| 8578202 | CV112581 | single nucleotide variant | NM_001038705.1(GPR149):c.1623+13938G>C | Lung cancer [RCV000093104] | uncertain significance | 3 | 154407101 | 154407101 | Human | | name |
| 405716960 | CV3255171 | single nucleotide variant | NM_001038705.3(GPR149):c.86C>T (p.Pro29Leu) | not specified [RCV004388319] | uncertain significance | 3 | 154429530 | 154429530 | Human | | name |
| 156093663 | CV2300240 | single nucleotide variant | NM_001038705.3(GPR149):c.119C>T (p.Thr40Ile) | not specified [RCV004153207] | uncertain significance | 3 | 154429497 | 154429497 | Human | | name |
| 156289500 | CV2309710 | single nucleotide variant | NM_001038705.3(GPR149):c.181A>G (p.Met61Val) | not specified [RCV004160843] | uncertain significance | 3 | 154429435 | 154429435 | Human | | name |
| 156176695 | CV2355800 | single nucleotide variant | NM_001038705.3(GPR149):c.130A>G (p.Thr44Ala) | not specified [RCV004201202] | uncertain significance | 3 | 154429486 | 154429486 | Human | | name |
| 405716898 | CV3255162 | single nucleotide variant | NM_001038705.3(GPR149):c.101T>G (p.Ile34Ser) | not specified [RCV004388310] | uncertain significance | 3 | 154429515 | 154429515 | Human | | name |
| 405716929 | CV3255166 | single nucleotide variant | NM_001038705.3(GPR149):c.230A>T (p.Asp77Val) | not specified [RCV004388314] | uncertain significance | 3 | 154429386 | 154429386 | Human | | name |
| 156089768 | CV2202087 | single nucleotide variant | NM_001038705.3(GPR149):c.479C>T (p.Ala160Val) | not specified [RCV004076000] | uncertain significance | 3 | 154429137 | 154429137 | Human | | name |
| 156114093 | CV2225027 | single nucleotide variant | NM_001038705.3(GPR149):c.980T>C (p.Met327Thr) | not specified [RCV004094857] | uncertain significance | 3 | 154428636 | 154428636 | Human | | name |
| 156027378 | CV2278427 | single nucleotide variant | NM_001038705.3(GPR149):c.788G>C (p.Arg263Pro) | not specified [RCV004132881] | uncertain significance | 3 | 154428828 | 154428828 | Human | | name |
| 155936642 | CV2375965 | single nucleotide variant | NM_001038705.3(GPR149):c.851G>A (p.Gly284Glu) | not specified [RCV004218171] | uncertain significance | 3 | 154428765 | 154428765 | Human | | name |
| 156035556 | CV2376773 | single nucleotide variant | NM_001038705.3(GPR149):c.454G>C (p.Gly152Arg) | not specified [RCV004227052] | uncertain significance | 3 | 154429162 | 154429162 | Human | | name |
| 156392090 | CV2378276 | single nucleotide variant | NM_001038705.3(GPR149):c.862T>C (p.Cys288Arg) | not specified [RCV004226311] | uncertain significance | 3 | 154428754 | 154428754 | Human | | name |
| 156156699 | CV2388881 | single nucleotide variant | NM_001038705.3(GPR149):c.665C>A (p.Pro222Gln) | not specified [RCV004239722] | uncertain significance | 3 | 154428951 | 154428951 | Human | | name |
| 156163986 | CV2389644 | single nucleotide variant | NM_001038705.3(GPR149):c.652T>C (p.Cys218Arg) | not specified [RCV004243699] | uncertain significance | 3 | 154428964 | 154428964 | Human | | name |
| 329353965 | CV2436684 | single nucleotide variant | NM_001038705.3(GPR149):c.530G>T (p.Arg177Leu) | not specified [RCV004258056] | uncertain significance | 3 | 154429086 | 154429086 | Human | | name |
| 329372974 | CV2451750 | single nucleotide variant | NM_001038705.3(GPR149):c.892G>C (p.Gly298Arg) | not specified [RCV004276442] | uncertain significance | 3 | 154428724 | 154428724 | Human | | name |
| 401719088 | CV2704950 | single nucleotide variant | NM_001038705.3(GPR149):c.700C>A (p.Arg234Ser) | not specified [RCV004307518] | uncertain significance | 3 | 154428916 | 154428916 | Human | | name |
| 401855981 | CV2754187 | single nucleotide variant | NM_001038705.3(GPR149):c.331A>T (p.Met111Leu) | not specified [RCV004334377] | likely benign | 3 | 154429285 | 154429285 | Human | | name |
| 405717676 | CV3255167 | single nucleotide variant | NM_001038705.3(GPR149):c.442G>A (p.Gly148Ser) | not specified [RCV004388315] | uncertain significance | 3 | 154429174 | 154429174 | Human | | name |
| 405716942 | CV3255168 | single nucleotide variant | NM_001038705.3(GPR149):c.620G>A (p.Gly207Asp) | not specified [RCV004388316] | uncertain significance | 3 | 154428996 | 154428996 | Human | | name |
| 405716948 | CV3255169 | single nucleotide variant | NM_001038705.3(GPR149):c.626C>T (p.Ser209Leu) | not specified [RCV004388317] | uncertain significance | 3 | 154428990 | 154428990 | Human | | name |
| 405716955 | CV3255170 | single nucleotide variant | NM_001038705.3(GPR149):c.847G>T (p.Ala283Ser) | not specified [RCV004388318] | uncertain significance | 3 | 154428769 | 154428769 | Human | | name |
| 407526209 | CV3436593 | single nucleotide variant | NM_001038705.3(GPR149):c.988A>G (p.Met330Val) | not specified [RCV004632364] | uncertain significance | 3 | 154427702 | 154427702 | Human | | name |
| 407526215 | CV3436595 | single nucleotide variant | NM_001038705.3(GPR149):c.725C>G (p.Pro242Arg) | not specified [RCV004632366] | uncertain significance | 3 | 154428891 | 154428891 | Human | | name |
| 407526186 | CV3440088 | single nucleotide variant | NM_001038705.3(GPR149):c.620G>T (p.Gly207Val) | not specified [RCV004632356] | uncertain significance | 3 | 154428996 | 154428996 | Human | | name |
| 407526190 | CV3440089 | single nucleotide variant | NM_001038705.3(GPR149):c.460G>A (p.Val154Met) | not specified [RCV004632357] | uncertain significance | 3 | 154429156 | 154429156 | Human | | name |
| 407526200 | CV3440093 | single nucleotide variant | NM_001038705.3(GPR149):c.800G>A (p.Cys267Tyr) | not specified [RCV004632361] | uncertain significance | 3 | 154428816 | 154428816 | Human | | name |
| 597789614 | CV3684774 | single nucleotide variant | NM_001038705.3(GPR149):c.469G>T (p.Val157Leu) | not specified [RCV004933034] | uncertain significance | 3 | 154429147 | 154429147 | Human | | name |
| 597744635 | CV3684775 | single nucleotide variant | NM_001038705.3(GPR149):c.608G>T (p.Gly203Val) | not specified [RCV004922299] | uncertain significance | 3 | 154429008 | 154429008 | Human | | name |
| 597744639 | CV3684777 | single nucleotide variant | NM_001038705.3(GPR149):c.907A>T (p.Thr303Ser) | not specified [RCV004922300] | uncertain significance | 3 | 154428709 | 154428709 | Human | | name |
| 597789620 | CV3684778 | single nucleotide variant | NM_001038705.3(GPR149):c.776C>A (p.Pro259Gln) | not specified [RCV004933036] | uncertain significance | 3 | 154428840 | 154428840 | Human | | name |
| 597789624 | CV3684779 | single nucleotide variant | NM_001038705.3(GPR149):c.517G>A (p.Gly173Ser) | not specified [RCV004933037] | uncertain significance | 3 | 154429099 | 154429099 | Human | | name |
| 598274214 | CV3971039 | single nucleotide variant | NM_001038705.3(GPR149):c.845C>T (p.Ala282Val) | not specified [RCV005351313] | uncertain significance | 3 | 154428771 | 154428771 | Human | | name |
| 598274216 | CV3971041 | single nucleotide variant | NM_001038705.3(GPR149):c.728C>T (p.Pro243Leu) | not specified [RCV005351314] | uncertain significance | 3 | 154428888 | 154428888 | Human | | name |
| 155914637 | CV2242779 | single nucleotide variant | NM_001038705.3(GPR149):c.1744A>G (p.Ile582Val) | not specified [RCV004107380] | uncertain significance | 3 | 154338151 | 154338151 | Human | | name |
| 156176147 | CV2278265 | single nucleotide variant | NM_001038705.3(GPR149):c.1420A>G (p.Thr474Ala) | not specified [RCV004147575] | uncertain significance | 3 | 154421242 | 154421242 | Human | | name |
| 156126616 | CV2283728 | single nucleotide variant | NM_001038705.3(GPR149):c.1490G>A (p.Gly497Glu) | not specified [RCV004142251] | likely benign | 3 | 154421172 | 154421172 | Human | | name |
| 156145707 | CV2292537 | single nucleotide variant | NM_001038705.3(GPR149):c.1789G>A (p.Val597Ile) | not specified [RCV004150310] | uncertain significance | 3 | 154338106 | 154338106 | Human | | name |
| 156291309 | CV2306059 | single nucleotide variant | NM_001038705.3(GPR149):c.1147T>C (p.Tyr383His) | not specified [RCV004161037] | uncertain significance | 3 | 154427543 | 154427543 | Human | | name |
| 156055919 | CV2326620 | single nucleotide variant | NM_001038705.3(GPR149):c.1382C>A (p.Ser461Tyr) | not specified [RCV004183158] | uncertain significance | 3 | 154421280 | 154421280 | Human | | name |
| 156263998 | CV2329413 | single nucleotide variant | NM_001038705.3(GPR149):c.1286A>T (p.Asn429Ile) | not specified [RCV004187421] | uncertain significance | 3 | 154421376 | 154421376 | Human | | name |
| 155914651 | CV2342047 | single nucleotide variant | NM_001038705.3(GPR149):c.1328G>C (p.Arg443Thr) | not specified [RCV004187028] | uncertain significance | 3 | 154421334 | 154421334 | Human | | name |
| 156125470 | CV2350195 | single nucleotide variant | NM_001038705.3(GPR149):c.1630G>A (p.Gly544Ser) | not specified [RCV004200109] | uncertain significance | 3 | 154338265 | 154338265 | Human | | name |
| 156108512 | CV2355407 | single nucleotide variant | NM_001038705.3(GPR149):c.1472C>A (p.Ala491Glu) | not specified [RCV004205263] | uncertain significance | 3 | 154421190 | 154421190 | Human | | name |
| 156178076 | CV2355903 | single nucleotide variant | NM_001038705.3(GPR149):c.1694G>A (p.Gly565Glu) | not specified [RCV004201291] | uncertain significance | 3 | 154338201 | 154338201 | Human | | name |
| 156153326 | CV2369363 | single nucleotide variant | NM_001038705.3(GPR149):c.1458C>A (p.Asn486Lys) | not specified [RCV004208266] | uncertain significance | 3 | 154421204 | 154421204 | Human | | name |
| 155927790 | CV2391528 | single nucleotide variant | NM_001038705.3(GPR149):c.1558A>T (p.Ser520Cys) | not specified [RCV004239913] | uncertain significance | 3 | 154421104 | 154421104 | Human | | name |
| 156228604 | CV2393028 | single nucleotide variant | NM_001038705.3(GPR149):c.1625G>A (p.Arg542His) | not specified [RCV004242880] | uncertain significance | 3 | 154338270 | 154338270 | Human | | name |
| 329381537 | CV2471224 | single nucleotide variant | NM_001038705.3(GPR149):c.1287C>A (p.Asn429Lys) | not specified [RCV004278463] | uncertain significance | 3 | 154421375 | 154421375 | Human | | name |
| 329393702 | CV2472096 | single nucleotide variant | NM_001038705.3(GPR149):c.1336C>A (p.Arg446Ser) | not specified [RCV004283232] | uncertain significance | 3 | 154421326 | 154421326 | Human | | name |
| 401743061 | CV2677756 | single nucleotide variant | NM_001038705.3(GPR149):c.1958G>A (p.Arg653His) | not specified [RCV004291831] | uncertain significance | 3 | 154337937 | 154337937 | Human | | name |
| 401734842 | CV2688631 | single nucleotide variant | NM_001038705.3(GPR149):c.1493G>A (p.Gly498Asp) | not specified [RCV004301580] | uncertain significance | 3 | 154421169 | 154421169 | Human | | name |
| 401866079 | CV2762516 | single nucleotide variant | NM_001038705.3(GPR149):c.1471G>A (p.Ala491Thr) | not specified [RCV004338051] | uncertain significance | 3 | 154421191 | 154421191 | Human | | name |
| 401897768 | CV2776562 | single nucleotide variant | NM_001038705.3(GPR149):c.2181A>C (p.Glu727Asp) | not specified [RCV004355657] | uncertain significance | 3 | 154337714 | 154337714 | Human | | name |
| 405716905 | CV3255163 | single nucleotide variant | NM_001038705.3(GPR149):c.1336C>T (p.Arg446Cys) | not specified [RCV004388311] | uncertain significance | 3 | 154421326 | 154421326 | Human | | name |
| 405716921 | CV3255165 | single nucleotide variant | NM_001038705.3(GPR149):c.1949C>T (p.Pro650Leu) | not specified [RCV004388313] | uncertain significance | 3 | 154337946 | 154337946 | Human | | name |
| 407526206 | CV3436592 | single nucleotide variant | NM_001038705.3(GPR149):c.2080G>A (p.Glu694Lys) | not specified [RCV004632363] | uncertain significance | 3 | 154337815 | 154337815 | Human | | name |
| 407526213 | CV3436594 | single nucleotide variant | NM_001038705.3(GPR149):c.1595G>A (p.Arg532Lys) | not specified [RCV004632365] | uncertain significance | 3 | 154421067 | 154421067 | Human | | name |
| 407526194 | CV3440091 | single nucleotide variant | NM_001038705.3(GPR149):c.1931C>T (p.Ser644Phe) | not specified [RCV004632359] | uncertain significance | 3 | 154337964 | 154337964 | Human | | name |
| 407526197 | CV3440092 | single nucleotide variant | NM_001038705.3(GPR149):c.1263T>G (p.Asp421Glu) | not specified [RCV004632360] | uncertain significance | 3 | 154421399 | 154421399 | Human | | name |
| 407526203 | CV3440094 | single nucleotide variant | NM_001038705.3(GPR149):c.1258G>T (p.Asp420Tyr) | not specified [RCV004632362] | uncertain significance | 3 | 154421404 | 154421404 | Human | | name |
| 597789610 | CV3684773 | single nucleotide variant | NM_001038705.3(GPR149):c.1468G>T (p.Asp490Tyr) | not specified [RCV004933033] | uncertain significance | 3 | 154421194 | 154421194 | Human | | name |
| 597789617 | CV3684776 | single nucleotide variant | NM_001038705.3(GPR149):c.1441G>A (p.Ala481Thr) | not specified [RCV004933035] | uncertain significance | 3 | 154421221 | 154421221 | Human | | name |
| 597789628 | CV3684780 | single nucleotide variant | NM_001038705.3(GPR149):c.1166G>A (p.Gly389Glu) | not specified [RCV004933038] | uncertain significance | 3 | 154427524 | 154427524 | Human | | name |
| 597789631 | CV3684781 | single nucleotide variant | NM_001038705.3(GPR149):c.1048C>T (p.Leu350Phe) | not specified [RCV004933039] | uncertain significance | 3 | 154427642 | 154427642 | Human | | name |
| 598274211 | CV3971037 | single nucleotide variant | NM_001038705.3(GPR149):c.1619G>A (p.Arg540His) | not specified [RCV005351311] | uncertain significance | 3 | 154421043 | 154421043 | Human | | name |
| 598274213 | CV3971038 | single nucleotide variant | NM_001038705.3(GPR149):c.1154T>C (p.Val385Ala) | not specified [RCV005351312] | uncertain significance | 3 | 154427536 | 154427536 | Human | | name |
| 598233652 | CV3971040 | single nucleotide variant | NM_001038705.3(GPR149):c.1379C>G (p.Pro460Arg) | not specified [RCV005342792] | uncertain significance | 3 | 154421283 | 154421283 | Human | | name |
| 598274218 | CV3971042 | single nucleotide variant | NM_001038705.3(GPR149):c.1928C>T (p.Ser643Phe) | not specified [RCV005351315] | uncertain significance | 3 | 154337967 | 154337967 | Human | | name |
| 38456903 | CV789731 | single nucleotide variant | NM_001038705.3(GPR149):c.1404A>C (p.Arg468Ser) | Hypertrophic cardiomyopathy [RCV001199399]|not provided [RCV004693422] | uncertain significance | 3 | 154421258 | 154421258 | Human | 2 | name |
| 8630658 | CV85813 | single nucleotide variant | NM_001038705.1(GPR149):c.1858G>A (p.Glu620Lys) | Malignant melanoma [RCV000065896] | not provided | 3 | 154338037 | 154338037 | Human | | name |
