Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110082I17Rik |
C |
A |
5: 139,349,812 (GRCm39) |
G79V |
probably damaging |
Het |
4930562C15Rik |
T |
A |
16: 4,684,082 (GRCm39) |
Y226N |
probably benign |
Het |
Arhgap45 |
G |
A |
10: 79,863,706 (GRCm39) |
A819T |
probably damaging |
Het |
Bach1 |
G |
A |
16: 87,519,390 (GRCm39) |
C560Y |
possibly damaging |
Het |
Capn13 |
T |
A |
17: 73,633,467 (GRCm39) |
|
probably null |
Het |
Casq2 |
G |
T |
3: 102,017,628 (GRCm39) |
A103S |
possibly damaging |
Het |
Cfap100 |
A |
G |
6: 90,394,656 (GRCm39) |
F57S |
|
Het |
Clca3a2 |
A |
T |
3: 144,783,653 (GRCm39) |
L654Q |
probably damaging |
Het |
Cntnap5c |
T |
A |
17: 58,411,765 (GRCm39) |
|
probably null |
Het |
Cplane2 |
A |
G |
4: 140,945,530 (GRCm39) |
H127R |
probably damaging |
Het |
Crtc2 |
G |
C |
3: 90,170,883 (GRCm39) |
G652A |
probably damaging |
Het |
Csnk1g2 |
A |
G |
10: 80,475,636 (GRCm39) |
D401G |
probably damaging |
Het |
Dars1 |
T |
C |
1: 128,304,002 (GRCm39) |
N242D |
probably null |
Het |
Dnah10 |
T |
C |
5: 124,877,946 (GRCm39) |
L2677P |
probably damaging |
Het |
Dnal1 |
G |
A |
12: 84,171,330 (GRCm39) |
A3T |
probably benign |
Het |
Dpep2 |
C |
T |
8: 106,722,849 (GRCm39) |
V60I |
|
Het |
Eeig1 |
T |
C |
2: 32,453,760 (GRCm39) |
I203T |
probably benign |
Het |
Ehmt2 |
T |
A |
17: 35,122,339 (GRCm39) |
I302N |
probably benign |
Het |
Eif3a |
C |
T |
19: 60,750,628 (GRCm39) |
R1309Q |
unknown |
Het |
Eno4 |
T |
A |
19: 58,935,084 (GRCm39) |
Y100N |
probably benign |
Het |
Ephx2 |
A |
T |
14: 66,349,602 (GRCm39) |
|
probably null |
Het |
Fbxw14 |
A |
T |
9: 109,106,284 (GRCm39) |
I251K |
probably benign |
Het |
Fcgbp |
T |
C |
7: 27,784,919 (GRCm39) |
|
probably null |
Het |
Foxm1 |
A |
C |
6: 128,348,671 (GRCm39) |
|
probably null |
Het |
Fscn3 |
T |
A |
6: 28,430,328 (GRCm39) |
I166N |
possibly damaging |
Het |
Gdpd4 |
G |
T |
7: 97,621,335 (GRCm39) |
V193L |
probably benign |
Het |
Gnpat |
T |
G |
8: 125,606,869 (GRCm39) |
C352G |
probably benign |
Het |
H2-Q7 |
T |
A |
17: 35,658,910 (GRCm39) |
Y120* |
probably null |
Het |
Klri1 |
G |
A |
6: 129,694,070 (GRCm39) |
R6C |
probably benign |
Het |
Kmo |
T |
C |
1: 175,476,729 (GRCm39) |
V154A |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,559,685 (GRCm39) |
L1031P |
probably damaging |
Het |
Lrrc14b |
T |
G |
13: 74,511,286 (GRCm39) |
T265P |
possibly damaging |
Het |
Lrrc2 |
C |
T |
9: 110,809,954 (GRCm39) |
T330I |
probably benign |
Het |
Lyn |
T |
A |
4: 3,783,050 (GRCm39) |
S428T |
probably damaging |
Het |
Lypd10 |
T |
A |
7: 24,412,000 (GRCm39) |
M60K |
probably benign |
Het |
Mfsd8 |
T |
A |
3: 40,791,550 (GRCm39) |
M59L |
probably benign |
Het |
Mok |
T |
A |
12: 110,774,799 (GRCm39) |
Q341L |
probably benign |
Het |
Muc21 |
T |
C |
17: 35,932,072 (GRCm39) |
T705A |
unknown |
Het |
Myh3 |
C |
A |
11: 66,979,856 (GRCm39) |
N598K |
probably benign |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Nlrp4e |
A |
G |
7: 23,019,931 (GRCm39) |
I139M |
probably benign |
Het |
Or11g25 |
T |
C |
14: 50,723,692 (GRCm39) |
V259A |
probably benign |
Het |
Or3a10 |
T |
A |
11: 73,935,707 (GRCm39) |
Q131L |
possibly damaging |
Het |
Or4b13 |
G |
A |
2: 90,082,442 (GRCm39) |
R297* |
probably null |
Het |
Or51g2 |
A |
G |
7: 102,622,545 (GRCm39) |
L218P |
probably damaging |
Het |
Or52n2b |
A |
T |
7: 104,565,619 (GRCm39) |
Y295N |
possibly damaging |
Het |
Osbpl7 |
G |
A |
11: 96,945,676 (GRCm39) |
S312N |
probably damaging |
Het |
Paxip1 |
A |
G |
5: 27,977,093 (GRCm39) |
L323P |
unknown |
Het |
Pcdh18 |
T |
A |
3: 49,699,684 (GRCm39) |
H926L |
probably damaging |
Het |
Pcm1 |
T |
G |
8: 41,763,153 (GRCm39) |
S1460R |
possibly damaging |
Het |
Pdha2 |
A |
G |
3: 140,917,155 (GRCm39) |
S118P |
possibly damaging |
Het |
Pdss1 |
A |
T |
2: 22,791,824 (GRCm39) |
Y86F |
probably benign |
Het |
Ppargc1a |
A |
T |
5: 51,631,026 (GRCm39) |
D534E |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,102,455 (GRCm39) |
K2538R |
probably benign |
Het |
Ptprq |
A |
T |
10: 107,418,351 (GRCm39) |
I1675N |
probably damaging |
Het |
Rgma |
C |
T |
7: 73,025,630 (GRCm39) |
P3L |
probably benign |
Het |
Ros1 |
A |
G |
10: 51,940,768 (GRCm39) |
|
probably null |
Het |
Sema4g |
C |
T |
19: 44,987,410 (GRCm39) |
R519W |
probably damaging |
Het |
Serpinc1 |
T |
A |
1: 160,820,971 (GRCm39) |
F139L |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,184,696 (GRCm39) |
I198T |
probably damaging |
Het |
Slc4a5 |
T |
C |
6: 83,280,373 (GRCm39) |
V1007A |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,147,783 (GRCm39) |
Y17C |
possibly damaging |
Het |
Tex261 |
C |
A |
6: 83,751,999 (GRCm39) |
|
probably null |
Het |
Timmdc1 |
T |
A |
16: 38,331,148 (GRCm39) |
T128S |
probably benign |
Het |
Tmem120b |
C |
A |
5: 123,237,999 (GRCm39) |
Y96* |
probably null |
Het |
Tmem196 |
T |
A |
12: 119,982,311 (GRCm39) |
F182I |
possibly damaging |
Het |
Tph1 |
T |
C |
7: 46,303,233 (GRCm39) |
|
silent |
Het |
Trmt9b |
A |
T |
8: 36,978,857 (GRCm39) |
K153N |
probably damaging |
Het |
Trpc1 |
G |
A |
9: 95,592,323 (GRCm39) |
Q551* |
probably null |
Het |
Tubgcp3 |
T |
C |
8: 12,666,099 (GRCm39) |
N828D |
probably benign |
Het |
Unc13a |
C |
A |
8: 72,108,933 (GRCm39) |
G478W |
probably damaging |
Het |
Usp15 |
T |
A |
10: 122,961,798 (GRCm39) |
T627S |
|
Het |
Vmn1r115 |
A |
T |
7: 20,578,144 (GRCm39) |
I256N |
probably damaging |
Het |
Vmn2r6 |
T |
A |
3: 64,447,310 (GRCm39) |
K585N |
probably benign |
Het |
Vsir |
G |
T |
10: 60,194,047 (GRCm39) |
|
probably null |
Het |
Xirp2 |
A |
G |
2: 67,343,543 (GRCm39) |
D1928G |
probably benign |
Het |
Xylt1 |
A |
G |
7: 117,249,846 (GRCm39) |
Y672C |
probably damaging |
Het |
Yrdc |
A |
G |
4: 124,744,880 (GRCm39) |
S105G |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,254,616 (GRCm39) |
N1403K |
probably damaging |
Het |
Zfp160 |
A |
T |
17: 21,247,298 (GRCm39) |
H616L |
probably damaging |
Het |
Zfp637 |
T |
A |
6: 117,822,252 (GRCm39) |
F127I |
probably damaging |
Het |
Zfp69 |
G |
T |
4: 120,787,731 (GRCm39) |
A528D |
probably damaging |
Het |
Zpr1 |
T |
A |
9: 46,189,645 (GRCm39) |
L342Q |
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 |
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 |
34,908,494 (GRCm39) |
missense |
probably benign |
0.03 |
R7690:Tnxb
|
UTSW |
17 |
34,908,501 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|
|