Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
A |
T |
4: 62,464,304 (GRCm39) |
R374* |
probably null |
Het |
5930422O12Rik |
A |
T |
8: 33,919,407 (GRCm39) |
R76* |
probably null |
Het |
A1cf |
G |
A |
19: 31,923,214 (GRCm39) |
A505T |
probably benign |
Het |
Abcc5 |
T |
A |
16: 20,241,150 (GRCm39) |
I12F |
probably damaging |
Het |
Abcf2 |
T |
C |
5: 24,771,562 (GRCm39) |
E555G |
probably damaging |
Het |
Acan |
A |
T |
7: 78,750,033 (GRCm39) |
E1601D |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adam2 |
T |
A |
14: 66,275,055 (GRCm39) |
K559N |
probably benign |
Het |
Akap11 |
A |
C |
14: 78,747,529 (GRCm39) |
D1619E |
possibly damaging |
Het |
Ankrd11 |
T |
C |
8: 123,622,307 (GRCm39) |
D515G |
probably benign |
Het |
Ankrd27 |
T |
A |
7: 35,318,796 (GRCm39) |
N562K |
probably damaging |
Het |
Atp10b |
T |
C |
11: 43,044,131 (GRCm39) |
I119T |
probably benign |
Het |
Bltp2 |
C |
T |
11: 78,162,750 (GRCm39) |
L871F |
possibly damaging |
Het |
Brd4 |
T |
A |
17: 32,432,514 (GRCm39) |
|
probably benign |
Het |
Catsperg2 |
C |
T |
7: 29,405,996 (GRCm39) |
C634Y |
possibly damaging |
Het |
Cep192 |
A |
G |
18: 67,961,553 (GRCm39) |
|
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,966,230 (GRCm39) |
I366F |
probably damaging |
Het |
Cnga4 |
G |
T |
7: 105,056,875 (GRCm39) |
R326L |
probably damaging |
Het |
Cntnap5b |
T |
A |
1: 99,999,878 (GRCm39) |
M212K |
probably benign |
Het |
Col6a6 |
T |
A |
9: 105,661,315 (GRCm39) |
M265L |
probably benign |
Het |
Cspg4b |
A |
T |
13: 113,505,677 (GRCm39) |
I727F |
probably damaging |
Het |
Cyp26b1 |
A |
T |
6: 84,551,538 (GRCm39) |
F417Y |
probably damaging |
Het |
Dhx15 |
A |
T |
5: 52,308,088 (GRCm39) |
M768K |
probably benign |
Het |
Drc7 |
G |
A |
8: 95,797,881 (GRCm39) |
R433H |
possibly damaging |
Het |
Duox2 |
C |
T |
2: 122,122,785 (GRCm39) |
V550M |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,138,810 (GRCm39) |
L456P |
probably damaging |
Het |
Fbxo39 |
T |
C |
11: 72,208,356 (GRCm39) |
I236T |
probably benign |
Het |
Fezf2 |
A |
G |
14: 12,343,977 (GRCm38) |
C305R |
probably damaging |
Het |
Fndc3b |
C |
A |
3: 27,511,155 (GRCm39) |
C785F |
probably benign |
Het |
Gm12253 |
T |
C |
11: 58,330,838 (GRCm39) |
|
probably benign |
Het |
Gnat2 |
T |
A |
3: 108,002,878 (GRCm39) |
Y95* |
probably null |
Het |
Gopc |
T |
C |
10: 52,226,774 (GRCm39) |
K220E |
probably damaging |
Het |
Hectd4 |
G |
A |
5: 121,392,314 (GRCm39) |
D193N |
possibly damaging |
Het |
Hexa |
G |
A |
9: 59,461,509 (GRCm39) |
|
probably null |
Het |
Hspa4l |
T |
C |
3: 40,739,840 (GRCm39) |
|
probably benign |
Het |
Hspa5 |
T |
C |
2: 34,664,332 (GRCm39) |
S301P |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,752,166 (GRCm39) |
S1307T |
possibly damaging |
Het |
Igtp |
T |
C |
11: 58,096,880 (GRCm39) |
L17P |
probably damaging |
Het |
Itk |
T |
C |
11: 46,244,743 (GRCm39) |
Y225C |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,830,088 (GRCm39) |
V560A |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,124,564 (GRCm39) |
N2875D |
probably damaging |
Het |
Lasp1 |
C |
A |
11: 97,697,677 (GRCm39) |
C32* |
probably null |
Het |
Lcp2 |
T |
A |
11: 34,019,854 (GRCm39) |
|
probably benign |
Het |
Lhx9 |
C |
T |
1: 138,760,642 (GRCm39) |
G236D |
probably benign |
Het |
Lrrc38 |
A |
T |
4: 143,076,979 (GRCm39) |
I81F |
probably damaging |
Het |
Ly6a |
C |
T |
15: 74,867,236 (GRCm39) |
V94M |
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,732,907 (GRCm39) |
E503G |
probably damaging |
Het |
Mertk |
T |
C |
2: 128,624,541 (GRCm39) |
|
probably benign |
Het |
Mrtfb |
T |
A |
16: 13,230,027 (GRCm39) |
I915N |
probably damaging |
Het |
Msantd2 |
G |
A |
9: 37,434,515 (GRCm39) |
D252N |
possibly damaging |
Het |
Mtmr12 |
T |
A |
15: 12,257,792 (GRCm39) |
L290* |
probably null |
Het |
Myo3a |
T |
C |
2: 22,250,409 (GRCm39) |
I92T |
probably benign |
Het |
Naglu |
T |
A |
11: 100,964,853 (GRCm39) |
N313K |
probably damaging |
Het |
Nceh1 |
T |
C |
3: 27,276,953 (GRCm39) |
V92A |
possibly damaging |
Het |
Ncf4 |
A |
G |
15: 78,135,083 (GRCm39) |
T47A |
probably damaging |
Het |
Nrp1 |
T |
A |
8: 129,187,164 (GRCm39) |
F403L |
probably damaging |
Het |
Nxph3 |
T |
C |
11: 95,402,082 (GRCm39) |
T111A |
possibly damaging |
Het |
Obscn |
T |
A |
11: 58,929,441 (GRCm39) |
E6061V |
probably damaging |
Het |
Obsl1 |
C |
A |
1: 75,469,571 (GRCm39) |
G1149W |
probably damaging |
Het |
Or14c39 |
A |
G |
7: 86,344,068 (GRCm39) |
T135A |
probably benign |
Het |
Or2k2 |
A |
T |
4: 58,784,981 (GRCm39) |
V247E |
probably damaging |
Het |
Or2p2 |
T |
A |
13: 21,256,544 (GRCm39) |
Y309F |
probably benign |
Het |
Or5b123 |
A |
G |
19: 13,596,849 (GRCm39) |
T65A |
probably benign |
Het |
Or5d14 |
C |
T |
2: 87,880,756 (GRCm39) |
V71I |
possibly damaging |
Het |
Or5p68 |
A |
C |
7: 107,946,121 (GRCm39) |
D22E |
probably benign |
Het |
Or6c70 |
T |
A |
10: 129,710,415 (GRCm39) |
L70F |
possibly damaging |
Het |
Pde9a |
T |
C |
17: 31,674,080 (GRCm39) |
V55A |
probably damaging |
Het |
Pip4k2c |
A |
T |
10: 127,041,690 (GRCm39) |
|
probably null |
Het |
Plvap |
T |
C |
8: 71,964,026 (GRCm39) |
N112S |
probably damaging |
Het |
Pop1 |
T |
A |
15: 34,530,004 (GRCm39) |
|
probably null |
Het |
Ppip5k2 |
T |
C |
1: 97,644,278 (GRCm39) |
H1113R |
possibly damaging |
Het |
Ptprk |
A |
T |
10: 28,449,388 (GRCm39) |
I962F |
probably damaging |
Het |
Rad51ap2 |
T |
C |
12: 11,507,043 (GRCm39) |
S322P |
possibly damaging |
Het |
Rasal1 |
A |
G |
5: 120,812,670 (GRCm39) |
T565A |
probably benign |
Het |
Rbm15 |
C |
A |
3: 107,238,471 (GRCm39) |
R642S |
probably damaging |
Het |
Rpsa |
G |
A |
9: 119,960,069 (GRCm39) |
E211K |
possibly damaging |
Het |
Ryr3 |
A |
G |
2: 112,517,155 (GRCm39) |
S3303P |
probably damaging |
Het |
Scg2 |
T |
A |
1: 79,413,229 (GRCm39) |
N458I |
possibly damaging |
Het |
Setx |
A |
G |
2: 29,069,655 (GRCm39) |
T2487A |
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,244,549 (GRCm39) |
|
probably benign |
Het |
Slc8a2 |
T |
A |
7: 15,874,914 (GRCm39) |
D387E |
probably benign |
Het |
Smarcc2 |
A |
G |
10: 128,310,591 (GRCm39) |
T407A |
probably benign |
Het |
Snap25 |
A |
G |
2: 136,619,384 (GRCm39) |
D179G |
probably damaging |
Het |
Socs4 |
T |
C |
14: 47,527,325 (GRCm39) |
S74P |
probably benign |
Het |
Sp6 |
T |
A |
11: 96,912,751 (GRCm39) |
Y155N |
probably benign |
Het |
Srrt |
C |
T |
5: 137,294,389 (GRCm39) |
|
probably benign |
Het |
Steap1 |
C |
T |
5: 5,786,431 (GRCm39) |
M335I |
probably benign |
Het |
Stra6 |
A |
T |
9: 58,052,772 (GRCm39) |
Y250F |
probably benign |
Het |
Svil |
T |
C |
18: 5,094,582 (GRCm39) |
S1421P |
probably damaging |
Het |
Tcea3 |
G |
A |
4: 135,998,677 (GRCm39) |
C317Y |
probably damaging |
Het |
Tmco6 |
T |
C |
18: 36,870,757 (GRCm39) |
L117S |
probably damaging |
Het |
Trp53bp1 |
T |
C |
2: 121,100,718 (GRCm39) |
K89E |
probably damaging |
Het |
Trp63 |
T |
A |
16: 25,583,052 (GRCm39) |
|
probably benign |
Het |
Ube2d2a |
A |
G |
18: 35,933,185 (GRCm39) |
Y74C |
probably damaging |
Het |
Usp19 |
T |
G |
9: 108,375,708 (GRCm39) |
F885V |
probably damaging |
Het |
Utp18 |
T |
A |
11: 93,773,003 (GRCm39) |
|
probably benign |
Het |
Vmn2r116 |
T |
C |
17: 23,620,387 (GRCm39) |
I707T |
possibly damaging |
Het |
Vmn2r68 |
T |
A |
7: 84,882,457 (GRCm39) |
|
probably benign |
Het |
Vmn2r68 |
C |
G |
7: 84,882,466 (GRCm39) |
|
probably null |
Het |
Zfp318 |
C |
T |
17: 46,723,540 (GRCm39) |
P1848S |
probably benign |
Het |
Zfp984 |
G |
T |
4: 147,839,722 (GRCm39) |
N376K |
probably benign |
Het |
|
Other mutations in Atr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00640:Atr
|
APN |
9 |
95,747,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00922:Atr
|
APN |
9 |
95,789,398 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01020:Atr
|
APN |
9 |
95,744,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01345:Atr
|
APN |
9 |
95,823,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01364:Atr
|
APN |
9 |
95,747,677 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01456:Atr
|
APN |
9 |
95,832,618 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01534:Atr
|
APN |
9 |
95,747,599 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01761:Atr
|
APN |
9 |
95,833,501 (GRCm39) |
splice site |
probably benign |
|
IGL01791:Atr
|
APN |
9 |
95,803,834 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01831:Atr
|
APN |
9 |
95,752,807 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01973:Atr
|
APN |
9 |
95,753,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Atr
|
APN |
9 |
95,763,473 (GRCm39) |
splice site |
probably benign |
|
IGL02016:Atr
|
APN |
9 |
95,809,228 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02035:Atr
|
APN |
9 |
95,748,735 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02058:Atr
|
APN |
9 |
95,753,540 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02081:Atr
|
APN |
9 |
95,765,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02224:Atr
|
APN |
9 |
95,760,682 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02234:Atr
|
APN |
9 |
95,829,303 (GRCm39) |
splice site |
probably benign |
|
IGL02367:Atr
|
APN |
9 |
95,781,194 (GRCm39) |
nonsense |
probably null |
|
IGL02621:Atr
|
APN |
9 |
95,790,453 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02728:Atr
|
APN |
9 |
95,818,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02833:Atr
|
APN |
9 |
95,744,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Atr
|
APN |
9 |
95,747,314 (GRCm39) |
missense |
probably benign |
|
IGL03107:Atr
|
APN |
9 |
95,779,783 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03382:Atr
|
APN |
9 |
95,802,875 (GRCm39) |
nonsense |
probably null |
|
PIT4812001:Atr
|
UTSW |
9 |
95,792,702 (GRCm39) |
missense |
probably benign |
0.41 |
R0042:Atr
|
UTSW |
9 |
95,809,409 (GRCm39) |
splice site |
probably benign |
|
R0042:Atr
|
UTSW |
9 |
95,809,409 (GRCm39) |
splice site |
probably benign |
|
R0282:Atr
|
UTSW |
9 |
95,744,851 (GRCm39) |
missense |
probably benign |
0.12 |
R0512:Atr
|
UTSW |
9 |
95,817,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R0547:Atr
|
UTSW |
9 |
95,781,218 (GRCm39) |
splice site |
probably benign |
|
R0567:Atr
|
UTSW |
9 |
95,747,882 (GRCm39) |
missense |
probably benign |
0.00 |
R0631:Atr
|
UTSW |
9 |
95,756,830 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1116:Atr
|
UTSW |
9 |
95,749,689 (GRCm39) |
nonsense |
probably null |
|
R1171:Atr
|
UTSW |
9 |
95,789,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Atr
|
UTSW |
9 |
95,832,689 (GRCm39) |
missense |
probably benign |
0.08 |
R1345:Atr
|
UTSW |
9 |
95,802,408 (GRCm39) |
missense |
probably benign |
0.25 |
R1400:Atr
|
UTSW |
9 |
95,744,901 (GRCm39) |
missense |
probably benign |
0.32 |
R1413:Atr
|
UTSW |
9 |
95,814,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Atr
|
UTSW |
9 |
95,752,096 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1557:Atr
|
UTSW |
9 |
95,753,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R1591:Atr
|
UTSW |
9 |
95,827,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1602:Atr
|
UTSW |
9 |
95,833,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Atr
|
UTSW |
9 |
95,818,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Atr
|
UTSW |
9 |
95,743,509 (GRCm39) |
missense |
probably benign |
0.38 |
R1709:Atr
|
UTSW |
9 |
95,753,129 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Atr
|
UTSW |
9 |
95,779,634 (GRCm39) |
missense |
probably benign |
0.01 |
R1729:Atr
|
UTSW |
9 |
95,779,634 (GRCm39) |
missense |
probably benign |
0.01 |
R1739:Atr
|
UTSW |
9 |
95,779,634 (GRCm39) |
missense |
probably benign |
0.01 |
R1816:Atr
|
UTSW |
9 |
95,748,747 (GRCm39) |
missense |
probably benign |
0.00 |
R1824:Atr
|
UTSW |
9 |
95,818,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Atr
|
UTSW |
9 |
95,787,870 (GRCm39) |
missense |
probably benign |
0.01 |
R1857:Atr
|
UTSW |
9 |
95,747,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Atr
|
UTSW |
9 |
95,747,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Atr
|
UTSW |
9 |
95,752,658 (GRCm39) |
splice site |
probably null |
|
R1913:Atr
|
UTSW |
9 |
95,748,786 (GRCm39) |
missense |
probably benign |
0.01 |
R2042:Atr
|
UTSW |
9 |
95,752,075 (GRCm39) |
missense |
probably benign |
0.00 |
R2210:Atr
|
UTSW |
9 |
95,789,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R2230:Atr
|
UTSW |
9 |
95,802,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2361:Atr
|
UTSW |
9 |
95,753,210 (GRCm39) |
missense |
probably benign |
0.41 |
R2399:Atr
|
UTSW |
9 |
95,753,652 (GRCm39) |
missense |
probably benign |
0.00 |
R2431:Atr
|
UTSW |
9 |
95,744,945 (GRCm39) |
missense |
probably benign |
0.24 |
R2860:Atr
|
UTSW |
9 |
95,756,296 (GRCm39) |
missense |
probably benign |
0.07 |
R2861:Atr
|
UTSW |
9 |
95,756,296 (GRCm39) |
missense |
probably benign |
0.07 |
R3019:Atr
|
UTSW |
9 |
95,787,871 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3684:Atr
|
UTSW |
9 |
95,802,453 (GRCm39) |
missense |
probably damaging |
0.96 |
R4155:Atr
|
UTSW |
9 |
95,770,177 (GRCm39) |
nonsense |
probably null |
|
R4295:Atr
|
UTSW |
9 |
95,756,479 (GRCm39) |
missense |
probably benign |
0.04 |
R4359:Atr
|
UTSW |
9 |
95,833,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R4506:Atr
|
UTSW |
9 |
95,747,290 (GRCm39) |
missense |
probably benign |
0.21 |
R4523:Atr
|
UTSW |
9 |
95,744,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Atr
|
UTSW |
9 |
95,756,471 (GRCm39) |
missense |
probably benign |
0.26 |
R4588:Atr
|
UTSW |
9 |
95,747,720 (GRCm39) |
missense |
probably benign |
|
R4646:Atr
|
UTSW |
9 |
95,753,250 (GRCm39) |
critical splice donor site |
probably null |
|
R4702:Atr
|
UTSW |
9 |
95,802,408 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4743:Atr
|
UTSW |
9 |
95,744,845 (GRCm39) |
missense |
probably benign |
0.14 |
R4782:Atr
|
UTSW |
9 |
95,744,850 (GRCm39) |
missense |
probably benign |
0.00 |
R4928:Atr
|
UTSW |
9 |
95,789,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R5031:Atr
|
UTSW |
9 |
95,747,755 (GRCm39) |
missense |
probably damaging |
0.98 |
R5138:Atr
|
UTSW |
9 |
95,819,649 (GRCm39) |
missense |
probably benign |
0.15 |
R5188:Atr
|
UTSW |
9 |
95,803,778 (GRCm39) |
missense |
probably benign |
0.00 |
R5219:Atr
|
UTSW |
9 |
95,763,291 (GRCm39) |
missense |
probably damaging |
0.99 |
R5307:Atr
|
UTSW |
9 |
95,760,597 (GRCm39) |
missense |
probably benign |
0.01 |
R5414:Atr
|
UTSW |
9 |
95,752,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5628:Atr
|
UTSW |
9 |
95,756,279 (GRCm39) |
nonsense |
probably null |
|
R5664:Atr
|
UTSW |
9 |
95,787,866 (GRCm39) |
missense |
probably benign |
0.00 |
R5678:Atr
|
UTSW |
9 |
95,833,540 (GRCm39) |
nonsense |
probably null |
|
R5724:Atr
|
UTSW |
9 |
95,748,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5759:Atr
|
UTSW |
9 |
95,756,455 (GRCm39) |
missense |
probably benign |
0.01 |
R5763:Atr
|
UTSW |
9 |
95,827,176 (GRCm39) |
missense |
probably benign |
0.04 |
R5922:Atr
|
UTSW |
9 |
95,785,735 (GRCm39) |
missense |
probably benign |
0.00 |
R6051:Atr
|
UTSW |
9 |
95,790,422 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6161:Atr
|
UTSW |
9 |
95,747,372 (GRCm39) |
missense |
probably benign |
|
R6171:Atr
|
UTSW |
9 |
95,763,324 (GRCm39) |
nonsense |
probably null |
|
R6532:Atr
|
UTSW |
9 |
95,790,461 (GRCm39) |
missense |
probably benign |
|
R6774:Atr
|
UTSW |
9 |
95,809,266 (GRCm39) |
missense |
probably benign |
0.00 |
R6894:Atr
|
UTSW |
9 |
95,809,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R6930:Atr
|
UTSW |
9 |
95,748,688 (GRCm39) |
missense |
probably benign |
0.21 |
R7018:Atr
|
UTSW |
9 |
95,748,747 (GRCm39) |
missense |
probably benign |
0.17 |
R7056:Atr
|
UTSW |
9 |
95,744,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R7103:Atr
|
UTSW |
9 |
95,747,425 (GRCm39) |
missense |
probably damaging |
0.98 |
R7154:Atr
|
UTSW |
9 |
95,747,098 (GRCm39) |
missense |
probably benign |
|
R7157:Atr
|
UTSW |
9 |
95,751,953 (GRCm39) |
missense |
probably benign |
0.00 |
R7188:Atr
|
UTSW |
9 |
95,744,844 (GRCm39) |
nonsense |
probably null |
|
R7189:Atr
|
UTSW |
9 |
95,744,844 (GRCm39) |
nonsense |
probably null |
|
R7300:Atr
|
UTSW |
9 |
95,747,423 (GRCm39) |
missense |
probably benign |
0.00 |
R7337:Atr
|
UTSW |
9 |
95,753,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7584:Atr
|
UTSW |
9 |
95,824,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R7602:Atr
|
UTSW |
9 |
95,789,436 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7633:Atr
|
UTSW |
9 |
95,829,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7640:Atr
|
UTSW |
9 |
95,789,346 (GRCm39) |
splice site |
probably null |
|
R7677:Atr
|
UTSW |
9 |
95,767,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Atr
|
UTSW |
9 |
95,757,743 (GRCm39) |
nonsense |
probably null |
|
R7700:Atr
|
UTSW |
9 |
95,757,743 (GRCm39) |
nonsense |
probably null |
|
R7790:Atr
|
UTSW |
9 |
95,756,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R8027:Atr
|
UTSW |
9 |
95,747,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R8147:Atr
|
UTSW |
9 |
95,781,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R8204:Atr
|
UTSW |
9 |
95,817,566 (GRCm39) |
missense |
|
|
R8306:Atr
|
UTSW |
9 |
95,802,423 (GRCm39) |
missense |
|
|
R8462:Atr
|
UTSW |
9 |
95,749,579 (GRCm39) |
missense |
probably benign |
|
R8716:Atr
|
UTSW |
9 |
95,789,468 (GRCm39) |
missense |
probably benign |
0.09 |
R8748:Atr
|
UTSW |
9 |
95,814,476 (GRCm39) |
missense |
probably benign |
0.00 |
R8795:Atr
|
UTSW |
9 |
95,749,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8891:Atr
|
UTSW |
9 |
95,787,813 (GRCm39) |
missense |
probably benign |
0.03 |
R8976:Atr
|
UTSW |
9 |
95,772,819 (GRCm39) |
missense |
probably benign |
0.00 |
R9024:Atr
|
UTSW |
9 |
95,789,416 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9116:Atr
|
UTSW |
9 |
95,747,851 (GRCm39) |
missense |
probably benign |
0.00 |
R9523:Atr
|
UTSW |
9 |
95,792,610 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9524:Atr
|
UTSW |
9 |
95,792,610 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9525:Atr
|
UTSW |
9 |
95,792,610 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9527:Atr
|
UTSW |
9 |
95,767,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Atr
|
UTSW |
9 |
95,802,833 (GRCm39) |
missense |
probably damaging |
0.98 |
R9629:Atr
|
UTSW |
9 |
95,747,098 (GRCm39) |
missense |
probably benign |
|
R9642:Atr
|
UTSW |
9 |
95,821,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R9652:Atr
|
UTSW |
9 |
95,756,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Atr
|
UTSW |
9 |
95,797,050 (GRCm39) |
missense |
probably benign |
0.40 |
R9678:Atr
|
UTSW |
9 |
95,792,610 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9728:Atr
|
UTSW |
9 |
95,797,050 (GRCm39) |
missense |
probably benign |
0.40 |
R9731:Atr
|
UTSW |
9 |
95,747,092 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9732:Atr
|
UTSW |
9 |
95,743,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Atr
|
UTSW |
9 |
95,819,703 (GRCm39) |
critical splice donor site |
probably null |
|
X0019:Atr
|
UTSW |
9 |
95,822,924 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Atr
|
UTSW |
9 |
95,767,373 (GRCm39) |
splice site |
probably null |
|
Z1177:Atr
|
UTSW |
9 |
95,770,153 (GRCm39) |
missense |
probably benign |
0.01 |
|