Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
G |
T |
13: 77,245,370 (GRCm38) |
|
probably benign |
Het |
Acot3 |
T |
G |
12: 84,053,943 (GRCm38) |
|
probably null |
Het |
Acox1 |
A |
T |
11: 116,174,682 (GRCm38) |
C523* |
probably null |
Het |
Adamts19 |
G |
A |
18: 58,972,825 (GRCm38) |
C764Y |
probably damaging |
Het |
Agrn |
GCTCT |
GCTCTCT |
4: 156,166,519 (GRCm38) |
|
probably null |
Het |
Apob |
A |
G |
12: 8,016,087 (GRCm38) |
K4319R |
probably benign |
Het |
AU016765 |
A |
C |
17: 64,555,438 (GRCm38) |
|
noncoding transcript |
Het |
Bpifb1 |
T |
A |
2: 154,213,983 (GRCm38) |
|
probably null |
Het |
Btn2a2 |
A |
G |
13: 23,481,936 (GRCm38) |
V242A |
probably benign |
Het |
Camta1 |
A |
G |
4: 151,084,024 (GRCm38) |
S1281P |
probably benign |
Het |
Ccdc116 |
T |
C |
16: 17,141,908 (GRCm38) |
K306E |
probably benign |
Het |
Cemip |
A |
G |
7: 83,935,658 (GRCm38) |
V1350A |
probably benign |
Het |
Clip2 |
A |
T |
5: 134,502,929 (GRCm38) |
L674* |
probably null |
Het |
Cyp2d12 |
T |
A |
15: 82,558,050 (GRCm38) |
D244E |
probably benign |
Het |
Cyp4x1 |
A |
G |
4: 115,111,670 (GRCm38) |
V379A |
possibly damaging |
Het |
Dnah9 |
T |
A |
11: 66,168,079 (GRCm38) |
H130L |
possibly damaging |
Het |
Enpp7 |
A |
G |
11: 118,990,983 (GRCm38) |
Y318C |
probably damaging |
Het |
Fras1 |
A |
T |
5: 96,554,889 (GRCm38) |
|
probably null |
Het |
Glra3 |
G |
T |
8: 55,940,907 (GRCm38) |
A18S |
probably benign |
Het |
Gm28042 |
T |
A |
2: 120,036,391 (GRCm38) |
S172T |
possibly damaging |
Het |
Gm7808 |
T |
A |
9: 19,928,003 (GRCm38) |
|
probably benign |
Het |
Gm8909 |
A |
G |
17: 36,161,784 (GRCm38) |
|
probably benign |
Het |
Gpr61 |
C |
T |
3: 108,150,380 (GRCm38) |
V322M |
possibly damaging |
Het |
Hapln3 |
A |
G |
7: 79,123,450 (GRCm38) |
V15A |
unknown |
Het |
Ip6k1 |
G |
A |
9: 108,040,996 (GRCm38) |
E77K |
possibly damaging |
Het |
Klk1b4 |
A |
G |
7: 44,209,672 (GRCm38) |
Y38C |
probably damaging |
Het |
Lrrfip1 |
A |
G |
1: 91,115,555 (GRCm38) |
K561E |
probably damaging |
Het |
Map3k1 |
A |
G |
13: 111,755,419 (GRCm38) |
C1101R |
probably benign |
Het |
Mcoln2 |
A |
G |
3: 146,190,474 (GRCm38) |
|
probably benign |
Het |
Mfsd2b |
G |
A |
12: 4,869,037 (GRCm38) |
T73I |
probably damaging |
Het |
Mfsd4b5 |
C |
T |
10: 39,975,203 (GRCm38) |
V19I |
probably benign |
Het |
Mgme1 |
T |
A |
2: 144,272,318 (GRCm38) |
D113E |
probably benign |
Het |
Mki67 |
A |
G |
7: 135,695,494 (GRCm38) |
S2604P |
probably damaging |
Het |
Mob3c |
A |
G |
4: 115,831,644 (GRCm38) |
I125V |
probably benign |
Het |
Mrps9 |
G |
A |
1: 42,903,399 (GRCm38) |
R339H |
probably damaging |
Het |
Ndst1 |
T |
C |
18: 60,707,803 (GRCm38) |
D269G |
probably damaging |
Het |
Nedd9 |
T |
C |
13: 41,338,926 (GRCm38) |
N30S |
probably damaging |
Het |
Notch4 |
G |
A |
17: 34,576,763 (GRCm38) |
|
probably benign |
Het |
Olfr1095 |
A |
T |
2: 86,851,187 (GRCm38) |
N170K |
probably benign |
Het |
Olfr250 |
A |
G |
9: 38,367,594 (GRCm38) |
D6G |
probably benign |
Het |
Olfr877 |
G |
A |
9: 37,855,453 (GRCm38) |
V212I |
probably benign |
Het |
Olfr995 |
T |
C |
2: 85,438,805 (GRCm38) |
M118V |
probably benign |
Het |
Papss1 |
C |
A |
3: 131,619,185 (GRCm38) |
R447S |
probably damaging |
Het |
Pla2g4a |
C |
T |
1: 149,871,523 (GRCm38) |
|
probably benign |
Het |
Rab11fip2 |
A |
G |
19: 59,935,649 (GRCm38) |
F266L |
probably damaging |
Het |
Ralgapb |
T |
A |
2: 158,443,280 (GRCm38) |
Y554* |
probably null |
Het |
Rem2 |
T |
C |
14: 54,479,150 (GRCm38) |
V240A |
probably damaging |
Het |
Retsat |
T |
C |
6: 72,602,671 (GRCm38) |
V143A |
probably benign |
Het |
Rnf141 |
G |
T |
7: 110,821,273 (GRCm38) |
Q175K |
probably damaging |
Het |
Rtcb |
C |
A |
10: 85,942,017 (GRCm38) |
G431V |
probably damaging |
Het |
Slc7a6os |
A |
G |
8: 106,204,339 (GRCm38) |
W222R |
probably damaging |
Het |
Smarcc2 |
T |
C |
10: 128,468,998 (GRCm38) |
|
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,448,833 (GRCm38) |
Y218N |
possibly damaging |
Het |
Sp110 |
G |
A |
1: 85,594,385 (GRCm38) |
H66Y |
probably benign |
Het |
Sprtn |
T |
C |
8: 124,898,357 (GRCm38) |
V67A |
probably damaging |
Het |
Tktl2 |
G |
A |
8: 66,512,347 (GRCm38) |
V186M |
probably damaging |
Het |
Tnks1bp1 |
G |
T |
2: 85,071,738 (GRCm38) |
E997D |
probably benign |
Het |
Tti1 |
A |
T |
2: 158,008,224 (GRCm38) |
V365E |
probably benign |
Het |
Tulp4 |
A |
G |
17: 6,222,440 (GRCm38) |
I590V |
probably benign |
Het |
Vmn2r61 |
A |
G |
7: 42,300,697 (GRCm38) |
D847G |
probably benign |
Het |
Zfp184 |
A |
G |
13: 21,959,272 (GRCm38) |
T383A |
possibly damaging |
Het |
Zik1 |
C |
A |
7: 10,492,342 (GRCm38) |
E33* |
probably null |
Het |
Zik1 |
T |
A |
7: 10,492,341 (GRCm38) |
E33V |
probably damaging |
Het |
|
Other mutations in Speg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:Speg
|
APN |
1 |
75,410,390 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL00979:Speg
|
APN |
1 |
75,410,734 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01122:Speg
|
APN |
1 |
75,410,035 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01293:Speg
|
APN |
1 |
75,388,102 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01304:Speg
|
APN |
1 |
75,428,197 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01351:Speg
|
APN |
1 |
75,411,276 (GRCm38) |
splice site |
probably benign |
|
IGL01473:Speg
|
APN |
1 |
75,428,285 (GRCm38) |
missense |
possibly damaging |
0.53 |
IGL01477:Speg
|
APN |
1 |
75,391,897 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01485:Speg
|
APN |
1 |
75,387,827 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01584:Speg
|
APN |
1 |
75,430,937 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01959:Speg
|
APN |
1 |
75,391,090 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02231:Speg
|
APN |
1 |
75,423,387 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02355:Speg
|
APN |
1 |
75,423,915 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL02362:Speg
|
APN |
1 |
75,423,915 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL03013:Speg
|
APN |
1 |
75,431,279 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL03168:Speg
|
APN |
1 |
75,388,187 (GRCm38) |
missense |
probably damaging |
1.00 |
H8562:Speg
|
UTSW |
1 |
75,415,597 (GRCm38) |
missense |
probably benign |
0.39 |
R0112:Speg
|
UTSW |
1 |
75,385,032 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0311:Speg
|
UTSW |
1 |
75,430,937 (GRCm38) |
missense |
probably damaging |
1.00 |
R0315:Speg
|
UTSW |
1 |
75,415,136 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0393:Speg
|
UTSW |
1 |
75,423,924 (GRCm38) |
missense |
possibly damaging |
0.46 |
R0403:Speg
|
UTSW |
1 |
75,430,784 (GRCm38) |
splice site |
probably benign |
|
R0483:Speg
|
UTSW |
1 |
75,385,032 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0648:Speg
|
UTSW |
1 |
75,427,978 (GRCm38) |
missense |
probably benign |
|
R0683:Speg
|
UTSW |
1 |
75,429,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R0800:Speg
|
UTSW |
1 |
75,423,489 (GRCm38) |
missense |
probably damaging |
1.00 |
R0815:Speg
|
UTSW |
1 |
75,415,392 (GRCm38) |
missense |
probably damaging |
1.00 |
R0835:Speg
|
UTSW |
1 |
75,375,674 (GRCm38) |
missense |
probably benign |
0.00 |
R0866:Speg
|
UTSW |
1 |
75,417,083 (GRCm38) |
missense |
probably damaging |
0.99 |
R0880:Speg
|
UTSW |
1 |
75,405,061 (GRCm38) |
missense |
probably damaging |
1.00 |
R1082:Speg
|
UTSW |
1 |
75,415,138 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1140:Speg
|
UTSW |
1 |
75,429,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R1252:Speg
|
UTSW |
1 |
75,427,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R1301:Speg
|
UTSW |
1 |
75,401,501 (GRCm38) |
missense |
probably damaging |
1.00 |
R1348:Speg
|
UTSW |
1 |
75,422,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R1388:Speg
|
UTSW |
1 |
75,430,460 (GRCm38) |
missense |
probably damaging |
0.99 |
R1465:Speg
|
UTSW |
1 |
75,428,484 (GRCm38) |
splice site |
probably benign |
|
R1505:Speg
|
UTSW |
1 |
75,375,542 (GRCm38) |
missense |
probably benign |
0.02 |
R1506:Speg
|
UTSW |
1 |
75,417,663 (GRCm38) |
missense |
probably benign |
0.03 |
R1531:Speg
|
UTSW |
1 |
75,401,222 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1543:Speg
|
UTSW |
1 |
75,421,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R1567:Speg
|
UTSW |
1 |
75,428,047 (GRCm38) |
missense |
probably benign |
|
R1630:Speg
|
UTSW |
1 |
75,422,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R1667:Speg
|
UTSW |
1 |
75,410,549 (GRCm38) |
splice site |
probably benign |
|
R1673:Speg
|
UTSW |
1 |
75,411,163 (GRCm38) |
missense |
possibly damaging |
0.60 |
R1718:Speg
|
UTSW |
1 |
75,421,744 (GRCm38) |
missense |
possibly damaging |
0.87 |
R1719:Speg
|
UTSW |
1 |
75,417,863 (GRCm38) |
missense |
probably benign |
0.00 |
R1759:Speg
|
UTSW |
1 |
75,401,162 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1861:Speg
|
UTSW |
1 |
75,389,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R1874:Speg
|
UTSW |
1 |
75,423,906 (GRCm38) |
missense |
probably benign |
|
R1936:Speg
|
UTSW |
1 |
75,431,408 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2192:Speg
|
UTSW |
1 |
75,417,727 (GRCm38) |
missense |
probably damaging |
1.00 |
R2204:Speg
|
UTSW |
1 |
75,430,477 (GRCm38) |
missense |
probably benign |
0.30 |
R2287:Speg
|
UTSW |
1 |
75,430,465 (GRCm38) |
missense |
possibly damaging |
0.76 |
R2696:Speg
|
UTSW |
1 |
75,406,926 (GRCm38) |
missense |
probably benign |
0.27 |
R2983:Speg
|
UTSW |
1 |
75,384,930 (GRCm38) |
missense |
possibly damaging |
0.83 |
R3110:Speg
|
UTSW |
1 |
75,422,682 (GRCm38) |
nonsense |
probably null |
|
R3112:Speg
|
UTSW |
1 |
75,422,682 (GRCm38) |
nonsense |
probably null |
|
R3154:Speg
|
UTSW |
1 |
75,401,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R3720:Speg
|
UTSW |
1 |
75,426,782 (GRCm38) |
missense |
probably damaging |
1.00 |
R3983:Speg
|
UTSW |
1 |
75,422,547 (GRCm38) |
missense |
probably benign |
0.27 |
R4133:Speg
|
UTSW |
1 |
75,427,904 (GRCm38) |
missense |
probably benign |
|
R4522:Speg
|
UTSW |
1 |
75,428,330 (GRCm38) |
missense |
probably damaging |
1.00 |
R4564:Speg
|
UTSW |
1 |
75,391,834 (GRCm38) |
missense |
probably damaging |
1.00 |
R4577:Speg
|
UTSW |
1 |
75,415,395 (GRCm38) |
missense |
probably damaging |
1.00 |
R4858:Speg
|
UTSW |
1 |
75,421,735 (GRCm38) |
missense |
probably damaging |
1.00 |
R4953:Speg
|
UTSW |
1 |
75,423,864 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4965:Speg
|
UTSW |
1 |
75,427,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R4967:Speg
|
UTSW |
1 |
75,387,869 (GRCm38) |
missense |
probably damaging |
1.00 |
R5152:Speg
|
UTSW |
1 |
75,428,098 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5156:Speg
|
UTSW |
1 |
75,428,087 (GRCm38) |
missense |
probably damaging |
0.99 |
R5371:Speg
|
UTSW |
1 |
75,431,393 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5550:Speg
|
UTSW |
1 |
75,429,100 (GRCm38) |
missense |
probably damaging |
1.00 |
R5562:Speg
|
UTSW |
1 |
75,427,056 (GRCm38) |
missense |
probably damaging |
1.00 |
R5687:Speg
|
UTSW |
1 |
75,419,129 (GRCm38) |
splice site |
probably null |
|
R5985:Speg
|
UTSW |
1 |
75,406,684 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6004:Speg
|
UTSW |
1 |
75,415,603 (GRCm38) |
nonsense |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,418,459 (GRCm38) |
critical splice donor site |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,418,459 (GRCm38) |
critical splice donor site |
probably null |
|
R6143:Speg
|
UTSW |
1 |
75,414,387 (GRCm38) |
missense |
probably damaging |
1.00 |
R6265:Speg
|
UTSW |
1 |
75,406,679 (GRCm38) |
nonsense |
probably null |
|
R6347:Speg
|
UTSW |
1 |
75,426,875 (GRCm38) |
missense |
probably benign |
0.00 |
R6453:Speg
|
UTSW |
1 |
75,417,972 (GRCm38) |
missense |
probably benign |
0.06 |
R6505:Speg
|
UTSW |
1 |
75,429,523 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6505:Speg
|
UTSW |
1 |
75,406,684 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6531:Speg
|
UTSW |
1 |
75,422,757 (GRCm38) |
missense |
probably benign |
0.03 |
R6566:Speg
|
UTSW |
1 |
75,388,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R6747:Speg
|
UTSW |
1 |
75,410,395 (GRCm38) |
critical splice donor site |
probably null |
|
R6819:Speg
|
UTSW |
1 |
75,391,812 (GRCm38) |
missense |
possibly damaging |
0.56 |
R6821:Speg
|
UTSW |
1 |
75,417,903 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6919:Speg
|
UTSW |
1 |
75,387,908 (GRCm38) |
nonsense |
probably null |
|
R6981:Speg
|
UTSW |
1 |
75,430,913 (GRCm38) |
missense |
probably damaging |
1.00 |
R7002:Speg
|
UTSW |
1 |
75,423,268 (GRCm38) |
missense |
probably damaging |
0.98 |
R7082:Speg
|
UTSW |
1 |
75,411,447 (GRCm38) |
missense |
probably damaging |
0.96 |
R7140:Speg
|
UTSW |
1 |
75,406,770 (GRCm38) |
critical splice donor site |
probably null |
|
R7175:Speg
|
UTSW |
1 |
75,422,490 (GRCm38) |
missense |
probably benign |
0.01 |
R7178:Speg
|
UTSW |
1 |
75,422,383 (GRCm38) |
missense |
possibly damaging |
0.46 |
R7345:Speg
|
UTSW |
1 |
75,384,835 (GRCm38) |
missense |
probably damaging |
0.97 |
R7420:Speg
|
UTSW |
1 |
75,430,905 (GRCm38) |
missense |
probably damaging |
1.00 |
R7537:Speg
|
UTSW |
1 |
75,401,464 (GRCm38) |
missense |
probably damaging |
1.00 |
R7562:Speg
|
UTSW |
1 |
75,431,279 (GRCm38) |
missense |
probably damaging |
0.97 |
R7615:Speg
|
UTSW |
1 |
75,429,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R7679:Speg
|
UTSW |
1 |
75,406,315 (GRCm38) |
missense |
probably damaging |
1.00 |
R7692:Speg
|
UTSW |
1 |
75,401,190 (GRCm38) |
missense |
probably benign |
0.04 |
R7696:Speg
|
UTSW |
1 |
75,429,161 (GRCm38) |
missense |
probably damaging |
1.00 |
R7719:Speg
|
UTSW |
1 |
75,375,825 (GRCm38) |
missense |
probably damaging |
1.00 |
R7794:Speg
|
UTSW |
1 |
75,388,870 (GRCm38) |
missense |
probably benign |
0.00 |
R7824:Speg
|
UTSW |
1 |
75,384,017 (GRCm38) |
splice site |
probably null |
|
R7834:Speg
|
UTSW |
1 |
75,384,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R7892:Speg
|
UTSW |
1 |
75,427,166 (GRCm38) |
missense |
probably damaging |
1.00 |
R8015:Speg
|
UTSW |
1 |
75,415,421 (GRCm38) |
splice site |
probably benign |
|
R8068:Speg
|
UTSW |
1 |
75,422,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R8085:Speg
|
UTSW |
1 |
75,415,353 (GRCm38) |
missense |
probably damaging |
1.00 |
R8130:Speg
|
UTSW |
1 |
75,415,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R8132:Speg
|
UTSW |
1 |
75,422,995 (GRCm38) |
missense |
probably damaging |
1.00 |
R8239:Speg
|
UTSW |
1 |
75,419,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R8287:Speg
|
UTSW |
1 |
75,422,236 (GRCm38) |
missense |
probably benign |
0.26 |
R8299:Speg
|
UTSW |
1 |
75,387,836 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8441:Speg
|
UTSW |
1 |
75,411,332 (GRCm38) |
missense |
possibly damaging |
0.60 |
R8468:Speg
|
UTSW |
1 |
75,431,309 (GRCm38) |
missense |
probably damaging |
1.00 |
R8555:Speg
|
UTSW |
1 |
75,402,264 (GRCm38) |
splice site |
probably null |
|
R8781:Speg
|
UTSW |
1 |
75,407,021 (GRCm38) |
missense |
probably damaging |
1.00 |
R8784:Speg
|
UTSW |
1 |
75,405,149 (GRCm38) |
critical splice donor site |
probably benign |
|
R8848:Speg
|
UTSW |
1 |
75,427,438 (GRCm38) |
critical splice donor site |
probably null |
|
R8881:Speg
|
UTSW |
1 |
75,401,151 (GRCm38) |
missense |
possibly damaging |
0.67 |
R8898:Speg
|
UTSW |
1 |
75,388,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R8935:Speg
|
UTSW |
1 |
75,422,606 (GRCm38) |
missense |
probably benign |
0.30 |
R9019:Speg
|
UTSW |
1 |
75,429,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R9027:Speg
|
UTSW |
1 |
75,388,432 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9066:Speg
|
UTSW |
1 |
75,385,010 (GRCm38) |
missense |
probably damaging |
0.99 |
R9092:Speg
|
UTSW |
1 |
75,422,734 (GRCm38) |
missense |
probably benign |
0.01 |
R9117:Speg
|
UTSW |
1 |
75,387,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R9202:Speg
|
UTSW |
1 |
75,390,993 (GRCm38) |
missense |
probably damaging |
1.00 |
R9246:Speg
|
UTSW |
1 |
75,384,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R9248:Speg
|
UTSW |
1 |
75,421,776 (GRCm38) |
missense |
probably damaging |
1.00 |
R9451:Speg
|
UTSW |
1 |
75,417,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R9452:Speg
|
UTSW |
1 |
75,422,508 (GRCm38) |
missense |
probably benign |
|
R9475:Speg
|
UTSW |
1 |
75,388,091 (GRCm38) |
missense |
probably damaging |
1.00 |
R9476:Speg
|
UTSW |
1 |
75,401,124 (GRCm38) |
missense |
probably damaging |
0.99 |
R9510:Speg
|
UTSW |
1 |
75,401,124 (GRCm38) |
missense |
probably damaging |
0.99 |
R9519:Speg
|
UTSW |
1 |
75,415,736 (GRCm38) |
missense |
probably damaging |
1.00 |
R9528:Speg
|
UTSW |
1 |
75,387,803 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9542:Speg
|
UTSW |
1 |
75,422,782 (GRCm38) |
missense |
probably benign |
0.08 |
R9553:Speg
|
UTSW |
1 |
75,418,001 (GRCm38) |
missense |
probably benign |
0.00 |
R9767:Speg
|
UTSW |
1 |
75,427,181 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9768:Speg
|
UTSW |
1 |
75,418,973 (GRCm38) |
nonsense |
probably null |
|
R9800:Speg
|
UTSW |
1 |
75,422,714 (GRCm38) |
missense |
probably benign |
0.03 |
X0025:Speg
|
UTSW |
1 |
75,422,457 (GRCm38) |
missense |
probably damaging |
1.00 |
X0026:Speg
|
UTSW |
1 |
75,423,475 (GRCm38) |
missense |
possibly damaging |
0.88 |
Z1176:Speg
|
UTSW |
1 |
75,406,594 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,427,683 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,430,455 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Speg
|
UTSW |
1 |
75,428,381 (GRCm38) |
missense |
probably damaging |
1.00 |
|