Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020L24Rik |
G |
T |
11: 83,331,232 (GRCm39) |
E48* |
probably null |
Het |
Acaca |
T |
C |
11: 84,169,783 (GRCm39) |
|
probably null |
Het |
Albfm1 |
T |
A |
5: 90,720,609 (GRCm39) |
L260* |
probably null |
Het |
Alkbh3 |
A |
G |
2: 93,835,097 (GRCm39) |
S83P |
possibly damaging |
Het |
Ammecr1l |
T |
C |
18: 31,904,872 (GRCm39) |
S38P |
probably benign |
Het |
Armc10 |
T |
C |
5: 21,858,390 (GRCm39) |
V145A |
probably damaging |
Het |
BC048671 |
A |
G |
6: 90,280,222 (GRCm39) |
K46R |
probably null |
Het |
C2cd3 |
A |
G |
7: 100,065,388 (GRCm39) |
T347A |
|
Het |
C8b |
G |
T |
4: 104,650,540 (GRCm39) |
E449D |
probably benign |
Het |
Camk4 |
T |
C |
18: 33,072,584 (GRCm39) |
S46P |
probably benign |
Het |
Ccdc113 |
G |
A |
8: 96,264,733 (GRCm39) |
R81H |
probably benign |
Het |
Cd177 |
A |
T |
7: 24,444,558 (GRCm39) |
C674* |
probably null |
Het |
Cdc6 |
T |
A |
11: 98,810,065 (GRCm39) |
V458D |
probably damaging |
Het |
Cenpo |
C |
T |
12: 4,265,307 (GRCm39) |
E238K |
probably benign |
Het |
Ckap2 |
G |
T |
8: 22,659,882 (GRCm39) |
P533Q |
possibly damaging |
Het |
Cma1 |
T |
A |
14: 56,181,273 (GRCm39) |
H44L |
probably damaging |
Het |
Cntnap5b |
T |
A |
1: 100,087,802 (GRCm39) |
I141N |
probably damaging |
Het |
Col6a4 |
T |
A |
9: 105,877,885 (GRCm39) |
T2031S |
possibly damaging |
Het |
Cplane1 |
C |
T |
15: 8,248,431 (GRCm39) |
T1660M |
probably benign |
Het |
Cxcr5 |
T |
A |
9: 44,424,683 (GRCm39) |
T325S |
possibly damaging |
Het |
Dhx32 |
A |
T |
7: 133,344,417 (GRCm39) |
L204Q |
probably damaging |
Het |
Dse |
A |
G |
10: 34,029,885 (GRCm39) |
Y402H |
probably damaging |
Het |
Ecpas |
A |
T |
4: 58,849,766 (GRCm39) |
L458I |
possibly damaging |
Het |
Exoc6 |
G |
T |
19: 37,565,458 (GRCm39) |
C178F |
probably damaging |
Het |
Fam149a |
A |
G |
8: 45,803,582 (GRCm39) |
V384A |
probably benign |
Het |
Fcrl5 |
T |
C |
3: 87,365,141 (GRCm39) |
*597Q |
probably null |
Het |
Fer1l6 |
A |
G |
15: 58,435,899 (GRCm39) |
K431E |
possibly damaging |
Het |
Fmo3 |
T |
A |
1: 162,796,434 (GRCm39) |
H46L |
probably benign |
Het |
Gcm2 |
T |
C |
13: 41,256,840 (GRCm39) |
D303G |
probably damaging |
Het |
Gk2 |
T |
C |
5: 97,603,534 (GRCm39) |
M435V |
probably damaging |
Het |
Gli1 |
C |
A |
10: 127,171,868 (GRCm39) |
M295I |
probably damaging |
Het |
Gm11444 |
G |
T |
11: 85,737,862 (GRCm39) |
H109Q |
|
Het |
Gtpbp1 |
T |
A |
15: 79,603,483 (GRCm39) |
D182E |
|
Het |
Hnf4g |
A |
T |
3: 3,713,185 (GRCm39) |
|
probably null |
Het |
Hsf2 |
G |
A |
10: 57,388,188 (GRCm39) |
R483H |
probably damaging |
Het |
Kcnq4 |
C |
T |
4: 120,561,596 (GRCm39) |
R491H |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,715,602 (GRCm39) |
V1686A |
possibly damaging |
Het |
Larp6 |
A |
G |
9: 60,631,638 (GRCm39) |
K137E |
probably damaging |
Het |
Mboat1 |
T |
G |
13: 30,379,772 (GRCm39) |
|
probably null |
Het |
Mdh1 |
T |
C |
11: 21,508,484 (GRCm39) |
Y286C |
probably damaging |
Het |
Mga |
G |
T |
2: 119,792,417 (GRCm39) |
K2607N |
probably damaging |
Het |
Morf4l1 |
C |
A |
9: 89,979,433 (GRCm39) |
V183F |
possibly damaging |
Het |
Mroh4 |
G |
A |
15: 74,497,993 (GRCm39) |
R196W |
probably benign |
Het |
Muc16 |
C |
A |
9: 18,503,976 (GRCm39) |
M6438I |
probably damaging |
Het |
Myom3 |
A |
G |
4: 135,530,589 (GRCm39) |
Y1167C |
probably damaging |
Het |
Neurl3 |
T |
C |
1: 36,308,302 (GRCm39) |
E170G |
possibly damaging |
Het |
Nsd3 |
T |
C |
8: 26,156,050 (GRCm39) |
I539T |
probably benign |
Het |
Nup155 |
T |
C |
15: 8,186,177 (GRCm39) |
F1313S |
probably benign |
Het |
Nxn |
A |
T |
11: 76,153,974 (GRCm39) |
V287E |
possibly damaging |
Het |
Or4a80 |
G |
A |
2: 89,582,443 (GRCm39) |
T243I |
probably benign |
Het |
Or7a38 |
A |
C |
10: 78,753,593 (GRCm39) |
L306F |
probably benign |
Het |
Or8c13 |
C |
A |
9: 38,091,748 (GRCm39) |
V124F |
probably damaging |
Het |
Pax6 |
A |
G |
2: 105,526,753 (GRCm39) |
N220D |
probably benign |
Het |
Pcdha11 |
G |
A |
18: 37,138,470 (GRCm39) |
R33H |
probably benign |
Het |
Pdzd8 |
A |
G |
19: 59,333,389 (GRCm39) |
F211L |
probably damaging |
Het |
Pear1 |
C |
A |
3: 87,661,945 (GRCm39) |
V477F |
possibly damaging |
Het |
Pex19 |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
GTCTCTTGTCTCCGAAGGTGCTCTTGATGATTTC |
1: 171,956,150 (GRCm39) |
|
probably null |
Het |
Pidd1 |
A |
T |
7: 141,020,400 (GRCm39) |
V539E |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,207,365 (GRCm38) |
I878F |
probably damaging |
Het |
Rabepk |
T |
C |
2: 34,675,711 (GRCm39) |
T140A |
probably benign |
Het |
Ranbp2 |
G |
T |
10: 58,299,728 (GRCm39) |
R454L |
probably damaging |
Het |
Rnf123 |
C |
T |
9: 107,935,735 (GRCm39) |
R943Q |
probably null |
Het |
Sash1 |
G |
A |
10: 8,605,481 (GRCm39) |
R970* |
probably null |
Het |
Serpinb2 |
C |
A |
1: 107,452,422 (GRCm39) |
F333L |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,387,728 (GRCm39) |
|
probably null |
Het |
Slc9a2 |
A |
C |
1: 40,765,539 (GRCm39) |
I310L |
probably damaging |
Het |
Strip2 |
T |
A |
6: 29,920,532 (GRCm39) |
|
probably null |
Het |
Thoc3 |
T |
C |
13: 54,611,565 (GRCm39) |
T241A |
probably damaging |
Het |
Tmem139 |
T |
A |
6: 42,240,199 (GRCm39) |
V2E |
probably damaging |
Het |
Usp24 |
G |
T |
4: 106,244,743 (GRCm39) |
V1233F |
probably damaging |
Het |
Vnn1 |
A |
G |
10: 23,776,645 (GRCm39) |
Q332R |
probably benign |
Het |
Wac |
T |
A |
18: 7,921,455 (GRCm39) |
H530Q |
probably damaging |
Het |
Wdr35 |
T |
A |
12: 9,028,659 (GRCm39) |
N92K |
probably benign |
Het |
Zbtb18 |
T |
G |
1: 177,274,820 (GRCm39) |
L60R |
probably damaging |
Het |
Zfp184 |
T |
A |
13: 22,144,162 (GRCm39) |
C623S |
probably damaging |
Het |
Zfp292 |
A |
G |
4: 34,806,796 (GRCm39) |
Y2088H |
probably damaging |
Het |
Zfp975 |
G |
T |
7: 42,312,096 (GRCm39) |
S172R |
probably benign |
Het |
Zswim2 |
G |
A |
2: 83,746,071 (GRCm39) |
Q456* |
probably null |
Het |
|
Other mutations in Cmya5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Cmya5
|
APN |
13 |
93,229,628 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00516:Cmya5
|
APN |
13 |
93,234,675 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00654:Cmya5
|
APN |
13 |
93,230,669 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00948:Cmya5
|
APN |
13 |
93,227,544 (GRCm39) |
missense |
probably benign |
|
IGL00966:Cmya5
|
APN |
13 |
93,234,414 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00988:Cmya5
|
APN |
13 |
93,234,441 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01106:Cmya5
|
APN |
13 |
93,221,120 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01331:Cmya5
|
APN |
13 |
93,233,454 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01392:Cmya5
|
APN |
13 |
93,225,714 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01508:Cmya5
|
APN |
13 |
93,230,535 (GRCm39) |
missense |
probably benign |
|
IGL01679:Cmya5
|
APN |
13 |
93,201,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01749:Cmya5
|
APN |
13 |
93,225,807 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01861:Cmya5
|
APN |
13 |
93,226,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02021:Cmya5
|
APN |
13 |
93,231,057 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02034:Cmya5
|
APN |
13 |
93,221,043 (GRCm39) |
splice site |
probably benign |
|
IGL02103:Cmya5
|
APN |
13 |
93,228,635 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02174:Cmya5
|
APN |
13 |
93,185,415 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02176:Cmya5
|
APN |
13 |
93,226,658 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02210:Cmya5
|
APN |
13 |
93,229,242 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02229:Cmya5
|
APN |
13 |
93,229,194 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02306:Cmya5
|
APN |
13 |
93,234,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02311:Cmya5
|
APN |
13 |
93,227,163 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02409:Cmya5
|
APN |
13 |
93,226,706 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02561:Cmya5
|
APN |
13 |
93,228,366 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Cmya5
|
APN |
13 |
93,229,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02683:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02685:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02686:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02724:Cmya5
|
APN |
13 |
93,233,163 (GRCm39) |
missense |
probably benign |
|
IGL02727:Cmya5
|
APN |
13 |
93,234,753 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02965:Cmya5
|
APN |
13 |
93,229,065 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03079:Cmya5
|
APN |
13 |
93,234,209 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03144:Cmya5
|
APN |
13 |
93,227,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03253:Cmya5
|
APN |
13 |
93,227,778 (GRCm39) |
nonsense |
probably null |
|
IGL03336:Cmya5
|
APN |
13 |
93,230,013 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03138:Cmya5
|
UTSW |
13 |
93,201,850 (GRCm39) |
missense |
probably damaging |
1.00 |
P0023:Cmya5
|
UTSW |
13 |
93,225,854 (GRCm39) |
missense |
probably benign |
0.22 |
P4748:Cmya5
|
UTSW |
13 |
93,210,983 (GRCm39) |
splice site |
probably benign |
|
R0123:Cmya5
|
UTSW |
13 |
93,232,412 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0206:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R0206:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R0242:Cmya5
|
UTSW |
13 |
93,232,108 (GRCm39) |
missense |
probably benign |
|
R0242:Cmya5
|
UTSW |
13 |
93,232,108 (GRCm39) |
missense |
probably benign |
|
R0331:Cmya5
|
UTSW |
13 |
93,280,911 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0363:Cmya5
|
UTSW |
13 |
93,231,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0382:Cmya5
|
UTSW |
13 |
93,229,256 (GRCm39) |
missense |
probably benign |
0.06 |
R0416:Cmya5
|
UTSW |
13 |
93,226,364 (GRCm39) |
missense |
probably benign |
0.05 |
R0446:Cmya5
|
UTSW |
13 |
93,230,164 (GRCm39) |
missense |
probably benign |
|
R0457:Cmya5
|
UTSW |
13 |
93,232,095 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0673:Cmya5
|
UTSW |
13 |
93,226,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Cmya5
|
UTSW |
13 |
93,229,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0692:Cmya5
|
UTSW |
13 |
93,230,357 (GRCm39) |
nonsense |
probably null |
|
R0698:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R1227:Cmya5
|
UTSW |
13 |
93,230,954 (GRCm39) |
missense |
probably damaging |
0.99 |
R1272:Cmya5
|
UTSW |
13 |
93,231,620 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1335:Cmya5
|
UTSW |
13 |
93,178,043 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1353:Cmya5
|
UTSW |
13 |
93,178,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R1354:Cmya5
|
UTSW |
13 |
93,228,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1458:Cmya5
|
UTSW |
13 |
93,201,835 (GRCm39) |
missense |
probably benign |
0.44 |
R1572:Cmya5
|
UTSW |
13 |
93,230,777 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1698:Cmya5
|
UTSW |
13 |
93,200,027 (GRCm39) |
missense |
probably benign |
0.27 |
R1735:Cmya5
|
UTSW |
13 |
93,226,297 (GRCm39) |
missense |
probably benign |
0.11 |
R1743:Cmya5
|
UTSW |
13 |
93,233,825 (GRCm39) |
missense |
probably benign |
0.33 |
R1750:Cmya5
|
UTSW |
13 |
93,232,171 (GRCm39) |
missense |
probably benign |
|
R1827:Cmya5
|
UTSW |
13 |
93,210,956 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2068:Cmya5
|
UTSW |
13 |
93,227,032 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2088:Cmya5
|
UTSW |
13 |
93,229,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Cmya5
|
UTSW |
13 |
93,205,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2216:Cmya5
|
UTSW |
13 |
93,230,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Cmya5
|
UTSW |
13 |
93,230,210 (GRCm39) |
missense |
probably benign |
0.15 |
R2497:Cmya5
|
UTSW |
13 |
93,234,513 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2509:Cmya5
|
UTSW |
13 |
93,230,066 (GRCm39) |
missense |
probably benign |
0.41 |
R2917:Cmya5
|
UTSW |
13 |
93,227,572 (GRCm39) |
nonsense |
probably null |
|
R2944:Cmya5
|
UTSW |
13 |
93,229,350 (GRCm39) |
nonsense |
probably null |
|
R3039:Cmya5
|
UTSW |
13 |
93,228,758 (GRCm39) |
missense |
probably benign |
0.12 |
R3078:Cmya5
|
UTSW |
13 |
93,185,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R3708:Cmya5
|
UTSW |
13 |
93,231,874 (GRCm39) |
nonsense |
probably null |
|
R3717:Cmya5
|
UTSW |
13 |
93,228,995 (GRCm39) |
missense |
probably benign |
0.12 |
R3768:Cmya5
|
UTSW |
13 |
93,233,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3769:Cmya5
|
UTSW |
13 |
93,233,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3840:Cmya5
|
UTSW |
13 |
93,231,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R3841:Cmya5
|
UTSW |
13 |
93,231,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R3882:Cmya5
|
UTSW |
13 |
93,227,727 (GRCm39) |
missense |
probably benign |
0.07 |
R3888:Cmya5
|
UTSW |
13 |
93,230,164 (GRCm39) |
missense |
probably benign |
|
R3897:Cmya5
|
UTSW |
13 |
93,233,189 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3952:Cmya5
|
UTSW |
13 |
93,225,707 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4366:Cmya5
|
UTSW |
13 |
93,228,464 (GRCm39) |
missense |
probably benign |
0.36 |
R4471:Cmya5
|
UTSW |
13 |
93,228,833 (GRCm39) |
missense |
probably benign |
0.01 |
R4493:Cmya5
|
UTSW |
13 |
93,230,573 (GRCm39) |
missense |
probably benign |
|
R4495:Cmya5
|
UTSW |
13 |
93,230,573 (GRCm39) |
missense |
probably benign |
|
R4544:Cmya5
|
UTSW |
13 |
93,228,426 (GRCm39) |
nonsense |
probably null |
|
R4545:Cmya5
|
UTSW |
13 |
93,228,426 (GRCm39) |
nonsense |
probably null |
|
R4624:Cmya5
|
UTSW |
13 |
93,200,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Cmya5
|
UTSW |
13 |
93,230,336 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4824:Cmya5
|
UTSW |
13 |
93,230,082 (GRCm39) |
missense |
probably benign |
0.04 |
R4965:Cmya5
|
UTSW |
13 |
93,232,295 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4967:Cmya5
|
UTSW |
13 |
93,227,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Cmya5
|
UTSW |
13 |
93,228,111 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5133:Cmya5
|
UTSW |
13 |
93,229,880 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5139:Cmya5
|
UTSW |
13 |
93,232,569 (GRCm39) |
missense |
probably benign |
0.00 |
R5220:Cmya5
|
UTSW |
13 |
93,228,804 (GRCm39) |
missense |
probably damaging |
0.99 |
R5332:Cmya5
|
UTSW |
13 |
93,232,703 (GRCm39) |
missense |
probably damaging |
0.96 |
R5337:Cmya5
|
UTSW |
13 |
93,219,781 (GRCm39) |
missense |
probably benign |
0.28 |
R5356:Cmya5
|
UTSW |
13 |
93,199,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Cmya5
|
UTSW |
13 |
93,228,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5438:Cmya5
|
UTSW |
13 |
93,231,707 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5604:Cmya5
|
UTSW |
13 |
93,229,271 (GRCm39) |
missense |
probably benign |
0.15 |
R5628:Cmya5
|
UTSW |
13 |
93,226,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Cmya5
|
UTSW |
13 |
93,182,457 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5687:Cmya5
|
UTSW |
13 |
93,234,684 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5695:Cmya5
|
UTSW |
13 |
93,182,374 (GRCm39) |
critical splice donor site |
probably null |
|
R5806:Cmya5
|
UTSW |
13 |
93,230,445 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5820:Cmya5
|
UTSW |
13 |
93,229,288 (GRCm39) |
missense |
probably benign |
0.04 |
R5872:Cmya5
|
UTSW |
13 |
93,233,943 (GRCm39) |
missense |
probably benign |
0.01 |
R5875:Cmya5
|
UTSW |
13 |
93,231,692 (GRCm39) |
missense |
probably benign |
0.13 |
R5896:Cmya5
|
UTSW |
13 |
93,182,373 (GRCm39) |
critical splice donor site |
probably null |
|
R5910:Cmya5
|
UTSW |
13 |
93,229,151 (GRCm39) |
missense |
probably damaging |
0.98 |
R5969:Cmya5
|
UTSW |
13 |
93,226,052 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6064:Cmya5
|
UTSW |
13 |
93,226,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6081:Cmya5
|
UTSW |
13 |
93,281,021 (GRCm39) |
unclassified |
probably benign |
|
R6102:Cmya5
|
UTSW |
13 |
93,230,739 (GRCm39) |
missense |
probably benign |
|
R6117:Cmya5
|
UTSW |
13 |
93,231,674 (GRCm39) |
missense |
probably damaging |
0.98 |
R6188:Cmya5
|
UTSW |
13 |
93,233,784 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6188:Cmya5
|
UTSW |
13 |
93,229,952 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6219:Cmya5
|
UTSW |
13 |
93,230,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Cmya5
|
UTSW |
13 |
93,229,814 (GRCm39) |
missense |
probably benign |
0.41 |
R6346:Cmya5
|
UTSW |
13 |
93,228,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Cmya5
|
UTSW |
13 |
93,210,972 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6436:Cmya5
|
UTSW |
13 |
93,225,723 (GRCm39) |
missense |
probably damaging |
0.98 |
R6598:Cmya5
|
UTSW |
13 |
93,226,316 (GRCm39) |
missense |
probably benign |
0.05 |
R6649:Cmya5
|
UTSW |
13 |
93,234,533 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6652:Cmya5
|
UTSW |
13 |
93,229,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R6652:Cmya5
|
UTSW |
13 |
93,229,403 (GRCm39) |
missense |
probably benign |
0.04 |
R6669:Cmya5
|
UTSW |
13 |
93,229,767 (GRCm39) |
missense |
probably benign |
0.03 |
R6881:Cmya5
|
UTSW |
13 |
93,226,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6909:Cmya5
|
UTSW |
13 |
93,227,760 (GRCm39) |
missense |
probably benign |
0.04 |
R6933:Cmya5
|
UTSW |
13 |
93,231,644 (GRCm39) |
missense |
probably benign |
0.03 |
R7021:Cmya5
|
UTSW |
13 |
93,230,063 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7022:Cmya5
|
UTSW |
13 |
93,205,786 (GRCm39) |
critical splice donor site |
probably null |
|
R7068:Cmya5
|
UTSW |
13 |
93,229,205 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7087:Cmya5
|
UTSW |
13 |
93,227,483 (GRCm39) |
missense |
probably benign |
0.00 |
R7126:Cmya5
|
UTSW |
13 |
93,226,448 (GRCm39) |
missense |
probably benign |
0.41 |
R7177:Cmya5
|
UTSW |
13 |
93,231,836 (GRCm39) |
missense |
probably benign |
0.00 |
R7188:Cmya5
|
UTSW |
13 |
93,182,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7217:Cmya5
|
UTSW |
13 |
93,226,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Cmya5
|
UTSW |
13 |
93,232,208 (GRCm39) |
missense |
probably damaging |
0.96 |
R7293:Cmya5
|
UTSW |
13 |
93,229,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7332:Cmya5
|
UTSW |
13 |
93,229,061 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7375:Cmya5
|
UTSW |
13 |
93,228,169 (GRCm39) |
missense |
probably damaging |
0.97 |
R7386:Cmya5
|
UTSW |
13 |
93,205,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R7489:Cmya5
|
UTSW |
13 |
93,228,346 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7529:Cmya5
|
UTSW |
13 |
93,233,942 (GRCm39) |
missense |
probably benign |
0.02 |
R7552:Cmya5
|
UTSW |
13 |
93,205,820 (GRCm39) |
missense |
probably benign |
0.41 |
R7624:Cmya5
|
UTSW |
13 |
93,226,865 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7637:Cmya5
|
UTSW |
13 |
93,219,720 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7673:Cmya5
|
UTSW |
13 |
93,230,629 (GRCm39) |
missense |
probably benign |
0.13 |
R7753:Cmya5
|
UTSW |
13 |
93,234,680 (GRCm39) |
missense |
probably benign |
0.18 |
R7757:Cmya5
|
UTSW |
13 |
93,234,780 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7806:Cmya5
|
UTSW |
13 |
93,230,770 (GRCm39) |
missense |
probably benign |
0.00 |
R7825:Cmya5
|
UTSW |
13 |
93,234,136 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7878:Cmya5
|
UTSW |
13 |
93,226,265 (GRCm39) |
missense |
probably damaging |
0.98 |
R7892:Cmya5
|
UTSW |
13 |
93,232,865 (GRCm39) |
missense |
probably damaging |
0.96 |
R7952:Cmya5
|
UTSW |
13 |
93,233,512 (GRCm39) |
small deletion |
probably benign |
|
R8127:Cmya5
|
UTSW |
13 |
93,231,122 (GRCm39) |
missense |
probably damaging |
0.99 |
R8256:Cmya5
|
UTSW |
13 |
93,229,986 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8339:Cmya5
|
UTSW |
13 |
93,228,142 (GRCm39) |
nonsense |
probably null |
|
R8446:Cmya5
|
UTSW |
13 |
93,230,336 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8553:Cmya5
|
UTSW |
13 |
93,230,304 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Cmya5
|
UTSW |
13 |
93,231,888 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8748:Cmya5
|
UTSW |
13 |
93,226,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8783:Cmya5
|
UTSW |
13 |
93,225,888 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8803:Cmya5
|
UTSW |
13 |
93,177,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Cmya5
|
UTSW |
13 |
93,200,048 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8937:Cmya5
|
UTSW |
13 |
93,232,840 (GRCm39) |
missense |
probably benign |
0.01 |
R8985:Cmya5
|
UTSW |
13 |
93,233,664 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9017:Cmya5
|
UTSW |
13 |
93,228,572 (GRCm39) |
missense |
probably benign |
0.03 |
R9087:Cmya5
|
UTSW |
13 |
93,233,711 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9133:Cmya5
|
UTSW |
13 |
93,234,108 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9156:Cmya5
|
UTSW |
13 |
93,233,878 (GRCm39) |
missense |
unknown |
|
R9209:Cmya5
|
UTSW |
13 |
93,226,866 (GRCm39) |
missense |
probably benign |
0.45 |
R9222:Cmya5
|
UTSW |
13 |
93,230,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9229:Cmya5
|
UTSW |
13 |
93,232,176 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9382:Cmya5
|
UTSW |
13 |
93,229,884 (GRCm39) |
missense |
probably benign |
|
R9385:Cmya5
|
UTSW |
13 |
93,230,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R9418:Cmya5
|
UTSW |
13 |
93,226,209 (GRCm39) |
missense |
probably benign |
0.22 |
R9452:Cmya5
|
UTSW |
13 |
93,232,394 (GRCm39) |
missense |
probably benign |
|
R9492:Cmya5
|
UTSW |
13 |
93,177,822 (GRCm39) |
makesense |
probably null |
|
R9600:Cmya5
|
UTSW |
13 |
93,226,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9712:Cmya5
|
UTSW |
13 |
93,201,881 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9742:Cmya5
|
UTSW |
13 |
93,231,935 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF020:Cmya5
|
UTSW |
13 |
93,205,799 (GRCm39) |
missense |
possibly damaging |
0.56 |
X0028:Cmya5
|
UTSW |
13 |
93,233,195 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1088:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
Z1176:Cmya5
|
UTSW |
13 |
93,233,298 (GRCm39) |
missense |
unknown |
|
Z1176:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
Z1177:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
|