Incidental Mutation 'R0416:Cmya5'
ID 40343
Institutional Source Beutler Lab
Gene Symbol Cmya5
Ensembl Gene ENSMUSG00000047419
Gene Name cardiomyopathy associated 5
Synonyms Myospryn, 2310076E21Rik, 2310076E16Rik
MMRRC Submission 038618-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.252) question?
Stock # R0416 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 93040713-93144724 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to G at 93089856 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Asparagine to Threonine at position 2908 (N2908T)
Ref Sequence ENSEMBL: ENSMUSP00000050408 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062122]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000062122
AA Change: N2908T

PolyPhen 2 Score 0.053 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000050408
Gene: ENSMUSG00000047419
AA Change: N2908T

DomainStartEndE-ValueType
low complexity region 20 46 N/A INTRINSIC
low complexity region 129 140 N/A INTRINSIC
internal_repeat_1 448 535 5.09e-18 PROSPERO
internal_repeat_1 543 625 5.09e-18 PROSPERO
low complexity region 626 645 N/A INTRINSIC
low complexity region 679 691 N/A INTRINSIC
low complexity region 734 741 N/A INTRINSIC
low complexity region 1001 1010 N/A INTRINSIC
low complexity region 1166 1183 N/A INTRINSIC
low complexity region 1259 1267 N/A INTRINSIC
low complexity region 1440 1449 N/A INTRINSIC
low complexity region 1876 1889 N/A INTRINSIC
low complexity region 2632 2645 N/A INTRINSIC
low complexity region 3048 3057 N/A INTRINSIC
FN3 3312 3399 7.29e-4 SMART
FN3 3411 3492 1.3e0 SMART
Pfam:SPRY 3551 3668 6.7e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224009
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 96.2%
  • 20x: 91.8%
Validation Efficiency 99% (74/75)
Allele List at MGI
Other mutations in this stock
Total: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsm2 A G 7: 119,563,556 (GRCm38) I18V probably benign Het
Adamdec1 T G 14: 68,568,712 (GRCm38) E438A possibly damaging Het
Adamts17 A G 7: 66,915,898 (GRCm38) probably null Het
Ankrd44 T G 1: 54,743,339 (GRCm38) I359L possibly damaging Het
Ap2s1 C A 7: 16,747,365 (GRCm38) N86K probably damaging Het
Arih1 T A 9: 59,426,710 (GRCm38) probably benign Het
Astn1 T A 1: 158,509,891 (GRCm38) I389N probably damaging Het
Brca2 T C 5: 150,569,392 (GRCm38) S3291P possibly damaging Het
Cacna1d T C 14: 30,100,688 (GRCm38) probably benign Het
Ccl7 C A 11: 82,045,866 (GRCm38) probably benign Het
Cd74 A T 18: 60,811,414 (GRCm38) Y232F possibly damaging Het
Cep128 A G 12: 91,230,867 (GRCm38) probably benign Het
Cep89 T A 7: 35,416,402 (GRCm38) probably benign Het
Coil T C 11: 88,981,986 (GRCm38) L391S possibly damaging Het
Cpd C T 11: 76,785,204 (GRCm38) V1208I probably benign Het
Ddx19a T C 8: 110,979,057 (GRCm38) D254G probably damaging Het
Desi2 T A 1: 178,256,321 (GRCm38) probably benign Het
Dnah11 A T 12: 117,911,058 (GRCm38) M4024K probably damaging Het
Ergic2 A T 6: 148,183,144 (GRCm38) L53H probably damaging Het
Etv2 T C 7: 30,634,633 (GRCm38) Y225C probably benign Het
F10 G A 8: 13,055,448 (GRCm38) A338T probably damaging Het
Fam228b T A 12: 4,762,382 (GRCm38) D132V probably damaging Het
Fat2 T A 11: 55,284,134 (GRCm38) I1918F possibly damaging Het
Fbxw5 C T 2: 25,503,239 (GRCm38) S214F probably damaging Het
Glyat G A 19: 12,651,453 (GRCm38) R204Q possibly damaging Het
Gm4825 T C 15: 85,510,981 (GRCm38) noncoding transcript Het
Ino80d G T 1: 63,086,276 (GRCm38) T9K possibly damaging Het
Lifr A T 15: 7,166,914 (GRCm38) D193V probably damaging Het
Lrp12 G T 15: 39,878,911 (GRCm38) probably benign Het
Lrp3 A G 7: 35,202,353 (GRCm38) V701A probably benign Het
Mfsd11 T A 11: 116,865,882 (GRCm38) probably benign Het
Mrto4 A T 4: 139,349,732 (GRCm38) probably null Het
Msi1 T C 5: 115,430,649 (GRCm38) F43L possibly damaging Het
Mthfsd T C 8: 121,101,237 (GRCm38) D168G probably damaging Het
Myo15 T A 11: 60,511,174 (GRCm38) V3099E probably damaging Het
Myrf T C 19: 10,215,812 (GRCm38) probably null Het
Nadk C A 4: 155,587,799 (GRCm38) probably benign Het
Nav1 T C 1: 135,471,126 (GRCm38) K573E possibly damaging Het
Ndufs3 A G 2: 90,898,388 (GRCm38) V207A probably damaging Het
Nlrp3 T C 11: 59,555,924 (GRCm38) probably benign Het
Nlrx1 T G 9: 44,262,914 (GRCm38) D330A probably benign Het
Olfr331 T C 11: 58,502,396 (GRCm38) I53M unknown Het
Olfr444 G A 6: 42,955,570 (GRCm38) C24Y probably benign Het
Osbpl3 C T 6: 50,348,018 (GRCm38) V167I probably benign Het
Pcnx A T 12: 81,974,466 (GRCm38) I1410F probably benign Het
Piezo2 G A 18: 63,024,491 (GRCm38) R2383C probably damaging Het
Pip5kl1 A T 2: 32,583,424 (GRCm38) K358* probably null Het
Polg T C 7: 79,452,240 (GRCm38) probably benign Het
Prr14l T A 5: 32,828,717 (GRCm38) I1145F probably benign Het
Psmb1 C T 17: 15,494,519 (GRCm38) V39I probably benign Het
Ptk6 T C 2: 181,202,308 (GRCm38) Y66C possibly damaging Het
Robo4 T C 9: 37,404,766 (GRCm38) probably benign Het
Sdk2 A G 11: 113,803,203 (GRCm38) Y1801H probably damaging Het
Serpinb3a C A 1: 107,049,386 (GRCm38) A95S probably benign Het
Setd1a CTGGTGGTGGTGGTGGTGGTAGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG CTGGTGGTGGTGGTGGTAGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGGTGG 7: 127,785,297 (GRCm38) probably benign Het
Sik2 A T 9: 50,995,632 (GRCm38) Y98N probably damaging Het
Slc30a1 C T 1: 191,909,726 (GRCm38) P495S probably benign Het
Smg1 A T 7: 118,184,461 (GRCm38) probably benign Het
Stk3 T A 15: 35,114,632 (GRCm38) I45L probably benign Het
Tapbp A G 17: 33,925,418 (GRCm38) T163A probably damaging Het
Tdrd5 T C 1: 156,285,481 (GRCm38) K410E probably damaging Het
Trim30b A T 7: 104,363,766 (GRCm38) M152K probably benign Het
Trpm6 G T 19: 18,783,025 (GRCm38) probably benign Het
Tsc22d1 T C 14: 76,505,303 (GRCm38) probably benign Het
U2surp A T 9: 95,485,607 (GRCm38) F444I probably damaging Het
Vmn2r95 C T 17: 18,441,402 (GRCm38) P470L probably damaging Het
Zc3h4 T G 7: 16,420,275 (GRCm38) Y163D probably damaging Het
Zfp62 A T 11: 49,215,676 (GRCm38) H198L probably damaging Het
Zmym1 A G 4: 127,058,820 (GRCm38) L56P probably benign Het
Other mutations in Cmya5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00489:Cmya5 APN 13 93,093,120 (GRCm38) missense probably benign 0.13
IGL00516:Cmya5 APN 13 93,098,167 (GRCm38) missense possibly damaging 0.73
IGL00654:Cmya5 APN 13 93,094,161 (GRCm38) missense probably benign 0.00
IGL00948:Cmya5 APN 13 93,091,036 (GRCm38) missense probably benign
IGL00966:Cmya5 APN 13 93,097,906 (GRCm38) missense probably benign 0.33
IGL00988:Cmya5 APN 13 93,097,933 (GRCm38) missense possibly damaging 0.96
IGL01106:Cmya5 APN 13 93,084,612 (GRCm38) missense probably damaging 1.00
IGL01331:Cmya5 APN 13 93,096,946 (GRCm38) missense possibly damaging 0.53
IGL01392:Cmya5 APN 13 93,089,206 (GRCm38) missense probably damaging 0.99
IGL01508:Cmya5 APN 13 93,094,027 (GRCm38) missense probably benign
IGL01679:Cmya5 APN 13 93,065,320 (GRCm38) missense probably damaging 1.00
IGL01749:Cmya5 APN 13 93,089,299 (GRCm38) missense probably benign 0.00
IGL01861:Cmya5 APN 13 93,089,748 (GRCm38) missense probably damaging 1.00
IGL02021:Cmya5 APN 13 93,094,549 (GRCm38) missense probably benign 0.00
IGL02034:Cmya5 APN 13 93,084,535 (GRCm38) splice site probably benign
IGL02103:Cmya5 APN 13 93,092,127 (GRCm38) missense probably benign 0.05
IGL02174:Cmya5 APN 13 93,048,907 (GRCm38) missense possibly damaging 0.76
IGL02176:Cmya5 APN 13 93,090,150 (GRCm38) missense probably damaging 1.00
IGL02210:Cmya5 APN 13 93,092,734 (GRCm38) missense probably benign 0.14
IGL02229:Cmya5 APN 13 93,092,686 (GRCm38) missense possibly damaging 0.54
IGL02306:Cmya5 APN 13 93,098,019 (GRCm38) missense probably damaging 1.00
IGL02311:Cmya5 APN 13 93,090,655 (GRCm38) missense probably benign 0.40
IGL02409:Cmya5 APN 13 93,090,198 (GRCm38) missense probably damaging 0.96
IGL02561:Cmya5 APN 13 93,091,858 (GRCm38) missense probably benign 0.00
IGL02676:Cmya5 APN 13 93,092,853 (GRCm38) missense probably damaging 1.00
IGL02683:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02685:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02686:Cmya5 APN 13 93,090,997 (GRCm38) nonsense probably null
IGL02724:Cmya5 APN 13 93,096,655 (GRCm38) missense probably benign
IGL02727:Cmya5 APN 13 93,098,245 (GRCm38) missense possibly damaging 0.73
IGL02965:Cmya5 APN 13 93,092,557 (GRCm38) missense probably benign 0.41
IGL03079:Cmya5 APN 13 93,097,701 (GRCm38) missense possibly damaging 0.85
IGL03144:Cmya5 APN 13 93,090,868 (GRCm38) missense probably damaging 1.00
IGL03253:Cmya5 APN 13 93,091,270 (GRCm38) nonsense probably null
IGL03336:Cmya5 APN 13 93,093,505 (GRCm38) missense possibly damaging 0.84
IGL03138:Cmya5 UTSW 13 93,065,342 (GRCm38) missense probably damaging 1.00
P0023:Cmya5 UTSW 13 93,089,346 (GRCm38) missense probably benign 0.22
P4748:Cmya5 UTSW 13 93,074,475 (GRCm38) splice site probably benign
R0123:Cmya5 UTSW 13 93,095,904 (GRCm38) missense possibly damaging 0.84
R0206:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R0206:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R0242:Cmya5 UTSW 13 93,095,600 (GRCm38) missense probably benign
R0242:Cmya5 UTSW 13 93,095,600 (GRCm38) missense probably benign
R0331:Cmya5 UTSW 13 93,144,403 (GRCm38) missense possibly damaging 0.53
R0363:Cmya5 UTSW 13 93,094,869 (GRCm38) missense possibly damaging 0.77
R0382:Cmya5 UTSW 13 93,092,748 (GRCm38) missense probably benign 0.06
R0446:Cmya5 UTSW 13 93,093,656 (GRCm38) missense probably benign
R0457:Cmya5 UTSW 13 93,095,587 (GRCm38) missense possibly damaging 0.84
R0673:Cmya5 UTSW 13 93,089,997 (GRCm38) missense probably damaging 1.00
R0674:Cmya5 UTSW 13 93,092,791 (GRCm38) missense probably damaging 1.00
R0692:Cmya5 UTSW 13 93,093,849 (GRCm38) nonsense probably null
R0698:Cmya5 UTSW 13 93,095,557 (GRCm38) missense probably damaging 0.98
R1227:Cmya5 UTSW 13 93,094,446 (GRCm38) missense probably damaging 0.99
R1272:Cmya5 UTSW 13 93,095,112 (GRCm38) missense possibly damaging 0.79
R1335:Cmya5 UTSW 13 93,041,535 (GRCm38) missense possibly damaging 0.65
R1353:Cmya5 UTSW 13 93,041,525 (GRCm38) missense probably damaging 1.00
R1354:Cmya5 UTSW 13 93,092,058 (GRCm38) missense possibly damaging 0.46
R1458:Cmya5 UTSW 13 93,065,327 (GRCm38) missense probably benign 0.44
R1572:Cmya5 UTSW 13 93,094,269 (GRCm38) missense possibly damaging 0.61
R1698:Cmya5 UTSW 13 93,063,519 (GRCm38) missense probably benign 0.27
R1735:Cmya5 UTSW 13 93,089,789 (GRCm38) missense probably benign 0.11
R1743:Cmya5 UTSW 13 93,097,317 (GRCm38) missense probably benign 0.33
R1750:Cmya5 UTSW 13 93,095,663 (GRCm38) missense probably benign
R1827:Cmya5 UTSW 13 93,074,448 (GRCm38) missense possibly damaging 0.80
R2068:Cmya5 UTSW 13 93,090,524 (GRCm38) missense possibly damaging 0.93
R2088:Cmya5 UTSW 13 93,092,812 (GRCm38) missense probably damaging 1.00
R2132:Cmya5 UTSW 13 93,069,383 (GRCm38) missense probably damaging 1.00
R2216:Cmya5 UTSW 13 93,093,495 (GRCm38) missense probably damaging 1.00
R2363:Cmya5 UTSW 13 93,093,702 (GRCm38) missense probably benign 0.15
R2497:Cmya5 UTSW 13 93,098,005 (GRCm38) missense possibly damaging 0.53
R2509:Cmya5 UTSW 13 93,093,558 (GRCm38) missense probably benign 0.41
R2917:Cmya5 UTSW 13 93,091,064 (GRCm38) nonsense probably null
R2944:Cmya5 UTSW 13 93,092,842 (GRCm38) nonsense probably null
R3039:Cmya5 UTSW 13 93,092,250 (GRCm38) missense probably benign 0.12
R3078:Cmya5 UTSW 13 93,048,927 (GRCm38) missense probably damaging 0.99
R3708:Cmya5 UTSW 13 93,095,366 (GRCm38) nonsense probably null
R3717:Cmya5 UTSW 13 93,092,487 (GRCm38) missense probably benign 0.12
R3768:Cmya5 UTSW 13 93,096,693 (GRCm38) missense possibly damaging 0.73
R3769:Cmya5 UTSW 13 93,096,693 (GRCm38) missense possibly damaging 0.73
R3840:Cmya5 UTSW 13 93,094,632 (GRCm38) missense probably damaging 0.96
R3841:Cmya5 UTSW 13 93,094,632 (GRCm38) missense probably damaging 0.96
R3882:Cmya5 UTSW 13 93,091,219 (GRCm38) missense probably benign 0.07
R3888:Cmya5 UTSW 13 93,093,656 (GRCm38) missense probably benign
R3897:Cmya5 UTSW 13 93,096,681 (GRCm38) missense possibly damaging 0.72
R3952:Cmya5 UTSW 13 93,089,199 (GRCm38) missense possibly damaging 0.89
R4366:Cmya5 UTSW 13 93,091,956 (GRCm38) missense probably benign 0.36
R4471:Cmya5 UTSW 13 93,092,325 (GRCm38) missense probably benign 0.01
R4493:Cmya5 UTSW 13 93,094,065 (GRCm38) missense probably benign
R4495:Cmya5 UTSW 13 93,094,065 (GRCm38) missense probably benign
R4544:Cmya5 UTSW 13 93,091,918 (GRCm38) nonsense probably null
R4545:Cmya5 UTSW 13 93,091,918 (GRCm38) nonsense probably null
R4624:Cmya5 UTSW 13 93,063,551 (GRCm38) missense probably damaging 1.00
R4648:Cmya5 UTSW 13 93,093,828 (GRCm38) missense possibly damaging 0.84
R4824:Cmya5 UTSW 13 93,093,574 (GRCm38) missense probably benign 0.04
R4965:Cmya5 UTSW 13 93,095,787 (GRCm38) missense possibly damaging 0.84
R4967:Cmya5 UTSW 13 93,090,585 (GRCm38) missense probably damaging 1.00
R5101:Cmya5 UTSW 13 93,091,603 (GRCm38) missense possibly damaging 0.61
R5133:Cmya5 UTSW 13 93,093,372 (GRCm38) missense possibly damaging 0.79
R5139:Cmya5 UTSW 13 93,096,061 (GRCm38) missense probably benign 0.00
R5220:Cmya5 UTSW 13 93,092,296 (GRCm38) missense probably damaging 0.99
R5332:Cmya5 UTSW 13 93,096,195 (GRCm38) missense probably damaging 0.96
R5337:Cmya5 UTSW 13 93,083,273 (GRCm38) missense probably benign 0.28
R5356:Cmya5 UTSW 13 93,063,485 (GRCm38) missense probably damaging 1.00
R5401:Cmya5 UTSW 13 93,091,968 (GRCm38) missense probably damaging 1.00
R5438:Cmya5 UTSW 13 93,095,199 (GRCm38) missense possibly damaging 0.89
R5604:Cmya5 UTSW 13 93,092,763 (GRCm38) missense probably benign 0.15
R5628:Cmya5 UTSW 13 93,089,710 (GRCm38) missense probably damaging 1.00
R5666:Cmya5 UTSW 13 93,045,949 (GRCm38) missense possibly damaging 0.75
R5687:Cmya5 UTSW 13 93,098,176 (GRCm38) missense possibly damaging 0.53
R5695:Cmya5 UTSW 13 93,045,866 (GRCm38) critical splice donor site probably null
R5806:Cmya5 UTSW 13 93,093,937 (GRCm38) missense possibly damaging 0.84
R5820:Cmya5 UTSW 13 93,092,780 (GRCm38) missense probably benign 0.04
R5872:Cmya5 UTSW 13 93,097,435 (GRCm38) missense probably benign 0.01
R5875:Cmya5 UTSW 13 93,095,184 (GRCm38) missense probably benign 0.13
R5896:Cmya5 UTSW 13 93,045,865 (GRCm38) critical splice donor site probably null
R5910:Cmya5 UTSW 13 93,092,643 (GRCm38) missense probably damaging 0.98
R5969:Cmya5 UTSW 13 93,089,544 (GRCm38) missense possibly damaging 0.78
R6064:Cmya5 UTSW 13 93,089,649 (GRCm38) missense probably damaging 1.00
R6081:Cmya5 UTSW 13 93,144,513 (GRCm38) unclassified probably benign
R6102:Cmya5 UTSW 13 93,094,231 (GRCm38) missense probably benign
R6117:Cmya5 UTSW 13 93,095,166 (GRCm38) missense probably damaging 0.98
R6188:Cmya5 UTSW 13 93,097,276 (GRCm38) missense possibly damaging 0.73
R6188:Cmya5 UTSW 13 93,093,444 (GRCm38) missense possibly damaging 0.61
R6219:Cmya5 UTSW 13 93,094,443 (GRCm38) missense probably damaging 1.00
R6229:Cmya5 UTSW 13 93,093,306 (GRCm38) missense probably benign 0.41
R6346:Cmya5 UTSW 13 93,092,190 (GRCm38) missense probably damaging 1.00
R6431:Cmya5 UTSW 13 93,074,464 (GRCm38) missense possibly damaging 0.60
R6436:Cmya5 UTSW 13 93,089,215 (GRCm38) missense probably damaging 0.98
R6598:Cmya5 UTSW 13 93,089,808 (GRCm38) missense probably benign 0.05
R6649:Cmya5 UTSW 13 93,098,025 (GRCm38) missense possibly damaging 0.91
R6652:Cmya5 UTSW 13 93,093,039 (GRCm38) missense probably damaging 0.99
R6652:Cmya5 UTSW 13 93,092,895 (GRCm38) missense probably benign 0.04
R6669:Cmya5 UTSW 13 93,093,259 (GRCm38) missense probably benign 0.03
R6881:Cmya5 UTSW 13 93,090,292 (GRCm38) missense probably damaging 1.00
R6909:Cmya5 UTSW 13 93,091,252 (GRCm38) missense probably benign 0.04
R6933:Cmya5 UTSW 13 93,095,136 (GRCm38) missense probably benign 0.03
R7021:Cmya5 UTSW 13 93,093,555 (GRCm38) missense possibly damaging 0.62
R7022:Cmya5 UTSW 13 93,069,278 (GRCm38) critical splice donor site probably null
R7068:Cmya5 UTSW 13 93,092,697 (GRCm38) missense possibly damaging 0.59
R7087:Cmya5 UTSW 13 93,090,975 (GRCm38) missense probably benign 0.00
R7088:Cmya5 UTSW 13 93,091,864 (GRCm38) missense possibly damaging 0.95
R7126:Cmya5 UTSW 13 93,089,940 (GRCm38) missense probably benign 0.41
R7177:Cmya5 UTSW 13 93,095,328 (GRCm38) missense probably benign 0.00
R7188:Cmya5 UTSW 13 93,046,038 (GRCm38) missense probably damaging 1.00
R7217:Cmya5 UTSW 13 93,090,430 (GRCm38) missense probably damaging 1.00
R7278:Cmya5 UTSW 13 93,095,700 (GRCm38) missense probably damaging 0.96
R7293:Cmya5 UTSW 13 93,092,797 (GRCm38) missense possibly damaging 0.90
R7332:Cmya5 UTSW 13 93,092,553 (GRCm38) missense possibly damaging 0.60
R7375:Cmya5 UTSW 13 93,091,661 (GRCm38) missense probably damaging 0.97
R7386:Cmya5 UTSW 13 93,069,323 (GRCm38) missense probably damaging 1.00
R7489:Cmya5 UTSW 13 93,091,838 (GRCm38) missense possibly damaging 0.87
R7529:Cmya5 UTSW 13 93,097,434 (GRCm38) missense probably benign 0.02
R7552:Cmya5 UTSW 13 93,069,312 (GRCm38) missense probably benign 0.41
R7624:Cmya5 UTSW 13 93,090,357 (GRCm38) missense possibly damaging 0.79
R7637:Cmya5 UTSW 13 93,083,212 (GRCm38) missense possibly damaging 0.87
R7673:Cmya5 UTSW 13 93,094,121 (GRCm38) missense probably benign 0.13
R7753:Cmya5 UTSW 13 93,098,172 (GRCm38) missense probably benign 0.18
R7757:Cmya5 UTSW 13 93,098,272 (GRCm38) missense possibly damaging 0.53
R7806:Cmya5 UTSW 13 93,094,262 (GRCm38) missense probably benign 0.00
R7825:Cmya5 UTSW 13 93,097,628 (GRCm38) missense possibly damaging 0.53
R7878:Cmya5 UTSW 13 93,089,757 (GRCm38) missense probably damaging 0.98
R7892:Cmya5 UTSW 13 93,096,357 (GRCm38) missense probably damaging 0.96
R7952:Cmya5 UTSW 13 93,097,004 (GRCm38) small deletion probably benign
R8127:Cmya5 UTSW 13 93,094,614 (GRCm38) missense probably damaging 0.99
R8256:Cmya5 UTSW 13 93,093,478 (GRCm38) missense possibly damaging 0.62
R8339:Cmya5 UTSW 13 93,091,634 (GRCm38) nonsense probably null
R8446:Cmya5 UTSW 13 93,093,828 (GRCm38) missense possibly damaging 0.84
R8553:Cmya5 UTSW 13 93,093,796 (GRCm38) missense probably benign 0.00
R8686:Cmya5 UTSW 13 93,095,380 (GRCm38) missense possibly damaging 0.91
R8748:Cmya5 UTSW 13 93,089,721 (GRCm38) missense probably damaging 1.00
R8783:Cmya5 UTSW 13 93,089,380 (GRCm38) missense possibly damaging 0.58
R8803:Cmya5 UTSW 13 93,041,483 (GRCm38) missense probably damaging 1.00
R8810:Cmya5 UTSW 13 93,063,540 (GRCm38) missense possibly damaging 0.47
R8937:Cmya5 UTSW 13 93,096,332 (GRCm38) missense probably benign 0.01
R8985:Cmya5 UTSW 13 93,097,156 (GRCm38) missense possibly damaging 0.73
R9017:Cmya5 UTSW 13 93,092,064 (GRCm38) missense probably benign 0.03
R9087:Cmya5 UTSW 13 93,097,203 (GRCm38) missense possibly damaging 0.72
R9133:Cmya5 UTSW 13 93,097,600 (GRCm38) missense possibly damaging 0.73
R9156:Cmya5 UTSW 13 93,097,370 (GRCm38) missense unknown
R9209:Cmya5 UTSW 13 93,090,358 (GRCm38) missense probably benign 0.45
R9222:Cmya5 UTSW 13 93,094,071 (GRCm38) missense probably benign 0.00
R9229:Cmya5 UTSW 13 93,095,668 (GRCm38) missense possibly damaging 0.92
R9382:Cmya5 UTSW 13 93,093,376 (GRCm38) missense probably benign
R9385:Cmya5 UTSW 13 93,094,372 (GRCm38) missense probably damaging 0.99
R9418:Cmya5 UTSW 13 93,089,701 (GRCm38) missense probably benign 0.22
R9452:Cmya5 UTSW 13 93,095,886 (GRCm38) missense probably benign
R9492:Cmya5 UTSW 13 93,041,314 (GRCm38) makesense probably null
R9600:Cmya5 UTSW 13 93,090,096 (GRCm38) missense probably damaging 1.00
R9712:Cmya5 UTSW 13 93,065,373 (GRCm38) critical splice acceptor site probably null
R9742:Cmya5 UTSW 13 93,095,427 (GRCm38) missense possibly damaging 0.89
RF020:Cmya5 UTSW 13 93,069,291 (GRCm38) missense possibly damaging 0.56
X0028:Cmya5 UTSW 13 93,096,687 (GRCm38) missense possibly damaging 0.53
Z1088:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Z1176:Cmya5 UTSW 13 93,096,790 (GRCm38) missense unknown
Z1176:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Z1177:Cmya5 UTSW 13 93,063,579 (GRCm38) missense probably benign
Predicted Primers PCR Primer
(F):5'- TGCTTGGCTCACTCTCCAGAACAC -3'
(R):5'- TTCCCAAGGCGACATTCTGACAC -3'

Sequencing Primer
(F):5'- TCTCCAGAACACAGCGGG -3'
(R):5'- GCGACATTCTGACACTGATG -3'
Posted On 2013-05-23