Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447C04Rik |
A |
T |
12: 72,956,502 (GRCm39) |
Y199* |
probably null |
Het |
Adhfe1 |
A |
T |
1: 9,637,029 (GRCm39) |
I394F |
probably benign |
Het |
Arhgap26 |
G |
T |
18: 39,379,893 (GRCm39) |
R485L |
probably damaging |
Het |
Atat1 |
T |
A |
17: 36,212,467 (GRCm39) |
N231I |
probably damaging |
Het |
B4galnt2 |
T |
C |
11: 95,760,100 (GRCm39) |
N309S |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,772,134 (GRCm39) |
F499I |
probably damaging |
Het |
Bcl9l |
A |
G |
9: 44,416,365 (GRCm39) |
D146G |
possibly damaging |
Het |
Bglap3 |
A |
T |
3: 88,283,671 (GRCm39) |
|
probably benign |
Het |
Bscl2 |
C |
A |
19: 8,825,344 (GRCm39) |
T376K |
probably benign |
Het |
Cercam |
A |
T |
2: 29,761,033 (GRCm39) |
|
probably null |
Het |
Clec4f |
C |
T |
6: 83,633,012 (GRCm39) |
M1I |
probably null |
Het |
Clec4n |
A |
T |
6: 123,209,066 (GRCm39) |
I14F |
probably benign |
Het |
Cog4 |
T |
A |
8: 111,578,915 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,352,856 (GRCm39) |
F1961L |
probably benign |
Het |
Cyp4a29 |
A |
T |
4: 115,104,196 (GRCm39) |
H88L |
probably benign |
Het |
Dhdh |
A |
G |
7: 45,128,530 (GRCm39) |
L216P |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,871,509 (GRCm39) |
F544S |
probably damaging |
Het |
Dthd1 |
C |
T |
5: 63,045,549 (GRCm39) |
T771I |
probably benign |
Het |
Emc10 |
A |
G |
7: 44,142,612 (GRCm39) |
|
probably null |
Het |
Fgg |
A |
T |
3: 82,920,072 (GRCm39) |
T284S |
probably benign |
Het |
Gask1a |
C |
T |
9: 121,794,784 (GRCm39) |
R313W |
probably damaging |
Het |
Gm3002 |
T |
A |
14: 3,824,737 (GRCm38) |
N24K |
probably damaging |
Het |
Gm8674 |
G |
A |
13: 50,056,034 (GRCm39) |
|
noncoding transcript |
Het |
Gpr63 |
G |
A |
4: 25,008,368 (GRCm39) |
W364* |
probably null |
Het |
Hcn4 |
C |
G |
9: 58,767,111 (GRCm39) |
P891A |
unknown |
Het |
Hcrtr1 |
A |
T |
4: 130,024,792 (GRCm39) |
F365I |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,244,176 (GRCm39) |
|
probably null |
Het |
Hoxc5 |
T |
A |
15: 102,923,786 (GRCm39) |
L194H |
probably damaging |
Het |
Ifna11 |
A |
G |
4: 88,738,287 (GRCm39) |
N31S |
probably null |
Het |
Ikbke |
GCC |
G |
1: 131,203,004 (GRCm39) |
|
probably null |
Het |
Iqgap2 |
A |
T |
13: 95,766,514 (GRCm39) |
D1496E |
probably benign |
Het |
Kif28 |
G |
T |
1: 179,536,007 (GRCm39) |
Q556K |
probably damaging |
Het |
Klhl42 |
C |
T |
6: 147,009,502 (GRCm39) |
T447I |
possibly damaging |
Het |
Lrp1b |
A |
C |
2: 41,678,986 (GRCm39) |
D35E |
probably damaging |
Het |
Lsm14b |
A |
G |
2: 179,675,692 (GRCm39) |
|
probably benign |
Het |
Map3k1 |
T |
C |
13: 111,909,272 (GRCm39) |
E226G |
probably damaging |
Het |
Map3k14 |
T |
A |
11: 103,130,357 (GRCm39) |
N187Y |
probably benign |
Het |
Mcm6 |
A |
T |
1: 128,263,586 (GRCm39) |
V645E |
probably damaging |
Het |
Mdh1b |
G |
T |
1: 63,759,022 (GRCm39) |
P190Q |
probably damaging |
Het |
Meiob |
T |
G |
17: 25,037,353 (GRCm39) |
L77R |
probably damaging |
Het |
Mrgpra3 |
A |
T |
7: 47,239,267 (GRCm39) |
F220I |
probably benign |
Het |
Mrtfa |
C |
A |
15: 80,929,476 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
A |
4: 148,575,817 (GRCm39) |
S1324T |
possibly damaging |
Het |
Myot |
T |
A |
18: 44,487,995 (GRCm39) |
D437E |
possibly damaging |
Het |
Ncoa6 |
G |
T |
2: 155,263,252 (GRCm39) |
T394K |
possibly damaging |
Het |
Nf1 |
T |
A |
11: 79,456,379 (GRCm39) |
|
probably null |
Het |
Nup210 |
T |
A |
6: 91,013,451 (GRCm39) |
T1190S |
possibly damaging |
Het |
Odf1 |
T |
A |
15: 38,226,652 (GRCm39) |
I184N |
probably damaging |
Het |
Or10d1 |
C |
T |
9: 39,484,054 (GRCm39) |
C167Y |
probably damaging |
Het |
Or13d1 |
T |
C |
4: 52,970,960 (GRCm39) |
V113A |
possibly damaging |
Het |
Or1n1b |
A |
G |
2: 36,780,719 (GRCm39) |
I47T |
probably damaging |
Het |
Or5k15 |
G |
T |
16: 58,709,957 (GRCm39) |
Q209K |
possibly damaging |
Het |
Padi1 |
A |
G |
4: 140,572,901 (GRCm39) |
V21A |
probably benign |
Het |
Pdzrn3 |
C |
T |
6: 101,128,551 (GRCm39) |
R705H |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,987,685 (GRCm39) |
I18V |
probably benign |
Het |
Pmpca |
T |
C |
2: 26,280,320 (GRCm39) |
S117P |
probably damaging |
Het |
Poteg |
T |
A |
8: 27,985,009 (GRCm39) |
|
probably benign |
Het |
Pramel32 |
T |
C |
4: 88,547,432 (GRCm39) |
T80A |
probably damaging |
Het |
Rab30 |
G |
A |
7: 92,478,771 (GRCm39) |
R72H |
probably damaging |
Het |
Ramp2 |
T |
A |
11: 101,138,383 (GRCm39) |
|
probably null |
Het |
Rbks |
G |
A |
5: 31,781,876 (GRCm39) |
T308I |
probably damaging |
Het |
Rnf112 |
A |
G |
11: 61,343,752 (GRCm39) |
|
probably benign |
Het |
Rnf38 |
G |
A |
4: 44,152,460 (GRCm39) |
P3S |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,302,883 (GRCm39) |
S2344P |
probably benign |
Het |
Slc16a8 |
C |
T |
15: 79,137,084 (GRCm39) |
V109M |
possibly damaging |
Het |
Slc28a1 |
A |
T |
7: 80,791,757 (GRCm39) |
T308S |
possibly damaging |
Het |
Slc39a3 |
T |
C |
10: 80,867,453 (GRCm39) |
T98A |
possibly damaging |
Het |
Smarcc2 |
T |
C |
10: 128,319,049 (GRCm39) |
F731L |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,925,572 (GRCm39) |
|
probably benign |
Het |
Sparcl1 |
T |
G |
5: 104,240,776 (GRCm39) |
D216A |
probably damaging |
Het |
Speg |
G |
A |
1: 75,364,513 (GRCm39) |
R192H |
probably damaging |
Het |
Sspo |
T |
C |
6: 48,441,539 (GRCm39) |
L1892P |
probably damaging |
Het |
Styxl2 |
A |
T |
1: 165,954,675 (GRCm39) |
V25E |
probably damaging |
Het |
Tacc2 |
A |
G |
7: 130,225,678 (GRCm39) |
N807D |
probably damaging |
Het |
Teddm1a |
A |
T |
1: 153,767,979 (GRCm39) |
K148* |
probably null |
Het |
Tex15 |
T |
A |
8: 34,064,498 (GRCm39) |
D1309E |
probably benign |
Het |
Thbs1 |
A |
T |
2: 117,945,259 (GRCm39) |
E277D |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,310,158 (GRCm39) |
R24Q |
probably damaging |
Het |
Tigd4 |
A |
G |
3: 84,502,460 (GRCm39) |
E459G |
probably benign |
Het |
Tln2 |
C |
A |
9: 67,262,407 (GRCm39) |
A615S |
probably damaging |
Het |
Tmprss5 |
T |
C |
9: 49,026,817 (GRCm39) |
V410A |
probably damaging |
Het |
Tnrc6a |
G |
T |
7: 122,789,095 (GRCm39) |
W1638L |
probably damaging |
Het |
Tpr |
A |
G |
1: 150,285,810 (GRCm39) |
D424G |
probably damaging |
Het |
Trim34a |
A |
T |
7: 103,910,271 (GRCm39) |
K358* |
probably null |
Het |
Tssk5 |
T |
A |
15: 76,258,856 (GRCm39) |
D10V |
possibly damaging |
Het |
Usp35 |
A |
C |
7: 96,962,782 (GRCm39) |
L470R |
probably damaging |
Het |
Usp42 |
T |
C |
5: 143,701,119 (GRCm39) |
D968G |
possibly damaging |
Het |
Utrn |
A |
G |
10: 12,331,164 (GRCm39) |
V2924A |
probably damaging |
Het |
Wdtc1 |
C |
A |
4: 133,021,654 (GRCm39) |
A627S |
probably damaging |
Het |
Xrra1 |
A |
G |
7: 99,555,730 (GRCm39) |
T366A |
probably damaging |
Het |
Zfp712 |
T |
A |
13: 67,188,773 (GRCm39) |
K585* |
probably null |
Het |
Zfp97 |
T |
A |
17: 17,365,393 (GRCm39) |
N297K |
probably damaging |
Het |
Zfp97 |
G |
T |
17: 17,364,938 (GRCm39) |
E146* |
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 |
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 |
R7088:Cmya5
|
UTSW |
13 |
93,228,372 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
|
|