Incidental Mutation 'R6547:Nrap'
ID 521335
Institutional Source Beutler Lab
Gene Symbol Nrap
Ensembl Gene ENSMUSG00000049134
Gene Name nebulin-related anchoring protein
Synonyms
MMRRC Submission 044672-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6547 (G1)
Quality Score 225.009
Status Validated
Chromosome 19
Chromosomal Location 56308473-56378466 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 56339998 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Asparagine at position 840 (H840N)
Ref Sequence ENSEMBL: ENSMUSP00000132582 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040711] [ENSMUST00000073536] [ENSMUST00000095947] [ENSMUST00000166203] [ENSMUST00000167239]
AlphaFold Q80XB4
Predicted Effect probably benign
Transcript: ENSMUST00000040711
AA Change: H841N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000048364
Gene: ENSMUSG00000049134
AA Change: H841N

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: H876N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000073228
Gene: ENSMUSG00000049134
AA Change: H876N

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: ENSMUST00000095947
AA Change: H759N

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000093640
Gene: ENSMUSG00000049134
AA Change: H759N

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: ENSMUST00000166203
AA Change: H840N

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000132582
Gene: ENSMUSG00000049134
AA Change: H840N

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: H841N

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000128196
Gene: ENSMUSG00000049134
AA Change: H841N

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.2%
  • 20x: 97.4%
Validation Efficiency 98% (53/54)
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik A T 2: 68,490,251 (GRCm39) probably benign Het
Abca13 T A 11: 9,224,757 (GRCm39) V490E probably benign Het
Abca2 G T 2: 25,323,350 (GRCm39) G106V possibly damaging Het
Ablim3 T C 18: 61,957,000 (GRCm39) T276A probably benign Het
Anxa7 A G 14: 20,519,461 (GRCm39) V119A probably benign Het
Arl9 A G 5: 77,158,257 (GRCm39) probably null Het
Atm T C 9: 53,351,457 (GRCm39) Y2964C probably damaging Het
Bbs9 T C 9: 22,425,365 (GRCm39) Y140H probably benign Het
Calcr A T 6: 3,717,177 (GRCm39) D94E probably damaging Het
Celsr3 T A 9: 108,706,327 (GRCm39) Y937N probably damaging Het
Cemip2 A T 19: 21,822,195 (GRCm39) T1197S probably benign Het
Clca3a1 C T 3: 144,442,708 (GRCm39) A779T probably damaging Het
Clec9a T A 6: 129,393,339 (GRCm39) V94D probably benign Het
Colec12 G T 18: 9,840,351 (GRCm39) L57F probably damaging Het
Fa2h T C 8: 112,074,652 (GRCm39) Y317C probably damaging Het
Flnc A G 6: 29,448,607 (GRCm39) T1282A probably damaging Het
Gm10801 AAGT AAGTAGT 2: 98,494,148 (GRCm39) probably null Het
Hcn2 G T 10: 79,552,986 (GRCm39) V162L probably benign Het
Hycc1 T C 5: 24,170,098 (GRCm39) N417S probably benign Het
Kbtbd11 T A 8: 15,077,641 (GRCm39) V80E possibly damaging Het
Lama4 A G 10: 38,949,652 (GRCm39) D915G probably damaging Het
Limch1 A T 5: 67,186,117 (GRCm39) E806V probably damaging Het
Mppe1 T C 18: 67,362,059 (GRCm39) I169V probably benign Het
Msc A C 1: 14,825,969 (GRCm39) S2A possibly damaging Het
Nploc4 A G 11: 120,319,348 (GRCm39) probably null Het
Nr3c2 A T 8: 77,635,438 (GRCm39) I180F possibly damaging Het
Or8a1 T A 9: 37,641,791 (GRCm39) M163L probably benign Het
Pate13 T A 9: 35,819,781 (GRCm39) M15K probably null Het
Pdlim1 G A 19: 40,211,564 (GRCm39) T243I probably damaging Het
Pfkl T A 10: 77,831,188 (GRCm39) M318L probably benign Het
Rap1gds1 C A 3: 138,661,099 (GRCm39) R426L probably damaging Het
Ric1 A G 19: 29,572,226 (GRCm39) N674D probably damaging Het
Rp1 G A 1: 4,240,528 (GRCm39) T875I unknown Het
Rtn1 G T 12: 72,355,535 (GRCm39) S137Y possibly damaging Het
Scn2a A G 2: 65,546,241 (GRCm39) I935V probably benign Het
Serpina1a C T 12: 103,822,180 (GRCm39) V251M probably damaging Het
Slc19a3 A G 1: 83,000,621 (GRCm39) V132A probably damaging Het
Slc26a6 T A 9: 108,737,981 (GRCm39) probably null Het
Slc2a5 T A 4: 150,220,076 (GRCm39) V164D possibly damaging Het
Slc4a1 T A 11: 102,247,561 (GRCm39) T441S probably damaging Het
Stk33 T C 7: 108,920,042 (GRCm39) I366V possibly damaging Het
Syt14 G T 1: 192,584,177 (GRCm39) H696N possibly damaging Het
Tcaim T A 9: 122,643,531 (GRCm39) V77D probably benign Het
Tefm T G 11: 80,031,210 (GRCm39) probably null Het
Tekt3 T A 11: 62,961,304 (GRCm39) S158T possibly damaging Het
Tspan11 T A 6: 127,926,766 (GRCm39) M238K possibly damaging Het
Unc5c A T 3: 141,495,780 (GRCm39) T476S probably benign Het
Usp9y A T Y: 1,444,612 (GRCm39) L109Q probably damaging Homo
Vmn2r111 T C 17: 22,778,032 (GRCm39) N549S possibly damaging Het
Vps13c C A 9: 67,880,647 (GRCm39) Q3495K probably damaging Het
Zbtb10 G A 3: 9,316,763 (GRCm39) A192T probably benign Het
Zfp316 A T 5: 143,239,952 (GRCm39) V689D probably damaging Het
Zswim1 A G 2: 164,666,716 (GRCm39) probably benign Het
Zswim5 T C 4: 116,844,100 (GRCm39) L1046P 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
R6270:Nrap UTSW 19 56,308,630 (GRCm39) missense probably benign 0.00
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
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'- CCTGAAACAGACATGCCAGG -3'
(R):5'- TACTCAGGTGAAATACAAAGAGGACTA -3'

Sequencing Primer
(F):5'- TCTTACACATGCTCTCACACAC -3'
(R):5'- GACTATGAAAGGTCCAGAGGG -3'
Posted On 2018-06-06