Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
T |
C |
3: 36,128,525 (GRCm39) |
Y129H |
probably damaging |
Het |
Adcy4 |
C |
T |
14: 56,016,486 (GRCm39) |
D322N |
probably damaging |
Het |
Adgre1 |
G |
A |
17: 57,748,321 (GRCm39) |
G507E |
probably damaging |
Het |
Agpat5 |
G |
A |
8: 18,918,971 (GRCm39) |
V118I |
probably benign |
Het |
Aif1 |
T |
C |
17: 35,390,074 (GRCm39) |
|
probably null |
Het |
Akr1c6 |
A |
T |
13: 4,488,608 (GRCm39) |
|
probably null |
Het |
Akt2 |
T |
A |
7: 27,337,597 (GRCm39) |
|
probably null |
Het |
Ankrd35 |
T |
A |
3: 96,590,989 (GRCm39) |
L425Q |
possibly damaging |
Het |
Arhgap40 |
A |
G |
2: 158,385,326 (GRCm39) |
T520A |
possibly damaging |
Het |
Arhgef28 |
T |
A |
13: 98,066,062 (GRCm39) |
D1597V |
possibly damaging |
Het |
Aspm |
A |
G |
1: 139,399,472 (GRCm39) |
D1079G |
probably benign |
Het |
Atp1a2 |
A |
T |
1: 172,119,009 (GRCm39) |
|
probably benign |
Het |
Cage1 |
C |
A |
13: 38,207,406 (GRCm39) |
E252D |
possibly damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,582 (GRCm39) |
S36P |
possibly damaging |
Het |
Cd300a |
T |
C |
11: 114,784,247 (GRCm39) |
V85A |
probably damaging |
Het |
Cd38 |
A |
C |
5: 44,064,887 (GRCm39) |
D235A |
possibly damaging |
Het |
Cdcp1 |
T |
C |
9: 123,009,088 (GRCm39) |
K530R |
probably benign |
Het |
Ceacam20 |
T |
A |
7: 19,705,651 (GRCm39) |
L214Q |
probably damaging |
Het |
Cntn4 |
G |
A |
6: 106,502,379 (GRCm39) |
A379T |
probably benign |
Het |
Col4a2 |
A |
T |
8: 11,479,505 (GRCm39) |
E796V |
probably benign |
Het |
Copa |
A |
G |
1: 171,910,453 (GRCm39) |
|
probably benign |
Het |
Cpa5 |
A |
G |
6: 30,631,363 (GRCm39) |
T426A |
possibly damaging |
Het |
Csmd1 |
A |
G |
8: 16,249,931 (GRCm39) |
F1016L |
probably damaging |
Het |
Cyb5r3 |
A |
T |
15: 83,042,822 (GRCm39) |
L290* |
probably null |
Het |
Ddx42 |
A |
G |
11: 106,133,766 (GRCm39) |
T581A |
probably damaging |
Het |
Deaf1 |
C |
T |
7: 140,902,381 (GRCm39) |
G221S |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,165,366 (GRCm39) |
S580P |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,754,017 (GRCm39) |
E1598G |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,350,262 (GRCm39) |
|
probably benign |
Het |
Eif3f |
C |
A |
7: 108,533,847 (GRCm39) |
|
probably benign |
Het |
Fam184a |
G |
T |
10: 53,574,901 (GRCm39) |
T236K |
probably benign |
Het |
Gas7 |
C |
T |
11: 67,550,876 (GRCm39) |
T126M |
possibly damaging |
Het |
Gckr |
T |
G |
5: 31,465,608 (GRCm39) |
F408C |
probably damaging |
Het |
Gm17472 |
A |
G |
6: 42,958,004 (GRCm39) |
D91G |
probably damaging |
Het |
Gm5117 |
G |
A |
8: 32,228,608 (GRCm39) |
|
noncoding transcript |
Het |
Gsto1 |
T |
A |
19: 47,843,759 (GRCm39) |
I47N |
probably damaging |
Het |
Hck |
C |
T |
2: 152,976,597 (GRCm39) |
P244S |
probably damaging |
Het |
Hif3a |
T |
C |
7: 16,784,490 (GRCm39) |
T250A |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,752,111 (GRCm39) |
|
probably benign |
Het |
Impa1 |
G |
A |
3: 10,380,340 (GRCm39) |
S247F |
probably damaging |
Het |
Ints14 |
G |
C |
9: 64,889,340 (GRCm39) |
R397P |
probably damaging |
Het |
Iqgap1 |
T |
C |
7: 80,373,524 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
C |
15: 101,722,377 (GRCm39) |
K436R |
probably damaging |
Het |
Lama3 |
G |
A |
18: 12,581,362 (GRCm39) |
C607Y |
probably damaging |
Het |
Loxl4 |
G |
T |
19: 42,599,133 (GRCm39) |
|
probably benign |
Het |
Lrrc8d |
C |
T |
5: 105,961,234 (GRCm39) |
T548M |
probably damaging |
Het |
Man1b1 |
T |
A |
2: 25,228,196 (GRCm39) |
D155E |
probably damaging |
Het |
Mapk8ip2 |
C |
T |
15: 89,341,431 (GRCm39) |
P214L |
probably benign |
Het |
Mast1 |
G |
A |
8: 85,645,357 (GRCm39) |
T696I |
probably damaging |
Het |
Muc15 |
C |
T |
2: 110,561,617 (GRCm39) |
P18S |
probably damaging |
Het |
Mybl2 |
T |
C |
2: 162,922,716 (GRCm39) |
S205P |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,809,331 (GRCm39) |
S1763P |
probably damaging |
Het |
Nek10 |
T |
A |
14: 14,860,986 (GRCm38) |
L513M |
possibly damaging |
Het |
Nfib |
A |
G |
4: 82,271,808 (GRCm39) |
M252T |
probably benign |
Het |
Nid2 |
C |
A |
14: 19,828,146 (GRCm39) |
Y261* |
probably null |
Het |
Nmd3 |
C |
T |
3: 69,638,970 (GRCm39) |
R187C |
possibly damaging |
Het |
Nomo1 |
G |
T |
7: 45,700,155 (GRCm39) |
|
probably benign |
Het |
Npy4r |
A |
G |
14: 33,868,437 (GRCm39) |
F284L |
probably damaging |
Het |
Nt5dc2 |
T |
C |
14: 30,860,878 (GRCm39) |
V351A |
possibly damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or5b121 |
T |
A |
19: 13,507,178 (GRCm39) |
L91Q |
probably null |
Het |
Or5g27 |
T |
A |
2: 85,410,069 (GRCm39) |
L162* |
probably null |
Het |
Pcdhb12 |
T |
A |
18: 37,569,209 (GRCm39) |
D118E |
probably damaging |
Het |
Pdcd11 |
C |
T |
19: 47,116,404 (GRCm39) |
T1518I |
probably benign |
Het |
Pde6a |
T |
A |
18: 61,364,434 (GRCm39) |
C163* |
probably null |
Het |
Pign |
A |
T |
1: 105,572,227 (GRCm39) |
W314R |
probably benign |
Het |
Pip5k1b |
T |
A |
19: 24,367,799 (GRCm39) |
H76L |
probably damaging |
Het |
Plcz1 |
T |
C |
6: 139,974,277 (GRCm39) |
N55S |
possibly damaging |
Het |
Pou5f1 |
A |
T |
17: 35,821,438 (GRCm39) |
H350L |
possibly damaging |
Het |
Rchy1 |
A |
T |
5: 92,110,487 (GRCm39) |
|
probably null |
Het |
Ric8b |
A |
G |
10: 84,793,946 (GRCm39) |
T270A |
possibly damaging |
Het |
Rprml |
A |
G |
11: 103,540,644 (GRCm39) |
E13G |
probably benign |
Het |
Secisbp2 |
T |
A |
13: 51,836,063 (GRCm39) |
I719N |
probably damaging |
Het |
Sergef |
C |
T |
7: 46,283,259 (GRCm39) |
R148H |
probably benign |
Het |
Serpina6 |
T |
A |
12: 103,618,221 (GRCm39) |
|
probably null |
Het |
Sirpb1b |
C |
A |
3: 15,613,887 (GRCm39) |
W65L |
probably damaging |
Het |
Slc32a1 |
A |
T |
2: 158,455,977 (GRCm39) |
I211F |
possibly damaging |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Smarce1 |
A |
G |
11: 99,105,977 (GRCm39) |
V226A |
probably benign |
Het |
Spata31d1b |
A |
T |
13: 59,864,097 (GRCm39) |
E415V |
probably damaging |
Het |
Suclg2 |
A |
C |
6: 95,543,417 (GRCm39) |
V338G |
probably damaging |
Het |
Tarbp1 |
T |
C |
8: 127,174,184 (GRCm39) |
E874G |
possibly damaging |
Het |
Tex14 |
G |
T |
11: 87,427,727 (GRCm39) |
|
probably null |
Het |
Trim36 |
T |
A |
18: 46,329,245 (GRCm39) |
D53V |
possibly damaging |
Het |
Tsga10ip |
T |
A |
19: 5,444,368 (GRCm39) |
Y21F |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,620,289 (GRCm39) |
V15849M |
probably damaging |
Het |
Ube3b |
T |
C |
5: 114,539,471 (GRCm39) |
S421P |
probably benign |
Het |
Unc5a |
A |
T |
13: 55,147,683 (GRCm39) |
M498L |
probably benign |
Het |
Vipr2 |
A |
G |
12: 116,107,876 (GRCm39) |
I420M |
probably benign |
Het |
Vmn1r179 |
T |
A |
7: 23,628,515 (GRCm39) |
H235Q |
probably damaging |
Het |
Vps35 |
T |
A |
8: 86,008,475 (GRCm39) |
I267F |
probably damaging |
Het |
Wdr26 |
G |
A |
1: 181,025,216 (GRCm39) |
R279W |
probably damaging |
Het |
Xpo6 |
C |
A |
7: 125,768,443 (GRCm39) |
R88L |
probably damaging |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp105 |
T |
A |
9: 122,758,880 (GRCm39) |
S184T |
probably benign |
Het |
Zfp574 |
G |
A |
7: 24,780,388 (GRCm39) |
R470H |
probably damaging |
Het |
Zswim9 |
T |
A |
7: 13,003,484 (GRCm39) |
H122L |
probably damaging |
Het |
|
Other mutations in Speg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:Speg
|
APN |
1 |
75,387,034 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00979:Speg
|
APN |
1 |
75,387,378 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01122:Speg
|
APN |
1 |
75,386,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Speg
|
APN |
1 |
75,364,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01304:Speg
|
APN |
1 |
75,404,841 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01351:Speg
|
APN |
1 |
75,387,920 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Speg
|
APN |
1 |
75,404,929 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01477:Speg
|
APN |
1 |
75,368,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Speg
|
APN |
1 |
75,364,471 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Speg
|
APN |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01959:Speg
|
APN |
1 |
75,367,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Speg
|
APN |
1 |
75,400,031 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02362:Speg
|
APN |
1 |
75,400,559 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03013:Speg
|
APN |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03168:Speg
|
APN |
1 |
75,364,831 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Speg
|
UTSW |
1 |
75,392,241 (GRCm39) |
missense |
probably benign |
0.39 |
R0112:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0311:Speg
|
UTSW |
1 |
75,407,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Speg
|
UTSW |
1 |
75,391,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0393:Speg
|
UTSW |
1 |
75,400,568 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0403:Speg
|
UTSW |
1 |
75,407,428 (GRCm39) |
splice site |
probably benign |
|
R0483:Speg
|
UTSW |
1 |
75,361,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0648:Speg
|
UTSW |
1 |
75,404,622 (GRCm39) |
missense |
probably benign |
|
R0683:Speg
|
UTSW |
1 |
75,405,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Speg
|
UTSW |
1 |
75,400,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Speg
|
UTSW |
1 |
75,392,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0835:Speg
|
UTSW |
1 |
75,352,318 (GRCm39) |
missense |
probably benign |
0.00 |
R0866:Speg
|
UTSW |
1 |
75,393,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R0880:Speg
|
UTSW |
1 |
75,381,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Speg
|
UTSW |
1 |
75,391,782 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1140:Speg
|
UTSW |
1 |
75,405,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Speg
|
UTSW |
1 |
75,403,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1301:Speg
|
UTSW |
1 |
75,378,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1348:Speg
|
UTSW |
1 |
75,399,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R1388:Speg
|
UTSW |
1 |
75,407,104 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Speg
|
UTSW |
1 |
75,405,128 (GRCm39) |
splice site |
probably benign |
|
R1505:Speg
|
UTSW |
1 |
75,352,186 (GRCm39) |
missense |
probably benign |
0.02 |
R1506:Speg
|
UTSW |
1 |
75,394,307 (GRCm39) |
missense |
probably benign |
0.03 |
R1531:Speg
|
UTSW |
1 |
75,377,866 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1543:Speg
|
UTSW |
1 |
75,398,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R1567:Speg
|
UTSW |
1 |
75,404,691 (GRCm39) |
missense |
probably benign |
|
R1630:Speg
|
UTSW |
1 |
75,399,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Speg
|
UTSW |
1 |
75,387,193 (GRCm39) |
splice site |
probably benign |
|
R1673:Speg
|
UTSW |
1 |
75,387,807 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1718:Speg
|
UTSW |
1 |
75,398,388 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1718:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Speg
|
UTSW |
1 |
75,394,507 (GRCm39) |
missense |
probably benign |
0.00 |
R1759:Speg
|
UTSW |
1 |
75,377,806 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1861:Speg
|
UTSW |
1 |
75,365,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Speg
|
UTSW |
1 |
75,400,550 (GRCm39) |
missense |
probably benign |
|
R1936:Speg
|
UTSW |
1 |
75,408,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2192:Speg
|
UTSW |
1 |
75,394,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R2204:Speg
|
UTSW |
1 |
75,407,121 (GRCm39) |
missense |
probably benign |
0.30 |
R2287:Speg
|
UTSW |
1 |
75,407,109 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2696:Speg
|
UTSW |
1 |
75,383,570 (GRCm39) |
missense |
probably benign |
0.27 |
R2983:Speg
|
UTSW |
1 |
75,361,574 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3110:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3112:Speg
|
UTSW |
1 |
75,399,326 (GRCm39) |
nonsense |
probably null |
|
R3154:Speg
|
UTSW |
1 |
75,378,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3720:Speg
|
UTSW |
1 |
75,403,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Speg
|
UTSW |
1 |
75,399,191 (GRCm39) |
missense |
probably benign |
0.27 |
R4133:Speg
|
UTSW |
1 |
75,404,548 (GRCm39) |
missense |
probably benign |
|
R4522:Speg
|
UTSW |
1 |
75,404,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R4564:Speg
|
UTSW |
1 |
75,368,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4577:Speg
|
UTSW |
1 |
75,392,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Speg
|
UTSW |
1 |
75,398,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Speg
|
UTSW |
1 |
75,404,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Speg
|
UTSW |
1 |
75,364,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5152:Speg
|
UTSW |
1 |
75,404,742 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5156:Speg
|
UTSW |
1 |
75,404,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R5371:Speg
|
UTSW |
1 |
75,408,037 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5550:Speg
|
UTSW |
1 |
75,405,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5562:Speg
|
UTSW |
1 |
75,403,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Speg
|
UTSW |
1 |
75,395,773 (GRCm39) |
splice site |
probably null |
|
R5985:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6004:Speg
|
UTSW |
1 |
75,392,247 (GRCm39) |
nonsense |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,395,103 (GRCm39) |
critical splice donor site |
probably null |
|
R6143:Speg
|
UTSW |
1 |
75,391,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Speg
|
UTSW |
1 |
75,383,323 (GRCm39) |
nonsense |
probably null |
|
R6347:Speg
|
UTSW |
1 |
75,403,519 (GRCm39) |
missense |
probably benign |
0.00 |
R6453:Speg
|
UTSW |
1 |
75,394,616 (GRCm39) |
missense |
probably benign |
0.06 |
R6505:Speg
|
UTSW |
1 |
75,406,167 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6505:Speg
|
UTSW |
1 |
75,383,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6531:Speg
|
UTSW |
1 |
75,399,401 (GRCm39) |
missense |
probably benign |
0.03 |
R6566:Speg
|
UTSW |
1 |
75,365,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Speg
|
UTSW |
1 |
75,387,039 (GRCm39) |
critical splice donor site |
probably null |
|
R6819:Speg
|
UTSW |
1 |
75,368,456 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6821:Speg
|
UTSW |
1 |
75,394,547 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6919:Speg
|
UTSW |
1 |
75,364,552 (GRCm39) |
nonsense |
probably null |
|
R6981:Speg
|
UTSW |
1 |
75,407,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Speg
|
UTSW |
1 |
75,399,912 (GRCm39) |
missense |
probably damaging |
0.98 |
R7082:Speg
|
UTSW |
1 |
75,388,091 (GRCm39) |
missense |
probably damaging |
0.96 |
R7140:Speg
|
UTSW |
1 |
75,383,414 (GRCm39) |
critical splice donor site |
probably null |
|
R7175:Speg
|
UTSW |
1 |
75,399,134 (GRCm39) |
missense |
probably benign |
0.01 |
R7178:Speg
|
UTSW |
1 |
75,399,027 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7345:Speg
|
UTSW |
1 |
75,361,479 (GRCm39) |
missense |
probably damaging |
0.97 |
R7420:Speg
|
UTSW |
1 |
75,407,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R7537:Speg
|
UTSW |
1 |
75,378,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7562:Speg
|
UTSW |
1 |
75,407,923 (GRCm39) |
missense |
probably damaging |
0.97 |
R7615:Speg
|
UTSW |
1 |
75,405,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Speg
|
UTSW |
1 |
75,382,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Speg
|
UTSW |
1 |
75,377,834 (GRCm39) |
missense |
probably benign |
0.04 |
R7696:Speg
|
UTSW |
1 |
75,405,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Speg
|
UTSW |
1 |
75,352,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Speg
|
UTSW |
1 |
75,365,514 (GRCm39) |
missense |
probably benign |
0.00 |
R7824:Speg
|
UTSW |
1 |
75,360,661 (GRCm39) |
splice site |
probably null |
|
R7834:Speg
|
UTSW |
1 |
75,361,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Speg
|
UTSW |
1 |
75,403,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R8015:Speg
|
UTSW |
1 |
75,392,065 (GRCm39) |
splice site |
probably benign |
|
R8068:Speg
|
UTSW |
1 |
75,398,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Speg
|
UTSW |
1 |
75,391,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8130:Speg
|
UTSW |
1 |
75,392,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R8132:Speg
|
UTSW |
1 |
75,399,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R8239:Speg
|
UTSW |
1 |
75,395,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8287:Speg
|
UTSW |
1 |
75,398,880 (GRCm39) |
missense |
probably benign |
0.26 |
R8299:Speg
|
UTSW |
1 |
75,364,480 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8441:Speg
|
UTSW |
1 |
75,387,976 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8468:Speg
|
UTSW |
1 |
75,407,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Speg
|
UTSW |
1 |
75,378,908 (GRCm39) |
splice site |
probably null |
|
R8781:Speg
|
UTSW |
1 |
75,383,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8784:Speg
|
UTSW |
1 |
75,381,793 (GRCm39) |
critical splice donor site |
probably benign |
|
R8848:Speg
|
UTSW |
1 |
75,404,082 (GRCm39) |
critical splice donor site |
probably null |
|
R8881:Speg
|
UTSW |
1 |
75,377,795 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8898:Speg
|
UTSW |
1 |
75,365,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:Speg
|
UTSW |
1 |
75,399,250 (GRCm39) |
missense |
probably benign |
0.30 |
R9019:Speg
|
UTSW |
1 |
75,405,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9027:Speg
|
UTSW |
1 |
75,365,076 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9066:Speg
|
UTSW |
1 |
75,361,654 (GRCm39) |
missense |
probably damaging |
0.99 |
R9092:Speg
|
UTSW |
1 |
75,399,378 (GRCm39) |
missense |
probably benign |
0.01 |
R9117:Speg
|
UTSW |
1 |
75,364,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9202:Speg
|
UTSW |
1 |
75,367,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Speg
|
UTSW |
1 |
75,361,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Speg
|
UTSW |
1 |
75,398,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Speg
|
UTSW |
1 |
75,394,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R9452:Speg
|
UTSW |
1 |
75,399,152 (GRCm39) |
missense |
probably benign |
|
R9475:Speg
|
UTSW |
1 |
75,364,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R9476:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9510:Speg
|
UTSW |
1 |
75,377,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9519:Speg
|
UTSW |
1 |
75,392,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9528:Speg
|
UTSW |
1 |
75,364,447 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9542:Speg
|
UTSW |
1 |
75,399,426 (GRCm39) |
missense |
probably benign |
0.08 |
R9553:Speg
|
UTSW |
1 |
75,394,645 (GRCm39) |
missense |
probably benign |
0.00 |
R9767:Speg
|
UTSW |
1 |
75,403,825 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9768:Speg
|
UTSW |
1 |
75,395,617 (GRCm39) |
nonsense |
probably null |
|
R9800:Speg
|
UTSW |
1 |
75,399,358 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Speg
|
UTSW |
1 |
75,399,101 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Speg
|
UTSW |
1 |
75,400,119 (GRCm39) |
missense |
possibly damaging |
0.88 |
Z1176:Speg
|
UTSW |
1 |
75,383,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,404,327 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,407,099 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Speg
|
UTSW |
1 |
75,405,025 (GRCm39) |
missense |
probably damaging |
1.00 |
|