Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
C |
G |
3: 124,199,999 (GRCm39) |
G531A |
probably damaging |
Het |
Abca8b |
C |
A |
11: 109,868,639 (GRCm39) |
G175V |
probably damaging |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Ap3d1 |
T |
C |
10: 80,559,383 (GRCm39) |
T264A |
probably benign |
Het |
Arhgef17 |
C |
G |
7: 100,578,635 (GRCm39) |
G771A |
probably benign |
Het |
Atg2b |
T |
A |
12: 105,624,588 (GRCm39) |
D637V |
probably benign |
Het |
Atp10b |
A |
G |
11: 43,103,302 (GRCm39) |
E562G |
probably damaging |
Het |
Atp1a1 |
A |
G |
3: 101,497,280 (GRCm39) |
V342A |
probably damaging |
Het |
Atp2a2 |
A |
G |
5: 122,599,810 (GRCm39) |
I527T |
probably benign |
Het |
Bach2 |
T |
A |
4: 32,562,683 (GRCm39) |
D383E |
probably benign |
Het |
Casq1 |
A |
T |
1: 172,046,983 (GRCm39) |
L92Q |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,952,832 (GRCm39) |
Y371N |
probably damaging |
Het |
Chd9 |
G |
A |
8: 91,723,777 (GRCm39) |
A617T |
probably damaging |
Het |
Cntrob |
T |
A |
11: 69,205,576 (GRCm39) |
R419S |
possibly damaging |
Het |
Corin |
C |
A |
5: 72,514,321 (GRCm39) |
G318C |
probably damaging |
Het |
Cpa3 |
A |
G |
3: 20,281,327 (GRCm39) |
|
probably null |
Het |
Cplane1 |
G |
A |
15: 8,290,174 (GRCm39) |
|
probably null |
Het |
Crybg1 |
T |
C |
10: 43,879,710 (GRCm39) |
S493G |
probably benign |
Het |
Ddc |
A |
G |
11: 11,826,321 (GRCm39) |
F80S |
probably damaging |
Het |
Dhrs2 |
A |
G |
14: 55,473,601 (GRCm39) |
S87G |
possibly damaging |
Het |
Dnah12 |
A |
G |
14: 26,414,641 (GRCm39) |
E14G |
possibly damaging |
Het |
Dtd1 |
A |
G |
2: 144,588,942 (GRCm39) |
E200G |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,155,099 (GRCm39) |
E895G |
probably damaging |
Het |
Ehhadh |
A |
C |
16: 21,581,442 (GRCm39) |
S517A |
probably benign |
Het |
Ephb2 |
C |
A |
4: 136,421,098 (GRCm39) |
Q417H |
possibly damaging |
Het |
Ephb4 |
A |
G |
5: 137,361,574 (GRCm39) |
T526A |
probably damaging |
Het |
Fam222b |
G |
A |
11: 78,044,594 (GRCm39) |
V52I |
probably damaging |
Het |
Galm |
G |
A |
17: 80,452,416 (GRCm39) |
W118* |
probably null |
Het |
Galm |
G |
T |
17: 80,452,417 (GRCm39) |
W118C |
probably damaging |
Het |
Gcfc2 |
A |
G |
6: 81,921,367 (GRCm39) |
N458D |
probably damaging |
Het |
Gm11595 |
G |
A |
11: 99,663,381 (GRCm39) |
R100C |
unknown |
Het |
Gykl1 |
A |
C |
18: 52,827,723 (GRCm39) |
R310S |
possibly damaging |
Het |
Gzmn |
A |
C |
14: 56,405,403 (GRCm39) |
V27G |
probably damaging |
Het |
H2-T23 |
T |
A |
17: 36,343,108 (GRCm39) |
M90L |
probably benign |
Het |
Hnrnpu |
T |
C |
1: 178,164,877 (GRCm39) |
E87G |
unknown |
Het |
Hps3 |
G |
A |
3: 20,066,865 (GRCm39) |
S567L |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,892,676 (GRCm39) |
V2148E |
probably damaging |
Het |
Ighv1-75 |
T |
C |
12: 115,797,572 (GRCm39) |
R117G |
probably damaging |
Het |
Itgae |
C |
T |
11: 73,036,464 (GRCm39) |
A1134V |
probably benign |
Het |
Kmt2b |
C |
T |
7: 30,281,098 (GRCm39) |
A1294T |
possibly damaging |
Het |
Leng8 |
C |
T |
7: 4,148,472 (GRCm39) |
T748I |
probably damaging |
Het |
Lrig3 |
G |
C |
10: 125,842,559 (GRCm39) |
D495H |
probably damaging |
Het |
Mctp1 |
G |
A |
13: 76,860,198 (GRCm39) |
|
probably null |
Het |
Mfsd3 |
T |
A |
15: 76,586,371 (GRCm39) |
L168* |
probably null |
Het |
Nherf1 |
T |
A |
11: 115,054,587 (GRCm39) |
I79N |
probably damaging |
Het |
Nlrp4d |
C |
A |
7: 10,096,709 (GRCm39) |
G921* |
probably null |
Het |
Nsun4 |
G |
A |
4: 115,891,335 (GRCm39) |
T348I |
probably damaging |
Het |
Nucb1 |
T |
C |
7: 45,147,842 (GRCm39) |
T246A |
probably damaging |
Het |
Nynrin |
A |
C |
14: 56,101,263 (GRCm39) |
S311R |
probably damaging |
Het |
Or4k37 |
T |
A |
2: 111,158,741 (GRCm39) |
|
probably null |
Het |
Or5ar1 |
T |
G |
2: 85,671,358 (GRCm39) |
Y259S |
probably damaging |
Het |
Ovch2 |
C |
A |
7: 107,391,341 (GRCm39) |
R303L |
probably benign |
Het |
Pcsk9 |
A |
G |
4: 106,304,371 (GRCm39) |
S490P |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,140,894 (GRCm39) |
F859L |
probably benign |
Het |
Pkd1l3 |
A |
G |
8: 110,367,424 (GRCm39) |
D1207G |
probably damaging |
Het |
Pnpla7 |
G |
A |
2: 24,911,964 (GRCm39) |
R710Q |
possibly damaging |
Het |
Prex2 |
T |
G |
1: 11,270,256 (GRCm39) |
S1314A |
probably damaging |
Het |
Rnf216 |
A |
G |
5: 143,078,757 (GRCm39) |
L64P |
probably damaging |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Slc6a20b |
T |
G |
9: 123,432,899 (GRCm39) |
S374R |
possibly damaging |
Het |
Slc8a1 |
G |
T |
17: 81,956,653 (GRCm39) |
N128K |
probably damaging |
Het |
Slfn5 |
A |
T |
11: 82,847,211 (GRCm39) |
D32V |
probably damaging |
Het |
Snrnp35 |
T |
C |
5: 124,628,553 (GRCm39) |
I122T |
possibly damaging |
Het |
Snx24 |
C |
T |
18: 53,473,283 (GRCm39) |
Q76* |
probably null |
Het |
Sspo |
T |
A |
6: 48,431,784 (GRCm39) |
H692Q |
probably damaging |
Het |
Stxbp3 |
T |
C |
3: 108,701,114 (GRCm39) |
D585G |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,072,677 (GRCm39) |
N2211D |
possibly damaging |
Het |
Tnfrsf18 |
G |
A |
4: 156,112,881 (GRCm39) |
|
probably null |
Het |
Tnik |
T |
G |
3: 28,596,121 (GRCm39) |
D171E |
probably damaging |
Het |
Ttc23l |
T |
A |
15: 10,533,745 (GRCm39) |
H266L |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,725,114 (GRCm39) |
S2037* |
probably null |
Het |
Tuba3a |
G |
A |
6: 125,258,273 (GRCm39) |
T239I |
probably damaging |
Het |
Usp25 |
T |
A |
16: 76,890,594 (GRCm39) |
D767E |
probably benign |
Het |
Whrn |
G |
T |
4: 63,350,080 (GRCm39) |
H546N |
probably benign |
Het |
Xirp2 |
C |
T |
2: 67,341,506 (GRCm39) |
T1249I |
probably damaging |
Het |
Zbtb1 |
T |
A |
12: 76,433,014 (GRCm39) |
D333E |
probably damaging |
Het |
Zfp689 |
T |
G |
7: 127,047,987 (GRCm39) |
E15A |
possibly damaging |
Het |
Zhx3 |
A |
G |
2: 160,621,788 (GRCm39) |
M793T |
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 |
|
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 |
|
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 |
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 |
|