| 150473085 | CV1217570 | single nucleotide variant | NM_001321142.2(CIDEC):c.*69C>G | not provided [RCV001615581] | benign | 3 | 9867065 | 9867065 | Human | | name |
| 150477904 | CV1252087 | single nucleotide variant | NM_001321142.2(CIDEC):c.*293T>C | not provided [RCV001672287] | benign | 3 | 9866841 | 9866841 | Human | | name |
| 150461945 | CV1272944 | single nucleotide variant | NM_001321142.2(CIDEC):c.*162G>A | not provided [RCV001693701] | benign | 3 | 9866972 | 9866972 | Human | | name |
| 150461898 | CV1234837 | single nucleotide variant | NM_001321142.2(CIDEC):c.53+77T>A | not provided [RCV001649419] | benign | 3 | 9878357 | 9878357 | Human | | name |
| 150433586 | CV1216959 | single nucleotide variant | NM_001321142.2(CIDEC):c.208-91C>T | not provided [RCV001608861] | benign | 3 | 9870413 | 9870413 | Human | | name |
| 150447182 | CV1261489 | single nucleotide variant | NM_001321142.2(CIDEC):c.-25-52G>T | not provided [RCV001680163] | benign | 3 | 9878563 | 9878563 | Human | | name |
| 405265909 | CV3215741 | single nucleotide variant | NM_001321142.2(CIDEC):c.366+10C>T | CIDEC-related disorder [RCV003946903] | likely benign | 3 | 9870154 | 9870154 | Human | | name , trait , alternate_id |
| 150505916 | CV1226216 | single nucleotide variant | NM_001321142.2(CIDEC):c.207+180G>A | not provided [RCV001635584] | benign | 3 | 9876886 | 9876886 | Human | | name |
| 401922085 | CV2819881 | single nucleotide variant | NM_001321142.2(CIDEC):c.208-143C>A | CIDEC-related disorder [RCV003980919]|not provided [RCV003433410] | benign | 3 | 9870465 | 9870465 | Human | 1 | name , trait , alternate_id |
| 8659308 | CV134221 | single nucleotide variant | NM_001321142.2(CIDEC):c.33C>G (p.Leu11=) | CIDEC-related disorder [RCV003975012]|not provided [RCV001596964]|not specified [RCV000116745] | benign|likely benign | 3 | 9878454 | 9878454 | Human | 1 | name , trait , alternate_id |
| 8659310 | CV134223 | single nucleotide variant | NM_001321142.2(CIDEC):c.96G>T (p.Leu32=) | CIDEC-related familial partial lipodystrophy [RCV001579016]|not provided [RCV001647130]|not specified [RCV000116747] | benign|likely benign | 3 | 9877177 | 9877177 | Human | 1 | name , trait , alternate_id |
| 15178786 | CV720666 | single nucleotide variant | NM_001321142.2(CIDEC):c.264T>C (p.Asp88=) | not provided [RCV000885140] | benign | 3 | 9870266 | 9870266 | Human | | name |
| 150484193 | CV1222439 | deletion | NM_001321142.2(CIDEC):c.207+294_207+308del | not provided [RCV001617442] | benign | 3 | 9876758 | 9876772 | Human | | name |
| 8659309 | CV134222 | single nucleotide variant | NM_001321142.2(CIDEC):c.600C>T (p.His200=) | CIDEC-related disorder [RCV003975013]|not provided [RCV001610402]|not specified [RCV000116746] | benign|likely benign | 3 | 9867251 | 9867251 | Human | 1 | name , trait , alternate_id |
| 155917538 | CV2198980 | single nucleotide variant | NM_001321142.2(CIDEC):c.88C>G (p.Gln30Glu) | not specified [RCV004080390] | uncertain significance | 3 | 9877185 | 9877185 | Human | | name |
| 405673620 | CV3293772 | single nucleotide variant | NM_001321142.2(CIDEC):c.97T>C (p.Ser33Pro) | not specified [RCV004441848] | uncertain significance | 3 | 9877176 | 9877176 | Human | | name |
| 13215326 | CV428237 | single nucleotide variant | NM_001321142.2(CIDEC):c.594A>G (p.Thr198=) | not provided [RCV000914315]|not specified [RCV000502185] | likely benign | 3 | 9867257 | 9867257 | Human | | name |
| 15199612 | CV720665 | single nucleotide variant | NM_001321142.2(CIDEC):c.387C>G (p.Ser129=) | not provided [RCV000890681] | likely benign | 3 | 9870049 | 9870049 | Human | | name |
| 15150772 | CV734332 | single nucleotide variant | NM_001321142.2(CIDEC):c.603A>G (p.Val201=) | CIDEC-related disorder [RCV003958140]|not provided [RCV000901224] | benign | 3 | 9867248 | 9867248 | Human | 1 | name , trait , alternate_id |
| 15098723 | CV748572 | single nucleotide variant | NM_001321142.2(CIDEC):c.588G>A (p.Gln196=) | not provided [RCV000914316] | likely benign | 3 | 9867263 | 9867263 | Human | | name |
| 151355837 | CV1327021 | single nucleotide variant | NM_001321142.2(CIDEC):c.160G>A (p.Val54Met) | not specified [RCV001822190] | uncertain significance | 3 | 9877113 | 9877113 | Human | | name |
| 8659306 | CV134219 | single nucleotide variant | NM_001321142.2(CIDEC):c.146C>T (p.Thr49Met) | not provided [RCV004707952]|not specified [RCV000116743] | benign | 3 | 9877127 | 9877127 | Human | | name |
| 8659307 | CV134220 | single nucleotide variant | NM_001321142.2(CIDEC):c.181T>C (p.Tyr61His) | CIDEC-related disorder [RCV003975011]|not provided [RCV001650951]|not specified [RCV000116744] | benign | 3 | 9877092 | 9877092 | Human | 1 | name , trait , alternate_id |
| 153303508 | CV1686298 | single nucleotide variant | NM_001321142.2(CIDEC):c.136C>T (p.Arg46Cys) | not provided [RCV002261731] | uncertain significance | 3 | 9877137 | 9877137 | Human | | name |
| 155916121 | CV2197231 | single nucleotide variant | NM_001321142.2(CIDEC):c.155G>A (p.Arg52Gln) | not specified [RCV004079013] | uncertain significance | 3 | 9877118 | 9877118 | Human | | name |
| 156081757 | CV2384780 | single nucleotide variant | NM_001321142.2(CIDEC):c.127C>T (p.Arg43Trp) | not specified [RCV004232543] | uncertain significance | 3 | 9877146 | 9877146 | Human | | name |
| 401896133 | CV2773625 | single nucleotide variant | NM_001321142.2(CIDEC):c.292T>C (p.Phe98Leu) | not specified [RCV004356319] | uncertain significance | 3 | 9870238 | 9870238 | Human | | name |
| 401961511 | CV2843855 | single nucleotide variant | NM_001321142.2(CIDEC):c.212G>A (p.Arg71Gln) | not provided [RCV003481694] | uncertain significance | 3 | 9870318 | 9870318 | Human | | name |
| 405673603 | CV3293767 | single nucleotide variant | NM_001321142.2(CIDEC):c.160G>C (p.Val54Leu) | not specified [RCV004441843] | uncertain significance | 3 | 9877113 | 9877113 | Human | | name |
| 597780975 | CV3650234 | single nucleotide variant | NM_001321142.2(CIDEC):c.112A>C (p.Lys38Gln) | not specified [RCV004899647] | uncertain significance | 3 | 9877161 | 9877161 | Human | | name |
| 597780978 | CV3650235 | single nucleotide variant | NM_001321142.2(CIDEC):c.161T>A (p.Val54Glu) | not specified [RCV004899648] | uncertain significance | 3 | 9877112 | 9877112 | Human | | name |
| 598218480 | CV3895509 | deletion | NM_001321142.2(CIDEC):c.668del (p.Lys223fs) | CIDEC-related familial partial lipodystrophy [RCV005360368] | uncertain significance | 3 | 9867183 | 9867183 | Human | 1 | name , trait , alternate_id |
| 598230704 | CV3948057 | single nucleotide variant | NM_001321142.2(CIDEC):c.128G>A (p.Arg43Gln) | not specified [RCV005319442] | uncertain significance | 3 | 9877145 | 9877145 | Human | | name |
| 15182980 | CV720667 | single nucleotide variant | NM_001321142.2(CIDEC):c.175A>G (p.Met59Val) | not provided [RCV000886120] | benign | 3 | 9877098 | 9877098 | Human | | name |
| 15180175 | CV720668 | single nucleotide variant | NM_001321142.2(CIDEC):c.139G>A (p.Val47Ile) | CIDEC-related disorder [RCV004758740]|not provided [RCV000885464]|not specified [RCV001817096] | likely benign | 3 | 9877134 | 9877134 | Human | 1 | name , trait , alternate_id |
| 151355836 | CV1327020 | single nucleotide variant | NM_001321142.2(CIDEC):c.545G>A (p.Arg182His) | not provided [RCV004692739]|not specified [RCV001822189] | uncertain significance | 3 | 9869891 | 9869891 | Human | | name |
| 155976832 | CV2246088 | single nucleotide variant | NM_001321142.2(CIDEC):c.356C>T (p.Pro119Leu) | not specified [RCV004113995] | uncertain significance | 3 | 9870174 | 9870174 | Human | | name |
| 156107589 | CV2254322 | single nucleotide variant | NM_001321142.2(CIDEC):c.676G>C (p.Ala226Pro) | not specified [RCV004123722] | uncertain significance | 3 | 9867175 | 9867175 | Human | | name |
| 156238085 | CV2285859 | single nucleotide variant | NM_001321142.2(CIDEC):c.389T>C (p.Leu130Pro) | not specified [RCV004143798] | uncertain significance | 3 | 9870047 | 9870047 | Human | | name |
| 156052428 | CV2320305 | single nucleotide variant | NM_001321142.2(CIDEC):c.680C>T (p.Ser227Leu) | not specified [RCV004178469] | uncertain significance | 3 | 9867171 | 9867171 | Human | | name |
| 156101262 | CV2393009 | single nucleotide variant | NM_001321142.2(CIDEC):c.585G>A (p.Met195Ile) | not specified [RCV004242861] | uncertain significance | 3 | 9867266 | 9867266 | Human | | name |
| 329393690 | CV2449796 | single nucleotide variant | NM_001321142.2(CIDEC):c.424C>T (p.Arg142Cys) | not specified [RCV004268901] | uncertain significance | 3 | 9870012 | 9870012 | Human | | name |
| 401896720 | CV2792022 | single nucleotide variant | NM_001321142.2(CIDEC):c.329T>C (p.Leu110Pro) | not specified [RCV004359429] | uncertain significance | 3 | 9870201 | 9870201 | Human | | name |
| 405283924 | CV3213414 | single nucleotide variant | NM_001321142.2(CIDEC):c.660G>T (p.Gln220His) | CIDEC-related disorder [RCV003922001] | likely benign | 3 | 9867191 | 9867191 | Human | | name , trait , alternate_id |
| 405673606 | CV3293768 | single nucleotide variant | NM_001321142.2(CIDEC):c.340C>G (p.Gln114Glu) | not specified [RCV004441844] | uncertain significance | 3 | 9870190 | 9870190 | Human | | name |
| 405673608 | CV3293769 | single nucleotide variant | NM_001321142.2(CIDEC):c.380C>T (p.Pro127Leu) | not specified [RCV004441845] | uncertain significance | 3 | 9870056 | 9870056 | Human | | name |
| 407456294 | CV3419111 | single nucleotide variant | NM_001321142.2(CIDEC):c.565C>T (p.Arg189Cys) | not specified [RCV004610671] | uncertain significance | 3 | 9867286 | 9867286 | Human | | name |
| 407456299 | CV3419113 | single nucleotide variant | NM_001321142.2(CIDEC):c.371C>T (p.Thr124Ile) | not specified [RCV004610673] | uncertain significance | 3 | 9870065 | 9870065 | Human | | name |
| 407456302 | CV3419114 | single nucleotide variant | NM_001321142.2(CIDEC):c.547A>T (p.Ile183Phe) | not specified [RCV004610674] | uncertain significance | 3 | 9869889 | 9869889 | Human | | name |
| 597780972 | CV3650233 | single nucleotide variant | NM_001321142.2(CIDEC):c.397A>C (p.Lys133Gln) | not specified [RCV004899646] | uncertain significance | 3 | 9870039 | 9870039 | Human | | name |
| 598230698 | CV3948056 | single nucleotide variant | NM_001321142.2(CIDEC):c.562T>C (p.Phe188Leu) | not specified [RCV005319441] | likely benign | 3 | 9867289 | 9867289 | Human | | name |
| 13216823 | CV428238 | single nucleotide variant | NM_001321142.2(CIDEC):c.467T>C (p.Ile156Thr) | not provided [RCV004791499]|not specified [RCV000504240] | uncertain significance | 3 | 9869969 | 9869969 | Human | | name |
| 8611940 | CV59522 | single nucleotide variant | NM_001321142.2(CIDEC):c.556G>T (p.Glu186Ter) | CIDEC-related familial partial lipodystrophy [RCV000043528] | pathogenic | 3 | 9867295 | 9867295 | Human | 1 | name , trait , alternate_id |
