| 15115606 | CV744117 | single nucleotide variant | NM_015245.3(ANKS1A):c.1424-8A>G | not provided [RCV000895056] | likely benign | 6 | 35017465 | 35017465 | Human | | name |
| 15192640 | CV730424 | single nucleotide variant | NM_015245.3(ANKS1A):c.2437-10C>T | not provided [RCV000888718] | benign | 6 | 35079811 | 35079811 | Human | | name |
| 8581865 | CV116313 | single nucleotide variant | NM_015245.2(ANKS1A):c.198-18282G>C | Lung cancer [RCV000096836] | uncertain significance | 6 | 34948957 | 34948957 | Human | | name |
| 8581866 | CV116314 | single nucleotide variant | NM_015245.2(ANKS1A):c.2011-10478G>A | Lung cancer [RCV000096837] | uncertain significance | 6 | 35043621 | 35043621 | Human | | name |
| 156155035 | CV2328714 | single nucleotide variant | NM_015245.3(ANKS1A):c.4G>A (p.Gly2Arg) | not specified [RCV004177949] | uncertain significance | 6 | 34889406 | 34889406 | Human | | name |
| 401885758 | CV2775077 | single nucleotide variant | NM_015245.3(ANKS1A):c.198C>T (p.Ser66=) | not specified [RCV004346445] | likely benign | 6 | 34967239 | 34967239 | Human | | name |
| 405694756 | CV3226516 | single nucleotide variant | NM_015245.3(ANKS1A):c.249C>G (p.Pro83=) | not provided [RCV003992909] | likely benign | 6 | 34967290 | 34967290 | Human | | name |
| 15115600 | CV735637 | single nucleotide variant | NM_015245.3(ANKS1A):c.321C>T (p.Asn107=) | not provided [RCV000895055] | likely benign | 6 | 34970052 | 34970052 | Human | | name |
| 405684016 | CV3282354 | single nucleotide variant | NM_015245.3(ANKS1A):c.179C>T (p.Pro60Leu) | not specified [RCV004422333] | uncertain significance | 6 | 34889581 | 34889581 | Human | | name |
| 597650954 | CV3561373 | single nucleotide variant | NM_015245.3(ANKS1A):c.167C>T (p.Ser56Phe) | not specified [RCV004833678] | uncertain significance | 6 | 34889569 | 34889569 | Human | | name |
| 597651189 | CV3561419 | single nucleotide variant | NM_015245.3(ANKS1A):c.119C>G (p.Ser40Cys) | not specified [RCV004833706] | uncertain significance | 6 | 34889521 | 34889521 | Human | | name |
| 598168646 | CV3982592 | single nucleotide variant | NM_015245.3(ANKS1A):c.289G>C (p.Glu97Gln) | not specified [RCV005369741] | uncertain significance | 6 | 34970020 | 34970020 | Human | | name |
| 15174611 | CV710468 | single nucleotide variant | NM_015245.3(ANKS1A):c.1890C>T (p.Leu630=) | not provided [RCV000972753] | benign | 6 | 35017939 | 35017939 | Human | | name |
| 15195708 | CV722008 | single nucleotide variant | NM_015245.3(ANKS1A):c.2835T>C (p.Asn945=) | not provided [RCV000889579] | benign | 6 | 35082816 | 35082816 | Human | | name |
| 156375062 | CV2204995 | single nucleotide variant | NM_015245.3(ANKS1A):c.952A>C (p.Thr318Pro) | not specified [RCV004077613] | uncertain significance | 6 | 34983365 | 34983365 | Human | | name |
| 156224095 | CV2219276 | single nucleotide variant | NM_015245.3(ANKS1A):c.700C>A (p.Leu234Ile) | not specified [RCV004095153] | uncertain significance | 6 | 34981954 | 34981954 | Human | | name |
| 401748446 | CV2704296 | single nucleotide variant | NM_015245.3(ANKS1A):c.545T>G (p.Phe182Cys) | not specified [RCV004311283] | uncertain significance | 6 | 34981799 | 34981799 | Human | | name |
| 401860334 | CV2762399 | single nucleotide variant | NM_015245.3(ANKS1A):c.343T>C (p.Tyr115His) | not specified [RCV004335505] | uncertain significance | 6 | 34970074 | 34970074 | Human | | name |
| 401920606 | CV2822977 | single nucleotide variant | NM_015245.3(ANKS1A):c.3267G>A (p.Pro1089=) | not provided [RCV003431820]|not specified [RCV005363114] | likely benign | 6 | 35085900 | 35085900 | Human | | name |
| 405260874 | CV3185955 | single nucleotide variant | NM_015245.3(ANKS1A):c.3225C>T (p.Gly1075=) | not provided [RCV003885031] | likely benign | 6 | 35085858 | 35085858 | Human | | name |
| 405684085 | CV3282368 | single nucleotide variant | NM_015245.3(ANKS1A):c.600G>A (p.Met200Ile) | not specified [RCV004422347] | uncertain significance | 6 | 34981854 | 34981854 | Human | | name |
| 405684091 | CV3282369 | single nucleotide variant | NM_015245.3(ANKS1A):c.739A>G (p.Met247Val) | not specified [RCV004422348] | uncertain significance | 6 | 34982758 | 34982758 | Human | | name |
| 407505264 | CV3447687 | single nucleotide variant | NM_015245.3(ANKS1A):c.437A>G (p.Asn146Ser) | not specified [RCV004646061] | uncertain significance | 6 | 34981691 | 34981691 | Human | | name |
| 407505298 | CV3447718 | single nucleotide variant | NM_015245.3(ANKS1A):c.347C>G (p.Pro116Arg) | not specified [RCV004646071] | uncertain significance | 6 | 34970078 | 34970078 | Human | | name |
| 597651434 | CV3561341 | single nucleotide variant | NM_015245.3(ANKS1A):c.891A>C (p.Gln297His) | not specified [RCV004833664] | uncertain significance | 6 | 34983195 | 34983195 | Human | | name |
| 597639423 | CV3561380 | single nucleotide variant | NM_015245.3(ANKS1A):c.857C>T (p.Thr286Ile) | not specified [RCV004825112] | uncertain significance | 6 | 34983161 | 34983161 | Human | | name |
| 597651570 | CV3561451 | single nucleotide variant | NM_015245.3(ANKS1A):c.302G>A (p.Arg101Lys) | not specified [RCV004833726] | uncertain significance | 6 | 34970033 | 34970033 | Human | | name |
| 597639822 | CV3561472 | single nucleotide variant | NM_015245.3(ANKS1A):c.865G>A (p.Glu289Lys) | not specified [RCV004825136] | uncertain significance | 6 | 34983169 | 34983169 | Human | | name |
| 598168499 | CV3982531 | single nucleotide variant | NM_015245.3(ANKS1A):c.388C>T (p.Arg130Trp) | not specified [RCV005369715] | uncertain significance | 6 | 34970119 | 34970119 | Human | | name |
| 598201697 | CV3982550 | single nucleotide variant | NM_015245.3(ANKS1A):c.959C>A (p.Pro320Gln) | not specified [RCV005376087] | uncertain significance | 6 | 34983372 | 34983372 | Human | | name |
| 15110554 | CV722009 | single nucleotide variant | NM_015245.3(ANKS1A):c.3285C>T (p.Val1095=) | not provided [RCV000894090] | benign | 6 | 35085918 | 35085918 | Human | | name |
| 8632027 | CV87233 | single nucleotide variant | NM_015245.2(ANKS1A):c.688G>A (p.Val230Met) | Malignant melanoma [RCV000067324] | not provided | 6 | 34981942 | 34981942 | Human | | name |
| 156027673 | CV2195538 | single nucleotide variant | NM_015245.3(ANKS1A):c.1433G>A (p.Arg478Gln) | not specified [RCV004082753] | uncertain significance | 6 | 35017482 | 35017482 | Human | | name |
| 156263181 | CV2201144 | single nucleotide variant | NM_015245.3(ANKS1A):c.1982C>T (p.Ser661Leu) | not specified [RCV004077302] | uncertain significance | 6 | 35018031 | 35018031 | Human | | name |
| 156373725 | CV2201356 | single nucleotide variant | NM_015245.3(ANKS1A):c.2062C>T (p.Arg688Trp) | not specified [RCV004077481] | uncertain significance | 6 | 35054150 | 35054150 | Human | | name |
| 156381918 | CV2212471 | single nucleotide variant | NM_015245.3(ANKS1A):c.2266G>T (p.Ala756Ser) | not specified [RCV004091365] | uncertain significance | 6 | 35078639 | 35078639 | Human | | name |
| 156249476 | CV2215559 | single nucleotide variant | NM_015245.3(ANKS1A):c.1567G>A (p.Ala523Thr) | not specified [RCV004089330] | likely benign | 6 | 35017616 | 35017616 | Human | | name |
| 156380019 | CV2218024 | single nucleotide variant | NM_015245.3(ANKS1A):c.1567G>C (p.Ala523Pro) | not specified [RCV004086466] | likely benign | 6 | 35017616 | 35017616 | Human | | name |
| 156028155 | CV2238203 | single nucleotide variant | NM_015245.3(ANKS1A):c.2216G>A (p.Arg739Gln) | not specified [RCV004113295] | uncertain significance | 6 | 35078589 | 35078589 | Human | | name |
| 156297370 | CV2240849 | single nucleotide variant | NM_015245.3(ANKS1A):c.2495G>A (p.Arg832Lys) | not specified [RCV004102138] | uncertain significance | 6 | 35079879 | 35079879 | Human | | name |
| 156081799 | CV2244351 | single nucleotide variant | NM_015245.3(ANKS1A):c.1432C>T (p.Arg478Trp) | not specified [RCV004100335] | uncertain significance | 6 | 35017481 | 35017481 | Human | | name |
| 155919764 | CV2254924 | single nucleotide variant | NM_015245.3(ANKS1A):c.2189C>G (p.Ser730Cys) | not specified [RCV004117163] | uncertain significance | 6 | 35078562 | 35078562 | Human | | name |
| 156339271 | CV2271392 | single nucleotide variant | NM_015245.3(ANKS1A):c.1948A>T (p.Asn650Tyr) | not specified [RCV004136502] | uncertain significance | 6 | 35017997 | 35017997 | Human | | name |
| 156251776 | CV2273434 | single nucleotide variant | NM_015245.3(ANKS1A):c.2980G>A (p.Asp994Asn) | not specified [RCV004132191] | uncertain significance | 6 | 35083489 | 35083489 | Human | | name |
| 156068086 | CV2280608 | single nucleotide variant | NM_015245.3(ANKS1A):c.2890G>A (p.Ala964Thr) | not specified [RCV004143085] | uncertain significance | 6 | 35083209 | 35083209 | Human | | name |
| 156257539 | CV2322073 | single nucleotide variant | NM_015245.3(ANKS1A):c.2170G>A (p.Asp724Asn) | not specified [RCV004173816] | uncertain significance | 6 | 35060239 | 35060239 | Human | | name |
| 156255451 | CV2325750 | single nucleotide variant | NM_015245.3(ANKS1A):c.2123T>C (p.Ile708Thr) | not specified [RCV004173643] | uncertain significance | 6 | 35060192 | 35060192 | Human | | name |
| 155919055 | CV2333124 | single nucleotide variant | NM_015245.3(ANKS1A):c.2773G>T (p.Val925Leu) | not specified [RCV004194417] | uncertain significance | 6 | 35082754 | 35082754 | Human | | name |
| 156197475 | CV2334279 | single nucleotide variant | NM_015245.3(ANKS1A):c.1695A>C (p.Arg565Ser) | not specified [RCV004188262] | uncertain significance | 6 | 35017744 | 35017744 | Human | | name |
| 156230628 | CV2348695 | single nucleotide variant | NM_015245.3(ANKS1A):c.1814G>A (p.Ser605Asn) | not specified [RCV004201108] | uncertain significance | 6 | 35017863 | 35017863 | Human | | name |
| 155925913 | CV2365665 | single nucleotide variant | NM_015245.3(ANKS1A):c.1579C>T (p.His527Tyr) | not specified [RCV004214219] | uncertain significance | 6 | 35017628 | 35017628 | Human | | name |
| 155906561 | CV2379063 | single nucleotide variant | NM_015245.3(ANKS1A):c.1219C>T (p.Pro407Ser) | not specified [RCV004233820] | uncertain significance | 6 | 34989233 | 34989233 | Human | | name |
| 156046589 | CV2382295 | single nucleotide variant | NM_015245.3(ANKS1A):c.2063G>A (p.Arg688Gln) | not specified [RCV004230645] | likely benign | 6 | 35054151 | 35054151 | Human | | name |
| 155902839 | CV2386349 | single nucleotide variant | NM_015245.3(ANKS1A):c.1463C>T (p.Ala488Val) | not specified [RCV004228684] | uncertain significance | 6 | 35017512 | 35017512 | Human | | name |
| 329354502 | CV2448304 | single nucleotide variant | NM_015245.3(ANKS1A):c.2741G>A (p.Arg914Gln) | not specified [RCV004256594] | uncertain significance | 6 | 35082722 | 35082722 | Human | | name |
| 329391772 | CV2453116 | single nucleotide variant | NM_015245.3(ANKS1A):c.1798C>T (p.Arg600Trp) | not specified [RCV004279507] | uncertain significance | 6 | 35017847 | 35017847 | Human | | name |
| 329395586 | CV2454374 | single nucleotide variant | NM_015245.3(ANKS1A):c.1135G>A (p.Gly379Arg) | not specified [RCV004267893] | uncertain significance | 6 | 34985204 | 34985204 | Human | | name |
| 329363870 | CV2460244 | single nucleotide variant | NM_015245.3(ANKS1A):c.1001A>G (p.Gln334Arg) | not specified [RCV004266802] | uncertain significance | 6 | 34983414 | 34983414 | Human | | name |
| 401720902 | CV2702182 | single nucleotide variant | NM_015245.3(ANKS1A):c.2758G>A (p.Ala920Thr) | not specified [RCV004314532] | uncertain significance | 6 | 35082739 | 35082739 | Human | | name |
| 401777263 | CV2707837 | single nucleotide variant | NM_015245.3(ANKS1A):c.2215C>T (p.Arg739Trp) | not specified [RCV004309120] | uncertain significance | 6 | 35078588 | 35078588 | Human | | name |
| 401757626 | CV2707883 | single nucleotide variant | NM_015245.3(ANKS1A):c.2097G>C (p.Gln699His) | not specified [RCV004309159] | uncertain significance | 6 | 35060166 | 35060166 | Human | | name |
| 401763418 | CV2720314 | single nucleotide variant | NM_015245.3(ANKS1A):c.2005G>A (p.Asp669Asn) | not specified [RCV004325638] | uncertain significance | 6 | 35018054 | 35018054 | Human | | name |
| 401780675 | CV2727506 | single nucleotide variant | NM_015245.3(ANKS1A):c.1531G>A (p.Glu511Lys) | not specified [RCV004329703] | uncertain significance | 6 | 35017580 | 35017580 | Human | | name |
| 401900047 | CV2780253 | single nucleotide variant | NM_015245.3(ANKS1A):c.1379C>G (p.Thr460Arg) | not specified [RCV004355886] | uncertain significance | 6 | 34994378 | 34994378 | Human | | name |
| 405684347 | CV3282348 | single nucleotide variant | NM_015245.3(ANKS1A):c.1514G>A (p.Gly505Asp) | not specified [RCV004422327] | uncertain significance | 6 | 35017563 | 35017563 | Human | | name |
| 405684216 | CV3282349 | single nucleotide variant | NM_015245.3(ANKS1A):c.1588G>A (p.Gly530Arg) | not specified [RCV004422328] | uncertain significance | 6 | 35017637 | 35017637 | Human | | name |
| 405684095 | CV3282350 | single nucleotide variant | NM_015245.3(ANKS1A):c.1613A>C (p.His538Pro) | not specified [RCV004422329] | uncertain significance | 6 | 35017662 | 35017662 | Human | | name |
| 405684002 | CV3282351 | single nucleotide variant | NM_015245.3(ANKS1A):c.1661C>A (p.Ala554Asp) | not specified [RCV004422330] | uncertain significance | 6 | 35017710 | 35017710 | Human | | name |
| 405684007 | CV3282352 | single nucleotide variant | NM_015245.3(ANKS1A):c.1769C>T (p.Pro590Leu) | not specified [RCV004422331] | uncertain significance | 6 | 35017818 | 35017818 | Human | | name |
| 405684011 | CV3282353 | single nucleotide variant | NM_015245.3(ANKS1A):c.1795G>A (p.Asp599Asn) | not specified [RCV004422332] | uncertain significance | 6 | 35017844 | 35017844 | Human | | name |
| 405684020 | CV3282355 | single nucleotide variant | NM_015245.3(ANKS1A):c.1828A>G (p.Thr610Ala) | not specified [RCV004422334] | uncertain significance | 6 | 35017877 | 35017877 | Human | | name |
| 405684027 | CV3282356 | single nucleotide variant | NM_015245.3(ANKS1A):c.2083C>T (p.Arg695Trp) | not specified [RCV004422335] | uncertain significance | 6 | 35060152 | 35060152 | Human | | name |
| 405684032 | CV3282357 | single nucleotide variant | NM_015245.3(ANKS1A):c.2116G>A (p.Glu706Lys) | not specified [RCV004422336] | uncertain significance | 6 | 35060185 | 35060185 | Human | | name |
| 405684039 | CV3282359 | single nucleotide variant | NM_015245.3(ANKS1A):c.2270G>A (p.Arg757His) | not specified [RCV004422338] | uncertain significance | 6 | 35078643 | 35078643 | Human | | name |
| 405684045 | CV3282360 | single nucleotide variant | NM_015245.3(ANKS1A):c.2438T>G (p.Val813Gly) | not specified [RCV004422339] | uncertain significance | 6 | 35079822 | 35079822 | Human | | name |
| 405684050 | CV3282361 | single nucleotide variant | NM_015245.3(ANKS1A):c.2509C>G (p.Pro837Ala) | not specified [RCV004422340] | uncertain significance | 6 | 35079893 | 35079893 | Human | | name |
| 405684056 | CV3282362 | single nucleotide variant | NM_015245.3(ANKS1A):c.2567C>T (p.Thr856Met) | not specified [RCV004422341] | uncertain significance | 6 | 35081016 | 35081016 | Human | | name |
| 405684063 | CV3282364 | single nucleotide variant | NM_015245.3(ANKS1A):c.2867G>A (p.Arg956Gln) | not specified [RCV004422343] | uncertain significance | 6 | 35083186 | 35083186 | Human | | name |
| 405684068 | CV3282365 | single nucleotide variant | NM_015245.3(ANKS1A):c.2946C>G (p.Ile982Met) | not specified [RCV004422344] | uncertain significance | 6 | 35083455 | 35083455 | Human | | name |
| 407505208 | CV3447658 | single nucleotide variant | NM_015245.3(ANKS1A):c.2696G>A (p.Arg899His) | not specified [RCV004646044] | uncertain significance | 6 | 35081145 | 35081145 | Human | | name |
| 407505215 | CV3447662 | single nucleotide variant | NM_015245.3(ANKS1A):c.2812G>A (p.Glu938Lys) | not specified [RCV004646047] | uncertain significance | 6 | 35082793 | 35082793 | Human | | name |
| 407505219 | CV3447667 | single nucleotide variant | NM_015245.3(ANKS1A):c.1387A>G (p.Thr463Ala) | not specified [RCV004646048] | uncertain significance | 6 | 34994386 | 34994386 | Human | | name |
| 407520276 | CV3447676 | single nucleotide variant | NM_015245.3(ANKS1A):c.1328A>G (p.His443Arg) | not specified [RCV004652135] | uncertain significance | 6 | 34994327 | 34994327 | Human | | name |
| 407520304 | CV3447698 | single nucleotide variant | NM_015245.3(ANKS1A):c.1073A>C (p.Glu358Ala) | not specified [RCV004652147] | uncertain significance | 6 | 34985142 | 34985142 | Human | | name |
| 407505283 | CV3447708 | single nucleotide variant | NM_015245.3(ANKS1A):c.2773G>C (p.Val925Leu) | not specified [RCV004646067] | uncertain significance | 6 | 35082754 | 35082754 | Human | | name |
| 597650838 | CV3561345 | single nucleotide variant | NM_015245.3(ANKS1A):c.1526T>C (p.Val509Ala) | not specified [RCV004833665] | uncertain significance | 6 | 35017575 | 35017575 | Human | | name |
| 597639369 | CV3561353 | single nucleotide variant | NM_015245.3(ANKS1A):c.2104G>A (p.Gly702Arg) | not specified [RCV004825102] | uncertain significance | 6 | 35060173 | 35060173 | Human | | name |
| 597651051 | CV3561390 | single nucleotide variant | NM_015245.3(ANKS1A):c.1291A>C (p.Thr431Pro) | not specified [RCV004833689] | uncertain significance | 6 | 34989305 | 34989305 | Human | | name |
| 597651163 | CV3561408 | single nucleotide variant | NM_015245.3(ANKS1A):c.1997C>T (p.Ser666Leu) | not specified [RCV004833703] | uncertain significance | 6 | 35018046 | 35018046 | Human | | name |
| 597639896 | CV3561428 | single nucleotide variant | NM_015245.3(ANKS1A):c.1192C>T (p.Pro398Ser) | not specified [RCV004825124] | uncertain significance | 6 | 34985261 | 34985261 | Human | | name |
| 597651469 | CV3561436 | single nucleotide variant | NM_015245.3(ANKS1A):c.1139G>A (p.Arg380Gln) | not specified [RCV004833714] | uncertain significance | 6 | 34985208 | 34985208 | Human | | name |
| 597651523 | CV3561443 | single nucleotide variant | NM_015245.3(ANKS1A):c.2704A>G (p.Ile902Val) | not specified [RCV004833720] | uncertain significance | 6 | 35081153 | 35081153 | Human | | name |
| 597639843 | CV3561461 | single nucleotide variant | NM_015245.3(ANKS1A):c.1343G>A (p.Arg448Gln) | not specified [RCV004825132] | likely benign | 6 | 34994342 | 34994342 | Human | | name |
| 597639807 | CV3561481 | single nucleotide variant | NM_015245.3(ANKS1A):c.2245C>T (p.Arg749Trp) | not specified [RCV004825139] | uncertain significance | 6 | 35078618 | 35078618 | Human | | name |
| 598201612 | CV3982495 | single nucleotide variant | NM_015245.3(ANKS1A):c.1477G>A (p.Gly493Arg) | not specified [RCV005376066] | uncertain significance | 6 | 35017526 | 35017526 | Human | | name |
| 598201616 | CV3982504 | single nucleotide variant | NM_015245.3(ANKS1A):c.2600C>T (p.Thr867Ile) | not specified [RCV005376067] | uncertain significance | 6 | 35081049 | 35081049 | Human | | name |
| 598201624 | CV3982514 | single nucleotide variant | NM_015245.3(ANKS1A):c.2606G>A (p.Arg869Gln) | not specified [RCV005376069] | uncertain significance | 6 | 35081055 | 35081055 | Human | | name |
| 598201643 | CV3982523 | single nucleotide variant | NM_015245.3(ANKS1A):c.1817G>A (p.Arg606Gln) | not specified [RCV005376074] | uncertain significance | 6 | 35017866 | 35017866 | Human | | name |
| 598201738 | CV3982562 | single nucleotide variant | NM_015245.3(ANKS1A):c.1612C>A (p.His538Asn) | not specified [RCV005376096] | uncertain significance | 6 | 35017661 | 35017661 | Human | | name |
| 598168598 | CV3982570 | single nucleotide variant | NM_015245.3(ANKS1A):c.1915G>A (p.Ala639Thr) | not specified [RCV005369732] | likely benign | 6 | 35017964 | 35017964 | Human | | name |
| 598168667 | CV3982598 | single nucleotide variant | NM_015245.3(ANKS1A):c.1313T>C (p.Met438Thr) | not specified [RCV005369745] | uncertain significance | 6 | 34994312 | 34994312 | Human | | name |
| 598168700 | CV3982608 | single nucleotide variant | NM_015245.3(ANKS1A):c.1958T>C (p.Ile653Thr) | not specified [RCV005369751] | uncertain significance | 6 | 35018007 | 35018007 | Human | | name |
| 15157722 | CV699558 | single nucleotide variant | NM_015245.3(ANKS1A):c.1417A>G (p.Thr473Ala) | not provided [RCV000946937] | benign | 6 | 34994416 | 34994416 | Human | | name |
| 15123025 | CV710467 | single nucleotide variant | NM_015245.3(ANKS1A):c.1732C>G (p.Arg578Gly) | not provided [RCV000963170] | benign | 6 | 35017781 | 35017781 | Human | | name |
| 156384965 | CV2231238 | single nucleotide variant | NM_015245.3(ANKS1A):c.3201G>C (p.Gln1067His) | not specified [RCV004094437] | uncertain significance | 6 | 35085834 | 35085834 | Human | | name |
| 156155252 | CV2266128 | single nucleotide variant | NM_015245.3(ANKS1A):c.3301G>A (p.Ala1101Thr) | not specified [RCV004128717] | uncertain significance | 6 | 35085934 | 35085934 | Human | | name |
| 156149215 | CV2307396 | single nucleotide variant | NM_015245.3(ANKS1A):c.3090G>T (p.Gln1030His) | not specified [RCV004166076] | uncertain significance | 6 | 35084216 | 35084216 | Human | | name |
| 156336189 | CV2333638 | single nucleotide variant | NM_015245.3(ANKS1A):c.3124G>A (p.Val1042Met) | not specified [RCV004192479] | uncertain significance | 6 | 35084250 | 35084250 | Human | | name |
| 155924972 | CV2348259 | single nucleotide variant | NM_015245.3(ANKS1A):c.3226G>A (p.Ala1076Thr) | not specified [RCV004191297] | uncertain significance | 6 | 35085859 | 35085859 | Human | | name |
| 156269071 | CV2372155 | single nucleotide variant | NM_015245.3(ANKS1A):c.3020G>A (p.Arg1007Gln) | not specified [RCV004223677] | uncertain significance | 6 | 35084146 | 35084146 | Human | | name |
| 155952759 | CV2393830 | single nucleotide variant | NM_015245.3(ANKS1A):c.3266C>G (p.Pro1089Arg) | not specified [RCV004233658] | uncertain significance | 6 | 35085899 | 35085899 | Human | | name |
| 405684081 | CV3282367 | single nucleotide variant | NM_015245.3(ANKS1A):c.3320T>C (p.Met1107Thr) | not specified [RCV004422346] | likely benign | 6 | 35086968 | 35086968 | Human | | name |
| 597651443 | CV3561362 | single nucleotide variant | NM_015245.3(ANKS1A):c.3047C>T (p.Pro1016Leu) | not specified [RCV004833671] | uncertain significance | 6 | 35084173 | 35084173 | Human | | name |
| 598168627 | CV3982581 | single nucleotide variant | NM_015245.3(ANKS1A):c.3112G>A (p.Val1038Met) | not specified [RCV005369737] | uncertain significance | 6 | 35084238 | 35084238 | Human | | name |