncertain significance | 3 | 138373068 | 138373068 | Human | | name |
| 14698079 | CV623613 | single nucleotide variant | NM_001085049.3(MRAS):c.203C>T (p.Thr68Ile) | Noonan syndrome 11 [RCV000787304]|RASopathy [RCV004732489]|not provided [RCV002536888] | pathogenic|likely pathogenic | 3 | 138397333 | 138397333 | Human | 2 | name |
| 14698080 | CV623614 | single nucleotide variant | NM_001085049.3(MRAS):c.212A>G (p.Gln71Arg) | Noonan syndrome 11 [RCV000787305]|RASopathy [RCV005252058] | pathogenic|likely pathogenic | 3 | 138397342 | 138397342 | Human | 2 | name |
| 40887276 | CV973340 | single nucleotide variant | NM_001085049.3(MRAS):c.197T>A (p.Leu66Gln) | Inborn genetic diseases [RCV001266777] | uncertain significance | 3 | 138397327 | 138397327 | Human | 1 | name |
| 150536882 | CV1303805 | single nucleotide variant | NM_001085049.3(MRAS):c.575G>A (p.Trp192Ter) | not provided [RCV001763908] | uncertain significance | 3 | 138402217 | 138402217 | Human | | name |
| 151236268 | CV1319724 | single nucleotide variant | NM_001085049.3(MRAS):c.488A>G (p.Asn163Ser) | not provided [RCV002034662]|not specified [RCV001797929] | benign|uncertain significance | 3 | 138400574 | 138400574 | Human | | name |
| 151777906 | CV1342769 | single nucleotide variant | NM_001085049.3(MRAS):c.313C>T (p.Arg105Cys) | Inborn genetic diseases [RCV004947006]|not provided [RCV001988860] | uncertain significance | 3 | 138397443 | 138397443 | Human | 1 | name |
| 151853867 | CV1370761 | single nucleotide variant | NM_001085049.3(MRAS):c.398T>C (p.Leu133Ser) | not provided [RCV001904445] | uncertain significance | 3 | 138398519 | 138398519 | Human | | name |
| 151755140 | CV1387696 | single nucleotide variant | NM_001085049.3(MRAS):c.410C>A (p.Thr137Asn) | not provided [RCV001969595] | uncertain significance | 3 | 138398531 | 138398531 | Human | | name |
| 151881522 | CV1395856 | single nucleotide variant | NM_001085049.3(MRAS):c.424A>C (p.Lys142Gln) | not provided [RCV002036958] | uncertain significance | 3 | 138398545 | 138398545 | Human | | name |
| 151852968 | CV1397664 | single nucleotide variant | NM_001085049.3(MRAS):c.300T>A (p.Phe100Leu) | Inborn genetic diseases [RCV002441092]|not provided [RCV001958240] | uncertain significance | 3 | 138397430 | 138397430 | Human | 1 | name |
| 151873928 | CV1430493 | single nucleotide variant | NM_001085049.3(MRAS):c.464C>G (p.Thr155Ser) | not provided [RCV002036020] | uncertain significance | 3 | 138400550 | 138400550 | Human | | name |
| 151832567 | CV1447872 | single nucleotide variant | NM_001085049.3(MRAS):c.363G>A (p.Met121Ile) | not provided [RCV001920634] | uncertain significance | 3 | 138398484 | 138398484 | Human | | name |
| 151753435 | CV1471103 | single nucleotide variant | NM_001085049.3(MRAS):c.378C>A (p.Asn126Lys) | Inborn genetic diseases [RCV002344072]|not provided [RCV001948381] | uncertain significance | 3 | 138398499 | 138398499 | Human | 1 | name |
| 151721589 | CV1491745 | single nucleotide variant | NM_001085049.3(MRAS):c.332T>G (p.Leu111Arg) | Inborn genetic diseases [RCV003170402]|MRAS-related disorder [RCV003893050]|not provided [RCV002003751] | uncertain significance | 3 | 138397462 | 138397462 | Human | 2 | name , trait , alternate_id |
| 151813812 | CV1494668 | single nucleotide variant | NM_001085049.3(MRAS):c.351G>T (p.Glu117Asp) | not provided [RCV001954086] | uncertain significance | 3 | 138398472 | 138398472 | Human | | name |
| 155663781 | CV1785797 | single nucleotide variant | NM_001085049.3(MRAS):c.337G>A (p.Val113Ile) | Inborn genetic diseases [RCV002451818] | uncertain significance | 3 | 138397467 | 138397467 | Human | 1 | name |
| 155744987 | CV1806407 | single nucleotide variant | NM_001085049.3(MRAS):c.532C>A (p.Gln178Lys) | Inborn genetic diseases [RCV002346822]|not provided [RCV003776090] | uncertain significance | 3 | 138402174 | 138402174 | Human | 1 | name |
| 155703262 | CV1810518 | single nucleotide variant | NM_001085049.3(MRAS):c.577C>T (p.Arg193Trp) | Inborn genetic diseases [RCV002359706] | uncertain significance | 3 | 138402219 | 138402219 | Human | 1 | name |
| 155703676 | CV1810569 | single nucleotide variant | NM_001085049.3(MRAS):c.578G>A (p.Arg193Gln) | Inborn genetic diseases [RCV002359757]|not provided [RCV003698928] | uncertain significance | 3 | 138402220 | 138402220 | Human | 1 | name |
| 155697795 | CV1854944 | single nucleotide variant | NM_001085049.3(MRAS):c.305A>G (p.His102Arg) | Inborn genetic diseases [RCV002444182] | uncertain significance | 3 | 138397435 | 138397435 | Human | 1 | name |
| 155934201 | CV1916203 | single nucleotide variant | NM_001085049.3(MRAS):c.567A>C (p.Lys189Asn) | Inborn genetic diseases [RCV004068885]|not provided [RCV002615184] | uncertain significance | 3 | 138402209 | 138402209 | Human | 1 | name |
| 156118501 | CV1982630 | single nucleotide variant | NM_001085049.3(MRAS):c.514G>A (p.Val172Ile) | not provided [RCV002622853] | uncertain significance | 3 | 138400600 | 138400600 | Human | | name |
| 155946309 | CV2028921 | single nucleotide variant | NM_001085049.3(MRAS):c.350A>G (p.Glu117Gly) | Inborn genetic diseases [RCV004067781]|not provided [RCV002730423] | uncertain significance | 3 | 138398471 | 138398471 | Human | 1 | name |
| 155938009 | CV2045199 | single nucleotide variant | NM_001085049.3(MRAS):c.586C>T (p.Arg196Trp) | not provided [RCV002775008] | uncertain significance | 3 | 138402228 | 138402228 | Human | | name |
| 156166649 | CV2056636 | single nucleotide variant | NM_001085049.3(MRAS):c.410C>T (p.Thr137Ile) | not provided [RCV002801823] | uncertain significance | 3 | 138398531 | 138398531 | Human | | name |
| 156331161 | CV2065402 | single nucleotide variant | NM_001085049.3(MRAS):c.537T>G (p.Ile179Met) | not provided [RCV002835307] | uncertain significance | 3 | 138402179 | 138402179 | Human | | name |
| 156100902 | CV2132280 | single nucleotide variant | NM_001085049.3(MRAS):c.608T>G (p.Leu203Arg) | not provided [RCV003002208] | uncertain significance | 3 | 138402250 | 138402250 | Human | | name |
| 156124419 | CV2144602 | single nucleotide variant | NM_001085049.3(MRAS):c.446A>G (p.Asn149Ser) | not provided [RCV003003111] | uncertain significance | 3 | 138398567 | 138398567 | Human | | name |
| 156201770 | CV2166094 | single nucleotide variant | NM_001085049.3(MRAS):c.334C>T (p.Arg112Cys) | not provided [RCV003041995] | uncertain significance | 3 | 138397464 | 138397464 | Human | | name |
| 156347379 | CV2172753 | single nucleotide variant | NM_001085049.3(MRAS):c.538C>G (p.Pro180Ala) | not provided [RCV003030633] | uncertain significance | 3 | 138402180 | 138402180 | Human | | name |
| 156229228 | CV2176650 | single nucleotide variant | NM_001085049.3(MRAS):c.557A>C (p.Lys186Thr) | not provided [RCV003059239] | uncertain significance | 3 | 138402199 | 138402199 | Human | | name |
| 329365428 | CV2433473 | single nucleotide variant | NM_001085049.3(MRAS):c.601C>T (p.His201Tyr) | Inborn genetic diseases [RCV003182230] | uncertain significance | 3 | 138402243 | 138402243 | Human | 1 | name |
| 401784078 | CV2721019 | single nucleotide variant | NM_001085049.3(MRAS):c.377A>G (p.Asn126Ser) | Inborn genetic diseases [RCV003310226]|not provided [RCV003481482] | uncertain significance | 3 | 138398498 | 138398498 | Human | 1 | name |
| 401880514 | CV2766214 | single nucleotide variant | NM_001085049.3(MRAS):c.539C>T (p.Pro180Leu) | Inborn genetic diseases [RCV003349682] | uncertain significance | 3 | 138402181 | 138402181 | Human | 1 | name |
| 401912715 | CV2824973 | single nucleotide variant | NM_001085049.3(MRAS):c.335G>A (p.Arg112His) | not provided [RCV003427422] | uncertain significance | 3 | 138397465 | 138397465 | Human | | name |
| 405717454 | CV2847044 | single nucleotide variant | NM_001085049.3(MRAS):c.359C>T (p.Pro120Leu) | Male infertility with azoospermia or oligozoospermia due to single gene mutation [RCV003991598] | likely pathogenic | 3 | 138398480 | 138398480 | Human | 1 | name |
| 402524352 | CV2940479 | single nucleotide variant | NM_001085049.3(MRAS):c.506A>G (p.His169Arg) | not provided [RCV003663541] | uncertain significance | 3 | 138400592 | 138400592 | Human | | name |
| 405214118 | CV2985170 | single nucleotide variant | NM_001085049.3(MRAS):c.510C>A (p.Asp170Glu) | not provided [RCV003709089] | uncertain significance | 3 | 138400596 | 138400596 | Human | | name |
| 404998306 | CV3008813 | single nucleotide variant | NM_001085049.3(MRAS):c.314G>A (p.Arg105His) | not provided [RCV003692909] | uncertain significance | 3 | 138397444 | 138397444 | Human | | name |
| 405232812 | CV3144948 | single nucleotide variant | NM_001085049.3(MRAS):c.307G>A (p.Val103Met) | not provided [RCV003853205] | uncertain significance | 3 | 138397437 | 138397437 | Human | | name |
| 405171749 | CV3150105 | single nucleotide variant | NM_001085049.3(MRAS):c.493G>A (p.Asp165Asn) | not provided [RCV003841576] | uncertain significance | 3 | 138400579 | 138400579 | Human | | name |
| 405241207 | CV3176898 | single nucleotide variant | NM_001085049.3(MRAS):c.431T>C (p.Met144Thr) | not provided [RCV003867336] | uncertain significance | 3 | 138398552 | 138398552 | Human | | name |
| 407519028 | CV3454068 | single nucleotide variant | NM_001085049.3(MRAS):c.593C>G (p.Thr198Arg) | Inborn genetic diseases [RCV004629101] | uncertain significance | 3 | 138402235 | 138402235 | Human | 1 | name |
| 408387894 | CV3520533 | single nucleotide variant | NM_001085049.3(MRAS):c.413G>A (p.Arg138Lys) | not provided [RCV004761365] | uncertain significance | 3 | 138398534 | 138398534 | Human | | name |
| 597663556 | CV3560767 | single nucleotide variant | NM_001085049.3(MRAS):c.313C>G (p.Arg105Gly) | Inborn genetic diseases [RCV004947155] | uncertain significance | 3 | 138397443 | 138397443 | Human | 1 | name |
| 597701889 | CV3560771 | single nucleotide variant | NM_001085049.3(MRAS):c.406A>G (p.Ile136Val) | Inborn genetic diseases [RCV004956615] | uncertain significance | 3 | 138398527 | 138398527 | Human | 1 | name |
| 597701875 | CV3560773 | single nucleotide variant | NM_001085049.3(MRAS):c.587G>A (p.Arg196Gln) | Inborn genetic diseases [RCV004956617] | uncertain significance | 3 | 138402229 | 138402229 | Human | 1 | name |
| 597913962 | CV3740575 | single nucleotide variant | NM_001085049.3(MRAS):c.457A>G (p.Ile153Val) | not provided [RCV005073912] | uncertain significance | 3 | 138400543 | 138400543 | Human | | name |
| 597944104 | CV3754949 | single nucleotide variant | NM_001085049.3(MRAS):c.434C>T (p.Ala145Val) | not provided [RCV005078138] | uncertain significance | 3 | 138398555 | 138398555 | Human | | name |
| 597883467 | CV3784255 | single nucleotide variant | NM_001085049.3(MRAS):c.457A>T (p.Ile153Leu) | not provided [RCV005124544] | uncertain significance | 3 | 138400543 | 138400543 | Human | | name |
| 597942379 | CV3815634 | single nucleotide variant | NM_001085049.3(MRAS):c.452C>T (p.Pro151Leu) | not provided [RCV005159323] | uncertain significance | 3 | 138400538 | 138400538 | Human | | name |
| 597849801 | CV3824505 | single nucleotide variant | NM_001085049.3(MRAS):c.394C>T (p.His132Tyr) | not provided [RCV005173544] | uncertain significance | 3 | 138398515 | 138398515 | Human | | name |
| 597976023 | CV3829041 | single nucleotide variant | NM_001085049.3(MRAS):c.370G>A (p.Val124Met) | not provided [RCV005169490] | uncertain significance | 3 | 138398491 | 138398491 | Human | | name |
| 598168657 | CV3982595 | single nucleotide variant | NM_001085049.3(MRAS):c.434C>A (p.Ala145Glu) | Inborn genetic diseases [RCV005369743] | uncertain significance | 3 | 138398555 | 138398555 | Human | 1 | name |
| 8630617 | CV85772 | single nucleotide variant | NM_001085049.2(MRAS):c.358C>T (p.Pro120Ser) | Malignant melanoma [RCV000065855] | not provided | 3 | 138398479 | 138398479 | Human | | name |
| 40816207 | CV969151 | single nucleotide variant | NM_001085049.3(MRAS):c.548G>A (p.Ser183Asn) | Inborn genetic diseases [RCV003353265]|not provided [RCV003669219]|not specified [RCV001260366] | uncertain significance | 3 | 138402190 | 138402190 | Human | 1 | name |
| 126728999 | CV985601 | single nucleotide variant | NM_001085049.3(MRAS):c.500C>G (p.Ala167Gly) | Inborn genetic diseases [RCV004639541]|not provided [RCV003770475]|not specified [RCV001293616] | uncertain significance | 3 | 138400586 | 138400586 | Human | 1 | name |
| 405190394 | CV2988050 | deletion | NM_001085049.3(MRAS):c.121_124del (p.Asp41fs) | not provided [RCV003706410] | uncertain significance | 3 | 138373002 | 138373005 | Human | | name |
| 34890860 | CV905900 | microsatellite | NM_001085049.3(MRAS):c.552GAA[4] (p.Lys189del) | MRAS-related disorder [RCV003945906]|not provided [RCV001873644]|not specified [RCV001174559] | likely benign|uncertain significance | 3 | 138402193 | 138402195 | Human | | name , trait , alternate_id |
| 597959904 | CV3746126 | microsatellite | NM_001085049.3(MRAS):c.552GAA[6] (p.Lys189_Thr190insLys) | not provided [RCV005081374] | uncertain significance | 3 | 138402192 | 138402193 | Human | | name |
| 405046913 | CV3017848 | duplication | NM_001085049.3(MRAS):c.500_508dup (p.His169_Asp170insAlaPheHis) | not provided [RCV003696666] | uncertain significance | 3 | 138400584 | 138400585 | Human | | name |
