Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
C |
18: 6,623,470 (GRCm39) |
R60P |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,393,354 (GRCm39) |
C1199S |
probably benign |
Het |
Arhgap18 |
G |
A |
10: 26,763,857 (GRCm39) |
M482I |
probably damaging |
Het |
Arhgap18 |
G |
T |
10: 26,763,858 (GRCm39) |
A483S |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
BC051019 |
T |
C |
7: 109,322,381 (GRCm39) |
T38A |
probably benign |
Het |
Bcam |
T |
C |
7: 19,499,543 (GRCm39) |
N192S |
probably null |
Het |
Bend5 |
A |
T |
4: 111,311,438 (GRCm39) |
K351* |
probably null |
Het |
Bicdl2 |
T |
A |
17: 23,884,923 (GRCm39) |
M208K |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,325,247 (GRCm39) |
|
probably null |
Het |
Cdc6 |
A |
T |
11: 98,803,043 (GRCm39) |
T328S |
probably damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,225,470 (GRCm39) |
N558K |
probably benign |
Het |
Cdkn1c |
C |
T |
7: 143,012,858 (GRCm39) |
R146K |
probably benign |
Het |
Ceacam18 |
G |
A |
7: 43,297,918 (GRCm39) |
C371Y |
probably benign |
Het |
Cep95 |
T |
A |
11: 106,697,177 (GRCm39) |
C233* |
probably null |
Het |
Chrnd |
A |
G |
1: 87,122,650 (GRCm39) |
I144V |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,957,299 (GRCm39) |
Q175L |
probably benign |
Het |
Cym |
A |
T |
3: 107,120,816 (GRCm39) |
V263E |
probably damaging |
Het |
Cyp2a4 |
G |
T |
7: 26,012,197 (GRCm39) |
V327F |
possibly damaging |
Het |
Dhx29 |
T |
A |
13: 113,084,774 (GRCm39) |
M664K |
probably damaging |
Het |
Dlec1 |
T |
G |
9: 118,975,075 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,792,863 (GRCm39) |
Y293H |
probably benign |
Het |
Dnase1l3 |
T |
A |
14: 7,974,104 (GRCm38) |
N196Y |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
Efcab14 |
A |
T |
4: 115,610,116 (GRCm39) |
|
probably null |
Het |
Entpd5 |
C |
T |
12: 84,432,985 (GRCm39) |
R189H |
probably benign |
Het |
Exoc4 |
A |
T |
6: 33,734,985 (GRCm39) |
K534M |
probably damaging |
Het |
Extl1 |
T |
A |
4: 134,098,449 (GRCm39) |
Y194F |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,323,299 (GRCm39) |
L161S |
possibly damaging |
Het |
Fam163b |
T |
C |
2: 27,002,874 (GRCm39) |
E41G |
possibly damaging |
Het |
Fam180a |
A |
C |
6: 35,292,287 (GRCm39) |
S40A |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,385,950 (GRCm39) |
S186P |
probably benign |
Het |
Fbxw19 |
A |
T |
9: 109,323,840 (GRCm39) |
L45* |
probably null |
Het |
Fgf14 |
G |
T |
14: 124,913,924 (GRCm39) |
T69N |
probably benign |
Het |
Flt1 |
A |
G |
5: 147,609,519 (GRCm39) |
Y432H |
probably damaging |
Het |
Frmd4b |
A |
T |
6: 97,283,725 (GRCm39) |
L374Q |
possibly damaging |
Het |
G6pc2 |
T |
A |
2: 69,053,321 (GRCm39) |
V125D |
probably damaging |
Het |
Gm10033 |
T |
C |
8: 69,826,210 (GRCm39) |
I119M |
unknown |
Het |
Gna15 |
A |
T |
10: 81,347,954 (GRCm39) |
L164Q |
probably damaging |
Het |
Gnaz |
C |
A |
10: 74,827,702 (GRCm39) |
D151E |
possibly damaging |
Het |
Has1 |
T |
C |
17: 18,070,562 (GRCm39) |
T120A |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,496,366 (GRCm39) |
D3919E |
possibly damaging |
Het |
Hs3st5 |
A |
G |
10: 36,709,165 (GRCm39) |
I233M |
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,314,438 (GRCm39) |
|
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,687,069 (GRCm39) |
L765* |
probably null |
Het |
Insr |
A |
T |
8: 3,209,561 (GRCm39) |
I1174N |
probably damaging |
Het |
Kash5 |
T |
A |
7: 44,838,227 (GRCm39) |
|
probably null |
Het |
Kcnq3 |
A |
G |
15: 65,877,755 (GRCm39) |
L445P |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,181,824 (GRCm39) |
N159Y |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,185,755 (GRCm39) |
D366V |
probably damaging |
Het |
Klk15 |
T |
C |
7: 43,587,757 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
G |
10: 38,979,497 (GRCm39) |
N1658K |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,060,586 (GRCm39) |
Y279C |
probably damaging |
Het |
Mast2 |
G |
T |
4: 116,164,156 (GRCm39) |
D1747E |
probably damaging |
Het |
Mest |
G |
A |
6: 30,745,138 (GRCm39) |
M235I |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,699,964 (GRCm39) |
|
probably null |
Het |
Mllt10 |
T |
A |
2: 18,167,657 (GRCm39) |
S449R |
probably damaging |
Het |
Mon2 |
T |
A |
10: 122,849,668 (GRCm39) |
T1211S |
probably benign |
Het |
Mrnip |
G |
A |
11: 50,067,688 (GRCm39) |
C27Y |
probably damaging |
Het |
Myh15 |
A |
T |
16: 48,983,498 (GRCm39) |
T1538S |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,989,634 (GRCm39) |
V250A |
probably benign |
Het |
Npy1r |
A |
G |
8: 67,157,177 (GRCm39) |
D199G |
possibly damaging |
Het |
Numbl |
A |
G |
7: 26,980,379 (GRCm39) |
T454A |
probably benign |
Het |
Nutm2 |
T |
G |
13: 50,627,152 (GRCm39) |
F436V |
probably damaging |
Het |
Opa1 |
T |
C |
16: 29,439,628 (GRCm39) |
S773P |
probably benign |
Het |
Or12e1 |
T |
A |
2: 87,022,042 (GRCm39) |
S4T |
probably benign |
Het |
Or2d3 |
A |
T |
7: 106,491,184 (GRCm39) |
|
probably null |
Het |
Or2d3 |
G |
T |
7: 106,491,185 (GRCm39) |
L44M |
probably damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,611 (GRCm39) |
L114S |
probably damaging |
Het |
Or2t48 |
A |
G |
11: 58,420,602 (GRCm39) |
L70P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,484 (GRCm39) |
S153P |
probably benign |
Het |
Or51m1 |
C |
T |
7: 103,578,932 (GRCm39) |
R301* |
probably null |
Het |
Or52e7 |
A |
G |
7: 104,685,157 (GRCm39) |
S251G |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,508 (GRCm39) |
Y127C |
probably damaging |
Het |
Or8b12c |
T |
A |
9: 37,715,599 (GRCm39) |
Y131N |
probably damaging |
Het |
Pde8a |
G |
C |
7: 80,950,471 (GRCm39) |
|
probably null |
Het |
Pgam1 |
T |
C |
19: 41,906,144 (GRCm39) |
F232S |
probably damaging |
Het |
Pgk1 |
T |
A |
X: 105,243,914 (GRCm39) |
V303E |
possibly damaging |
Het |
Pirb |
A |
T |
7: 3,720,189 (GRCm39) |
C395S |
probably damaging |
Het |
Plxnc1 |
C |
T |
10: 94,680,184 (GRCm39) |
V824I |
probably benign |
Het |
Ppp6r1 |
A |
G |
7: 4,636,691 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
C |
A |
2: 72,056,131 (GRCm39) |
|
probably benign |
Het |
Rars1 |
T |
A |
11: 35,700,465 (GRCm39) |
T539S |
probably damaging |
Het |
Rbm44 |
G |
T |
1: 91,081,679 (GRCm39) |
|
probably null |
Het |
Samd4b |
A |
G |
7: 28,113,317 (GRCm39) |
I216T |
probably benign |
Het |
Serpine2 |
A |
C |
1: 79,794,532 (GRCm39) |
F134V |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,683,790 (GRCm39) |
Y341H |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,917,561 (GRCm39) |
V226F |
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,933,896 (GRCm39) |
I69T |
probably damaging |
Het |
Slc37a1 |
C |
A |
17: 31,552,652 (GRCm39) |
T319K |
possibly damaging |
Het |
Slc6a4 |
A |
T |
11: 76,904,078 (GRCm39) |
T178S |
probably damaging |
Het |
Smarca4 |
G |
A |
9: 21,612,479 (GRCm39) |
A1588T |
possibly damaging |
Het |
Spag17 |
A |
T |
3: 99,934,668 (GRCm39) |
Y650F |
possibly damaging |
Het |
Stab2 |
C |
T |
10: 86,838,872 (GRCm39) |
G65S |
probably damaging |
Het |
Stambpl1 |
C |
G |
19: 34,204,121 (GRCm39) |
N70K |
probably damaging |
Het |
Stip1 |
C |
A |
19: 6,999,165 (GRCm39) |
C471F |
probably damaging |
Het |
Taf1 |
T |
C |
X: 100,584,500 (GRCm39) |
S223P |
probably benign |
Het |
Tchh |
C |
A |
3: 93,350,882 (GRCm39) |
N107K |
possibly damaging |
Het |
Tenm3 |
A |
C |
8: 48,685,139 (GRCm39) |
H2432Q |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,168,548 (GRCm39) |
N110S |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,662,076 (GRCm39) |
I306F |
probably benign |
Het |
Trpm4 |
A |
G |
7: 44,958,036 (GRCm39) |
I811T |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,710,950 (GRCm39) |
|
probably null |
Het |
Ttc28 |
A |
T |
5: 111,425,034 (GRCm39) |
I1589F |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,699,686 (GRCm39) |
|
probably benign |
Het |
U2af2 |
C |
A |
7: 5,070,544 (GRCm39) |
R78S |
probably benign |
Het |
Wdr17 |
A |
T |
8: 55,126,689 (GRCm39) |
D388E |
possibly damaging |
Het |
Wdr3 |
A |
T |
3: 100,061,186 (GRCm39) |
S261T |
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,066 (GRCm39) |
N245D |
possibly damaging |
Het |
Zfp692 |
A |
G |
11: 58,201,002 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
C |
13: 67,767,370 (GRCm39) |
H953R |
probably benign |
Het |
|
Other mutations in Trank1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00234:Trank1
|
APN |
9 |
111,221,677 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00467:Trank1
|
APN |
9 |
111,193,734 (GRCm39) |
splice site |
probably benign |
|
IGL00569:Trank1
|
APN |
9 |
111,174,579 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00585:Trank1
|
APN |
9 |
111,178,358 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01070:Trank1
|
APN |
9 |
111,195,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01134:Trank1
|
APN |
9 |
111,220,849 (GRCm39) |
missense |
probably benign |
|
IGL01154:Trank1
|
APN |
9 |
111,215,468 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01355:Trank1
|
APN |
9 |
111,194,588 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01407:Trank1
|
APN |
9 |
111,193,790 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01410:Trank1
|
APN |
9 |
111,194,117 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01410:Trank1
|
APN |
9 |
111,194,327 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01504:Trank1
|
APN |
9 |
111,202,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01744:Trank1
|
APN |
9 |
111,178,431 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02043:Trank1
|
APN |
9 |
111,193,028 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02104:Trank1
|
APN |
9 |
111,219,780 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02193:Trank1
|
APN |
9 |
111,196,344 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02581:Trank1
|
APN |
9 |
111,212,193 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02630:Trank1
|
APN |
9 |
111,202,143 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02839:Trank1
|
APN |
9 |
111,193,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02897:Trank1
|
APN |
9 |
111,196,585 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03065:Trank1
|
APN |
9 |
111,219,361 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL03123:Trank1
|
APN |
9 |
111,196,475 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Trank1
|
APN |
9 |
111,195,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03323:Trank1
|
APN |
9 |
111,181,184 (GRCm39) |
missense |
probably damaging |
1.00 |
1mM(1):Trank1
|
UTSW |
9 |
111,222,049 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Trank1
|
UTSW |
9 |
111,219,175 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Trank1
|
UTSW |
9 |
111,176,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Trank1
|
UTSW |
9 |
111,195,844 (GRCm39) |
missense |
probably benign |
0.00 |
R0064:Trank1
|
UTSW |
9 |
111,172,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0064:Trank1
|
UTSW |
9 |
111,172,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Trank1
|
UTSW |
9 |
111,221,978 (GRCm39) |
missense |
probably benign |
0.00 |
R0207:Trank1
|
UTSW |
9 |
111,195,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Trank1
|
UTSW |
9 |
111,195,092 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0334:Trank1
|
UTSW |
9 |
111,222,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Trank1
|
UTSW |
9 |
111,194,421 (GRCm39) |
missense |
probably benign |
0.00 |
R0383:Trank1
|
UTSW |
9 |
111,220,545 (GRCm39) |
missense |
probably benign |
0.08 |
R0421:Trank1
|
UTSW |
9 |
111,220,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Trank1
|
UTSW |
9 |
111,220,361 (GRCm39) |
missense |
probably benign |
0.19 |
R0518:Trank1
|
UTSW |
9 |
111,162,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Trank1
|
UTSW |
9 |
111,220,154 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0637:Trank1
|
UTSW |
9 |
111,219,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Trank1
|
UTSW |
9 |
111,194,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Trank1
|
UTSW |
9 |
111,195,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Trank1
|
UTSW |
9 |
111,176,537 (GRCm39) |
missense |
probably benign |
0.45 |
R0827:Trank1
|
UTSW |
9 |
111,178,485 (GRCm39) |
unclassified |
probably benign |
|
R1005:Trank1
|
UTSW |
9 |
111,162,789 (GRCm39) |
missense |
probably benign |
0.13 |
R1108:Trank1
|
UTSW |
9 |
111,194,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1155:Trank1
|
UTSW |
9 |
111,196,038 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1470:Trank1
|
UTSW |
9 |
111,172,300 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1470:Trank1
|
UTSW |
9 |
111,172,300 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1596:Trank1
|
UTSW |
9 |
111,195,358 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1601:Trank1
|
UTSW |
9 |
111,202,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Trank1
|
UTSW |
9 |
111,220,547 (GRCm39) |
missense |
probably benign |
|
R1754:Trank1
|
UTSW |
9 |
111,221,939 (GRCm39) |
missense |
probably benign |
0.00 |
R1767:Trank1
|
UTSW |
9 |
111,220,547 (GRCm39) |
missense |
probably benign |
|
R1809:Trank1
|
UTSW |
9 |
111,221,893 (GRCm39) |
missense |
probably benign |
0.34 |
R1912:Trank1
|
UTSW |
9 |
111,219,777 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Trank1
|
UTSW |
9 |
111,176,996 (GRCm39) |
critical splice donor site |
probably null |
|
R1960:Trank1
|
UTSW |
9 |
111,220,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1993:Trank1
|
UTSW |
9 |
111,207,900 (GRCm39) |
missense |
probably benign |
0.20 |
R2012:Trank1
|
UTSW |
9 |
111,194,096 (GRCm39) |
missense |
probably benign |
|
R2025:Trank1
|
UTSW |
9 |
111,221,107 (GRCm39) |
missense |
probably benign |
0.01 |
R2050:Trank1
|
UTSW |
9 |
111,193,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Trank1
|
UTSW |
9 |
111,196,001 (GRCm39) |
missense |
probably benign |
0.00 |
R2912:Trank1
|
UTSW |
9 |
111,221,551 (GRCm39) |
missense |
probably damaging |
0.98 |
R2962:Trank1
|
UTSW |
9 |
111,181,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Trank1
|
UTSW |
9 |
111,220,598 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3821:Trank1
|
UTSW |
9 |
111,207,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3822:Trank1
|
UTSW |
9 |
111,207,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R3892:Trank1
|
UTSW |
9 |
111,193,827 (GRCm39) |
missense |
probably benign |
0.03 |
R4105:Trank1
|
UTSW |
9 |
111,181,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Trank1
|
UTSW |
9 |
111,202,592 (GRCm39) |
nonsense |
probably null |
|
R4237:Trank1
|
UTSW |
9 |
111,196,103 (GRCm39) |
missense |
probably benign |
0.04 |
R4239:Trank1
|
UTSW |
9 |
111,196,103 (GRCm39) |
missense |
probably benign |
0.04 |
R4394:Trank1
|
UTSW |
9 |
111,194,265 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4417:Trank1
|
UTSW |
9 |
111,195,036 (GRCm39) |
missense |
probably benign |
0.17 |
R4611:Trank1
|
UTSW |
9 |
111,191,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Trank1
|
UTSW |
9 |
111,221,129 (GRCm39) |
missense |
probably benign |
0.40 |
R4731:Trank1
|
UTSW |
9 |
111,219,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Trank1
|
UTSW |
9 |
111,195,146 (GRCm39) |
missense |
probably benign |
0.00 |
R4852:Trank1
|
UTSW |
9 |
111,220,963 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4859:Trank1
|
UTSW |
9 |
111,194,078 (GRCm39) |
missense |
probably benign |
0.17 |
R4868:Trank1
|
UTSW |
9 |
111,194,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5080:Trank1
|
UTSW |
9 |
111,218,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R5156:Trank1
|
UTSW |
9 |
111,219,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Trank1
|
UTSW |
9 |
111,194,627 (GRCm39) |
missense |
probably benign |
0.00 |
R5234:Trank1
|
UTSW |
9 |
111,215,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Trank1
|
UTSW |
9 |
111,191,470 (GRCm39) |
missense |
probably benign |
0.12 |
R5419:Trank1
|
UTSW |
9 |
111,220,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Trank1
|
UTSW |
9 |
111,220,958 (GRCm39) |
missense |
probably benign |
0.00 |
R5444:Trank1
|
UTSW |
9 |
111,222,026 (GRCm39) |
missense |
probably benign |
0.04 |
R5543:Trank1
|
UTSW |
9 |
111,195,180 (GRCm39) |
missense |
probably damaging |
0.97 |
R5560:Trank1
|
UTSW |
9 |
111,219,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5772:Trank1
|
UTSW |
9 |
111,195,744 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5774:Trank1
|
UTSW |
9 |
111,220,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Trank1
|
UTSW |
9 |
111,194,928 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5858:Trank1
|
UTSW |
9 |
111,221,604 (GRCm39) |
missense |
probably benign |
|
R5878:Trank1
|
UTSW |
9 |
111,195,753 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5900:Trank1
|
UTSW |
9 |
111,220,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5917:Trank1
|
UTSW |
9 |
111,191,485 (GRCm39) |
missense |
probably benign |
0.38 |
R5954:Trank1
|
UTSW |
9 |
111,194,201 (GRCm39) |
missense |
probably benign |
0.13 |
R6041:Trank1
|
UTSW |
9 |
111,206,864 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6112:Trank1
|
UTSW |
9 |
111,220,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R6165:Trank1
|
UTSW |
9 |
111,220,940 (GRCm39) |
missense |
probably benign |
0.00 |
R6255:Trank1
|
UTSW |
9 |
111,181,314 (GRCm39) |
critical splice donor site |
probably null |
|
R6395:Trank1
|
UTSW |
9 |
111,196,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R6567:Trank1
|
UTSW |
9 |
111,176,589 (GRCm39) |
missense |
probably benign |
0.02 |
R6644:Trank1
|
UTSW |
9 |
111,193,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6724:Trank1
|
UTSW |
9 |
111,194,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Trank1
|
UTSW |
9 |
111,219,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Trank1
|
UTSW |
9 |
111,206,967 (GRCm39) |
missense |
probably benign |
0.00 |
R6934:Trank1
|
UTSW |
9 |
111,202,158 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Trank1
|
UTSW |
9 |
111,194,864 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7206:Trank1
|
UTSW |
9 |
111,174,583 (GRCm39) |
critical splice donor site |
probably null |
|
R7236:Trank1
|
UTSW |
9 |
111,202,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7247:Trank1
|
UTSW |
9 |
111,196,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Trank1
|
UTSW |
9 |
111,206,938 (GRCm39) |
missense |
probably benign |
0.02 |
R7310:Trank1
|
UTSW |
9 |
111,196,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Trank1
|
UTSW |
9 |
111,191,470 (GRCm39) |
missense |
probably benign |
0.12 |
R7448:Trank1
|
UTSW |
9 |
111,195,417 (GRCm39) |
missense |
probably benign |
0.01 |
R7477:Trank1
|
UTSW |
9 |
111,194,025 (GRCm39) |
missense |
probably benign |
0.00 |
R7514:Trank1
|
UTSW |
9 |
111,193,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7595:Trank1
|
UTSW |
9 |
111,195,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Trank1
|
UTSW |
9 |
111,194,364 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7648:Trank1
|
UTSW |
9 |
111,220,753 (GRCm39) |
missense |
probably benign |
|
R7737:Trank1
|
UTSW |
9 |
111,195,080 (GRCm39) |
nonsense |
probably null |
|
R7784:Trank1
|
UTSW |
9 |
111,193,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Trank1
|
UTSW |
9 |
111,221,584 (GRCm39) |
missense |
probably benign |
|
R7912:Trank1
|
UTSW |
9 |
111,220,596 (GRCm39) |
missense |
probably benign |
0.04 |
R7938:Trank1
|
UTSW |
9 |
111,194,096 (GRCm39) |
missense |
probably benign |
|
R7979:Trank1
|
UTSW |
9 |
111,206,967 (GRCm39) |
missense |
probably benign |
0.00 |
R8064:Trank1
|
UTSW |
9 |
111,181,144 (GRCm39) |
nonsense |
probably null |
|
R8100:Trank1
|
UTSW |
9 |
111,221,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Trank1
|
UTSW |
9 |
111,207,995 (GRCm39) |
missense |
probably benign |
0.31 |
R8198:Trank1
|
UTSW |
9 |
111,219,880 (GRCm39) |
missense |
probably benign |
0.09 |
R8219:Trank1
|
UTSW |
9 |
111,193,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Trank1
|
UTSW |
9 |
111,194,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R8316:Trank1
|
UTSW |
9 |
111,178,370 (GRCm39) |
missense |
probably benign |
0.38 |
R8347:Trank1
|
UTSW |
9 |
111,196,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R8436:Trank1
|
UTSW |
9 |
111,220,450 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8489:Trank1
|
UTSW |
9 |
111,219,343 (GRCm39) |
missense |
probably benign |
0.01 |
R8682:Trank1
|
UTSW |
9 |
111,194,412 (GRCm39) |
missense |
probably benign |
0.01 |
R8768:Trank1
|
UTSW |
9 |
111,218,344 (GRCm39) |
missense |
probably benign |
0.00 |
R8770:Trank1
|
UTSW |
9 |
111,219,892 (GRCm39) |
missense |
probably benign |
0.00 |
R8829:Trank1
|
UTSW |
9 |
111,176,591 (GRCm39) |
missense |
probably benign |
|
R8838:Trank1
|
UTSW |
9 |
111,193,973 (GRCm39) |
missense |
probably benign |
0.03 |
R8855:Trank1
|
UTSW |
9 |
111,141,289 (GRCm39) |
missense |
unknown |
|
R8929:Trank1
|
UTSW |
9 |
111,208,003 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9047:Trank1
|
UTSW |
9 |
111,191,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R9090:Trank1
|
UTSW |
9 |
111,174,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9114:Trank1
|
UTSW |
9 |
111,162,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9133:Trank1
|
UTSW |
9 |
111,220,770 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9177:Trank1
|
UTSW |
9 |
111,221,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9178:Trank1
|
UTSW |
9 |
111,196,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Trank1
|
UTSW |
9 |
111,174,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Trank1
|
UTSW |
9 |
111,195,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R9373:Trank1
|
UTSW |
9 |
111,194,259 (GRCm39) |
missense |
probably benign |
0.25 |
R9380:Trank1
|
UTSW |
9 |
111,221,738 (GRCm39) |
missense |
probably benign |
0.07 |
R9435:Trank1
|
UTSW |
9 |
111,193,890 (GRCm39) |
missense |
probably benign |
0.04 |
R9501:Trank1
|
UTSW |
9 |
111,176,943 (GRCm39) |
missense |
probably benign |
0.00 |
R9593:Trank1
|
UTSW |
9 |
111,191,365 (GRCm39) |
missense |
probably benign |
0.30 |
R9601:Trank1
|
UTSW |
9 |
111,202,193 (GRCm39) |
missense |
probably benign |
0.18 |
R9729:Trank1
|
UTSW |
9 |
111,220,537 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Trank1
|
UTSW |
9 |
111,172,304 (GRCm39) |
missense |
possibly damaging |
0.57 |
Z1088:Trank1
|
UTSW |
9 |
111,193,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Trank1
|
UTSW |
9 |
111,221,938 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Trank1
|
UTSW |
9 |
111,196,445 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Trank1
|
UTSW |
9 |
111,140,970 (GRCm39) |
missense |
unknown |
|
|