Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
G |
A |
12: 118,831,611 (GRCm39) |
T1247I |
probably benign |
Het |
Afdn |
T |
C |
17: 14,108,869 (GRCm39) |
L1479P |
probably damaging |
Het |
Alox12e |
T |
C |
11: 70,210,534 (GRCm39) |
R363G |
probably damaging |
Het |
Ank2 |
A |
T |
3: 126,740,590 (GRCm39) |
S1765T |
unknown |
Het |
Anks6 |
T |
C |
4: 47,046,268 (GRCm39) |
|
probably null |
Het |
Apob |
A |
C |
12: 8,057,034 (GRCm39) |
I1839L |
probably benign |
Het |
Bdp1 |
C |
A |
13: 100,186,478 (GRCm39) |
R1658I |
probably damaging |
Het |
Ccs |
T |
A |
19: 4,883,390 (GRCm39) |
D136V |
probably damaging |
Het |
Cd200 |
T |
C |
16: 45,220,578 (GRCm39) |
|
probably null |
Het |
Cirbp |
T |
C |
10: 80,006,297 (GRCm39) |
S130P |
probably benign |
Het |
Cpb1 |
A |
G |
3: 20,317,927 (GRCm39) |
I199T |
probably benign |
Het |
Csn3 |
C |
T |
5: 88,077,586 (GRCm39) |
R31C |
probably damaging |
Het |
Dcaf1 |
A |
T |
9: 106,735,775 (GRCm39) |
I908F |
probably benign |
Het |
Dhcr7 |
C |
T |
7: 143,399,227 (GRCm39) |
T199I |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 66,024,463 (GRCm39) |
Q277L |
probably benign |
Het |
Echdc2 |
C |
A |
4: 108,031,366 (GRCm39) |
P237T |
probably damaging |
Het |
Efcab3 |
T |
C |
11: 104,838,237 (GRCm39) |
V3625A |
unknown |
Het |
Eif4g3 |
A |
G |
4: 137,853,526 (GRCm39) |
N364S |
probably damaging |
Het |
Eml6 |
T |
A |
11: 29,734,231 (GRCm39) |
I1170L |
probably benign |
Het |
Epha3 |
C |
T |
16: 63,403,863 (GRCm39) |
R746Q |
probably damaging |
Het |
Exosc5 |
G |
A |
7: 25,363,794 (GRCm39) |
C102Y |
probably damaging |
Het |
Fam91a1 |
A |
T |
15: 58,302,527 (GRCm39) |
Y289F |
probably benign |
Het |
Fbxo38 |
A |
C |
18: 62,648,544 (GRCm39) |
F665V |
probably benign |
Het |
Fcrl5 |
T |
C |
3: 87,353,645 (GRCm39) |
V330A |
probably benign |
Het |
Fer |
T |
A |
17: 64,231,090 (GRCm39) |
D280E |
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,373,113 (GRCm39) |
H16R |
probably benign |
Het |
Gzmg |
C |
T |
14: 56,396,979 (GRCm39) |
M1I |
probably null |
Het |
Hectd4 |
C |
T |
5: 121,411,692 (GRCm39) |
A456V |
possibly damaging |
Het |
Hk2 |
T |
A |
6: 82,711,830 (GRCm39) |
Q613L |
probably benign |
Het |
Inhca |
A |
G |
9: 103,128,988 (GRCm39) |
|
probably null |
Het |
Itsn1 |
T |
C |
16: 91,664,938 (GRCm39) |
F1121L |
unknown |
Het |
Lztr1 |
G |
T |
16: 17,340,895 (GRCm39) |
C557F |
possibly damaging |
Het |
Mdn1 |
A |
G |
4: 32,694,634 (GRCm39) |
Y1119C |
probably damaging |
Het |
Nfkb1 |
A |
T |
3: 135,319,751 (GRCm39) |
L248Q |
probably damaging |
Het |
Or1a1 |
T |
A |
11: 74,087,004 (GRCm39) |
L225* |
probably null |
Het |
Or1p1b |
T |
C |
11: 74,130,803 (GRCm39) |
F138L |
probably benign |
Het |
Or2g7 |
T |
A |
17: 38,378,370 (GRCm39) |
S103T |
probably damaging |
Het |
Or52e19 |
T |
C |
7: 102,959,054 (GRCm39) |
V42A |
probably benign |
Het |
Otulinl |
A |
C |
15: 27,658,374 (GRCm39) |
D165E |
probably damaging |
Het |
Pate1 |
T |
G |
9: 35,596,408 (GRCm39) |
D119A |
probably damaging |
Het |
Pcdhgc4 |
T |
C |
18: 37,949,424 (GRCm39) |
V280A |
possibly damaging |
Het |
Pik3ap1 |
T |
C |
19: 41,275,929 (GRCm39) |
D717G |
probably damaging |
Het |
Prdm13 |
A |
T |
4: 21,679,473 (GRCm39) |
L339Q |
unknown |
Het |
Rasgrf1 |
T |
A |
9: 89,862,802 (GRCm39) |
N519K |
probably benign |
Het |
Rergl |
A |
G |
6: 139,473,533 (GRCm39) |
V39A |
probably benign |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Sema4b |
T |
A |
7: 79,848,402 (GRCm39) |
M1K |
probably null |
Het |
Slc20a1 |
T |
G |
2: 129,052,662 (GRCm39) |
L648R |
probably damaging |
Het |
Spata31h1 |
T |
A |
10: 82,122,583 (GRCm39) |
S3476C |
probably damaging |
Het |
Spns1 |
T |
C |
7: 125,972,961 (GRCm39) |
D215G |
probably damaging |
Het |
Tle4 |
A |
T |
19: 14,429,071 (GRCm39) |
V717E |
probably damaging |
Het |
Trim50 |
T |
A |
5: 135,382,151 (GRCm39) |
M1K |
probably null |
Het |
Trpa1 |
A |
G |
1: 14,963,431 (GRCm39) |
V597A |
possibly damaging |
Het |
Usp13 |
C |
T |
3: 32,971,757 (GRCm39) |
Q746* |
probably null |
Het |
Vmn1r35 |
A |
T |
6: 66,655,906 (GRCm39) |
W255R |
probably benign |
Het |
Vps35 |
A |
T |
8: 85,990,189 (GRCm39) |
|
probably null |
Het |
Vps54 |
T |
C |
11: 21,265,028 (GRCm39) |
|
probably null |
Het |
Zfp318 |
T |
A |
17: 46,697,774 (GRCm39) |
L210Q |
probably damaging |
Het |
Zfp319 |
C |
A |
8: 96,055,410 (GRCm39) |
K264N |
probably damaging |
Het |
Zfp62 |
C |
T |
11: 49,107,580 (GRCm39) |
S557L |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,357,239 (GRCm39) |
S822P |
probably damaging |
Het |
Zxdc |
A |
G |
6: 90,346,645 (GRCm39) |
D2G |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,742,727 (GRCm39) |
I769T |
possibly 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 |
R4953:Speg
|
UTSW |
1 |
75,400,508 (GRCm39) |
missense |
possibly damaging |
0.72 |
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 |
|
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 |
|