Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,585,043 (GRCm39) |
I844V |
probably damaging |
Het |
Acnat1 |
T |
A |
4: 49,450,784 (GRCm39) |
Y109F |
probably benign |
Het |
Alox12b |
T |
C |
11: 69,054,033 (GRCm39) |
V205A |
probably benign |
Het |
Arl6ip1 |
G |
A |
7: 117,721,208 (GRCm39) |
R77C |
probably damaging |
Het |
Atp8b1 |
A |
G |
18: 64,666,730 (GRCm39) |
C1156R |
possibly damaging |
Het |
Atp8b3 |
A |
C |
10: 80,372,156 (GRCm39) |
N24K |
probably damaging |
Het |
Bdh1 |
T |
C |
16: 31,273,954 (GRCm39) |
V209A |
possibly damaging |
Het |
Blm |
A |
T |
7: 80,113,596 (GRCm39) |
C1234S |
probably damaging |
Het |
Caml |
A |
G |
13: 55,779,740 (GRCm39) |
D271G |
possibly damaging |
Het |
Capn11 |
T |
C |
17: 45,944,006 (GRCm39) |
D545G |
probably benign |
Het |
Catspere1 |
T |
C |
1: 177,765,304 (GRCm39) |
|
noncoding transcript |
Het |
Cep128 |
T |
C |
12: 91,200,969 (GRCm39) |
E347G |
probably damaging |
Het |
Cngb3 |
A |
G |
4: 19,415,713 (GRCm39) |
T408A |
possibly damaging |
Het |
Coa8 |
A |
G |
12: 111,679,823 (GRCm39) |
T33A |
possibly damaging |
Het |
Cog1 |
G |
A |
11: 113,548,253 (GRCm39) |
R18Q |
possibly damaging |
Het |
Cps1 |
T |
C |
1: 67,259,671 (GRCm39) |
F1338L |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,059,369 (GRCm39) |
H2122R |
probably benign |
Het |
Ctu2 |
T |
G |
8: 123,207,851 (GRCm39) |
S26A |
probably benign |
Het |
Dbf4 |
G |
A |
5: 8,453,062 (GRCm39) |
|
probably benign |
Het |
Ddx23 |
A |
T |
15: 98,545,116 (GRCm39) |
D663E |
probably benign |
Het |
Dpep2 |
T |
C |
8: 106,717,388 (GRCm39) |
T123A |
possibly damaging |
Het |
Eed |
A |
G |
7: 89,613,976 (GRCm39) |
I274T |
probably damaging |
Het |
Eif3b |
A |
G |
5: 140,405,255 (GRCm39) |
D47G |
probably benign |
Het |
Epas1 |
T |
C |
17: 87,113,186 (GRCm39) |
V124A |
probably damaging |
Het |
Fer1l6 |
T |
C |
15: 58,449,798 (GRCm39) |
L668P |
probably damaging |
Het |
Fnip2 |
C |
A |
3: 79,373,028 (GRCm39) |
E1017* |
probably null |
Het |
Gm43517 |
A |
T |
12: 49,436,690 (GRCm39) |
|
probably benign |
Het |
Got1 |
A |
G |
19: 43,491,345 (GRCm39) |
|
probably null |
Het |
H2-Eb2 |
T |
A |
17: 34,553,375 (GRCm39) |
V187E |
probably damaging |
Het |
H2-Q1 |
T |
C |
17: 35,540,242 (GRCm39) |
|
probably benign |
Het |
Hpgd |
T |
C |
8: 56,751,454 (GRCm39) |
V94A |
probably damaging |
Het |
Htra1 |
T |
A |
7: 130,586,756 (GRCm39) |
N446K |
probably benign |
Het |
Igkv3-4 |
T |
A |
6: 70,649,269 (GRCm39) |
S89R |
probably damaging |
Het |
Immt |
C |
T |
6: 71,829,720 (GRCm39) |
T142I |
probably damaging |
Het |
Itpkb |
C |
A |
1: 180,245,759 (GRCm39) |
P759T |
probably damaging |
Het |
Jmjd1c |
G |
A |
10: 67,060,571 (GRCm39) |
V688I |
possibly damaging |
Het |
Kbtbd13 |
G |
T |
9: 65,298,025 (GRCm39) |
R304S |
probably benign |
Het |
Lama5 |
A |
C |
2: 179,827,734 (GRCm39) |
L2176R |
probably damaging |
Het |
Lrp1b |
G |
C |
2: 40,551,544 (GRCm39) |
L418V |
probably null |
Het |
Lrrc4b |
C |
A |
7: 44,111,796 (GRCm39) |
|
probably null |
Het |
Lyst |
A |
G |
13: 13,915,182 (GRCm39) |
N3292S |
probably damaging |
Het |
Mep1b |
A |
T |
18: 21,219,241 (GRCm39) |
I132F |
probably benign |
Het |
Mettl2 |
A |
G |
11: 105,017,436 (GRCm39) |
|
probably null |
Het |
Nherf2 |
T |
C |
17: 24,863,873 (GRCm39) |
M1V |
probably null |
Het |
Niban1 |
A |
T |
1: 151,591,445 (GRCm39) |
D529V |
probably damaging |
Het |
Nmd3 |
T |
C |
3: 69,652,569 (GRCm39) |
L385S |
probably benign |
Het |
Nol4 |
T |
C |
18: 23,045,683 (GRCm39) |
E243G |
probably damaging |
Het |
Odad1 |
T |
A |
7: 45,597,804 (GRCm39) |
S571R |
probably damaging |
Het |
Or4l1 |
T |
A |
14: 50,166,726 (GRCm39) |
I92F |
probably damaging |
Het |
Or51k1 |
A |
G |
7: 103,661,795 (GRCm39) |
I38T |
probably benign |
Het |
Or5j3 |
A |
T |
2: 86,129,042 (GRCm39) |
N294I |
possibly damaging |
Het |
Or8b52 |
A |
G |
9: 38,576,519 (GRCm39) |
I207T |
probably benign |
Het |
Pcnp |
A |
G |
16: 55,837,522 (GRCm39) |
|
probably benign |
Het |
Pla2g6 |
A |
C |
15: 79,171,818 (GRCm39) |
C680G |
probably damaging |
Het |
Plekha7 |
G |
T |
7: 115,744,178 (GRCm39) |
D661E |
probably damaging |
Het |
Prim1 |
A |
T |
10: 127,862,887 (GRCm39) |
|
probably benign |
Het |
Psg29 |
T |
A |
7: 16,944,460 (GRCm39) |
N323K |
probably benign |
Het |
Ptrh2 |
G |
A |
11: 86,580,833 (GRCm39) |
R150H |
probably damaging |
Het |
Rasa1 |
A |
G |
13: 85,398,621 (GRCm39) |
|
probably benign |
Het |
Rasa3 |
T |
C |
8: 13,627,501 (GRCm39) |
D667G |
probably benign |
Het |
Rnase2a |
T |
C |
14: 51,493,201 (GRCm39) |
N55D |
probably damaging |
Het |
Rsf1 |
GCGGCGGCGGCGGCGGCGGC |
GCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
7: 97,229,123 (GRCm39) |
|
probably benign |
Het |
Sbp |
T |
A |
17: 24,164,218 (GRCm39) |
N133K |
probably damaging |
Het |
Scml4 |
A |
G |
10: 42,833,743 (GRCm39) |
|
probably benign |
Het |
Sema5b |
T |
A |
16: 35,483,552 (GRCm39) |
N1063K |
probably damaging |
Het |
Serpind1 |
C |
T |
16: 17,154,272 (GRCm39) |
T33M |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slc15a2 |
A |
T |
16: 36,602,057 (GRCm39) |
L80* |
probably null |
Het |
Sorcs3 |
A |
G |
19: 48,782,602 (GRCm39) |
D1039G |
probably benign |
Het |
Spon1 |
A |
G |
7: 113,639,102 (GRCm39) |
E776G |
probably damaging |
Het |
Tdp1 |
C |
T |
12: 99,868,623 (GRCm39) |
A259V |
possibly damaging |
Het |
Tex46 |
C |
A |
4: 136,337,991 (GRCm39) |
P61Q |
probably benign |
Het |
Tnr |
T |
A |
1: 159,724,636 (GRCm39) |
L1109Q |
probably damaging |
Het |
Tpra1 |
G |
A |
6: 88,887,661 (GRCm39) |
|
probably benign |
Het |
Trim43c |
A |
T |
9: 88,729,705 (GRCm39) |
H383L |
possibly damaging |
Het |
Trip6 |
A |
G |
5: 137,308,433 (GRCm39) |
C439R |
probably damaging |
Het |
Tsen2 |
C |
T |
6: 115,552,894 (GRCm39) |
S398L |
possibly damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,576,074 (GRCm39) |
D863G |
probably damaging |
Het |
Ube2d2a |
A |
G |
18: 35,903,498 (GRCm39) |
|
probably benign |
Het |
Umad1 |
T |
A |
6: 8,427,181 (GRCm39) |
F145I |
probably damaging |
Het |
Unc5c |
A |
T |
3: 141,534,278 (GRCm39) |
E933V |
probably damaging |
Het |
Vmn1r208 |
A |
G |
13: 22,956,646 (GRCm39) |
F284L |
probably benign |
Het |
Vmn2r53 |
T |
A |
7: 12,334,692 (GRCm39) |
R323* |
probably null |
Het |
Zan |
G |
A |
5: 137,387,281 (GRCm39) |
T4924I |
unknown |
Het |
Zfp597 |
G |
T |
16: 3,683,851 (GRCm39) |
Q302K |
probably benign |
Het |
|
Other mutations in Tns2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01575:Tns2
|
APN |
15 |
102,021,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Tns2
|
APN |
15 |
102,020,069 (GRCm39) |
splice site |
probably null |
|
IGL01994:Tns2
|
APN |
15 |
102,019,814 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02025:Tns2
|
APN |
15 |
102,020,484 (GRCm39) |
nonsense |
probably null |
|
IGL02135:Tns2
|
APN |
15 |
102,021,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02355:Tns2
|
APN |
15 |
102,020,725 (GRCm39) |
missense |
probably benign |
|
IGL02362:Tns2
|
APN |
15 |
102,020,725 (GRCm39) |
missense |
probably benign |
|
IGL02439:Tns2
|
APN |
15 |
102,022,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02488:Tns2
|
APN |
15 |
102,021,178 (GRCm39) |
missense |
probably benign |
|
IGL02546:Tns2
|
APN |
15 |
102,019,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02616:Tns2
|
APN |
15 |
102,019,850 (GRCm39) |
missense |
probably benign |
|
IGL02628:Tns2
|
APN |
15 |
102,020,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02658:Tns2
|
APN |
15 |
102,016,231 (GRCm39) |
splice site |
probably benign |
|
IGL03267:Tns2
|
APN |
15 |
102,013,813 (GRCm39) |
critical splice donor site |
probably null |
|
P0005:Tns2
|
UTSW |
15 |
102,022,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R0586:Tns2
|
UTSW |
15 |
102,018,020 (GRCm39) |
splice site |
probably benign |
|
R0791:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0817:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0820:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1451:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1453:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1454:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1455:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1510:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Tns2
|
UTSW |
15 |
102,019,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1698:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Tns2
|
UTSW |
15 |
102,021,568 (GRCm39) |
splice site |
probably null |
|
R1923:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2051:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2087:Tns2
|
UTSW |
15 |
102,015,554 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2100:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Tns2
|
UTSW |
15 |
102,021,100 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2105:Tns2
|
UTSW |
15 |
102,015,941 (GRCm39) |
missense |
probably benign |
0.27 |
R2224:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2225:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2253:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Tns2
|
UTSW |
15 |
102,020,458 (GRCm39) |
missense |
probably damaging |
0.99 |
R2304:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2318:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2446:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2447:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2448:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2897:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2898:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3159:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3162:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3162:Tns2
|
UTSW |
15 |
102,021,771 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3196:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3237:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3426:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3427:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3695:Tns2
|
UTSW |
15 |
102,021,184 (GRCm39) |
missense |
probably null |
|
R3767:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R3911:Tns2
|
UTSW |
15 |
102,022,272 (GRCm39) |
critical splice donor site |
probably null |
|
R4113:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4157:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4395:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4439:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4441:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4537:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4538:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4541:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4602:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4773:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4775:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Tns2
|
UTSW |
15 |
102,020,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R4989:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5058:Tns2
|
UTSW |
15 |
102,016,295 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5253:Tns2
|
UTSW |
15 |
102,019,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Tns2
|
UTSW |
15 |
102,019,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5351:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5453:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5631:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5685:Tns2
|
UTSW |
15 |
102,015,538 (GRCm39) |
missense |
probably benign |
0.02 |
R5844:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Tns2
|
UTSW |
15 |
102,019,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R6067:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6079:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6130:Tns2
|
UTSW |
15 |
102,019,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Tns2
|
UTSW |
15 |
102,015,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R6138:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6199:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6210:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6426:Tns2
|
UTSW |
15 |
102,015,472 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6544:Tns2
|
UTSW |
15 |
102,022,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6594:Tns2
|
UTSW |
15 |
102,018,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6596:Tns2
|
UTSW |
15 |
102,018,994 (GRCm39) |
missense |
probably benign |
0.00 |
R6734:Tns2
|
UTSW |
15 |
102,011,551 (GRCm39) |
missense |
probably damaging |
0.96 |
R7061:Tns2
|
UTSW |
15 |
102,012,914 (GRCm39) |
start codon destroyed |
probably null |
|
R7070:Tns2
|
UTSW |
15 |
102,012,968 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7110:Tns2
|
UTSW |
15 |
102,013,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R7410:Tns2
|
UTSW |
15 |
102,018,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Tns2
|
UTSW |
15 |
102,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Tns2
|
UTSW |
15 |
102,018,163 (GRCm39) |
missense |
probably benign |
0.02 |
R8052:Tns2
|
UTSW |
15 |
102,021,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8114:Tns2
|
UTSW |
15 |
102,019,825 (GRCm39) |
missense |
probably benign |
0.01 |
R8906:Tns2
|
UTSW |
15 |
102,020,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8964:Tns2
|
UTSW |
15 |
102,011,553 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9192:Tns2
|
UTSW |
15 |
102,021,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Tns2
|
UTSW |
15 |
102,021,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Tns2
|
UTSW |
15 |
102,018,996 (GRCm39) |
missense |
probably damaging |
0.97 |
R9402:Tns2
|
UTSW |
15 |
102,021,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R9612:Tns2
|
UTSW |
15 |
102,015,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Tns2
|
UTSW |
15 |
102,012,933 (GRCm39) |
missense |
probably benign |
0.03 |
U15987:Tns2
|
UTSW |
15 |
102,017,369 (GRCm39) |
missense |
probably damaging |
1.00 |
X0009:Tns2
|
UTSW |
15 |
102,020,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0026:Tns2
|
UTSW |
15 |
102,018,937 (GRCm39) |
missense |
probably damaging |
1.00 |
|