| 405272891 | CV3197554 | single nucleotide variant | NM_012183.3(FOXD3):c.432C>T (p.Tyr144=) | FOXD3-related disorder [RCV003901522] | likely benign | 1 | 63323490 | 63323490 | Human | | name , trait , alternate_id |
| 405279494 | CV3206933 | single nucleotide variant | NM_012183.3(FOXD3):c.804G>C (p.Ala268=) | FOXD3-related disorder [RCV003919491] | likely benign | 1 | 63323862 | 63323862 | Human | | name , trait , alternate_id |
| 405279006 | CV3217310 | single nucleotide variant | NM_012183.3(FOXD3):c.720C>T (p.His240=) | FOXD3-related disorder [RCV003976754] | likely benign | 1 | 63323778 | 63323778 | Human | | name , trait , alternate_id |
| 15194725 | CV696830 | single nucleotide variant | NM_012183.3(FOXD3):c.639C>T (p.Asn213=) | not provided [RCV000955723] | benign|likely benign | 1 | 63323697 | 63323697 | Human | | name |
| 401891974 | CV2775856 | single nucleotide variant | NM_012183.3(FOXD3):c.257C>T (p.Ala86Val) | not specified [RCV004344889] | uncertain significance | 1 | 63323315 | 63323315 | Human | | name |
| 401927818 | CV2808947 | single nucleotide variant | NM_012183.3(FOXD3):c.1080C>G (p.Ala360=) | not provided [RCV003406544] | likely benign | 1 | 63324138 | 63324138 | Human | | name |
| 405258804 | CV3194171 | single nucleotide variant | NM_012183.3(FOXD3):c.266G>A (p.Gly89Glu) | FOXD3-related disorder [RCV003893752] | uncertain significance | 1 | 63323324 | 63323324 | Human | | name , trait , alternate_id |
| 405275725 | CV3199452 | single nucleotide variant | NM_012183.3(FOXD3):c.286G>T (p.Val96Leu) | FOXD3-related disorder [RCV003916856] | benign | 1 | 63323344 | 63323344 | Human | | name , trait , alternate_id |
| 405267332 | CV3205378 | single nucleotide variant | NM_012183.3(FOXD3):c.1074G>T (p.Ala358=) | FOXD3-related disorder [RCV003947343] | likely benign | 1 | 63324132 | 63324132 | Human | | name , trait , alternate_id |
| 405295348 | CV3209569 | single nucleotide variant | NM_012183.3(FOXD3):c.1308G>A (p.Ser436=) | FOXD3-related disorder [RCV003937293] | likely benign | 1 | 63324366 | 63324366 | Human | | name , trait , alternate_id |
| 405747129 | CV3253910 | single nucleotide variant | NM_012183.3(FOXD3):c.139C>A (p.Pro47Thr) | not specified [RCV004392174] | uncertain significance | 1 | 63323197 | 63323197 | Human | | name |
| 405747144 | CV3253912 | single nucleotide variant | NM_012183.3(FOXD3):c.149C>T (p.Pro50Leu) | not specified [RCV004392176] | uncertain significance | 1 | 63323207 | 63323207 | Human | | name |
| 405747150 | CV3253913 | single nucleotide variant | NM_012183.3(FOXD3):c.245C>T (p.Pro82Leu) | not specified [RCV004392177] | uncertain significance | 1 | 63323303 | 63323303 | Human | | name |
| 407510521 | CV3432626 | single nucleotide variant | NM_012183.3(FOXD3):c.191C>A (p.Ala64Glu) | not specified [RCV004626146] | uncertain significance | 1 | 63323249 | 63323249 | Human | | name |
| 598158318 | CV3973734 | single nucleotide variant | NM_012183.3(FOXD3):c.265G>A (p.Gly89Arg) | not specified [RCV005327991] | uncertain significance | 1 | 63323323 | 63323323 | Human | | name |
| 598216306 | CV3973737 | single nucleotide variant | NM_012183.3(FOXD3):c.184C>A (p.Pro62Thr) | not specified [RCV005339844] | uncertain significance | 1 | 63323242 | 63323242 | Human | | name |
| 598216314 | CV3973738 | single nucleotide variant | NM_012183.3(FOXD3):c.128G>A (p.Gly43Asp) | not specified [RCV005339845] | uncertain significance | 1 | 63323186 | 63323186 | Human | | name |
| 598216352 | CV3973743 | single nucleotide variant | NM_012183.3(FOXD3):c.109G>A (p.Glu37Lys) | not specified [RCV005339850] | uncertain significance | 1 | 63323167 | 63323167 | Human | | name |
| 155921058 | CV2210960 | single nucleotide variant | NM_012183.3(FOXD3):c.395C>A (p.Pro132Gln) | not specified [RCV004086033] | uncertain significance | 1 | 63323453 | 63323453 | Human | | name |
| 156247217 | CV2215312 | single nucleotide variant | NM_012183.3(FOXD3):c.803C>G (p.Ala268Gly) | not specified [RCV004087343] | uncertain significance | 1 | 63323861 | 63323861 | Human | | name |
| 155968181 | CV2261963 | single nucleotide variant | NM_012183.3(FOXD3):c.404C>G (p.Pro135Arg) | not specified [RCV004126457] | uncertain significance | 1 | 63323462 | 63323462 | Human | | name |
| 156096371 | CV2375373 | single nucleotide variant | NM_012183.3(FOXD3):c.797G>C (p.Gly266Ala) | not specified [RCV004232773] | uncertain significance | 1 | 63323855 | 63323855 | Human | | name |
| 156054436 | CV2388608 | single nucleotide variant | NM_012183.3(FOXD3):c.791C>G (p.Ala264Gly) | not specified [RCV004239492] | uncertain significance | 1 | 63323849 | 63323849 | Human | | name |
| 155906123 | CV2393880 | single nucleotide variant | NM_012183.3(FOXD3):c.361G>A (p.Gly121Ser) | not specified [RCV004233703] | uncertain significance | 1 | 63323419 | 63323419 | Human | | name |
| 329360662 | CV2452375 | single nucleotide variant | NM_012183.3(FOXD3):c.970G>A (p.Gly324Ser) | not specified [RCV004272696] | uncertain significance | 1 | 63324028 | 63324028 | Human | | name |
| 329359831 | CV2462323 | single nucleotide variant | NM_012183.3(FOXD3):c.826G>C (p.Gly276Arg) | not specified [RCV004266310] | uncertain significance | 1 | 63323884 | 63323884 | Human | | name |
| 401719884 | CV2675712 | single nucleotide variant | NM_012183.3(FOXD3):c.880G>T (p.Ala294Ser) | not specified [RCV004287961] | uncertain significance | 1 | 63323938 | 63323938 | Human | | name |
| 401731857 | CV2690174 | single nucleotide variant | NM_012183.3(FOXD3):c.358C>A (p.Pro120Thr) | not specified [RCV004302187] | uncertain significance | 1 | 63323416 | 63323416 | Human | | name |
| 401749189 | CV2709938 | single nucleotide variant | NM_012183.3(FOXD3):c.982C>T (p.Arg328Cys) | not specified [RCV004315011] | uncertain significance | 1 | 63324040 | 63324040 | Human | | name |
| 401782131 | CV2719191 | single nucleotide variant | NM_012183.3(FOXD3):c.682G>C (p.Gly228Arg) | not specified [RCV004324851] | uncertain significance | 1 | 63323740 | 63323740 | Human | | name |
| 401880409 | CV2763030 | single nucleotide variant | NM_012183.3(FOXD3):c.835C>A (p.Pro279Thr) | not specified [RCV004336091] | uncertain significance | 1 | 63323893 | 63323893 | Human | | name |
| 405747157 | CV3253914 | single nucleotide variant | NM_012183.3(FOXD3):c.749C>T (p.Ala250Val) | not specified [RCV004392178] | uncertain significance | 1 | 63323807 | 63323807 | Human | | name |
| 405747163 | CV3253915 | single nucleotide variant | NM_012183.3(FOXD3):c.842C>T (p.Ala281Val) | not specified [RCV004392179] | uncertain significance | 1 | 63323900 | 63323900 | Human | | name |
| 405747169 | CV3253916 | single nucleotide variant | NM_012183.3(FOXD3):c.859T>A (p.Ser287Thr) | not specified [RCV004392180] | uncertain significance | 1 | 63323917 | 63323917 | Human | | name |
| 405747177 | CV3253917 | single nucleotide variant | NM_012183.3(FOXD3):c.968C>T (p.Ser323Leu) | not specified [RCV004392181] | uncertain significance | 1 | 63324026 | 63324026 | Human | | name |
| 407510512 | CV3432623 | single nucleotide variant | NM_012183.3(FOXD3):c.854C>T (p.Ala285Val) | not specified [RCV004626143] | uncertain significance | 1 | 63323912 | 63323912 | Human | | name |
| 407510515 | CV3432624 | single nucleotide variant | NM_012183.3(FOXD3):c.803C>T (p.Ala268Val) | not specified [RCV004626144] | uncertain significance | 1 | 63323861 | 63323861 | Human | | name |
| 407510518 | CV3432625 | single nucleotide variant | NM_012183.3(FOXD3):c.535A>G (p.Arg179Gly) | not specified [RCV004626145] | uncertain significance | 1 | 63323593 | 63323593 | Human | | name |
| 597725798 | CV3673054 | single nucleotide variant | NM_012183.3(FOXD3):c.848C>G (p.Ala283Gly) | not specified [RCV004919251] | uncertain significance | 1 | 63323906 | 63323906 | Human | | name |
| 597725814 | CV3673056 | single nucleotide variant | NM_012183.3(FOXD3):c.710T>C (p.Phe237Ser) | not specified [RCV004919253] | uncertain significance | 1 | 63323768 | 63323768 | Human | | name |
| 597725820 | CV3673057 | single nucleotide variant | NM_012183.3(FOXD3):c.979G>A (p.Gly327Ser) | not specified [RCV004919254] | uncertain significance | 1 | 63324037 | 63324037 | Human | | name |
| 598216291 | CV3973735 | single nucleotide variant | NM_012183.3(FOXD3):c.806G>C (p.Gly269Ala) | not specified [RCV005339842] | uncertain significance | 1 | 63323864 | 63323864 | Human | | name |
| 598216299 | CV3973736 | single nucleotide variant | NM_012183.3(FOXD3):c.992C>T (p.Ala331Val) | not specified [RCV005339843] | uncertain significance | 1 | 63324050 | 63324050 | Human | | name |
| 598216328 | CV3973740 | single nucleotide variant | NM_012183.3(FOXD3):c.352G>A (p.Gly118Ser) | not specified [RCV005339847] | uncertain significance | 1 | 63323410 | 63323410 | Human | | name |
| 598216336 | CV3973741 | single nucleotide variant | NM_012183.3(FOXD3):c.544T>A (p.Phe182Ile) | not specified [RCV005339848] | uncertain significance | 1 | 63323602 | 63323602 | Human | | name |
| 598216344 | CV3973742 | single nucleotide variant | NM_012183.3(FOXD3):c.505G>A (p.Glu169Lys) | not specified [RCV005339849] | uncertain significance | 1 | 63323563 | 63323563 | Human | | name |
| 598216370 | CV3973745 | single nucleotide variant | NM_012183.3(FOXD3):c.715C>A (p.Arg239Ser) | not specified [RCV005339852] | uncertain significance | 1 | 63323773 | 63323773 | Human | | name |
| 126910631 | CV1037046 | single nucleotide variant | NM_012183.3(FOXD3):c.1024C>A (p.Gln342Lys) | not provided [RCV001354632] | uncertain significance | 1 | 63324082 | 63324082 | Human | | name |
| 156397737 | CV2197500 | single nucleotide variant | NM_012183.3(FOXD3):c.1177G>T (p.Gly393Cys) | not specified [RCV004081228] | uncertain significance | 1 | 63324235 | 63324235 | Human | | name |
| 156162396 | CV2246512 | single nucleotide variant | NM_012183.3(FOXD3):c.1169C>G (p.Ala390Gly) | not specified [RCV004110268] | uncertain significance | 1 | 63324227 | 63324227 | Human | | name |
| 156291787 | CV2246513 | single nucleotide variant | NM_012183.3(FOXD3):c.1174G>A (p.Gly392Arg) | not specified [RCV004110269] | uncertain significance | 1 | 63324232 | 63324232 | Human | | name |
| 156162407 | CV2246514 | single nucleotide variant | NM_012183.3(FOXD3):c.1177G>A (p.Gly393Ser) | not specified [RCV004110270] | uncertain significance | 1 | 63324235 | 63324235 | Human | | name |
| 156168822 | CV2373828 | single nucleotide variant | NM_012183.3(FOXD3):c.1396G>T (p.Ala466Ser) | not specified [RCV004224764] | uncertain significance | 1 | 63324454 | 63324454 | Human | | name |
| 156348024 | CV2383029 | single nucleotide variant | NM_012183.3(FOXD3):c.1202C>T (p.Ala401Val) | not specified [RCV004217612] | uncertain significance | 1 | 63324260 | 63324260 | Human | | name |
| 329388160 | CV2437143 | single nucleotide variant | NM_012183.3(FOXD3):c.1372C>A (p.Gln458Lys) | not specified [RCV004262949] | uncertain significance | 1 | 63324430 | 63324430 | Human | | name |
| 401744002 | CV2688076 | single nucleotide variant | NM_012183.3(FOXD3):c.1111G>A (p.Glu371Lys) | not specified [RCV004305139] | uncertain significance | 1 | 63324169 | 63324169 | Human | | name |
| 401731179 | CV2693654 | single nucleotide variant | NM_012183.3(FOXD3):c.1226G>A (p.Gly409Asp) | not specified [RCV004297989] | uncertain significance | 1 | 63324284 | 63324284 | Human | | name |
| 401750369 | CV2715611 | single nucleotide variant | NM_012183.3(FOXD3):c.1037A>G (p.Asn346Ser) | not specified [RCV004326999] | uncertain significance | 1 | 63324095 | 63324095 | Human | | name |
| 405747099 | CV3253905 | single nucleotide variant | NM_012183.3(FOXD3):c.1055C>T (p.Ala352Val) | not specified [RCV004392169] | uncertain significance | 1 | 63324113 | 63324113 | Human | | name |
| 405747106 | CV3253906 | single nucleotide variant | NM_012183.3(FOXD3):c.1163C>T (p.Pro388Leu) | not specified [RCV004392170] | uncertain significance | 1 | 63324221 | 63324221 | Human | | name |
| 405747117 | CV3253908 | single nucleotide variant | NM_012183.3(FOXD3):c.1228G>A (p.Gly410Ser) | not specified [RCV004392172] | uncertain significance | 1 | 63324286 | 63324286 | Human | | name |
| 405747123 | CV3253909 | single nucleotide variant | NM_012183.3(FOXD3):c.1241A>G (p.Gln414Arg) | not specified [RCV004392173] | uncertain significance | 1 | 63324299 | 63324299 | Human | | name |
| 597725789 | CV3673053 | single nucleotide variant | NM_012183.3(FOXD3):c.1001G>A (p.Gly334Asp) | not specified [RCV004919250] | uncertain significance | 1 | 63324059 | 63324059 | Human | | name |
| 597725806 | CV3673055 | single nucleotide variant | NM_012183.3(FOXD3):c.1192G>A (p.Ala398Thr) | not specified [RCV004919252] | uncertain significance | 1 | 63324250 | 63324250 | Human | | name |
| 597725828 | CV3673058 | single nucleotide variant | NM_012183.3(FOXD3):c.1031A>G (p.Gln344Arg) | not specified [RCV004919255] | uncertain significance | 1 | 63324089 | 63324089 | Human | | name |
| 597725835 | CV3673059 | single nucleotide variant | NM_012183.3(FOXD3):c.1427C>T (p.Pro476Leu) | not specified [RCV004919256] | uncertain significance | 1 | 63324485 | 63324485 | Human | | name |
| 598216322 | CV3973739 | single nucleotide variant | NM_012183.3(FOXD3):c.1178G>A (p.Gly393Asp) | not specified [RCV005339846] | uncertain significance | 1 | 63324236 | 63324236 | Human | | name |
