Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
T |
C |
1: 138,781,380 (GRCm39) |
T90A |
probably damaging |
Het |
A930011G23Rik |
T |
C |
5: 99,381,784 (GRCm39) |
D326G |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,795,581 (GRCm39) |
I446F |
probably damaging |
Het |
Adam34l |
T |
C |
8: 44,080,176 (GRCm39) |
K16R |
probably benign |
Het |
Adamts14 |
A |
G |
10: 61,034,439 (GRCm39) |
Y1150H |
probably benign |
Het |
Adgrl2 |
A |
G |
3: 148,522,880 (GRCm39) |
I217T |
possibly damaging |
Het |
Afap1l1 |
A |
T |
18: 61,874,842 (GRCm39) |
Y446* |
probably null |
Het |
Aimp2 |
G |
A |
5: 143,843,548 (GRCm39) |
A14V |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,535,586 (GRCm39) |
H143Y |
probably damaging |
Het |
Aldh2 |
A |
T |
5: 121,714,026 (GRCm39) |
V207E |
possibly damaging |
Het |
Aoc1l2 |
T |
A |
6: 48,907,703 (GRCm39) |
H234Q |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,986,861 (GRCm39) |
E230G |
probably damaging |
Het |
Arrdc3 |
G |
A |
13: 81,031,808 (GRCm39) |
D14N |
probably damaging |
Het |
Atn1 |
A |
G |
6: 124,722,291 (GRCm39) |
|
probably benign |
Het |
Atxn7l1 |
G |
A |
12: 33,408,743 (GRCm39) |
D302N |
probably damaging |
Het |
Bbs1 |
T |
A |
19: 4,941,736 (GRCm39) |
H518L |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,054,181 (GRCm39) |
H3100L |
probably benign |
Het |
Bmpr1a |
C |
A |
14: 34,147,050 (GRCm39) |
G241C |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Calcrl |
T |
C |
2: 84,200,855 (GRCm39) |
Y63C |
probably damaging |
Het |
Cand2 |
A |
G |
6: 115,762,093 (GRCm39) |
H173R |
possibly damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Card14 |
A |
T |
11: 119,212,647 (GRCm39) |
|
probably null |
Het |
Cd3d |
T |
A |
9: 44,896,299 (GRCm39) |
Y29* |
probably null |
Het |
Cd4 |
A |
G |
6: 124,844,651 (GRCm39) |
V378A |
possibly damaging |
Het |
Cluh |
A |
T |
11: 74,550,828 (GRCm39) |
H318L |
probably damaging |
Het |
Clvs1 |
T |
A |
4: 9,281,899 (GRCm39) |
D114E |
probably benign |
Het |
Cnot4 |
T |
A |
6: 35,000,344 (GRCm39) |
T548S |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crebbp |
A |
T |
16: 3,946,561 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
G |
1: 53,621,835 (GRCm39) |
K1097Q |
possibly damaging |
Het |
Doc2a |
T |
A |
7: 126,450,979 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
T |
1: 123,832,833 (GRCm39) |
V48E |
probably null |
Het |
Dsg2 |
A |
G |
18: 20,734,530 (GRCm39) |
K836R |
probably damaging |
Het |
Egr2 |
T |
C |
10: 67,375,857 (GRCm39) |
V164A |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,970,221 (GRCm39) |
S1132T |
probably benign |
Het |
Espn |
T |
A |
4: 152,213,012 (GRCm39) |
|
probably null |
Het |
Fam83b |
A |
G |
9: 76,399,304 (GRCm39) |
S600P |
probably benign |
Het |
Fanca |
A |
T |
8: 124,024,551 (GRCm39) |
N425K |
possibly damaging |
Het |
Flot2 |
C |
T |
11: 77,949,445 (GRCm39) |
L294F |
probably damaging |
Het |
Frs2 |
A |
G |
10: 116,910,459 (GRCm39) |
V301A |
probably benign |
Het |
Fv1 |
T |
A |
4: 147,953,618 (GRCm39) |
N61K |
possibly damaging |
Het |
Fxr2 |
A |
G |
11: 69,540,659 (GRCm39) |
E339G |
possibly damaging |
Het |
Gck |
T |
C |
11: 5,856,515 (GRCm39) |
Y214C |
probably damaging |
Het |
Golga3 |
C |
G |
5: 110,340,839 (GRCm39) |
T551R |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,625 (GRCm39) |
S59P |
probably damaging |
Het |
Gsdme |
C |
T |
6: 50,185,102 (GRCm39) |
V451M |
probably damaging |
Het |
H2-T13 |
A |
C |
17: 36,391,938 (GRCm39) |
I216S |
probably damaging |
Het |
Herc4 |
T |
A |
10: 63,081,743 (GRCm39) |
V22E |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
A |
T |
6: 52,141,576 (GRCm39) |
S17T |
probably damaging |
Het |
Hs3st5 |
A |
G |
10: 36,708,882 (GRCm39) |
Y139C |
probably damaging |
Het |
Ism1 |
G |
A |
2: 139,587,937 (GRCm39) |
V221I |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,796,108 (GRCm39) |
L1222F |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,419,261 (GRCm39) |
N476S |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,261,631 (GRCm39) |
D602G |
possibly damaging |
Het |
Ktn1 |
A |
G |
14: 47,932,978 (GRCm39) |
K711E |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Macf1 |
A |
G |
4: 123,350,488 (GRCm39) |
S3792P |
probably damaging |
Het |
Maml3 |
C |
T |
3: 51,598,178 (GRCm39) |
M189I |
probably benign |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mep1a |
T |
G |
17: 43,813,573 (GRCm39) |
I13L |
probably benign |
Het |
Mkrn2 |
G |
T |
6: 115,586,562 (GRCm39) |
C16F |
probably damaging |
Het |
Mlh1 |
C |
T |
9: 111,057,631 (GRCm39) |
A727T |
probably damaging |
Het |
Muc21 |
A |
T |
17: 35,929,600 (GRCm39) |
S1529T |
probably benign |
Het |
Naa16 |
T |
C |
14: 79,593,931 (GRCm39) |
Y344C |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,752,628 (GRCm39) |
Y585F |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,587,753 (GRCm39) |
K149R |
probably damaging |
Het |
Nufip1 |
T |
A |
14: 76,372,287 (GRCm39) |
I467N |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,632,960 (GRCm39) |
I1057T |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,886,653 (GRCm39) |
|
probably benign |
Het |
Or10ag52 |
T |
A |
2: 87,043,588 (GRCm39) |
C117* |
probably null |
Het |
Or5k1 |
A |
G |
16: 58,617,309 (GRCm39) |
V300A |
probably benign |
Het |
Or5k14 |
A |
C |
16: 58,692,874 (GRCm39) |
I213R |
probably benign |
Het |
Pi4k2a |
A |
T |
19: 42,104,377 (GRCm39) |
I380F |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pik3cg |
A |
T |
12: 32,254,024 (GRCm39) |
D654E |
possibly damaging |
Het |
Poli |
G |
T |
18: 70,642,058 (GRCm39) |
P714Q |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,378,230 (GRCm39) |
N201D |
probably benign |
Het |
Prorp |
A |
G |
12: 55,384,991 (GRCm39) |
D89G |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,747 (GRCm39) |
K81N |
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,271,948 (GRCm39) |
|
probably null |
Het |
Sec24a |
C |
T |
11: 51,627,190 (GRCm39) |
V241I |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,950,567 (GRCm39) |
T160A |
possibly damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,375 (GRCm39) |
I497T |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,532 (GRCm39) |
D512V |
probably damaging |
Het |
Slc43a3 |
C |
T |
2: 84,788,084 (GRCm39) |
R489C |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,452,089 (GRCm39) |
F327L |
probably benign |
Het |
Slitrk3 |
A |
G |
3: 72,957,104 (GRCm39) |
V556A |
possibly damaging |
Het |
Spata6l |
A |
G |
19: 28,926,024 (GRCm39) |
F130L |
probably damaging |
Het |
Spib |
T |
C |
7: 44,178,281 (GRCm39) |
E180G |
probably benign |
Het |
Spint2 |
T |
A |
7: 28,958,833 (GRCm39) |
N128Y |
probably damaging |
Het |
Spx |
G |
A |
6: 142,364,245 (GRCm39) |
G102E |
probably benign |
Het |
Spz1 |
T |
A |
13: 92,712,166 (GRCm39) |
E103D |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,495 (GRCm39) |
I138T |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,000,448 (GRCm39) |
I206N |
possibly damaging |
Het |
Tcaf2 |
T |
C |
6: 42,606,791 (GRCm39) |
T388A |
probably benign |
Het |
Tdpoz8 |
G |
T |
3: 92,981,344 (GRCm39) |
A121S |
probably benign |
Het |
Thap12 |
T |
C |
7: 98,365,572 (GRCm39) |
V580A |
possibly damaging |
Het |
Tlr5 |
T |
A |
1: 182,801,912 (GRCm39) |
D405E |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim43a |
T |
G |
9: 88,466,312 (GRCm39) |
L211R |
probably damaging |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Ttll8 |
T |
C |
15: 88,798,654 (GRCm39) |
T694A |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,953,535 (GRCm39) |
A823V |
probably damaging |
Het |
Ubqln5 |
C |
A |
7: 103,778,741 (GRCm39) |
V28F |
probably damaging |
Het |
Ulk1 |
T |
A |
5: 110,935,017 (GRCm39) |
Q972L |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,994,062 (GRCm39) |
Y398H |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,531 (GRCm39) |
D615G |
probably benign |
Het |
Utp15 |
A |
G |
13: 98,387,420 (GRCm39) |
C385R |
probably benign |
Het |
Vmn2r91 |
T |
A |
17: 18,356,142 (GRCm39) |
V603D |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Yjefn3 |
A |
T |
8: 70,341,645 (GRCm39) |
|
probably null |
Het |
Ywhab |
A |
T |
2: 163,853,807 (GRCm39) |
I95F |
probably damaging |
Het |
Zfp143 |
C |
T |
7: 109,660,489 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
C |
G |
7: 27,401,949 (GRCm39) |
T135R |
possibly damaging |
Het |
Zfp970 |
A |
G |
2: 177,166,663 (GRCm39) |
Q79R |
possibly damaging |
Het |
|
Other mutations in Tnxb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Tnxb
|
APN |
17 |
34,904,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00424:Tnxb
|
APN |
17 |
34,933,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00486:Tnxb
|
APN |
17 |
34,911,356 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00952:Tnxb
|
APN |
17 |
34,932,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00974:Tnxb
|
APN |
17 |
34,937,707 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01017:Tnxb
|
APN |
17 |
34,912,782 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01082:Tnxb
|
APN |
17 |
34,933,584 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01397:Tnxb
|
APN |
17 |
34,933,647 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01473:Tnxb
|
APN |
17 |
34,904,675 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01642:Tnxb
|
APN |
17 |
34,937,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01774:Tnxb
|
APN |
17 |
34,907,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01971:Tnxb
|
APN |
17 |
34,891,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02016:Tnxb
|
APN |
17 |
34,891,249 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02160:Tnxb
|
APN |
17 |
34,933,719 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02473:Tnxb
|
APN |
17 |
34,936,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Tnxb
|
APN |
17 |
34,903,913 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02831:Tnxb
|
APN |
17 |
34,922,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02838:Tnxb
|
APN |
17 |
34,908,606 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02965:Tnxb
|
APN |
17 |
34,928,628 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03155:Tnxb
|
APN |
17 |
34,932,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Tnxb
|
APN |
17 |
34,914,921 (GRCm39) |
nonsense |
probably null |
|
IGL03215:Tnxb
|
APN |
17 |
34,911,499 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03256:Tnxb
|
APN |
17 |
34,907,694 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
BB018:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Tnxb
|
UTSW |
17 |
34,897,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Tnxb
|
UTSW |
17 |
34,901,266 (GRCm39) |
missense |
probably benign |
0.07 |
R0049:Tnxb
|
UTSW |
17 |
34,928,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0050:Tnxb
|
UTSW |
17 |
34,892,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Tnxb
|
UTSW |
17 |
34,918,007 (GRCm39) |
missense |
probably benign |
0.32 |
R0233:Tnxb
|
UTSW |
17 |
34,918,007 (GRCm39) |
missense |
probably benign |
0.32 |
R0311:Tnxb
|
UTSW |
17 |
34,935,958 (GRCm39) |
missense |
probably damaging |
0.97 |
R0326:Tnxb
|
UTSW |
17 |
34,917,153 (GRCm39) |
missense |
probably benign |
0.32 |
R0387:Tnxb
|
UTSW |
17 |
34,902,548 (GRCm39) |
missense |
probably benign |
0.30 |
R0396:Tnxb
|
UTSW |
17 |
34,890,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Tnxb
|
UTSW |
17 |
34,937,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R0540:Tnxb
|
UTSW |
17 |
34,890,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0563:Tnxb
|
UTSW |
17 |
34,935,921 (GRCm39) |
missense |
probably benign |
0.05 |
R0575:Tnxb
|
UTSW |
17 |
34,936,180 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0586:Tnxb
|
UTSW |
17 |
34,891,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Tnxb
|
UTSW |
17 |
34,890,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:Tnxb
|
UTSW |
17 |
34,937,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Tnxb
|
UTSW |
17 |
34,902,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Tnxb
|
UTSW |
17 |
34,908,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0898:Tnxb
|
UTSW |
17 |
34,889,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R0970:Tnxb
|
UTSW |
17 |
34,917,917 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0972:Tnxb
|
UTSW |
17 |
34,904,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R1118:Tnxb
|
UTSW |
17 |
34,904,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Tnxb
|
UTSW |
17 |
34,904,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R1226:Tnxb
|
UTSW |
17 |
34,907,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Tnxb
|
UTSW |
17 |
34,890,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Tnxb
|
UTSW |
17 |
34,929,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R1349:Tnxb
|
UTSW |
17 |
34,929,267 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1356:Tnxb
|
UTSW |
17 |
34,914,446 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1372:Tnxb
|
UTSW |
17 |
34,929,267 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1521:Tnxb
|
UTSW |
17 |
34,930,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Tnxb
|
UTSW |
17 |
34,937,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Tnxb
|
UTSW |
17 |
34,929,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R1735:Tnxb
|
UTSW |
17 |
34,936,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Tnxb
|
UTSW |
17 |
34,902,548 (GRCm39) |
missense |
probably benign |
0.30 |
R1802:Tnxb
|
UTSW |
17 |
34,922,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R1824:Tnxb
|
UTSW |
17 |
34,911,307 (GRCm39) |
nonsense |
probably null |
|
R1838:Tnxb
|
UTSW |
17 |
34,897,884 (GRCm39) |
missense |
probably damaging |
0.96 |
R1863:Tnxb
|
UTSW |
17 |
34,889,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Tnxb
|
UTSW |
17 |
34,922,431 (GRCm39) |
nonsense |
probably null |
|
R1867:Tnxb
|
UTSW |
17 |
34,890,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Tnxb
|
UTSW |
17 |
34,908,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1884:Tnxb
|
UTSW |
17 |
34,908,539 (GRCm39) |
missense |
probably benign |
0.01 |
R1889:Tnxb
|
UTSW |
17 |
34,914,799 (GRCm39) |
missense |
probably damaging |
0.97 |
R1969:Tnxb
|
UTSW |
17 |
34,898,055 (GRCm39) |
missense |
probably benign |
0.20 |
R1989:Tnxb
|
UTSW |
17 |
34,912,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Tnxb
|
UTSW |
17 |
34,902,351 (GRCm39) |
missense |
probably benign |
0.08 |
R1991:Tnxb
|
UTSW |
17 |
34,901,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Tnxb
|
UTSW |
17 |
34,890,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Tnxb
|
UTSW |
17 |
34,911,553 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2018:Tnxb
|
UTSW |
17 |
34,890,724 (GRCm39) |
missense |
probably benign |
0.04 |
R2030:Tnxb
|
UTSW |
17 |
34,937,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Tnxb
|
UTSW |
17 |
34,918,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Tnxb
|
UTSW |
17 |
34,901,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Tnxb
|
UTSW |
17 |
34,891,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Tnxb
|
UTSW |
17 |
34,928,391 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2207:Tnxb
|
UTSW |
17 |
34,928,391 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2215:Tnxb
|
UTSW |
17 |
34,923,114 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2413:Tnxb
|
UTSW |
17 |
34,937,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R2680:Tnxb
|
UTSW |
17 |
34,922,594 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2910:Tnxb
|
UTSW |
17 |
34,891,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R2984:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R3120:Tnxb
|
UTSW |
17 |
34,911,329 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3429:Tnxb
|
UTSW |
17 |
34,922,561 (GRCm39) |
missense |
probably damaging |
0.98 |
R3429:Tnxb
|
UTSW |
17 |
34,891,605 (GRCm39) |
nonsense |
probably null |
|
R3552:Tnxb
|
UTSW |
17 |
34,937,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R3698:Tnxb
|
UTSW |
17 |
34,909,407 (GRCm39) |
critical splice donor site |
probably null |
|
R3720:Tnxb
|
UTSW |
17 |
34,931,938 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3841:Tnxb
|
UTSW |
17 |
34,917,897 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3848:Tnxb
|
UTSW |
17 |
34,909,369 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3886:Tnxb
|
UTSW |
17 |
34,937,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Tnxb
|
UTSW |
17 |
34,890,845 (GRCm39) |
missense |
probably benign |
0.22 |
R4159:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4160:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4161:Tnxb
|
UTSW |
17 |
34,930,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R4181:Tnxb
|
UTSW |
17 |
34,928,428 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4210:Tnxb
|
UTSW |
17 |
34,929,951 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4275:Tnxb
|
UTSW |
17 |
34,917,205 (GRCm39) |
missense |
probably damaging |
0.98 |
R4329:Tnxb
|
UTSW |
17 |
34,912,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4394:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4395:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4397:Tnxb
|
UTSW |
17 |
34,897,636 (GRCm39) |
nonsense |
probably null |
|
R4540:Tnxb
|
UTSW |
17 |
34,922,309 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4673:Tnxb
|
UTSW |
17 |
34,891,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R4719:Tnxb
|
UTSW |
17 |
34,908,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Tnxb
|
UTSW |
17 |
34,918,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R4753:Tnxb
|
UTSW |
17 |
34,914,909 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4777:Tnxb
|
UTSW |
17 |
34,890,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Tnxb
|
UTSW |
17 |
34,936,981 (GRCm39) |
missense |
probably damaging |
0.98 |
R4898:Tnxb
|
UTSW |
17 |
34,914,566 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4938:Tnxb
|
UTSW |
17 |
34,932,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Tnxb
|
UTSW |
17 |
34,936,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Tnxb
|
UTSW |
17 |
34,929,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R5223:Tnxb
|
UTSW |
17 |
34,923,052 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5269:Tnxb
|
UTSW |
17 |
34,922,582 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5333:Tnxb
|
UTSW |
17 |
34,909,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Tnxb
|
UTSW |
17 |
34,928,599 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5470:Tnxb
|
UTSW |
17 |
34,935,947 (GRCm39) |
missense |
probably null |
1.00 |
R5475:Tnxb
|
UTSW |
17 |
34,908,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Tnxb
|
UTSW |
17 |
34,929,998 (GRCm39) |
missense |
probably benign |
|
R5596:Tnxb
|
UTSW |
17 |
34,907,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Tnxb
|
UTSW |
17 |
34,909,179 (GRCm39) |
missense |
probably benign |
0.22 |
R5599:Tnxb
|
UTSW |
17 |
34,909,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Tnxb
|
UTSW |
17 |
34,902,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Tnxb
|
UTSW |
17 |
34,936,504 (GRCm39) |
nonsense |
probably null |
|
R5625:Tnxb
|
UTSW |
17 |
34,904,185 (GRCm39) |
missense |
probably benign |
0.30 |
R5734:Tnxb
|
UTSW |
17 |
34,917,884 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5896:Tnxb
|
UTSW |
17 |
34,891,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R5961:Tnxb
|
UTSW |
17 |
34,937,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Tnxb
|
UTSW |
17 |
34,904,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Tnxb
|
UTSW |
17 |
34,929,338 (GRCm39) |
missense |
probably damaging |
0.98 |
R6134:Tnxb
|
UTSW |
17 |
34,890,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R6325:Tnxb
|
UTSW |
17 |
34,911,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6358:Tnxb
|
UTSW |
17 |
34,897,968 (GRCm39) |
missense |
probably damaging |
0.98 |
R6362:Tnxb
|
UTSW |
17 |
34,913,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R6432:Tnxb
|
UTSW |
17 |
34,936,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6461:Tnxb
|
UTSW |
17 |
34,890,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Tnxb
|
UTSW |
17 |
34,912,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Tnxb
|
UTSW |
17 |
34,909,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R6477:Tnxb
|
UTSW |
17 |
34,938,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Tnxb
|
UTSW |
17 |
34,937,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Tnxb
|
UTSW |
17 |
34,928,606 (GRCm39) |
nonsense |
probably null |
|
R6787:Tnxb
|
UTSW |
17 |
34,929,710 (GRCm39) |
missense |
probably benign |
0.02 |
R6805:Tnxb
|
UTSW |
17 |
34,917,127 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6860:Tnxb
|
UTSW |
17 |
34,932,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R6883:Tnxb
|
UTSW |
17 |
34,937,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R7049:Tnxb
|
UTSW |
17 |
34,936,242 (GRCm39) |
critical splice donor site |
probably null |
|
R7107:Tnxb
|
UTSW |
17 |
34,890,314 (GRCm39) |
missense |
unknown |
|
R7172:Tnxb
|
UTSW |
17 |
34,914,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R7206:Tnxb
|
UTSW |
17 |
34,923,075 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7219:Tnxb
|
UTSW |
17 |
34,898,039 (GRCm39) |
missense |
probably benign |
0.08 |
R7237:Tnxb
|
UTSW |
17 |
34,901,170 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7257:Tnxb
|
UTSW |
17 |
34,935,475 (GRCm39) |
missense |
probably benign |
0.44 |
R7269:Tnxb
|
UTSW |
17 |
34,914,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7302:Tnxb
|
UTSW |
17 |
34,897,875 (GRCm39) |
missense |
probably benign |
0.41 |
R7372:Tnxb
|
UTSW |
17 |
34,936,228 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7384:Tnxb
|
UTSW |
17 |
34,937,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Tnxb
|
UTSW |
17 |
34,937,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Tnxb
|
UTSW |
17 |
34,922,335 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7480:Tnxb
|
UTSW |
17 |
34,934,747 (GRCm39) |
missense |
probably damaging |
0.96 |
R7506:Tnxb
|
UTSW |
17 |
34,934,665 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7586:Tnxb
|
UTSW |
17 |
34,935,382 (GRCm39) |
missense |
probably damaging |
0.98 |
R7688:Tnxb
|
UTSW |
17 |
34,890,880 (GRCm39) |
missense |
probably benign |
0.23 |
R7690:Tnxb
|
UTSW |
17 |
34,908,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7690:Tnxb
|
UTSW |
17 |
34,908,494 (GRCm39) |
missense |
probably benign |
0.03 |
R7732:Tnxb
|
UTSW |
17 |
34,913,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Tnxb
|
UTSW |
17 |
34,890,398 (GRCm39) |
missense |
unknown |
|
R7760:Tnxb
|
UTSW |
17 |
34,931,911 (GRCm39) |
missense |
probably damaging |
0.96 |
R7874:Tnxb
|
UTSW |
17 |
34,930,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Tnxb
|
UTSW |
17 |
34,911,428 (GRCm39) |
missense |
probably benign |
0.02 |
R7922:Tnxb
|
UTSW |
17 |
34,933,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Tnxb
|
UTSW |
17 |
34,907,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Tnxb
|
UTSW |
17 |
34,936,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R7953:Tnxb
|
UTSW |
17 |
34,929,077 (GRCm39) |
missense |
probably benign |
0.03 |
R7953:Tnxb
|
UTSW |
17 |
34,928,509 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7977:Tnxb
|
UTSW |
17 |
34,929,194 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7985:Tnxb
|
UTSW |
17 |
34,935,984 (GRCm39) |
critical splice donor site |
probably null |
|
R7987:Tnxb
|
UTSW |
17 |
34,929,194 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8040:Tnxb
|
UTSW |
17 |
34,935,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Tnxb
|
UTSW |
17 |
34,923,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R8074:Tnxb
|
UTSW |
17 |
34,922,955 (GRCm39) |
missense |
probably benign |
0.32 |
R8089:Tnxb
|
UTSW |
17 |
34,891,763 (GRCm39) |
missense |
unknown |
|
R8169:Tnxb
|
UTSW |
17 |
34,918,181 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8348:Tnxb
|
UTSW |
17 |
34,929,102 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8352:Tnxb
|
UTSW |
17 |
34,908,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Tnxb
|
UTSW |
17 |
34,931,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R8452:Tnxb
|
UTSW |
17 |
34,908,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R8527:Tnxb
|
UTSW |
17 |
34,907,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Tnxb
|
UTSW |
17 |
34,934,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8813:Tnxb
|
UTSW |
17 |
34,938,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R8936:Tnxb
|
UTSW |
17 |
34,904,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R8986:Tnxb
|
UTSW |
17 |
34,897,646 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9001:Tnxb
|
UTSW |
17 |
34,922,410 (GRCm39) |
missense |
probably benign |
0.32 |
R9215:Tnxb
|
UTSW |
17 |
34,891,564 (GRCm39) |
missense |
unknown |
|
R9226:Tnxb
|
UTSW |
17 |
34,904,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Tnxb
|
UTSW |
17 |
34,929,134 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9279:Tnxb
|
UTSW |
17 |
34,898,088 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9363:Tnxb
|
UTSW |
17 |
34,917,294 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9367:Tnxb
|
UTSW |
17 |
34,931,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Tnxb
|
UTSW |
17 |
34,904,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9606:Tnxb
|
UTSW |
17 |
34,914,578 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9650:Tnxb
|
UTSW |
17 |
34,930,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R9677:Tnxb
|
UTSW |
17 |
34,917,878 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9690:Tnxb
|
UTSW |
17 |
34,936,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Tnxb
|
UTSW |
17 |
34,903,987 (GRCm39) |
missense |
probably benign |
0.32 |
X0004:Tnxb
|
UTSW |
17 |
34,922,389 (GRCm39) |
missense |
possibly damaging |
0.71 |
X0010:Tnxb
|
UTSW |
17 |
34,890,908 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Tnxb
|
UTSW |
17 |
34,913,163 (GRCm39) |
missense |
possibly damaging |
0.51 |
X0063:Tnxb
|
UTSW |
17 |
34,922,482 (GRCm39) |
missense |
probably damaging |
0.98 |
X0064:Tnxb
|
UTSW |
17 |
34,913,006 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnxb
|
UTSW |
17 |
34,937,700 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Tnxb
|
UTSW |
17 |
34,902,305 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnxb
|
UTSW |
17 |
34,890,740 (GRCm39) |
missense |
unknown |
|
|