| 405276859 | CV3193512 | duplication | NM_133462.4(TTC14):c.287-3dup | TTC14-related disorder [RCV003974680] | benign | 3 | 180603109 | 180603110 | Human | | name , trait , alternate_id |
| 407528775 | CV3487164 | single nucleotide variant | NM_133462.4(TTC14):c.26C>T (p.Ser9Leu) | not specified [RCV004680563] | uncertain significance | 3 | 180602287 | 180602287 | Human | | name |
| 155972265 | CV2334315 | single nucleotide variant | NM_133462.4(TTC14):c.83A>G (p.Asn28Ser) | not specified [RCV004188295] | uncertain significance | 3 | 180602344 | 180602344 | Human | | name |
| 155914361 | CV2341980 | single nucleotide variant | NM_133462.4(TTC14):c.36C>G (p.Cys12Trp) | not specified [RCV004184922] | uncertain significance | 3 | 180602297 | 180602297 | Human | | name |
| 405278834 | CV3212649 | single nucleotide variant | NM_133462.4(TTC14):c.888T>C (p.Ser296=) | TTC14-related disorder [RCV003954681] | benign | 3 | 180605796 | 180605796 | Human | | name , trait , alternate_id |
| 405295453 | CV3216027 | single nucleotide variant | NM_133462.4(TTC14):c.939C>T (p.Ile313=) | TTC14-related disorder [RCV003937402] | likely benign | 3 | 180606262 | 180606262 | Human | | name , trait , alternate_id |
| 156232067 | CV2199709 | single nucleotide variant | NM_133462.4(TTC14):c.206C>T (p.Ser69Phe) | not specified [RCV004072440] | uncertain significance | 3 | 180602935 | 180602935 | Human | | name |
| 156140942 | CV2212241 | single nucleotide variant | NM_133462.4(TTC14):c.280A>G (p.Ser94Gly) | not specified [RCV004089122] | uncertain significance | 3 | 180603009 | 180603009 | Human | | name |
| 156066021 | CV2340873 | single nucleotide variant | NM_133462.4(TTC14):c.293A>G (p.Tyr98Cys) | not specified [RCV004188229] | uncertain significance | 3 | 180603130 | 180603130 | Human | | name |
| 155925732 | CV2365635 | single nucleotide variant | NM_133462.4(TTC14):c.254C>T (p.Pro85Leu) | not specified [RCV004214196] | uncertain significance | 3 | 180602983 | 180602983 | Human | | name |
| 401783497 | CV2723635 | single nucleotide variant | NM_133462.4(TTC14):c.181A>G (p.Asn61Asp) | not specified [RCV004325814] | uncertain significance | 3 | 180602910 | 180602910 | Human | | name |
| 405279957 | CV3191600 | single nucleotide variant | NM_133462.4(TTC14):c.1056G>A (p.Ala352=) | TTC14-related disorder [RCV003919745] | benign | 3 | 180606487 | 180606487 | Human | | name , trait , alternate_id |
| 405268725 | CV3199024 | single nucleotide variant | NM_133462.4(TTC14):c.1143C>T (p.Leu381=) | TTC14-related disorder [RCV003912131] | likely benign | 3 | 180606574 | 180606574 | Human | | name , trait , alternate_id |
| 405274603 | CV3208994 | single nucleotide variant | NM_133462.4(TTC14):c.1806C>T (p.Asn602=) | TTC14-related disorder [RCV003951764] | likely benign | 3 | 180610035 | 180610035 | Human | | name , trait , alternate_id |
| 405282414 | CV3212908 | single nucleotide variant | NM_133462.4(TTC14):c.2034T>C (p.Ser678=) | TTC14-related disorder [RCV003957029] | likely benign | 3 | 180610263 | 180610263 | Human | | name , trait , alternate_id |
| 405803826 | CV3337321 | single nucleotide variant | NM_133462.4(TTC14):c.268A>C (p.Ile90Leu) | not specified [RCV004478969] | uncertain significance | 3 | 180602997 | 180602997 | Human | | name |
| 597789056 | CV3625214 | single nucleotide variant | NM_133462.4(TTC14):c.235T>C (p.Ser79Pro) | not specified [RCV004876004] | uncertain significance | 3 | 180602964 | 180602964 | Human | | name |
| 156151078 | CV2307529 | single nucleotide variant | NM_133462.4(TTC14):c.707G>C (p.Ser236Thr) | not specified [RCV004166173] | uncertain significance | 3 | 180604857 | 180604857 | Human | | name |
| 156268204 | CV2314716 | single nucleotide variant | NM_133462.4(TTC14):c.406A>G (p.Ile136Val) | not specified [RCV004170861] | uncertain significance | 3 | 180603243 | 180603243 | Human | | name |
| 156256704 | CV2322011 | single nucleotide variant | NM_133462.4(TTC14):c.362G>A (p.Arg121Gln) | not specified [RCV004173767] | uncertain significance | 3 | 180603199 | 180603199 | Human | | name |
| 156213711 | CV2367120 | single nucleotide variant | NM_133462.4(TTC14):c.803A>G (p.Glu268Gly) | not specified [RCV004215562] | likely benign | 3 | 180604953 | 180604953 | Human | | name |
| 155905552 | CV2393096 | single nucleotide variant | NM_133462.4(TTC14):c.790G>C (p.Glu264Gln) | not specified [RCV004226579] | uncertain significance | 3 | 180604940 | 180604940 | Human | | name |
| 401769704 | CV2689899 | single nucleotide variant | NM_133462.4(TTC14):c.707G>A (p.Ser236Asn) | not specified [RCV004297792] | uncertain significance | 3 | 180604857 | 180604857 | Human | | name |
| 405803828 | CV3337322 | single nucleotide variant | NM_133462.4(TTC14):c.337A>G (p.Met113Val) | not specified [RCV004478970] | uncertain significance | 3 | 180603174 | 180603174 | Human | | name |
| 405803831 | CV3337323 | single nucleotide variant | NM_133462.4(TTC14):c.458T>A (p.Met153Lys) | not specified [RCV004478971] | uncertain significance | 3 | 180603295 | 180603295 | Human | | name |
| 405803833 | CV3337324 | single nucleotide variant | NM_133462.4(TTC14):c.469G>A (p.Ala157Thr) | not specified [RCV004478972] | uncertain significance | 3 | 180603306 | 180603306 | Human | | name |
| 407528780 | CV3487166 | single nucleotide variant | NM_133462.4(TTC14):c.569G>A (p.Arg190Gln) | not specified [RCV004680565] | uncertain significance | 3 | 180604307 | 180604307 | Human | | name |
| 407528782 | CV3487167 | single nucleotide variant | NM_133462.4(TTC14):c.877G>T (p.Asp293Tyr) | not specified [RCV004680566] | uncertain significance | 3 | 180605785 | 180605785 | Human | | name |
| 597788993 | CV3625198 | single nucleotide variant | NM_133462.4(TTC14):c.728C>A (p.Ser243Tyr) | not specified [RCV004875989] | uncertain significance | 3 | 180604878 | 180604878 | Human | | name |
| 597789012 | CV3625204 | single nucleotide variant | NM_133462.4(TTC14):c.913T>C (p.Ser305Pro) | not specified [RCV004875994] | uncertain significance | 3 | 180605821 | 180605821 | Human | | name |
| 597789016 | CV3625205 | single nucleotide variant | NM_133462.4(TTC14):c.939C>G (p.Ile313Met) | not specified [RCV004875995] | uncertain significance | 3 | 180606262 | 180606262 | Human | | name |
| 597789047 | CV3625212 | single nucleotide variant | NM_133462.4(TTC14):c.814A>G (p.Ile272Val) | not specified [RCV004876002] | uncertain significance | 3 | 180604964 | 180604964 | Human | | name |
| 598252869 | CV3925097 | single nucleotide variant | NM_133462.4(TTC14):c.680A>G (p.Glu227Gly) | not specified [RCV005298971] | uncertain significance | 3 | 180604586 | 180604586 | Human | | name |
| 156027518 | CV2195499 | single nucleotide variant | NM_133462.4(TTC14):c.1514A>G (p.His505Arg) | not specified [RCV004082721] | uncertain significance | 3 | 180609743 | 180609743 | Human | | name |
| 156377739 | CV2211425 | single nucleotide variant | NM_133462.4(TTC14):c.1735C>G (p.Leu579Val) | not specified [RCV004090332] | uncertain significance | 3 | 180609964 | 180609964 | Human | | name |
| 156375208 | CV2213530 | single nucleotide variant | NM_133462.4(TTC14):c.1540C>T (p.Arg514Cys) | not specified [RCV004087492] | uncertain significance | 3 | 180609769 | 180609769 | Human | | name |
| 156186885 | CV2236283 | single nucleotide variant | NM_133462.4(TTC14):c.1340A>C (p.Lys447Thr) | not specified [RCV004107983] | uncertain significance | 3 | 180608750 | 180608750 | Human | | name |
| 155943176 | CV2244929 | single nucleotide variant | NM_133462.4(TTC14):c.2120C>T (p.Thr707Ile) | not specified [RCV004104675] | uncertain significance | 3 | 180610349 | 180610349 | Human | | name |
| 155919679 | CV2279460 | single nucleotide variant | NM_133462.4(TTC14):c.1363G>A (p.Ala455Thr) | not specified [RCV004141989] | uncertain significance | 3 | 180608773 | 180608773 | Human | | name |
| 156096826 | CV2294407 | single nucleotide variant | NM_133462.4(TTC14):c.1811A>C (p.Tyr604Ser) | not specified [RCV004159917] | uncertain significance | 3 | 180610040 | 180610040 | Human | | name |
| 155902235 | CV2301406 | single nucleotide variant | NM_133462.4(TTC14):c.2005T>C (p.Ser669Pro) | not specified [RCV004162342] | uncertain significance | 3 | 180610234 | 180610234 | Human | | name |
| 155906702 | CV2303363 | single nucleotide variant | NM_133462.4(TTC14):c.1721A>G (p.Lys574Arg) | not specified [RCV004159096] | uncertain significance | 3 | 180609950 | 180609950 | Human | | name |
| 156349395 | CV2305580 | single nucleotide variant | NM_133462.4(TTC14):c.1788T>G (p.Asp596Glu) | not specified [RCV004165602] | uncertain significance | 3 | 180610017 | 180610017 | Human | | name |
| 155914172 | CV2341938 | single nucleotide variant | NM_133462.4(TTC14):c.2065G>A (p.Ala689Thr) | not specified [RCV004184882] | likely benign | 3 | 180610294 | 180610294 | Human | | name |
| 156004966 | CV2397015 | single nucleotide variant | NM_133462.4(TTC14):c.1684G>A (p.Asp562Asn) | not specified [RCV004236167] | uncertain significance | 3 | 180609913 | 180609913 | Human | | name |
| 156255776 | CV2397686 | single nucleotide variant | NM_133462.4(TTC14):c.2288A>G (p.Glu763Gly) | not specified [RCV004237129] | uncertain significance | 3 | 180610517 | 180610517 | Human | | name |
| 329363192 | CV2445953 | single nucleotide variant | NM_133462.4(TTC14):c.2137G>A (p.Glu713Lys) | not specified [RCV004270550] | uncertain significance | 3 | 180610366 | 180610366 | Human | | name |
| 401861985 | CV2766533 | single nucleotide variant | NM_133462.4(TTC14):c.2125C>A (p.Gln709Lys) | not specified [RCV004347153] | uncertain significance | 3 | 180610354 | 180610354 | Human | | name |
| 401887667 | CV2770075 | single nucleotide variant | NM_133462.4(TTC14):c.1526G>A (p.Arg509His) | not specified [RCV004355991] | uncertain significance | 3 | 180609755 | 180609755 | Human | | name |
| 401894472 | CV2788167 | single nucleotide variant | NM_133462.4(TTC14):c.1624A>G (p.Asn542Asp) | not specified [RCV004352785] | uncertain significance | 3 | 180609853 | 180609853 | Human | | name |
| 405274099 | CV3211546 | single nucleotide variant | NM_133462.4(TTC14):c.1513C>T (p.His505Tyr) | TTC14-related disorder [RCV003951383] | likely benign | 3 | 180609742 | 180609742 | Human | | name , trait , alternate_id |
| 405282834 | CV3213052 | single nucleotide variant | NM_133462.4(TTC14):c.2177T>C (p.Val726Ala) | TTC14-related disorder [RCV003957146]|not specified [RCV004369863] | likely benign|uncertain significance | 3 | 180610406 | 180610406 | Human | | name , trait , alternate_id |
| 405803815 | CV3337316 | single nucleotide variant | NM_133462.4(TTC14):c.1156G>A (p.Val386Ile) | not specified [RCV004478964] | uncertain significance | 3 | 180606587 | 180606587 | Human | | name |
| 405803817 | CV3337317 | single nucleotide variant | NM_133462.4(TTC14):c.1439G>A (p.Ser480Asn) | not specified [RCV004478965] | uncertain significance | 3 | 180609668 | 180609668 | Human | | name |
| 405803820 | CV3337318 | single nucleotide variant | NM_133462.4(TTC14):c.1571C>A (p.Ser524Tyr) | not specified [RCV004478966] | uncertain significance | 3 | 180609800 | 180609800 | Human | | name |
| 405803822 | CV3337319 | single nucleotide variant | NM_133462.4(TTC14):c.1810T>A (p.Tyr604Asn) | not specified [RCV004478967] | uncertain significance | 3 | 180610039 | 180610039 | Human | | name |
| 407528777 | CV3487165 | single nucleotide variant | NM_133462.4(TTC14):c.1850A>G (p.Tyr617Cys) | not specified [RCV004680564] | uncertain significance | 3 | 180610079 | 180610079 | Human | | name |
| 597788996 | CV3625199 | single nucleotide variant | NM_133462.4(TTC14):c.2014C>T (p.Pro672Ser) | not specified [RCV004875990] | uncertain significance | 3 | 180610243 | 180610243 | Human | | name |
| 597789000 | CV3625201 | single nucleotide variant | NM_133462.4(TTC14):c.1021G>A (p.Val341Met) | not specified [RCV004875991] | uncertain significance | 3 | 180606344 | 180606344 | Human | | name |
| 597789004 | CV3625202 | single nucleotide variant | NM_133462.4(TTC14):c.1986A>T (p.Glu662Asp) | not specified [RCV004875992] | uncertain significance | 3 | 180610215 | 180610215 | Human | | name |
| 597789008 | CV3625203 | single nucleotide variant | NM_133462.4(TTC14):c.1802A>G (p.Tyr601Cys) | not specified [RCV004875993] | uncertain significance | 3 | 180610031 | 180610031 | Human | | name |
| 597789020 | CV3625206 | single nucleotide variant | NM_133462.4(TTC14):c.1429T>A (p.Ser477Thr) | not specified [RCV004875996] | uncertain significance | 3 | 180609658 | 180609658 | Human | | name |
| 597789025 | CV3625207 | single nucleotide variant | NM_133462.4(TTC14):c.1223C>G (p.Ala408Gly) | not specified [RCV004875997] | uncertain significance | 3 | 180607698 | 180607698 | Human | | name |
| 597789030 | CV3625208 | single nucleotide variant | NM_133462.4(TTC14):c.1952T>C (p.Ile651Thr) | not specified [RCV004875998] | likely benign | 3 | 180610181 | 180610181 | Human | | name |
| 597789034 | CV3625209 | single nucleotide variant | NM_133462.4(TTC14):c.2191G>A (p.Ala731Thr) | not specified [RCV004875999] | uncertain significance | 3 | 180610420 | 180610420 | Human | | name |
| 597789038 | CV3625210 | single nucleotide variant | NM_133462.4(TTC14):c.1565G>T (p.Arg522Met) | not specified [RCV004876000] | uncertain significance | 3 | 180609794 | 180609794 | Human | | name |
| 597789043 | CV3625211 | single nucleotide variant | NM_133462.4(TTC14):c.1475C>T (p.Ser492Leu) | not specified [RCV004876001] | uncertain significance | 3 | 180609704 | 180609704 | Human | | name |
| 597789052 | CV3625213 | single nucleotide variant | NM_133462.4(TTC14):c.2150A>G (p.Asn717Ser) | not specified [RCV004876003] | uncertain significance | 3 | 180610379 | 180610379 | Human | | name |
| 597789061 | CV3625215 | single nucleotide variant | NM_133462.4(TTC14):c.1720A>G (p.Lys574Glu) | not specified [RCV004876005] | uncertain significance | 3 | 180609949 | 180609949 | Human | | name |
| 598252863 | CV3925095 | single nucleotide variant | NM_133462.4(TTC14):c.1808G>C (p.Ser603Thr) | not specified [RCV005298970] | uncertain significance | 3 | 180610037 | 180610037 | Human | | name |
| 598252875 | CV3925098 | single nucleotide variant | NM_133462.4(TTC14):c.2204A>G (p.Lys735Arg) | not specified [RCV005298972] | uncertain significance | 3 | 180610433 | 180610433 | Human | | name |
| 598230045 | CV3925099 | single nucleotide variant | NM_133462.4(TTC14):c.1888T>G (p.Ser630Ala) | not specified [RCV005294987] | uncertain significance | 3 | 180610117 | 180610117 | Human | | name |
| 598230051 | CV3925100 | single nucleotide variant | NM_133462.4(TTC14):c.1593T>A (p.Asn531Lys) | not specified [RCV005294988] | uncertain significance | 3 | 180609822 | 180609822 | Human | | name |
