| 405655958 | CV3287847 | single nucleotide variant | NM_020710.3(LRRC47):c.13G>A (p.Ala5Thr) | not specified [RCV004415635] | uncertain significance | 1 | 3796464 | 3796464 | Human | | name |
| 597632862 | CV3693471 | single nucleotide variant | NM_020710.3(LRRC47):c.16G>C (p.Val6Leu) | not specified [RCV004940113] | uncertain significance | 1 | 3796461 | 3796461 | Human | | name |
| 598251136 | CV3984742 | single nucleotide variant | NM_020710.3(LRRC47):c.14C>A (p.Ala5Glu) | not specified [RCV005366628] | uncertain significance | 1 | 3796463 | 3796463 | Human | | name |
| 598222532 | CV3984740 | single nucleotide variant | NM_020710.3(LRRC47):c.89G>C (p.Gly30Ala) | not specified [RCV005379904] | uncertain significance | 1 | 3796388 | 3796388 | Human | | name |
| 401880721 | CV2792948 | single nucleotide variant | NM_020710.3(LRRC47):c.164T>C (p.Leu55Ser) | not specified [RCV004365673] | uncertain significance | 1 | 3796313 | 3796313 | Human | | name |
| 405655966 | CV3287850 | single nucleotide variant | NM_020710.3(LRRC47):c.238C>G (p.Leu80Val) | not specified [RCV004415638] | uncertain significance | 1 | 3796239 | 3796239 | Human | | name |
| 598222506 | CV3984736 | single nucleotide variant | NM_020710.3(LRRC47):c.271C>G (p.Leu91Val) | not specified [RCV005379901] | uncertain significance | 1 | 3796206 | 3796206 | Human | | name |
| 156400612 | CV2199301 | single nucleotide variant | NM_020710.3(LRRC47):c.944C>T (p.Ser315Phe) | not specified [RCV004082650] | uncertain significance | 1 | 3786982 | 3786982 | Human | | name |
| 156239877 | CV2203698 | single nucleotide variant | NM_020710.3(LRRC47):c.778G>A (p.Val260Ile) | not specified [RCV004074348] | uncertain significance | 1 | 3787148 | 3787148 | Human | | name |
| 156193542 | CV2214113 | single nucleotide variant | NM_020710.3(LRRC47):c.468G>C (p.Gln156His) | not specified [RCV004086120] | uncertain significance | 1 | 3796009 | 3796009 | Human | | name |
| 155983643 | CV2241033 | single nucleotide variant | NM_020710.3(LRRC47):c.760A>G (p.Ile254Val) | not specified [RCV004104084] | uncertain significance | 1 | 3787166 | 3787166 | Human | | name |
| 156077476 | CV2318556 | single nucleotide variant | NM_020710.3(LRRC47):c.989G>A (p.Arg330Gln) | not specified [RCV004173463] | uncertain significance | 1 | 3786937 | 3786937 | Human | | name |
| 156346833 | CV2353759 | single nucleotide variant | NM_020710.3(LRRC47):c.955G>A (p.Val319Ile) | not specified [RCV004201768] | uncertain significance | 1 | 3786971 | 3786971 | Human | | name |
| 156201458 | CV2363030 | single nucleotide variant | NM_020710.3(LRRC47):c.787C>T (p.Arg263Cys) | not specified [RCV004211164] | uncertain significance | 1 | 3787139 | 3787139 | Human | | name |
| 329362979 | CV2449611 | single nucleotide variant | NM_020710.3(LRRC47):c.298G>A (p.Ala100Thr) | not specified [RCV004268530] | uncertain significance | 1 | 3796179 | 3796179 | Human | | name |
| 329356982 | CV2460640 | single nucleotide variant | NM_020710.3(LRRC47):c.752C>T (p.Thr251Ile) | not specified [RCV004270692] | uncertain significance | 1 | 3787174 | 3787174 | Human | | name |
| 329398229 | CV2464927 | single nucleotide variant | NM_020710.3(LRRC47):c.673C>T (p.Pro225Ser) | not specified [RCV004284856] | uncertain significance | 1 | 3787253 | 3787253 | Human | | name |
| 401743175 | CV2684034 | single nucleotide variant | NM_020710.3(LRRC47):c.482C>G (p.Thr161Ser) | not specified [RCV004295638] | uncertain significance | 1 | 3795995 | 3795995 | Human | | name |
| 401733170 | CV2712997 | single nucleotide variant | NM_020710.3(LRRC47):c.347C>G (p.Pro116Arg) | not specified [RCV004314703] | uncertain significance | 1 | 3796130 | 3796130 | Human | | name |
| 401899750 | CV2762137 | single nucleotide variant | NM_020710.3(LRRC47):c.824C>T (p.Ser275Leu) | not specified [RCV004341951] | uncertain significance | 1 | 3787102 | 3787102 | Human | | name |
| 401877258 | CV2790105 | single nucleotide variant | NM_020710.3(LRRC47):c.565A>C (p.Asn189His) | not specified [RCV004364050] | uncertain significance | 1 | 3795912 | 3795912 | Human | | name |
| 405655970 | CV3287852 | single nucleotide variant | NM_020710.3(LRRC47):c.547G>A (p.Glu183Lys) | not specified [RCV004415640] | uncertain significance | 1 | 3795930 | 3795930 | Human | | name |
| 405655975 | CV3287854 | single nucleotide variant | NM_020710.3(LRRC47):c.952C>G (p.Pro318Ala) | not specified [RCV004415642] | uncertain significance | 1 | 3786974 | 3786974 | Human | | name |
| 405655978 | CV3287855 | single nucleotide variant | NM_020710.3(LRRC47):c.988C>T (p.Arg330Trp) | not specified [RCV004415643] | uncertain significance | 1 | 3786938 | 3786938 | Human | | name |
| 405655980 | CV3287856 | single nucleotide variant | NM_020710.3(LRRC47):c.997C>T (p.Arg333Trp) | not specified [RCV004415644] | uncertain significance | 1 | 3786929 | 3786929 | Human | | name |
| 597632853 | CV3693469 | single nucleotide variant | NM_020710.3(LRRC47):c.617C>T (p.Thr206Met) | not specified [RCV004940111] | uncertain significance | 1 | 3787309 | 3787309 | Human | | name |
| 597632858 | CV3693470 | single nucleotide variant | NM_020710.3(LRRC47):c.910G>A (p.Ala304Thr) | not specified [RCV004940112] | uncertain significance | 1 | 3787016 | 3787016 | Human | | name |
| 597632867 | CV3693472 | single nucleotide variant | NM_020710.3(LRRC47):c.511G>A (p.Glu171Lys) | not specified [RCV004940114] | uncertain significance | 1 | 3795966 | 3795966 | Human | | name |
| 597633242 | CV3693475 | single nucleotide variant | NM_020710.3(LRRC47):c.503T>C (p.Phe168Ser) | not specified [RCV004940116] | uncertain significance | 1 | 3795974 | 3795974 | Human | | name |
| 156361582 | CV2269275 | single nucleotide variant | NM_020710.3(LRRC47):c.1361C>T (p.Ala454Val) | not specified [RCV004130423] | uncertain significance | 1 | 3782713 | 3782713 | Human | | name |
| 155968267 | CV2312816 | single nucleotide variant | NM_020710.3(LRRC47):c.1073C>T (p.Ser358Leu) | not specified [RCV004171317] | uncertain significance | 1 | 3786853 | 3786853 | Human | | name |
| 156363733 | CV2330026 | single nucleotide variant | NM_020710.3(LRRC47):c.1744G>A (p.Val582Met) | not specified [RCV004185518] | uncertain significance | 1 | 3781096 | 3781096 | Human | | name |
| 156075865 | CV2377089 | single nucleotide variant | NM_020710.3(LRRC47):c.1142G>A (p.Arg381His) | not provided [RCV004691550]|not specified [RCV004229762] | uncertain significance | 1 | 3785139 | 3785139 | Human | | name |
| 329381217 | CV2464571 | single nucleotide variant | NM_020710.3(LRRC47):c.1663G>A (p.Val555Met) | not specified [RCV004278264] | uncertain significance | 1 | 3781177 | 3781177 | Human | | name |
| 401736041 | CV2672808 | single nucleotide variant | NM_020710.3(LRRC47):c.1060C>T (p.Arg354Cys) | not specified [RCV004281587] | uncertain significance | 1 | 3786866 | 3786866 | Human | | name |
| 401741369 | CV2680392 | single nucleotide variant | NM_020710.3(LRRC47):c.1727C>T (p.Pro576Leu) | not specified [RCV004288638] | uncertain significance | 1 | 3781113 | 3781113 | Human | | name |
| 401728323 | CV2686006 | single nucleotide variant | NM_020710.3(LRRC47):c.1197T>G (p.Ile399Met) | not specified [RCV004297022] | uncertain significance | 1 | 3784109 | 3784109 | Human | | name |
| 401747618 | CV2688962 | single nucleotide variant | NM_020710.3(LRRC47):c.1012G>A (p.Gly338Arg) | not specified [RCV004305749] | uncertain significance | 1 | 3786914 | 3786914 | Human | | name |
| 401855954 | CV2754151 | single nucleotide variant | NM_020710.3(LRRC47):c.1006A>G (p.Ile336Val) | not specified [RCV004334344] | uncertain significance | 1 | 3786920 | 3786920 | Human | | name |
| 405655956 | CV3287846 | single nucleotide variant | NM_020710.3(LRRC47):c.1240C>T (p.Arg414Trp) | not specified [RCV004415634] | uncertain significance | 1 | 3784066 | 3784066 | Human | | name |
| 405655961 | CV3287848 | single nucleotide variant | NM_020710.3(LRRC47):c.1483G>A (p.Val495Ile) | not specified [RCV004415636] | likely benign | 1 | 3781532 | 3781532 | Human | | name |
| 405655963 | CV3287849 | single nucleotide variant | NM_020710.3(LRRC47):c.1645G>T (p.Val549Leu) | not specified [RCV004415637] | uncertain significance | 1 | 3781195 | 3781195 | Human | | name |
| 407501029 | CV3456542 | single nucleotide variant | NM_020710.3(LRRC47):c.1141C>T (p.Arg381Cys) | not specified [RCV004644768] | uncertain significance | 1 | 3785140 | 3785140 | Human | | name |
| 597633248 | CV3693473 | single nucleotide variant | NM_020710.3(LRRC47):c.1509G>T (p.Met503Ile) | not specified [RCV004940115] | uncertain significance | 1 | 3781331 | 3781331 | Human | | name |
| 598222515 | CV3984737 | single nucleotide variant | NM_020710.3(LRRC47):c.1046G>A (p.Gly349Glu) | not specified [RCV005379902] | uncertain significance | 1 | 3786880 | 3786880 | Human | | name |
| 598222524 | CV3984738 | single nucleotide variant | NM_020710.3(LRRC47):c.1166A>G (p.Tyr389Cys) | not specified [RCV005379903] | uncertain significance | 1 | 3785115 | 3785115 | Human | | name |
| 598251131 | CV3984739 | single nucleotide variant | NM_020710.3(LRRC47):c.1669G>C (p.Asp557His) | not specified [RCV005366627] | uncertain significance | 1 | 3781171 | 3781171 | Human | | name |
