Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta2 |
C |
A |
19: 34,243,418 (GRCm38) |
A297S |
probably benign |
Het |
Ada |
A |
G |
2: 163,735,368 (GRCm38) |
Y67H |
probably benign |
Het |
Adcy9 |
A |
G |
16: 4,304,380 (GRCm38) |
I839T |
probably benign |
Het |
Arg1 |
C |
T |
10: 24,916,791 (GRCm38) |
V182I |
possibly damaging |
Het |
Cbx7 |
G |
A |
15: 79,933,823 (GRCm38) |
T26M |
unknown |
Het |
Ceacam5 |
A |
G |
7: 17,759,392 (GRCm38) |
Y780C |
probably damaging |
Het |
Ces2h |
A |
G |
8: 105,018,400 (GRCm38) |
M389V |
probably benign |
Het |
Chst11 |
A |
T |
10: 83,191,186 (GRCm38) |
E149V |
possibly damaging |
Het |
Clstn1 |
T |
C |
4: 149,631,871 (GRCm38) |
W265R |
probably damaging |
Het |
Col4a4 |
A |
G |
1: 82,489,698 (GRCm38) |
|
probably null |
Het |
Csrp3 |
T |
G |
7: 48,833,797 (GRCm38) |
K119T |
probably benign |
Het |
Ddx39a |
T |
C |
8: 83,719,600 (GRCm38) |
|
probably null |
Het |
Ddx41 |
A |
G |
13: 55,531,921 (GRCm38) |
I437T |
probably damaging |
Het |
Eif1ad4 |
T |
A |
12: 87,895,499 (GRCm38) |
C44S |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,761,818 (GRCm38) |
D282E |
probably damaging |
Het |
Folh1 |
G |
A |
7: 86,726,098 (GRCm38) |
T527I |
probably damaging |
Het |
Gch1 |
T |
A |
14: 47,188,961 (GRCm38) |
T103S |
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,530,715 (GRCm38) |
S674P |
probably damaging |
Het |
Hecw1 |
G |
T |
13: 14,234,342 (GRCm38) |
R1127S |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,770,279 (GRCm38) |
C723S |
probably benign |
Het |
Impg2 |
T |
C |
16: 56,267,150 (GRCm38) |
S1111P |
probably damaging |
Het |
Insl3 |
T |
C |
8: 71,689,340 (GRCm38) |
L28P |
probably damaging |
Het |
Kifc1 |
T |
C |
17: 33,884,740 (GRCm38) |
D203G |
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,862,923 (GRCm38) |
S849T |
unknown |
Het |
Krt33b |
A |
G |
11: 100,025,258 (GRCm38) |
|
probably null |
Het |
Lpin3 |
A |
G |
2: 160,895,390 (GRCm38) |
D119G |
possibly damaging |
Het |
Maml2 |
AGC |
AGCCGC |
9: 13,621,254 (GRCm38) |
|
probably benign |
Het |
Maml2 |
AGC |
AGCCGC |
9: 13,621,275 (GRCm38) |
|
probably benign |
Het |
Maml2 |
GCA |
GCACCA |
9: 13,621,276 (GRCm38) |
|
probably benign |
Het |
Nsun7 |
T |
A |
5: 66,276,541 (GRCm38) |
L178* |
probably null |
Het |
Or6c1b |
A |
G |
10: 129,436,931 (GRCm38) |
N40D |
probably damaging |
Het |
Or6c205 |
A |
T |
10: 129,250,995 (GRCm38) |
I154F |
probably benign |
Het |
Or8g55 |
A |
T |
9: 39,874,082 (GRCm38) |
D269V |
probably benign |
Het |
Orc6 |
T |
A |
8: 85,303,408 (GRCm38) |
S136T |
possibly damaging |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 (GRCm38) |
|
probably benign |
Het |
Plxnc1 |
A |
G |
10: 94,943,515 (GRCm38) |
|
probably null |
Het |
Prkdc |
G |
A |
16: 15,806,096 (GRCm38) |
D3308N |
probably null |
Het |
Rtkn2 |
G |
A |
10: 67,979,813 (GRCm38) |
|
probably null |
Het |
Sele |
T |
C |
1: 164,050,694 (GRCm38) |
S201P |
possibly damaging |
Het |
Shq1 |
A |
G |
6: 100,671,045 (GRCm38) |
F6S |
probably damaging |
Het |
Sparc |
A |
T |
11: 55,409,971 (GRCm38) |
I5N |
probably damaging |
Het |
Spata31e3 |
A |
G |
13: 50,246,190 (GRCm38) |
V700A |
probably benign |
Het |
Srm |
T |
C |
4: 148,593,945 (GRCm38) |
I238T |
probably damaging |
Het |
Stx2 |
C |
A |
5: 128,993,563 (GRCm38) |
E97* |
probably null |
Het |
Sugp2 |
C |
T |
8: 70,252,072 (GRCm38) |
P753L |
probably benign |
Het |
Tff3 |
T |
C |
17: 31,129,570 (GRCm38) |
T3A |
probably benign |
Het |
Tmem38a |
C |
T |
8: 72,572,120 (GRCm38) |
A6V |
probably benign |
Het |
Trbv16 |
G |
A |
6: 41,151,995 (GRCm38) |
A38T |
not run |
Het |
Trim30a |
G |
A |
7: 104,411,397 (GRCm38) |
Q391* |
probably null |
Het |
Ttn |
T |
G |
2: 76,776,371 (GRCm38) |
Y18065S |
probably damaging |
Het |
Ubr5 |
G |
A |
15: 37,979,832 (GRCm38) |
A2434V |
probably null |
Het |
Vmn2r24 |
T |
A |
6: 123,780,479 (GRCm38) |
M102K |
probably benign |
Het |
Vmn2r69 |
G |
T |
7: 85,407,116 (GRCm38) |
H605N |
probably benign |
Het |
Washc1 |
T |
A |
17: 66,119,060 (GRCm38) |
M451K |
possibly damaging |
Het |
Washc3 |
G |
T |
10: 88,216,075 (GRCm38) |
|
probably null |
Het |
Washc5 |
A |
T |
15: 59,368,459 (GRCm38) |
Y112N |
probably damaging |
Het |
Zbtb40 |
T |
A |
4: 137,017,327 (GRCm38) |
T261S |
probably benign |
Het |
|
Other mutations in Tenm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Tenm2
|
APN |
11 |
36,206,899 (GRCm38) |
splice site |
probably benign |
|
IGL00834:Tenm2
|
APN |
11 |
36,024,258 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00911:Tenm2
|
APN |
11 |
36,008,733 (GRCm38) |
nonsense |
probably null |
|
IGL00937:Tenm2
|
APN |
11 |
36,024,623 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01154:Tenm2
|
APN |
11 |
36,041,544 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01313:Tenm2
|
APN |
11 |
36,024,248 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01346:Tenm2
|
APN |
11 |
36,027,405 (GRCm38) |
nonsense |
probably null |
|
IGL01539:Tenm2
|
APN |
11 |
36,106,827 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01629:Tenm2
|
APN |
11 |
36,864,884 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01780:Tenm2
|
APN |
11 |
36,046,941 (GRCm38) |
missense |
probably benign |
|
IGL01821:Tenm2
|
APN |
11 |
36,023,883 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01988:Tenm2
|
APN |
11 |
36,027,251 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02002:Tenm2
|
APN |
11 |
36,207,095 (GRCm38) |
missense |
probably benign |
|
IGL02449:Tenm2
|
APN |
11 |
36,023,622 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02505:Tenm2
|
APN |
11 |
36,051,916 (GRCm38) |
nonsense |
probably null |
|
IGL02649:Tenm2
|
APN |
11 |
36,207,085 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL02688:Tenm2
|
APN |
11 |
36,068,458 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02801:Tenm2
|
APN |
11 |
36,047,030 (GRCm38) |
nonsense |
probably null |
|
IGL02928:Tenm2
|
APN |
11 |
36,027,170 (GRCm38) |
missense |
possibly damaging |
0.69 |
IGL02940:Tenm2
|
APN |
11 |
36,041,644 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03202:Tenm2
|
APN |
11 |
36,024,548 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03213:Tenm2
|
APN |
11 |
36,023,330 (GRCm38) |
missense |
probably benign |
0.05 |
IGL03276:Tenm2
|
APN |
11 |
36,072,776 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL03296:Tenm2
|
APN |
11 |
36,052,025 (GRCm38) |
splice site |
probably null |
|
IGL03381:Tenm2
|
APN |
11 |
36,068,411 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03398:Tenm2
|
APN |
11 |
36,024,543 (GRCm38) |
missense |
probably damaging |
1.00 |
browser
|
UTSW |
11 |
36,046,765 (GRCm38) |
critical splice donor site |
probably null |
|
mosaic
|
UTSW |
11 |
36,063,775 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02799:Tenm2
|
UTSW |
11 |
36,273,408 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4260001:Tenm2
|
UTSW |
11 |
36,163,730 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4382001:Tenm2
|
UTSW |
11 |
36,063,902 (GRCm38) |
missense |
probably damaging |
0.99 |
R0004:Tenm2
|
UTSW |
11 |
36,023,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R0420:Tenm2
|
UTSW |
11 |
36,207,124 (GRCm38) |
splice site |
probably benign |
|
R0537:Tenm2
|
UTSW |
11 |
36,163,730 (GRCm38) |
missense |
probably damaging |
1.00 |
R0599:Tenm2
|
UTSW |
11 |
36,024,780 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0636:Tenm2
|
UTSW |
11 |
36,943,976 (GRCm38) |
missense |
probably damaging |
1.00 |
R0693:Tenm2
|
UTSW |
11 |
36,024,809 (GRCm38) |
missense |
probably damaging |
1.00 |
R0991:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0992:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1167:Tenm2
|
UTSW |
11 |
36,864,684 (GRCm38) |
missense |
probably benign |
0.30 |
R1177:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1178:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1179:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1180:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1181:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1193:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1194:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1195:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1259:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1265:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1267:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1268:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1269:Tenm2
|
UTSW |
11 |
36,008,358 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1270:Tenm2
|
UTSW |
11 |
36,041,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R1272:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1273:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1311:Tenm2
|
UTSW |
11 |
36,068,594 (GRCm38) |
splice site |
probably benign |
|
R1374:Tenm2
|
UTSW |
11 |
36,008,454 (GRCm38) |
missense |
probably benign |
0.00 |
R1542:Tenm2
|
UTSW |
11 |
36,300,220 (GRCm38) |
missense |
probably damaging |
0.99 |
R1573:Tenm2
|
UTSW |
11 |
36,047,069 (GRCm38) |
missense |
probably damaging |
1.00 |
R1579:Tenm2
|
UTSW |
11 |
36,106,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R1697:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1722:Tenm2
|
UTSW |
11 |
36,008,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R1756:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1793:Tenm2
|
UTSW |
11 |
36,023,382 (GRCm38) |
missense |
probably damaging |
0.99 |
R1950:Tenm2
|
UTSW |
11 |
36,063,177 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1954:Tenm2
|
UTSW |
11 |
36,047,547 (GRCm38) |
missense |
possibly damaging |
0.87 |
R2025:Tenm2
|
UTSW |
11 |
36,047,264 (GRCm38) |
nonsense |
probably null |
|
R2117:Tenm2
|
UTSW |
11 |
36,024,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R2244:Tenm2
|
UTSW |
11 |
36,864,862 (GRCm38) |
missense |
probably damaging |
0.98 |
R2298:Tenm2
|
UTSW |
11 |
36,046,777 (GRCm38) |
missense |
possibly damaging |
0.62 |
R2432:Tenm2
|
UTSW |
11 |
36,027,191 (GRCm38) |
missense |
probably damaging |
1.00 |
R3014:Tenm2
|
UTSW |
11 |
36,023,973 (GRCm38) |
missense |
probably damaging |
1.00 |
R3115:Tenm2
|
UTSW |
11 |
36,023,366 (GRCm38) |
missense |
probably damaging |
1.00 |
R3684:Tenm2
|
UTSW |
11 |
36,051,817 (GRCm38) |
missense |
probably benign |
0.00 |
R3685:Tenm2
|
UTSW |
11 |
36,051,817 (GRCm38) |
missense |
probably benign |
0.00 |
R3705:Tenm2
|
UTSW |
11 |
36,068,326 (GRCm38) |
missense |
probably damaging |
0.97 |
R3820:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3821:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3822:Tenm2
|
UTSW |
11 |
36,024,320 (GRCm38) |
missense |
probably damaging |
0.98 |
R3844:Tenm2
|
UTSW |
11 |
36,047,538 (GRCm38) |
missense |
probably damaging |
0.98 |
R3878:Tenm2
|
UTSW |
11 |
36,139,574 (GRCm38) |
critical splice donor site |
probably null |
|
R4019:Tenm2
|
UTSW |
11 |
36,047,074 (GRCm38) |
missense |
probably benign |
0.04 |
R4062:Tenm2
|
UTSW |
11 |
36,008,655 (GRCm38) |
missense |
probably damaging |
1.00 |
R4367:Tenm2
|
UTSW |
11 |
36,027,398 (GRCm38) |
missense |
probably benign |
|
R4395:Tenm2
|
UTSW |
11 |
36,024,624 (GRCm38) |
missense |
probably benign |
0.23 |
R4508:Tenm2
|
UTSW |
11 |
36,008,345 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4534:Tenm2
|
UTSW |
11 |
36,063,104 (GRCm38) |
missense |
possibly damaging |
0.64 |
R4539:Tenm2
|
UTSW |
11 |
36,046,780 (GRCm38) |
missense |
probably damaging |
1.00 |
R4644:Tenm2
|
UTSW |
11 |
36,047,136 (GRCm38) |
missense |
probably benign |
0.00 |
R4661:Tenm2
|
UTSW |
11 |
36,024,448 (GRCm38) |
missense |
probably damaging |
0.99 |
R4669:Tenm2
|
UTSW |
11 |
36,010,487 (GRCm38) |
missense |
probably damaging |
1.00 |
R4687:Tenm2
|
UTSW |
11 |
36,049,097 (GRCm38) |
missense |
probably benign |
|
R4711:Tenm2
|
UTSW |
11 |
36,300,212 (GRCm38) |
missense |
probably damaging |
0.98 |
R4816:Tenm2
|
UTSW |
11 |
36,027,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R4843:Tenm2
|
UTSW |
11 |
36,024,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R4850:Tenm2
|
UTSW |
11 |
36,023,488 (GRCm38) |
nonsense |
probably null |
|
R4870:Tenm2
|
UTSW |
11 |
36,078,569 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Tenm2
|
UTSW |
11 |
36,207,080 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5071:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5073:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5074:Tenm2
|
UTSW |
11 |
36,068,381 (GRCm38) |
missense |
probably damaging |
0.99 |
R5081:Tenm2
|
UTSW |
11 |
36,024,633 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5093:Tenm2
|
UTSW |
11 |
36,944,162 (GRCm38) |
missense |
probably damaging |
1.00 |
R5170:Tenm2
|
UTSW |
11 |
36,024,806 (GRCm38) |
missense |
probably damaging |
0.98 |
R5253:Tenm2
|
UTSW |
11 |
36,047,201 (GRCm38) |
nonsense |
probably null |
|
R5343:Tenm2
|
UTSW |
11 |
36,069,503 (GRCm38) |
missense |
probably benign |
0.00 |
R5493:Tenm2
|
UTSW |
11 |
36,864,676 (GRCm38) |
missense |
probably benign |
0.01 |
R5600:Tenm2
|
UTSW |
11 |
36,163,714 (GRCm38) |
splice site |
probably null |
|
R5677:Tenm2
|
UTSW |
11 |
36,141,683 (GRCm38) |
missense |
probably damaging |
0.98 |
R5703:Tenm2
|
UTSW |
11 |
36,023,799 (GRCm38) |
missense |
probably benign |
0.34 |
R5707:Tenm2
|
UTSW |
11 |
36,047,182 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6026:Tenm2
|
UTSW |
11 |
36,072,729 (GRCm38) |
critical splice donor site |
probably null |
|
R6063:Tenm2
|
UTSW |
11 |
36,163,717 (GRCm38) |
critical splice donor site |
probably null |
|
R6086:Tenm2
|
UTSW |
11 |
36,008,646 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6151:Tenm2
|
UTSW |
11 |
36,008,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R6169:Tenm2
|
UTSW |
11 |
36,139,690 (GRCm38) |
missense |
probably damaging |
0.99 |
R6193:Tenm2
|
UTSW |
11 |
36,046,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R6405:Tenm2
|
UTSW |
11 |
36,864,859 (GRCm38) |
missense |
probably benign |
0.44 |
R6477:Tenm2
|
UTSW |
11 |
36,010,507 (GRCm38) |
critical splice acceptor site |
probably null |
|
R6607:Tenm2
|
UTSW |
11 |
36,063,775 (GRCm38) |
critical splice donor site |
probably null |
|
R6668:Tenm2
|
UTSW |
11 |
36,046,765 (GRCm38) |
critical splice donor site |
probably null |
|
R6825:Tenm2
|
UTSW |
11 |
36,046,884 (GRCm38) |
missense |
probably benign |
0.02 |
R6885:Tenm2
|
UTSW |
11 |
36,023,580 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7017:Tenm2
|
UTSW |
11 |
36,171,409 (GRCm38) |
missense |
probably damaging |
0.98 |
R7115:Tenm2
|
UTSW |
11 |
36,163,817 (GRCm38) |
missense |
probably damaging |
0.99 |
R7153:Tenm2
|
UTSW |
11 |
36,024,182 (GRCm38) |
missense |
probably damaging |
0.98 |
R7173:Tenm2
|
UTSW |
11 |
36,041,551 (GRCm38) |
missense |
probably damaging |
0.99 |
R7199:Tenm2
|
UTSW |
11 |
36,171,436 (GRCm38) |
missense |
probably damaging |
1.00 |
R7205:Tenm2
|
UTSW |
11 |
36,049,129 (GRCm38) |
missense |
probably damaging |
0.99 |
R7250:Tenm2
|
UTSW |
11 |
36,072,798 (GRCm38) |
missense |
probably damaging |
1.00 |
R7290:Tenm2
|
UTSW |
11 |
36,023,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R7366:Tenm2
|
UTSW |
11 |
36,069,414 (GRCm38) |
missense |
probably benign |
0.09 |
R7432:Tenm2
|
UTSW |
11 |
36,864,941 (GRCm38) |
missense |
probably benign |
|
R7504:Tenm2
|
UTSW |
11 |
36,139,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R7513:Tenm2
|
UTSW |
11 |
36,051,900 (GRCm38) |
missense |
probably benign |
0.34 |
R7523:Tenm2
|
UTSW |
11 |
36,078,581 (GRCm38) |
splice site |
probably null |
|
R7527:Tenm2
|
UTSW |
11 |
36,206,976 (GRCm38) |
missense |
probably damaging |
1.00 |
R7648:Tenm2
|
UTSW |
11 |
36,106,736 (GRCm38) |
missense |
probably damaging |
1.00 |
R7653:Tenm2
|
UTSW |
11 |
36,047,347 (GRCm38) |
missense |
probably benign |
0.09 |
R7717:Tenm2
|
UTSW |
11 |
36,864,935 (GRCm38) |
missense |
probably damaging |
0.97 |
R7739:Tenm2
|
UTSW |
11 |
36,069,561 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7762:Tenm2
|
UTSW |
11 |
36,023,306 (GRCm38) |
missense |
possibly damaging |
0.74 |
R7786:Tenm2
|
UTSW |
11 |
36,010,449 (GRCm38) |
missense |
probably damaging |
0.99 |
R7834:Tenm2
|
UTSW |
11 |
36,024,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R7838:Tenm2
|
UTSW |
11 |
36,106,799 (GRCm38) |
missense |
probably benign |
0.02 |
R8073:Tenm2
|
UTSW |
11 |
36,139,644 (GRCm38) |
missense |
possibly damaging |
0.56 |
R8076:Tenm2
|
UTSW |
11 |
36,027,221 (GRCm38) |
missense |
probably benign |
0.23 |
R8109:Tenm2
|
UTSW |
11 |
36,008,310 (GRCm38) |
missense |
probably benign |
|
R8306:Tenm2
|
UTSW |
11 |
36,069,369 (GRCm38) |
missense |
possibly damaging |
0.52 |
R8352:Tenm2
|
UTSW |
11 |
36,023,601 (GRCm38) |
missense |
probably damaging |
0.98 |
R8452:Tenm2
|
UTSW |
11 |
36,023,601 (GRCm38) |
missense |
probably damaging |
0.98 |
R8864:Tenm2
|
UTSW |
11 |
36,027,195 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8880:Tenm2
|
UTSW |
11 |
36,051,961 (GRCm38) |
missense |
probably damaging |
0.99 |
R8943:Tenm2
|
UTSW |
11 |
36,944,034 (GRCm38) |
missense |
probably damaging |
0.98 |
R8969:Tenm2
|
UTSW |
11 |
36,051,861 (GRCm38) |
missense |
probably damaging |
0.99 |
R9168:Tenm2
|
UTSW |
11 |
36,039,895 (GRCm38) |
missense |
probably damaging |
1.00 |
R9279:Tenm2
|
UTSW |
11 |
36,068,476 (GRCm38) |
missense |
probably benign |
0.00 |
R9294:Tenm2
|
UTSW |
11 |
36,024,500 (GRCm38) |
missense |
probably damaging |
0.98 |
R9320:Tenm2
|
UTSW |
11 |
36,023,647 (GRCm38) |
missense |
probably damaging |
0.99 |
R9373:Tenm2
|
UTSW |
11 |
36,039,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R9408:Tenm2
|
UTSW |
11 |
36,069,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R9410:Tenm2
|
UTSW |
11 |
36,141,569 (GRCm38) |
missense |
probably damaging |
0.99 |
R9454:Tenm2
|
UTSW |
11 |
36,221,459 (GRCm38) |
missense |
probably benign |
|
R9489:Tenm2
|
UTSW |
11 |
36,943,964 (GRCm38) |
missense |
probably damaging |
0.99 |
R9711:Tenm2
|
UTSW |
11 |
36,024,514 (GRCm38) |
missense |
probably damaging |
0.99 |
RF021:Tenm2
|
UTSW |
11 |
36,024,203 (GRCm38) |
missense |
possibly damaging |
0.95 |
X0018:Tenm2
|
UTSW |
11 |
36,024,200 (GRCm38) |
missense |
probably damaging |
1.00 |
X0063:Tenm2
|
UTSW |
11 |
36,024,730 (GRCm38) |
missense |
probably benign |
|
Z1088:Tenm2
|
UTSW |
11 |
36,273,267 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Tenm2
|
UTSW |
11 |
36,385,130 (GRCm38) |
missense |
probably benign |
0.01 |
Z1177:Tenm2
|
UTSW |
11 |
36,300,335 (GRCm38) |
missense |
probably damaging |
0.98 |
Z1177:Tenm2
|
UTSW |
11 |
36,008,234 (GRCm38) |
missense |
possibly damaging |
0.95 |
|