Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot5 |
A |
T |
12: 84,122,261 (GRCm39) |
I282F |
probably benign |
Het |
Adam19 |
C |
A |
11: 46,029,744 (GRCm39) |
Q730K |
probably benign |
Het |
Adgrv1 |
A |
G |
13: 81,636,066 (GRCm39) |
V3481A |
possibly damaging |
Het |
Akr1c20 |
T |
C |
13: 4,537,207 (GRCm39) |
D316G |
probably benign |
Het |
Ap3b1 |
G |
A |
13: 94,630,225 (GRCm39) |
V827I |
unknown |
Het |
Aph1a |
T |
A |
3: 95,802,821 (GRCm39) |
D140E |
probably damaging |
Het |
Arhgef19 |
G |
T |
4: 140,976,929 (GRCm39) |
V502L |
possibly damaging |
Het |
Arl9 |
T |
C |
5: 77,154,473 (GRCm39) |
F67S |
probably damaging |
Het |
B430305J03Rik |
G |
A |
3: 61,271,361 (GRCm39) |
|
probably benign |
Het |
B4galnt2 |
A |
G |
11: 95,781,809 (GRCm39) |
F119L |
probably damaging |
Het |
Bcap29 |
T |
A |
12: 31,680,839 (GRCm39) |
N49I |
probably damaging |
Het |
Capn11 |
T |
A |
17: 45,943,327 (GRCm39) |
K616* |
probably null |
Het |
Cdh12 |
T |
A |
15: 21,520,452 (GRCm39) |
Y306N |
probably damaging |
Het |
Cep350 |
T |
A |
1: 155,828,960 (GRCm39) |
N315Y |
probably damaging |
Het |
Cfap300 |
A |
C |
9: 8,027,266 (GRCm39) |
S91A |
probably benign |
Het |
Cited2 |
C |
A |
10: 17,599,794 (GRCm39) |
P34Q |
probably damaging |
Het |
Cmya5 |
A |
T |
13: 93,226,297 (GRCm39) |
D2930E |
probably benign |
Het |
Cog3 |
T |
A |
14: 75,966,761 (GRCm39) |
K470* |
probably null |
Het |
Commd10 |
A |
G |
18: 47,123,552 (GRCm39) |
T136A |
probably benign |
Het |
Csf2ra |
C |
A |
19: 61,214,782 (GRCm39) |
D181Y |
probably damaging |
Het |
Csmd1 |
T |
A |
8: 15,982,610 (GRCm39) |
I2686F |
probably damaging |
Het |
Dhx29 |
T |
C |
13: 113,081,620 (GRCm39) |
S415P |
probably benign |
Het |
Dsel |
A |
T |
1: 111,788,645 (GRCm39) |
F630Y |
probably damaging |
Het |
Ell |
T |
A |
8: 71,031,590 (GRCm39) |
I96N |
possibly damaging |
Het |
Ephx2 |
T |
A |
14: 66,325,752 (GRCm39) |
I358L |
probably benign |
Het |
Fam162b |
A |
G |
10: 51,463,307 (GRCm39) |
I120T |
probably damaging |
Het |
Fam187a |
T |
C |
11: 102,776,606 (GRCm39) |
Y137H |
probably damaging |
Het |
Fastk |
T |
C |
5: 24,646,801 (GRCm39) |
E403G |
probably damaging |
Het |
Fcrlb |
C |
A |
1: 170,734,901 (GRCm39) |
V409F |
probably benign |
Het |
Flot2 |
G |
T |
11: 77,948,831 (GRCm39) |
A269S |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,245,563 (GRCm39) |
N419K |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,552,350 (GRCm39) |
M61K |
probably null |
Het |
Htr2a |
T |
C |
14: 74,943,568 (GRCm39) |
F383L |
probably damaging |
Het |
Kctd6 |
C |
T |
14: 8,222,253 (GRCm38) |
R32C |
probably damaging |
Het |
Khdc1a |
A |
G |
1: 21,421,189 (GRCm39) |
T125A |
probably benign |
Het |
Klhl40 |
T |
C |
9: 121,609,004 (GRCm39) |
S390P |
probably benign |
Het |
Lonp1 |
G |
A |
17: 56,921,956 (GRCm39) |
T808I |
probably damaging |
Het |
Loxhd1 |
A |
C |
18: 77,492,585 (GRCm39) |
D1342A |
probably damaging |
Het |
Lrat |
T |
C |
3: 82,804,417 (GRCm39) |
I187V |
probably benign |
Het |
Lrif1 |
T |
C |
3: 106,643,162 (GRCm39) |
*238Q |
probably null |
Het |
Lrp2bp |
T |
C |
8: 46,465,025 (GRCm39) |
F48S |
probably benign |
Het |
Mafg |
A |
G |
11: 120,520,504 (GRCm39) |
M32T |
possibly damaging |
Het |
Map4 |
C |
T |
9: 109,864,023 (GRCm39) |
T416I |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,965,659 (GRCm39) |
F1236S |
probably damaging |
Het |
Nfatc3 |
A |
G |
8: 106,810,466 (GRCm39) |
D414G |
probably damaging |
Het |
Nhsl3 |
G |
T |
4: 129,117,370 (GRCm39) |
S476R |
probably damaging |
Het |
Nrip2 |
T |
G |
6: 128,382,037 (GRCm39) |
V50G |
probably damaging |
Het |
Or10aa3 |
A |
T |
1: 173,878,365 (GRCm39) |
K142I |
probably benign |
Het |
Or10j5 |
A |
G |
1: 172,784,374 (GRCm39) |
N4S |
probably benign |
Het |
Or52ae7 |
T |
A |
7: 103,119,353 (GRCm39) |
F36I |
possibly damaging |
Het |
Or5b24 |
T |
A |
19: 12,912,207 (GRCm39) |
I35N |
probably damaging |
Het |
Pcdhb18 |
A |
T |
18: 37,623,822 (GRCm39) |
H384L |
probably benign |
Het |
Pik3r1 |
A |
T |
13: 101,822,882 (GRCm39) |
Y607N |
probably damaging |
Het |
Plagl2 |
G |
A |
2: 153,074,397 (GRCm39) |
T168I |
probably damaging |
Het |
Polr2a |
A |
G |
11: 69,633,222 (GRCm39) |
S912P |
probably damaging |
Het |
Ppp1r16b |
A |
G |
2: 158,603,415 (GRCm39) |
K447E |
possibly damaging |
Het |
Prkd1 |
T |
C |
12: 50,388,822 (GRCm39) |
E907G |
possibly damaging |
Het |
Rabep2 |
A |
G |
7: 126,043,712 (GRCm39) |
R470G |
probably damaging |
Het |
Rasal2 |
T |
C |
1: 157,001,730 (GRCm39) |
Y518C |
probably damaging |
Het |
Rbmxl1 |
A |
G |
8: 79,232,711 (GRCm39) |
Y211H |
probably damaging |
Het |
Rdh7 |
T |
C |
10: 127,720,454 (GRCm39) |
Y306C |
probably benign |
Het |
Rtn3 |
T |
C |
19: 7,435,276 (GRCm39) |
I220V |
probably damaging |
Het |
Scn8a |
A |
G |
15: 100,913,742 (GRCm39) |
N1045D |
possibly damaging |
Het |
Scube1 |
T |
C |
15: 83,491,638 (GRCm39) |
H952R |
probably damaging |
Het |
Sf3b1 |
A |
G |
1: 55,039,811 (GRCm39) |
I690T |
probably damaging |
Het |
Sharpin |
T |
C |
15: 76,232,136 (GRCm39) |
K240R |
probably benign |
Het |
Skint5 |
A |
G |
4: 113,420,656 (GRCm39) |
I1108T |
unknown |
Het |
Snip1 |
A |
G |
4: 124,964,994 (GRCm39) |
D133G |
probably benign |
Het |
St3gal3 |
T |
C |
4: 117,871,971 (GRCm39) |
Y77C |
probably damaging |
Het |
Sytl3 |
T |
C |
17: 6,982,880 (GRCm39) |
V112A |
probably benign |
Het |
Ttc24 |
A |
T |
3: 87,980,401 (GRCm39) |
|
probably null |
Het |
Ubr3 |
A |
T |
2: 69,839,473 (GRCm39) |
E1529V |
probably damaging |
Het |
Utrn |
T |
A |
10: 12,585,882 (GRCm39) |
H965L |
probably benign |
Het |
Xrn2 |
T |
A |
2: 146,903,343 (GRCm39) |
L781Q |
probably damaging |
Het |
Zbtb11 |
T |
C |
16: 55,811,045 (GRCm39) |
I401T |
probably benign |
Het |
Zc3h14 |
C |
T |
12: 98,724,839 (GRCm39) |
P167L |
probably damaging |
Het |
Zfp609 |
G |
T |
9: 65,610,374 (GRCm39) |
S863* |
probably null |
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 |
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 |
R1992: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 |
|
|