Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933402N03Rik |
G |
T |
7: 130,747,859 (GRCm39) |
N44K |
probably benign |
Het |
Acd |
C |
A |
8: 106,425,524 (GRCm39) |
A270S |
possibly damaging |
Het |
Acnat1 |
G |
A |
4: 49,451,042 (GRCm39) |
T23I |
probably benign |
Het |
Adam26a |
T |
G |
8: 44,023,226 (GRCm39) |
E88A |
possibly damaging |
Het |
Adgrb1 |
G |
A |
15: 74,413,676 (GRCm39) |
V589M |
probably benign |
Het |
Agbl2 |
T |
A |
2: 90,646,720 (GRCm39) |
|
probably benign |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Amh |
AGCGCCTTGG |
AG |
10: 80,641,419 (GRCm39) |
|
probably null |
Het |
Asap2 |
T |
C |
12: 21,253,999 (GRCm39) |
L170P |
probably damaging |
Het |
Btg2 |
T |
C |
1: 134,006,769 (GRCm39) |
D8G |
probably benign |
Het |
Cacna1g |
A |
T |
11: 94,334,118 (GRCm39) |
V841E |
probably damaging |
Het |
Cacna2d1 |
C |
T |
5: 16,469,286 (GRCm39) |
P230L |
probably benign |
Het |
Cacna2d2 |
A |
T |
9: 107,401,843 (GRCm39) |
D766V |
probably damaging |
Het |
Carns1 |
A |
G |
19: 4,223,156 (GRCm39) |
W23R |
possibly damaging |
Het |
Cdk11b |
T |
A |
4: 155,713,137 (GRCm39) |
|
probably null |
Het |
Chrna3 |
T |
C |
9: 54,923,341 (GRCm39) |
S156G |
probably damaging |
Het |
Cpne7 |
C |
A |
8: 123,861,263 (GRCm39) |
P541T |
probably damaging |
Het |
Cracd |
A |
G |
5: 77,005,522 (GRCm39) |
I628V |
unknown |
Het |
Csmd1 |
A |
T |
8: 15,967,303 (GRCm39) |
L3187I |
probably damaging |
Het |
Dbt |
A |
G |
3: 116,339,943 (GRCm39) |
I404V |
probably benign |
Het |
Dgki |
A |
T |
6: 36,893,369 (GRCm39) |
I819K |
probably damaging |
Het |
Dip2b |
T |
A |
15: 100,076,347 (GRCm39) |
S782T |
probably benign |
Het |
Dlc1 |
A |
T |
8: 37,325,244 (GRCm39) |
|
probably null |
Het |
Dnajc13 |
A |
T |
9: 104,098,676 (GRCm39) |
V459E |
probably damaging |
Het |
Enam |
A |
G |
5: 88,651,086 (GRCm39) |
E790G |
probably damaging |
Het |
Epb41l4a |
G |
C |
18: 33,961,261 (GRCm39) |
Y424* |
probably null |
Het |
Extl1 |
A |
G |
4: 134,089,999 (GRCm39) |
S370P |
probably benign |
Het |
Fan1 |
T |
C |
7: 64,022,761 (GRCm39) |
Y164C |
probably benign |
Het |
Fbxw15 |
G |
A |
9: 109,387,314 (GRCm39) |
S227F |
probably damaging |
Het |
Fbxw25 |
A |
T |
9: 109,479,141 (GRCm39) |
I370N |
probably benign |
Het |
Fcgbp |
T |
A |
7: 27,792,868 (GRCm39) |
Y957* |
probably null |
Het |
Gkap1 |
C |
A |
13: 58,384,857 (GRCm39) |
E77* |
probably null |
Het |
Gkn1 |
A |
T |
6: 87,326,105 (GRCm39) |
N28K |
unknown |
Het |
Gls2 |
A |
G |
10: 128,037,194 (GRCm39) |
E245G |
probably damaging |
Het |
Glyat |
G |
A |
19: 12,623,679 (GRCm39) |
V32I |
probably benign |
Het |
Gm2431 |
A |
T |
7: 141,811,762 (GRCm39) |
C47* |
probably null |
Het |
Gm5431 |
T |
C |
11: 48,785,658 (GRCm39) |
D239G |
probably benign |
Het |
Ift70a1 |
C |
T |
2: 75,810,599 (GRCm39) |
V495I |
probably benign |
Het |
Inpp5d |
T |
C |
1: 87,626,803 (GRCm39) |
F540L |
probably damaging |
Het |
Kcna1 |
A |
C |
6: 126,619,771 (GRCm39) |
I183S |
probably benign |
Het |
Kpna2 |
G |
T |
11: 106,882,271 (GRCm39) |
L212I |
probably damaging |
Het |
Krt36 |
C |
G |
11: 99,994,884 (GRCm39) |
R229S |
probably benign |
Het |
Krt78 |
G |
A |
15: 101,854,812 (GRCm39) |
H1000Y |
probably benign |
Het |
Krt90 |
A |
G |
15: 101,461,800 (GRCm39) |
|
probably benign |
Het |
Ldlrad4 |
C |
A |
18: 68,239,758 (GRCm39) |
F59L |
probably benign |
Het |
Lrrc3b |
T |
C |
14: 15,358,601 (GRCm38) |
N2D |
probably benign |
Het |
Madd |
T |
C |
2: 90,998,236 (GRCm39) |
D239G |
probably damaging |
Het |
Mapk8ip3 |
C |
T |
17: 25,133,433 (GRCm39) |
G332S |
probably null |
Het |
Mastl |
A |
T |
2: 23,036,093 (GRCm39) |
L141* |
probably null |
Het |
Mdh1b |
T |
C |
1: 63,758,681 (GRCm39) |
N304D |
probably benign |
Het |
Mfsd4b3-ps |
G |
T |
10: 39,823,929 (GRCm39) |
N110K |
probably benign |
Het |
Mtus2 |
T |
C |
5: 148,214,443 (GRCm39) |
S1035P |
probably damaging |
Het |
Muc21 |
T |
A |
17: 35,931,940 (GRCm39) |
|
probably benign |
Het |
Myh11 |
T |
A |
16: 14,018,622 (GRCm39) |
D1908V |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,033,654 (GRCm39) |
E1080G |
probably damaging |
Het |
Mypn |
A |
C |
10: 62,971,976 (GRCm39) |
M688R |
probably benign |
Het |
Nat8l |
G |
T |
5: 34,158,130 (GRCm39) |
C180F |
probably damaging |
Het |
Nip7 |
T |
A |
8: 107,784,018 (GRCm39) |
L86Q |
probably damaging |
Het |
Nisch |
C |
T |
14: 30,896,839 (GRCm39) |
|
probably benign |
Het |
Nop2 |
A |
G |
6: 125,114,601 (GRCm39) |
I283V |
probably benign |
Het |
Oas1h |
T |
A |
5: 121,009,840 (GRCm39) |
|
probably null |
Het |
Or10ag56 |
T |
C |
2: 87,139,196 (GRCm39) |
V41A |
probably benign |
Het |
Or2g25 |
A |
C |
17: 37,970,564 (GRCm39) |
I220S |
probably damaging |
Het |
Or4c101 |
C |
A |
2: 88,390,402 (GRCm39) |
D185E |
possibly damaging |
Het |
Or4c104 |
T |
C |
2: 88,586,117 (GRCm39) |
R301G |
probably benign |
Het |
Or56b1b |
A |
T |
7: 108,164,564 (GRCm39) |
L146* |
probably null |
Het |
Or5w17 |
T |
A |
2: 87,583,530 (GRCm39) |
D269V |
probably damaging |
Het |
Or8b42 |
T |
A |
9: 38,341,986 (GRCm39) |
M136K |
probably damaging |
Het |
P4hb |
A |
G |
11: 120,453,546 (GRCm39) |
V373A |
probably damaging |
Het |
Pappa2 |
C |
A |
1: 158,590,720 (GRCm39) |
E1645* |
probably null |
Het |
Pcdh10 |
G |
T |
3: 45,336,316 (GRCm39) |
E877* |
probably null |
Het |
Pcdhb17 |
C |
T |
18: 37,618,764 (GRCm39) |
R185C |
probably damaging |
Het |
Pcdhb17 |
A |
G |
18: 37,620,070 (GRCm39) |
H620R |
possibly damaging |
Het |
Pdcl3 |
T |
A |
1: 39,034,946 (GRCm39) |
F168I |
probably damaging |
Het |
Pde4a |
T |
A |
9: 21,114,528 (GRCm39) |
I365N |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,385,950 (GRCm39) |
V940A |
probably damaging |
Het |
Picalm |
T |
A |
7: 89,840,390 (GRCm39) |
S399T |
possibly damaging |
Het |
Pigk |
A |
T |
3: 152,450,101 (GRCm39) |
I249F |
probably damaging |
Het |
Plxnb1 |
C |
A |
9: 108,940,836 (GRCm39) |
H1570Q |
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,635,359 (GRCm39) |
Y1321H |
probably damaging |
Het |
Ppm1g |
G |
A |
5: 31,363,560 (GRCm39) |
S114F |
probably damaging |
Het |
Rassf4 |
A |
G |
6: 116,617,228 (GRCm39) |
M259T |
probably damaging |
Het |
Rbm47 |
T |
C |
5: 66,176,653 (GRCm39) |
K557E |
possibly damaging |
Het |
Rhobtb1 |
A |
G |
10: 69,115,236 (GRCm39) |
K21R |
probably damaging |
Het |
Selenoi |
T |
C |
5: 30,462,771 (GRCm39) |
F212S |
probably benign |
Het |
Shc3 |
T |
G |
13: 51,603,328 (GRCm39) |
Y259S |
probably damaging |
Het |
Skic3 |
T |
A |
13: 76,288,720 (GRCm39) |
L951Q |
possibly damaging |
Het |
Slc11a2 |
T |
C |
15: 100,299,168 (GRCm39) |
N134S |
probably damaging |
Het |
Slc9a7 |
A |
T |
X: 20,028,717 (GRCm39) |
M368K |
probably damaging |
Het |
Slx4ip |
T |
A |
2: 136,888,669 (GRCm39) |
C117S |
probably damaging |
Het |
Spata31d1d |
T |
A |
13: 59,876,509 (GRCm39) |
Q342L |
probably benign |
Het |
Spink13 |
T |
A |
18: 62,740,820 (GRCm39) |
Y93F |
probably damaging |
Het |
St6galnac5 |
A |
T |
3: 152,551,958 (GRCm39) |
I203N |
possibly damaging |
Het |
Syne2 |
T |
A |
12: 76,099,579 (GRCm39) |
C5335S |
probably damaging |
Het |
Tagap |
T |
A |
17: 8,148,742 (GRCm39) |
D173E |
probably benign |
Het |
Tekt3 |
A |
C |
11: 62,960,867 (GRCm39) |
Y12S |
probably damaging |
Het |
Tmem81 |
T |
A |
1: 132,435,321 (GRCm39) |
N42K |
probably damaging |
Het |
Tnc |
A |
G |
4: 63,890,972 (GRCm39) |
W1728R |
probably damaging |
Het |
Ttc33 |
C |
T |
15: 5,241,579 (GRCm39) |
R135* |
probably null |
Het |
Unc5c |
A |
G |
3: 141,533,278 (GRCm39) |
D842G |
possibly damaging |
Het |
Usp43 |
A |
T |
11: 67,770,779 (GRCm39) |
H618Q |
probably damaging |
Het |
Vmn2r50 |
T |
G |
7: 9,786,915 (GRCm39) |
N64T |
possibly damaging |
Het |
Vmn2r53 |
T |
C |
7: 12,315,632 (GRCm39) |
Y729C |
probably damaging |
Het |
Vmn2r59 |
T |
A |
7: 41,695,251 (GRCm39) |
H387L |
possibly damaging |
Het |
Vstm2a |
G |
T |
11: 16,213,166 (GRCm39) |
V184F |
possibly damaging |
Het |
Wdr53 |
T |
G |
16: 32,070,935 (GRCm39) |
N93K |
probably damaging |
Het |
Wdr95 |
A |
G |
5: 149,505,351 (GRCm39) |
|
probably null |
Het |
Xpot |
A |
T |
10: 121,438,932 (GRCm39) |
|
probably null |
Het |
Xrcc5 |
C |
T |
1: 72,364,246 (GRCm39) |
Q233* |
probably null |
Het |
Zbtb18 |
T |
A |
1: 177,275,077 (GRCm39) |
C137S |
possibly damaging |
Het |
Zfp58 |
C |
A |
13: 67,639,598 (GRCm39) |
G298* |
probably null |
Het |
Zfp963 |
A |
G |
8: 70,196,100 (GRCm39) |
S118P |
possibly damaging |
Het |
Zmynd15 |
A |
T |
11: 70,353,393 (GRCm39) |
Q336L |
probably benign |
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 |
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 |
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 |
|
|