Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
A |
T |
7: 119,140,075 (GRCm39) |
E492V |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
Bdkrb2 |
G |
T |
12: 105,558,416 (GRCm39) |
R219L |
probably benign |
Het |
Bhmt2 |
A |
T |
13: 93,798,837 (GRCm39) |
M328K |
probably benign |
Het |
Btbd3 |
A |
G |
2: 138,125,881 (GRCm39) |
D286G |
probably benign |
Het |
Bub1b |
T |
G |
2: 118,437,167 (GRCm39) |
L122V |
probably benign |
Het |
Caml |
T |
C |
13: 55,772,820 (GRCm39) |
S155P |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,824,150 (GRCm39) |
K74E |
probably benign |
Het |
Chst4 |
A |
G |
8: 110,757,255 (GRCm39) |
S120P |
probably damaging |
Het |
Col11a1 |
A |
G |
3: 113,860,213 (GRCm39) |
D213G |
unknown |
Het |
Cripto |
C |
A |
9: 110,772,235 (GRCm39) |
V54L |
probably benign |
Het |
Cxcl10 |
TACTCAC |
TACTCACTCAC |
5: 92,495,941 (GRCm39) |
|
probably null |
Het |
Cxcl10 |
CAC |
CACTAAC |
5: 92,495,945 (GRCm39) |
|
probably null |
Het |
Cyp26b1 |
A |
T |
6: 84,553,653 (GRCm39) |
I167N |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,406,921 (GRCm39) |
S2195P |
probably benign |
Het |
Ddx25 |
T |
A |
9: 35,458,142 (GRCm39) |
K326* |
probably null |
Het |
Dip2c |
A |
T |
13: 9,543,162 (GRCm39) |
Y36F |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,586,068 (GRCm39) |
D538G |
probably damaging |
Het |
E4f1 |
C |
T |
17: 24,670,523 (GRCm39) |
D55N |
probably damaging |
Het |
Emp1 |
G |
T |
6: 135,358,077 (GRCm39) |
W141L |
probably damaging |
Het |
Faim2 |
T |
A |
15: 99,398,135 (GRCm39) |
H271L |
probably benign |
Het |
Fbxw9 |
T |
C |
8: 85,792,707 (GRCm39) |
M352T |
possibly damaging |
Het |
Fcrl2 |
A |
T |
3: 87,164,167 (GRCm39) |
F321I |
probably benign |
Het |
Frzb |
C |
T |
2: 80,268,834 (GRCm39) |
|
probably null |
Het |
Gal3st1 |
G |
T |
11: 3,948,931 (GRCm39) |
K379N |
probably damaging |
Het |
Gm5519 |
G |
A |
19: 33,800,372 (GRCm39) |
C22Y |
possibly damaging |
Het |
Gpn3 |
T |
C |
5: 122,516,583 (GRCm39) |
F71L |
probably benign |
Het |
H2-M9 |
A |
G |
17: 36,952,545 (GRCm39) |
V167A |
probably benign |
Het |
Hars1 |
A |
G |
18: 36,904,467 (GRCm39) |
F182L |
possibly damaging |
Het |
Hid1 |
T |
C |
11: 115,243,543 (GRCm39) |
T502A |
probably benign |
Het |
Hipk3 |
G |
T |
2: 104,302,021 (GRCm39) |
T57K |
probably benign |
Het |
Iqsec2 |
A |
G |
X: 150,927,727 (GRCm39) |
S87G |
probably benign |
Het |
Itpk1 |
G |
A |
12: 102,572,378 (GRCm39) |
L112F |
probably damaging |
Het |
Klk1b9 |
T |
A |
7: 43,443,817 (GRCm39) |
D110E |
possibly damaging |
Het |
Lemd3 |
A |
T |
10: 120,785,246 (GRCm39) |
M535K |
possibly damaging |
Het |
Lipg |
A |
T |
18: 75,078,894 (GRCm39) |
S453T |
possibly damaging |
Het |
Lrrc75a |
A |
T |
11: 62,500,069 (GRCm39) |
W150R |
probably damaging |
Het |
Lyg1 |
T |
C |
1: 37,986,305 (GRCm39) |
E143G |
probably damaging |
Het |
Map3k1 |
A |
G |
13: 111,892,177 (GRCm39) |
V1026A |
probably benign |
Het |
Mgat3 |
T |
A |
15: 80,095,838 (GRCm39) |
F222I |
probably benign |
Het |
Mindy4 |
A |
T |
6: 55,232,601 (GRCm39) |
N348I |
possibly damaging |
Het |
Ms4a20 |
T |
C |
19: 11,089,741 (GRCm39) |
Y48C |
probably damaging |
Het |
Myo1b |
A |
C |
1: 51,817,684 (GRCm39) |
F532C |
probably damaging |
Het |
Naif1 |
T |
A |
2: 32,342,558 (GRCm39) |
N36K |
probably damaging |
Het |
Nkpd1 |
C |
A |
7: 19,258,012 (GRCm39) |
A597E |
possibly damaging |
Het |
Npr2 |
A |
G |
4: 43,647,260 (GRCm39) |
D772G |
possibly damaging |
Het |
Or52n4 |
T |
G |
7: 104,294,204 (GRCm39) |
D123A |
probably damaging |
Het |
Or6a2 |
T |
C |
7: 106,600,791 (GRCm39) |
N92S |
probably benign |
Het |
Pcolce2 |
A |
T |
9: 95,576,793 (GRCm39) |
M355L |
probably benign |
Het |
Pdgfra |
A |
T |
5: 75,334,108 (GRCm39) |
I394F |
probably damaging |
Het |
Pdzrn3 |
G |
A |
6: 101,127,838 (GRCm39) |
R943C |
probably damaging |
Het |
Pml |
A |
G |
9: 58,141,821 (GRCm39) |
V337A |
probably damaging |
Het |
Pnpla2 |
T |
A |
7: 141,038,794 (GRCm39) |
M321K |
probably benign |
Het |
Poln |
A |
T |
5: 34,261,284 (GRCm39) |
N546K |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prss28 |
T |
A |
17: 25,529,029 (GRCm39) |
F123L |
possibly damaging |
Het |
Psg18 |
A |
G |
7: 18,080,004 (GRCm39) |
V399A |
probably benign |
Het |
Rab5a |
T |
C |
17: 53,813,443 (GRCm39) |
C212R |
probably damaging |
Het |
Ranbp6 |
A |
T |
19: 29,789,679 (GRCm39) |
D224E |
probably benign |
Het |
Recql4 |
T |
C |
15: 76,588,239 (GRCm39) |
I1104M |
possibly damaging |
Het |
Rev1 |
A |
T |
1: 38,127,581 (GRCm39) |
N226K |
possibly damaging |
Het |
Rhbdl3 |
T |
A |
11: 80,244,418 (GRCm39) |
V375E |
possibly damaging |
Het |
Senp6 |
T |
A |
9: 80,024,007 (GRCm39) |
N423K |
possibly damaging |
Het |
Sertad2 |
C |
G |
11: 20,598,091 (GRCm39) |
L96V |
probably benign |
Het |
Slc33a1 |
T |
A |
3: 63,861,315 (GRCm39) |
T296S |
probably benign |
Het |
Smurf2 |
G |
A |
11: 106,743,444 (GRCm39) |
P188S |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,039,180 (GRCm39) |
Y1174* |
probably null |
Het |
Stra6l |
A |
T |
4: 45,864,982 (GRCm39) |
T103S |
probably benign |
Het |
Swt1 |
C |
T |
1: 151,281,272 (GRCm39) |
A352T |
probably damaging |
Het |
Thoc2l |
T |
C |
5: 104,668,769 (GRCm39) |
V1097A |
possibly damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,361 (GRCm39) |
N409K |
possibly damaging |
Het |
Tlr6 |
G |
T |
5: 65,112,593 (GRCm39) |
H105N |
probably benign |
Het |
Tmprss9 |
A |
C |
10: 80,715,692 (GRCm39) |
T15P |
possibly damaging |
Het |
Tnik |
C |
T |
3: 28,587,089 (GRCm39) |
T120M |
probably damaging |
Het |
Tnr |
T |
A |
1: 159,685,780 (GRCm39) |
I337N |
probably damaging |
Het |
Top3a |
A |
G |
11: 60,641,419 (GRCm39) |
Y422H |
probably benign |
Het |
Trim67 |
A |
G |
8: 125,555,820 (GRCm39) |
N768S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,536,310 (GRCm39) |
V35016A |
probably benign |
Het |
Utrn |
A |
C |
10: 12,357,052 (GRCm39) |
S312R |
probably damaging |
Het |
Vdac2 |
A |
G |
14: 21,887,879 (GRCm39) |
Y62C |
probably damaging |
Het |
Vwa5b2 |
A |
G |
16: 20,423,734 (GRCm39) |
T1216A |
probably benign |
Het |
Wfdc16 |
T |
C |
2: 164,480,403 (GRCm39) |
K31E |
possibly damaging |
Het |
Wtip |
C |
T |
7: 33,824,921 (GRCm39) |
C221Y |
probably damaging |
Het |
Xrn1 |
A |
G |
9: 95,873,064 (GRCm39) |
D640G |
possibly damaging |
Het |
Zdhhc5 |
T |
C |
2: 84,522,685 (GRCm39) |
R293G |
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,269,059 (GRCm39) |
D119G |
probably damaging |
Het |
Zfp81 |
T |
C |
17: 33,554,254 (GRCm39) |
T187A |
probably benign |
Het |
Zfp810 |
C |
T |
9: 22,190,122 (GRCm39) |
G262D |
possibly damaging |
Het |
Zfp963 |
A |
C |
8: 70,195,669 (GRCm39) |
I203M |
possibly damaging |
Het |
Zfpm2 |
T |
C |
15: 40,965,075 (GRCm39) |
M520T |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,763,181 (GRCm39) |
R360Q |
possibly damaging |
Het |
Zwilch |
T |
A |
9: 64,065,999 (GRCm39) |
H254L |
possibly damaging |
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 |
|
R0281:Atr
|
UTSW |
9 |
95,819,619 (GRCm39) |
missense |
probably benign |
0.26 |
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 |
|
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 |
|