Incidental Mutation 'R6270:Nrap'
ID 507309
Institutional Source Beutler Lab
Gene Symbol Nrap
Ensembl Gene ENSMUSG00000049134
Gene Name nebulin-related anchoring protein
Synonyms
MMRRC Submission 044441-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6270 (G1)
Quality Score 216.009
Status Validated
Chromosome 19
Chromosomal Location 56308473-56378466 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 56308630 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 1485 (M1485I)
Ref Sequence ENSEMBL: ENSMUSP00000128196 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040711] [ENSMUST00000073536] [ENSMUST00000078284] [ENSMUST00000095947] [ENSMUST00000095948] [ENSMUST00000163502] [ENSMUST00000166203] [ENSMUST00000167239] [ENSMUST00000165522] [ENSMUST00000166049] [ENSMUST00000171341]
AlphaFold Q80XB4
Predicted Effect probably benign
Transcript: ENSMUST00000040711
AA Change: M1693I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000048364
Gene: ENSMUSG00000049134
AA Change: M1693I

DomainStartEndE-ValueType
LIM 5 57 5.39e-11 SMART
NEBU 64 94 2.17e1 SMART
NEBU 168 197 1.94e-4 SMART
NEBU 202 232 1.39e-5 SMART
NEBU 239 268 2.23e-4 SMART
NEBU 308 337 2.83e-6 SMART
NEBU 346 376 3.82e-3 SMART
NEBU 382 412 1.18e-3 SMART
NEBU 450 480 8.97e-9 SMART
NEBU 485 515 1.73e-10 SMART
NEBU 521 551 8.12e-7 SMART
NEBU 555 585 1.73e-1 SMART
NEBU 590 620 2.33e-7 SMART
NEBU 621 651 1.49e-5 SMART
NEBU 655 686 5.12e-4 SMART
NEBU 689 719 8.12e-7 SMART
NEBU 724 754 2.64e-6 SMART
NEBU 760 790 3.48e-6 SMART
NEBU 798 828 2.35e-3 SMART
NEBU 833 863 6.11e-2 SMART
NEBU 864 894 1.69e-4 SMART
NEBU 899 929 3.88e-4 SMART
NEBU 932 962 4e-6 SMART
NEBU 967 997 4.22e-5 SMART
NEBU 1003 1033 2.64e-6 SMART
NEBU 1041 1071 3.68e-5 SMART
NEBU 1076 1106 4.16e-4 SMART
NEBU 1107 1137 1.1e-3 SMART
NEBU 1142 1172 1.68e1 SMART
NEBU 1175 1205 4.59e-6 SMART
NEBU 1210 1240 4.06e-7 SMART
NEBU 1246 1276 1.99e-1 SMART
NEBU 1284 1314 1.85e-1 SMART
NEBU 1319 1349 1.39e-5 SMART
NEBU 1350 1380 4.03e-2 SMART
NEBU 1385 1415 1.76e-2 SMART
NEBU 1418 1448 2.09e0 SMART
NEBU 1453 1483 6.4e-5 SMART
NEBU 1489 1519 8.63e-1 SMART
NEBU 1527 1557 1.33e-2 SMART
NEBU 1562 1592 1.84e-5 SMART
NEBU 1593 1623 7.24e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000073536
AA Change: M1728I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000073228
Gene: ENSMUSG00000049134
AA Change: M1728I

DomainStartEndE-ValueType
LIM 5 57 5.39e-11 SMART
NEBU 64 94 2.17e1 SMART
NEBU 168 197 1.94e-4 SMART
NEBU 202 232 1.39e-5 SMART
NEBU 239 268 2.23e-4 SMART
NEBU 308 337 2.83e-6 SMART
NEBU 346 376 7.24e-4 SMART
NEBU 381 411 3.46e-1 SMART
NEBU 417 447 1.18e-3 SMART
NEBU 485 515 8.97e-9 SMART
NEBU 520 550 1.73e-10 SMART
NEBU 556 586 8.12e-7 SMART
NEBU 590 620 1.73e-1 SMART
NEBU 625 655 2.33e-7 SMART
NEBU 656 686 1.49e-5 SMART
NEBU 690 721 5.12e-4 SMART
NEBU 724 754 8.12e-7 SMART
NEBU 759 789 2.64e-6 SMART
NEBU 795 825 3.48e-6 SMART
NEBU 833 863 2.35e-3 SMART
NEBU 868 898 6.11e-2 SMART
NEBU 899 929 1.69e-4 SMART
NEBU 934 964 3.88e-4 SMART
NEBU 967 997 4e-6 SMART
NEBU 1002 1032 4.22e-5 SMART
NEBU 1038 1068 2.64e-6 SMART
NEBU 1076 1106 3.68e-5 SMART
NEBU 1111 1141 4.16e-4 SMART
NEBU 1142 1172 1.1e-3 SMART
NEBU 1177 1207 1.68e1 SMART
NEBU 1210 1240 4.59e-6 SMART
NEBU 1245 1275 4.06e-7 SMART
NEBU 1281 1311 1.99e-1 SMART
NEBU 1319 1349 1.85e-1 SMART
NEBU 1354 1384 1.39e-5 SMART
NEBU 1385 1415 4.03e-2 SMART
NEBU 1420 1450 1.76e-2 SMART
NEBU 1453 1483 2.09e0 SMART
NEBU 1488 1518 6.4e-5 SMART
NEBU 1524 1554 8.63e-1 SMART
NEBU 1562 1592 1.33e-2 SMART
NEBU 1597 1627 1.84e-5 SMART
NEBU 1628 1658 7.24e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000078284
SMART Domains Protein: ENSMUSP00000077402
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 28 42 N/A INTRINSIC
EGF 70 103 4.66e-6 SMART
EGF 108 142 3.97e0 SMART
EGF 147 182 2.26e-4 SMART
KR 186 272 2.72e-39 SMART
Tryp_SPc 307 544 1.47e-90 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000095947
AA Change: M1611I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000093640
Gene: ENSMUSG00000049134
AA Change: M1611I

DomainStartEndE-ValueType
NEBU 86 115 1.2e-6 SMART
NEBU 120 150 9.1e-8 SMART
NEBU 157 186 1.4e-6 SMART
NEBU 226 255 1.8e-8 SMART
NEBU 264 294 2.5e-5 SMART
NEBU 300 330 7.8e-6 SMART
NEBU 368 398 6e-11 SMART
NEBU 403 433 1.1e-12 SMART
NEBU 439 469 5.2e-9 SMART
NEBU 473 503 1.1e-3 SMART
NEBU 508 538 1.5e-9 SMART
NEBU 539 569 1e-7 SMART
NEBU 573 604 3.3e-6 SMART
NEBU 607 637 5.4e-9 SMART
NEBU 642 672 1.7e-8 SMART
NEBU 678 708 2.3e-8 SMART
NEBU 716 746 1.5e-5 SMART
NEBU 751 781 4.1e-4 SMART
NEBU 782 812 1.1e-6 SMART
NEBU 817 847 2.6e-6 SMART
NEBU 850 880 2.6e-8 SMART
NEBU 885 915 2.7e-7 SMART
NEBU 921 951 1.7e-8 SMART
NEBU 959 989 2.4e-7 SMART
NEBU 994 1024 2.7e-6 SMART
NEBU 1025 1055 7.2e-6 SMART
NEBU 1060 1090 1.1e-1 SMART
NEBU 1093 1123 3e-8 SMART
NEBU 1128 1158 2.6e-9 SMART
NEBU 1164 1194 1.3e-3 SMART
NEBU 1202 1232 1.2e-3 SMART
NEBU 1237 1267 8.8e-8 SMART
NEBU 1268 1298 2.7e-4 SMART
NEBU 1303 1333 1.2e-4 SMART
NEBU 1336 1366 1.4e-2 SMART
NEBU 1371 1401 4.3e-7 SMART
NEBU 1407 1437 5.6e-3 SMART
NEBU 1445 1475 8.8e-5 SMART
NEBU 1480 1510 1.2e-7 SMART
NEBU 1511 1541 4.8e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000095948
SMART Domains Protein: ENSMUSP00000093641
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
EGF 33 66 4.66e-6 SMART
EGF 71 105 3.97e0 SMART
EGF 110 145 2.26e-4 SMART
KR 149 235 2.72e-39 SMART
Tryp_SPc 270 507 1.47e-90 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000163502
SMART Domains Protein: ENSMUSP00000128964
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
KR 1 41 5.87e-6 SMART
Tryp_SPc 76 220 5.6e-14 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000166203
AA Change: M1692I

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000132582
Gene: ENSMUSG00000049134
AA Change: M1692I

DomainStartEndE-ValueType
LIM 5 57 5.39e-11 SMART
NEBU 64 94 2.17e1 SMART
NEBU 168 197 1.94e-4 SMART
NEBU 202 232 1.39e-5 SMART
NEBU 239 268 2.23e-4 SMART
NEBU 308 337 2.83e-6 SMART
NEBU 346 376 7.24e-4 SMART
NEBU 381 411 3.46e-1 SMART
NEBU 417 447 1.18e-3 SMART
NEBU 485 515 8.97e-9 SMART
NEBU 520 550 1.06e-10 SMART
NEBU 554 584 1.73e-1 SMART
NEBU 589 619 2.33e-7 SMART
NEBU 620 650 1.49e-5 SMART
NEBU 654 685 5.12e-4 SMART
NEBU 688 718 8.12e-7 SMART
NEBU 723 753 2.64e-6 SMART
NEBU 759 789 3.48e-6 SMART
NEBU 797 827 2.35e-3 SMART
NEBU 832 862 6.11e-2 SMART
NEBU 863 893 1.69e-4 SMART
NEBU 898 928 3.88e-4 SMART
NEBU 931 961 4e-6 SMART
NEBU 966 996 4.22e-5 SMART
NEBU 1002 1032 2.64e-6 SMART
NEBU 1040 1070 3.68e-5 SMART
NEBU 1075 1105 4.16e-4 SMART
NEBU 1106 1136 1.1e-3 SMART
NEBU 1141 1171 1.68e1 SMART
NEBU 1174 1204 4.59e-6 SMART
NEBU 1209 1239 4.06e-7 SMART
NEBU 1245 1275 1.99e-1 SMART
NEBU 1283 1313 1.85e-1 SMART
NEBU 1318 1348 1.39e-5 SMART
NEBU 1349 1379 4.03e-2 SMART
NEBU 1384 1414 1.76e-2 SMART
NEBU 1417 1447 2.09e0 SMART
NEBU 1452 1482 6.4e-5 SMART
NEBU 1488 1518 8.63e-1 SMART
NEBU 1526 1556 1.33e-2 SMART
NEBU 1561 1591 1.84e-5 SMART
NEBU 1592 1622 7.24e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000167239
AA Change: M1485I

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000128196
Gene: ENSMUSG00000049134
AA Change: M1485I

DomainStartEndE-ValueType
LIM 5 57 5.39e-11 SMART
NEBU 64 94 2.17e1 SMART
NEBU 168 197 1.94e-4 SMART
NEBU 202 232 1.39e-5 SMART
NEBU 239 268 2.23e-4 SMART
NEBU 308 337 2.83e-6 SMART
NEBU 346 376 3.82e-3 SMART
NEBU 382 412 1.18e-3 SMART
NEBU 450 480 8.97e-9 SMART
NEBU 485 515 1.73e-10 SMART
NEBU 521 551 8.12e-7 SMART
NEBU 555 585 1.73e-1 SMART
NEBU 590 620 2.33e-7 SMART
NEBU 621 651 1.49e-5 SMART
NEBU 655 686 5.12e-4 SMART
NEBU 689 719 8.12e-7 SMART
NEBU 724 754 2.64e-6 SMART
NEBU 760 790 3.48e-6 SMART
NEBU 798 828 2.35e-3 SMART
NEBU 833 863 6.11e-2 SMART
NEBU 864 894 1.69e-4 SMART
NEBU 899 929 3.88e-4 SMART
NEBU 932 962 4e-6 SMART
NEBU 967 997 4.22e-5 SMART
NEBU 1003 1033 2.64e-6 SMART
NEBU 1041 1071 3.68e-5 SMART
NEBU 1076 1106 4.16e-4 SMART
NEBU 1107 1137 1.1e-3 SMART
NEBU 1142 1172 1.68e1 SMART
NEBU 1175 1205 4.59e-6 SMART
NEBU 1210 1240 4.06e-7 SMART
NEBU 1246 1276 1.99e-1 SMART
NEBU 1284 1314 1.85e-1 SMART
NEBU 1319 1349 1.39e-5 SMART
NEBU 1350 1380 4.03e-2 SMART
NEBU 1385 1415 3.06e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000169099
SMART Domains Protein: ENSMUSP00000125889
Gene: ENSMUSG00000049134

DomainStartEndE-ValueType
NEBU 32 61 2.83e-6 SMART
NEBU 70 100 7.24e-4 SMART
NEBU 105 135 3.46e-1 SMART
NEBU 141 171 1.18e-3 SMART
NEBU 209 239 8.97e-9 SMART
NEBU 244 274 1.73e-10 SMART
NEBU 280 310 8.12e-7 SMART
NEBU 314 344 1.73e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000165522
SMART Domains Protein: ENSMUSP00000130809
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
Pfam:Trypsin 41 106 6.4e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000166049
SMART Domains Protein: ENSMUSP00000132444
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 28 42 N/A INTRINSIC
EGF 70 103 4.66e-6 SMART
EGF 108 142 3.97e0 SMART
EGF 147 182 2.26e-4 SMART
KR 186 272 2.72e-39 SMART
Tryp_SPc 302 539 1.47e-90 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000171341
SMART Domains Protein: ENSMUSP00000126235
Gene: ENSMUSG00000025075

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
low complexity region 28 42 N/A INTRINSIC
EGF 70 103 4.66e-6 SMART
EGF 108 142 3.97e0 SMART
EGF 147 182 2.26e-4 SMART
KR 186 272 2.72e-39 SMART
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.6%
Validation Efficiency 98% (51/52)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 A G 11: 54,242,933 (GRCm39) E648G probably benign Het
Ak7 A G 12: 105,734,960 (GRCm39) H642R probably benign Het
Akap11 T C 14: 78,756,239 (GRCm39) E53G probably damaging Het
Ark2n T C 18: 77,762,117 (GRCm39) D65G probably damaging Het
Ddr2 T G 1: 169,816,109 (GRCm39) T533P probably benign Het
Dhx40 A G 11: 86,690,431 (GRCm39) S197P possibly damaging Het
Dolpp1 C A 2: 30,282,281 (GRCm39) probably benign Het
Eng A G 2: 32,563,655 (GRCm39) D347G probably benign Het
Esrra C T 19: 6,891,488 (GRCm39) probably null Het
Fap T C 2: 62,378,132 (GRCm39) I159V probably damaging Het
Fn1 C T 1: 71,676,434 (GRCm39) C599Y probably damaging Het
Fnbp4 T C 2: 90,587,807 (GRCm39) V395A probably damaging Het
Foxn3 T C 12: 99,354,676 (GRCm39) R163G probably damaging Het
Gphn T G 12: 78,569,724 (GRCm39) L306R probably benign Het
Gse1 T C 8: 121,295,902 (GRCm39) probably benign Het
Habp2 A G 19: 56,295,295 (GRCm39) D62G possibly damaging Het
Hdac7 AGGG AGGGG 15: 97,706,376 (GRCm39) probably null Het
Hyls1 G A 9: 35,472,480 (GRCm39) S312F probably benign Het
Kit A G 5: 75,770,169 (GRCm39) T194A probably benign Het
Krt16 C A 11: 100,138,029 (GRCm39) A316S possibly damaging Het
Krt7 A G 15: 101,317,439 (GRCm39) D244G probably damaging Het
Lhfpl3 T A 5: 23,478,349 (GRCm39) Y77* probably null Het
Lrrc18 A T 14: 32,731,078 (GRCm39) M206L probably benign Het
Magel2 C A 7: 62,030,406 (GRCm39) C1103* probably null Het
Mcf2l T C 8: 13,068,701 (GRCm39) V1058A probably damaging Het
Nbas G A 12: 13,374,294 (GRCm39) A541T probably damaging Het
Nudt18 T C 14: 70,816,830 (GRCm39) Y145H probably benign Het
Or51b6b T C 7: 103,309,620 (GRCm39) Y279C possibly damaging Het
Or51f1d T C 7: 102,700,538 (GRCm39) L11P probably benign Het
Or5k8 A T 16: 58,644,782 (GRCm39) C97S probably damaging Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Pcdhb12 A T 18: 37,569,838 (GRCm39) Q328L possibly damaging Het
Pde6c T C 19: 38,146,884 (GRCm39) W431R probably damaging Het
Pga5 T C 19: 10,652,225 (GRCm39) E139G probably benign Het
Pkdrej G T 15: 85,705,306 (GRCm39) S210* probably null Het
Pnpla1 G A 17: 29,100,342 (GRCm39) G403E probably benign Het
Sema3d A T 5: 12,498,074 (GRCm39) M27L probably benign Het
Serinc5 T C 13: 92,825,170 (GRCm39) S200P probably damaging Het
Sf3b3 T C 8: 111,568,452 (GRCm39) D174G probably damaging Het
Sult1b1 A T 5: 87,665,413 (GRCm39) probably null Het
Tasor2 C T 13: 3,631,891 (GRCm39) R870H possibly damaging Het
Tcaf3 T C 6: 42,570,725 (GRCm39) I342M probably benign Het
Tenm3 G A 8: 48,820,429 (GRCm39) T136M probably damaging Het
Tet3 T C 6: 83,352,773 (GRCm39) T1008A possibly damaging Het
Tgif1 T C 17: 71,151,861 (GRCm39) probably null Het
Trav15-2-dv6-2 A G 14: 53,887,323 (GRCm39) D81G probably benign Het
Trpv5 T A 6: 41,651,293 (GRCm39) H251L possibly damaging Het
Ttc14 C A 3: 33,854,537 (GRCm39) T37K possibly damaging Het
Vmn2r80 A T 10: 79,030,159 (GRCm39) I662L probably benign Het
Vmn2r81 A G 10: 79,129,649 (GRCm39) I847V probably benign Het
Zfp474 A G 18: 52,771,436 (GRCm39) T30A probably benign Het
Zswim4 C T 8: 84,957,580 (GRCm39) V163M probably damaging Het
Other mutations in Nrap
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00500:Nrap APN 19 56,361,341 (GRCm39) missense probably damaging 1.00
IGL00570:Nrap APN 19 56,326,545 (GRCm39) missense probably benign 0.10
IGL00946:Nrap APN 19 56,329,058 (GRCm39) splice site probably null
IGL01070:Nrap APN 19 56,317,516 (GRCm39) missense probably damaging 1.00
IGL01111:Nrap APN 19 56,333,990 (GRCm39) missense probably damaging 1.00
IGL01138:Nrap APN 19 56,343,970 (GRCm39) missense probably damaging 1.00
IGL01290:Nrap APN 19 56,350,180 (GRCm39) missense probably damaging 1.00
IGL01352:Nrap APN 19 56,368,268 (GRCm39) missense probably benign 0.00
IGL01372:Nrap APN 19 56,317,534 (GRCm39) critical splice acceptor site probably null
IGL01395:Nrap APN 19 56,350,225 (GRCm39) missense probably damaging 1.00
IGL01413:Nrap APN 19 56,377,823 (GRCm39) missense probably damaging 0.99
IGL01734:Nrap APN 19 56,338,741 (GRCm39) missense probably damaging 1.00
IGL01933:Nrap APN 19 56,377,250 (GRCm39) missense probably damaging 1.00
IGL02156:Nrap APN 19 56,309,432 (GRCm39) missense probably damaging 1.00
IGL02415:Nrap APN 19 56,370,741 (GRCm39) missense probably damaging 1.00
IGL02447:Nrap APN 19 56,333,951 (GRCm39) nonsense probably null
IGL02864:Nrap APN 19 56,338,806 (GRCm39) missense probably damaging 1.00
IGL02993:Nrap APN 19 56,333,965 (GRCm39) missense probably damaging 1.00
IGL03003:Nrap APN 19 56,310,384 (GRCm39) missense probably damaging 1.00
IGL03006:Nrap APN 19 56,335,596 (GRCm39) missense probably benign 0.02
IGL03084:Nrap APN 19 56,353,886 (GRCm39) missense probably damaging 1.00
IGL03136:Nrap APN 19 56,330,687 (GRCm39) missense possibly damaging 0.69
IGL03272:Nrap APN 19 56,334,000 (GRCm39) intron probably benign
IGL03389:Nrap APN 19 56,340,148 (GRCm39) missense probably benign 0.10
R0116:Nrap UTSW 19 56,343,978 (GRCm39) missense probably damaging 1.00
R0374:Nrap UTSW 19 56,340,054 (GRCm39) missense probably damaging 1.00
R0715:Nrap UTSW 19 56,345,757 (GRCm39) missense probably damaging 0.98
R0828:Nrap UTSW 19 56,333,990 (GRCm39) missense probably damaging 1.00
R0883:Nrap UTSW 19 56,333,906 (GRCm39) missense probably damaging 1.00
R1416:Nrap UTSW 19 56,315,725 (GRCm39) missense possibly damaging 0.60
R1459:Nrap UTSW 19 56,372,562 (GRCm39) missense probably benign 0.00
R1616:Nrap UTSW 19 56,378,255 (GRCm39) missense probably damaging 1.00
R1676:Nrap UTSW 19 56,323,687 (GRCm39) missense probably damaging 1.00
R1687:Nrap UTSW 19 56,343,961 (GRCm39) missense probably damaging 0.99
R1766:Nrap UTSW 19 56,323,474 (GRCm39) missense probably damaging 0.99
R1792:Nrap UTSW 19 56,367,590 (GRCm39) missense probably benign 0.00
R1817:Nrap UTSW 19 56,372,487 (GRCm39) unclassified probably benign
R1972:Nrap UTSW 19 56,345,785 (GRCm39) missense probably damaging 1.00
R1982:Nrap UTSW 19 56,372,537 (GRCm39) missense probably damaging 0.99
R2258:Nrap UTSW 19 56,310,394 (GRCm39) missense possibly damaging 0.80
R2448:Nrap UTSW 19 56,310,462 (GRCm39) missense possibly damaging 0.90
R3034:Nrap UTSW 19 56,352,437 (GRCm39) missense probably damaging 1.00
R3801:Nrap UTSW 19 56,310,211 (GRCm39) missense probably damaging 1.00
R3804:Nrap UTSW 19 56,310,211 (GRCm39) missense probably damaging 1.00
R3923:Nrap UTSW 19 56,368,688 (GRCm39) missense probably damaging 0.99
R3964:Nrap UTSW 19 56,330,576 (GRCm39) missense probably damaging 1.00
R3965:Nrap UTSW 19 56,330,576 (GRCm39) missense probably damaging 1.00
R3966:Nrap UTSW 19 56,330,576 (GRCm39) missense probably damaging 1.00
R3980:Nrap UTSW 19 56,369,984 (GRCm39) missense probably benign 0.01
R4182:Nrap UTSW 19 56,338,759 (GRCm39) missense probably damaging 1.00
R4499:Nrap UTSW 19 56,339,913 (GRCm39) missense probably damaging 0.97
R4573:Nrap UTSW 19 56,330,770 (GRCm39) critical splice acceptor site probably null
R4603:Nrap UTSW 19 56,323,456 (GRCm39) critical splice donor site probably null
R4689:Nrap UTSW 19 56,374,458 (GRCm39) missense probably damaging 0.97
R4749:Nrap UTSW 19 56,368,669 (GRCm39) missense probably damaging 0.96
R4845:Nrap UTSW 19 56,339,902 (GRCm39) missense probably benign 0.16
R4937:Nrap UTSW 19 56,335,652 (GRCm39) missense probably damaging 1.00
R4962:Nrap UTSW 19 56,366,575 (GRCm39) missense probably damaging 1.00
R5156:Nrap UTSW 19 56,360,277 (GRCm39) missense possibly damaging 0.94
R5181:Nrap UTSW 19 56,333,960 (GRCm39) missense possibly damaging 0.85
R5202:Nrap UTSW 19 56,323,583 (GRCm39) missense probably damaging 1.00
R5262:Nrap UTSW 19 56,308,655 (GRCm39) missense possibly damaging 0.95
R5301:Nrap UTSW 19 56,367,541 (GRCm39) missense probably damaging 1.00
R5380:Nrap UTSW 19 56,370,035 (GRCm39) missense probably damaging 1.00
R5576:Nrap UTSW 19 56,310,414 (GRCm39) missense probably damaging 0.99
R5631:Nrap UTSW 19 56,342,553 (GRCm39) missense probably benign 0.19
R5754:Nrap UTSW 19 56,377,916 (GRCm39) missense possibly damaging 0.55
R5799:Nrap UTSW 19 56,330,601 (GRCm39) nonsense probably null
R5899:Nrap UTSW 19 56,329,006 (GRCm39) missense possibly damaging 0.80
R5910:Nrap UTSW 19 56,330,743 (GRCm39) missense probably benign 0.00
R5994:Nrap UTSW 19 56,340,031 (GRCm39) nonsense probably null
R6124:Nrap UTSW 19 56,374,458 (GRCm39) missense probably damaging 0.97
R6149:Nrap UTSW 19 56,377,885 (GRCm39) missense possibly damaging 0.79
R6182:Nrap UTSW 19 56,350,130 (GRCm39) missense probably benign
R6245:Nrap UTSW 19 56,368,307 (GRCm39) missense possibly damaging 0.80
R6245:Nrap UTSW 19 56,342,653 (GRCm39) missense probably damaging 1.00
R6274:Nrap UTSW 19 56,350,153 (GRCm39) missense probably benign 0.21
R6340:Nrap UTSW 19 56,335,616 (GRCm39) missense probably damaging 1.00
R6547:Nrap UTSW 19 56,339,998 (GRCm39) missense probably benign 0.00
R6734:Nrap UTSW 19 56,333,941 (GRCm39) missense probably damaging 0.99
R6770:Nrap UTSW 19 56,370,969 (GRCm39) splice site probably null
R6812:Nrap UTSW 19 56,340,108 (GRCm39) missense probably damaging 1.00
R6843:Nrap UTSW 19 56,368,651 (GRCm39) missense probably damaging 1.00
R7207:Nrap UTSW 19 56,333,953 (GRCm39) missense probably damaging 1.00
R7214:Nrap UTSW 19 56,366,567 (GRCm39) missense probably benign 0.09
R7313:Nrap UTSW 19 56,330,700 (GRCm39) missense probably damaging 0.97
R7515:Nrap UTSW 19 56,354,859 (GRCm39) missense possibly damaging 0.94
R7662:Nrap UTSW 19 56,308,715 (GRCm39) missense probably benign 0.00
R7819:Nrap UTSW 19 56,323,720 (GRCm39) missense probably benign
R7836:Nrap UTSW 19 56,338,729 (GRCm39) missense probably benign 0.00
R7895:Nrap UTSW 19 56,342,584 (GRCm39) missense probably benign 0.00
R8041:Nrap UTSW 19 56,352,768 (GRCm39) nonsense probably null
R8046:Nrap UTSW 19 56,308,683 (GRCm39) missense possibly damaging 0.46
R8066:Nrap UTSW 19 56,342,562 (GRCm39) missense possibly damaging 0.94
R8129:Nrap UTSW 19 56,355,068 (GRCm39) splice site probably null
R8188:Nrap UTSW 19 56,325,010 (GRCm39) nonsense probably null
R8323:Nrap UTSW 19 56,378,255 (GRCm39) missense probably benign 0.00
R8353:Nrap UTSW 19 56,312,352 (GRCm39) missense probably damaging 1.00
R8453:Nrap UTSW 19 56,312,352 (GRCm39) missense probably damaging 1.00
R8693:Nrap UTSW 19 56,310,384 (GRCm39) missense probably damaging 1.00
R8703:Nrap UTSW 19 56,323,703 (GRCm39) missense probably damaging 1.00
R8810:Nrap UTSW 19 56,352,843 (GRCm39) critical splice acceptor site probably benign
R8872:Nrap UTSW 19 56,308,627 (GRCm39) makesense probably null
R8980:Nrap UTSW 19 56,343,970 (GRCm39) missense probably damaging 1.00
R9201:Nrap UTSW 19 56,340,093 (GRCm39) missense probably damaging 1.00
R9229:Nrap UTSW 19 56,310,339 (GRCm39) missense probably benign 0.01
R9235:Nrap UTSW 19 56,330,760 (GRCm39) nonsense probably null
R9323:Nrap UTSW 19 56,378,255 (GRCm39) missense probably benign 0.00
R9327:Nrap UTSW 19 56,340,100 (GRCm39) missense probably benign 0.25
R9329:Nrap UTSW 19 56,350,277 (GRCm39) missense probably damaging 1.00
R9468:Nrap UTSW 19 56,330,632 (GRCm39) missense possibly damaging 0.52
R9517:Nrap UTSW 19 56,360,277 (GRCm39) missense probably benign 0.00
R9639:Nrap UTSW 19 56,333,948 (GRCm39) missense possibly damaging 0.63
R9657:Nrap UTSW 19 56,352,377 (GRCm39) missense probably benign 0.27
R9709:Nrap UTSW 19 56,317,453 (GRCm39) missense probably benign 0.08
R9709:Nrap UTSW 19 56,317,452 (GRCm39) missense probably damaging 0.98
X0028:Nrap UTSW 19 56,323,652 (GRCm39) nonsense probably null
Z1176:Nrap UTSW 19 56,333,949 (GRCm39) frame shift probably null
Z1177:Nrap UTSW 19 56,333,196 (GRCm39) missense probably benign 0.01
Z1177:Nrap UTSW 19 56,326,524 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCATGCAGCCATCAGAGAGAAG -3'
(R):5'- ATGTTTGCCGGGCATCTTAGC -3'

Sequencing Primer
(F):5'- GCCATCAGAGAGAAGCCCCC -3'
(R):5'- GGCATCTTAGCACGGCTTG -3'
Posted On 2018-03-15