Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
G |
A |
7: 41,276,400 (GRCm39) |
G701D |
probably damaging |
Het |
6030468B19Rik |
T |
A |
11: 117,693,780 (GRCm39) |
N82K |
probably damaging |
Het |
Abca17 |
A |
T |
17: 24,554,564 (GRCm39) |
V130E |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,399,348 (GRCm39) |
K2077* |
probably null |
Het |
Aox1 |
T |
C |
1: 58,322,651 (GRCm39) |
F73S |
probably benign |
Het |
Ap3b1 |
T |
A |
13: 94,668,542 (GRCm39) |
C965* |
probably null |
Het |
Arhgef10 |
T |
A |
8: 14,980,030 (GRCm39) |
V90E |
probably damaging |
Het |
Bicdl1 |
G |
T |
5: 115,789,916 (GRCm39) |
Q511K |
possibly damaging |
Het |
Capn15 |
A |
T |
17: 26,184,228 (GRCm39) |
N150K |
probably damaging |
Het |
Card6 |
A |
T |
15: 5,129,591 (GRCm39) |
W602R |
probably benign |
Het |
Clnk |
A |
T |
5: 38,927,234 (GRCm39) |
S82T |
possibly damaging |
Het |
Cmah |
T |
C |
13: 24,620,612 (GRCm39) |
I282T |
probably damaging |
Het |
Cog8 |
A |
G |
8: 107,779,131 (GRCm39) |
I382T |
probably benign |
Het |
Dhrs7c |
G |
T |
11: 67,700,722 (GRCm39) |
|
probably null |
Het |
Dhrs9 |
T |
A |
2: 69,223,502 (GRCm39) |
D83E |
probably damaging |
Het |
Dmac2l |
A |
T |
12: 69,788,562 (GRCm39) |
N154Y |
probably benign |
Het |
Dmgdh |
G |
A |
13: 93,852,043 (GRCm39) |
G624E |
probably damaging |
Het |
Dnajc30 |
C |
A |
5: 135,093,569 (GRCm39) |
F155L |
probably damaging |
Het |
Drc7 |
A |
C |
8: 95,800,778 (GRCm39) |
K600T |
probably damaging |
Het |
Efhb |
A |
C |
17: 53,707,928 (GRCm39) |
I745S |
probably damaging |
Het |
Elp1 |
ACTTCTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTCTTC |
4: 56,781,176 (GRCm39) |
|
probably benign |
Het |
Fasn |
T |
A |
11: 120,701,291 (GRCm39) |
K1988* |
probably null |
Het |
Gad2 |
T |
C |
2: 22,525,035 (GRCm39) |
L273P |
probably damaging |
Het |
Gm45861 |
A |
T |
8: 28,032,536 (GRCm39) |
K887* |
probably null |
Het |
Gm45861 |
A |
T |
8: 28,032,537 (GRCm39) |
K887I |
unknown |
Het |
Gm9195 |
A |
G |
14: 72,718,221 (GRCm39) |
Y152H |
probably damaging |
Het |
Grip1 |
G |
A |
10: 119,781,061 (GRCm39) |
D237N |
probably damaging |
Het |
Hamp |
A |
C |
7: 30,641,961 (GRCm39) |
C65G |
possibly damaging |
Het |
Hes3 |
A |
G |
4: 152,372,581 (GRCm39) |
|
probably benign |
Het |
Hgh1 |
T |
C |
15: 76,254,650 (GRCm39) |
I342T |
probably damaging |
Het |
Hlcs |
T |
A |
16: 94,069,023 (GRCm39) |
K66* |
probably null |
Het |
Ift80 |
A |
T |
3: 68,898,277 (GRCm39) |
C19* |
probably null |
Het |
Kbtbd12 |
C |
T |
6: 88,595,650 (GRCm39) |
C60Y |
probably damaging |
Het |
Kdm4c |
T |
A |
4: 74,263,804 (GRCm39) |
V696E |
probably benign |
Het |
Lect2 |
A |
G |
13: 56,690,803 (GRCm39) |
I117T |
unknown |
Het |
Lipn |
T |
A |
19: 34,054,390 (GRCm39) |
Y209* |
probably null |
Het |
Lpin3 |
G |
A |
2: 160,740,627 (GRCm39) |
V391I |
probably benign |
Het |
Mocs2 |
A |
T |
13: 114,961,143 (GRCm39) |
I47L |
probably benign |
Het |
Mogs |
T |
A |
6: 83,095,488 (GRCm39) |
H768Q |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,276,317 (GRCm39) |
I686N |
probably damaging |
Het |
Nbeal1 |
T |
A |
1: 60,299,793 (GRCm39) |
C1376* |
probably null |
Het |
Ninl |
A |
G |
2: 150,791,263 (GRCm39) |
Y1087H |
possibly damaging |
Het |
Or10a3 |
A |
G |
7: 108,480,475 (GRCm39) |
F113L |
probably benign |
Het |
Or10ak14 |
A |
G |
4: 118,611,615 (GRCm39) |
V42A |
possibly damaging |
Het |
Or4k5 |
A |
G |
14: 50,385,689 (GRCm39) |
L214S |
probably damaging |
Het |
Or51b6b |
A |
C |
7: 103,309,788 (GRCm39) |
L223R |
probably damaging |
Het |
Or6s1 |
A |
G |
14: 51,308,616 (GRCm39) |
V78A |
possibly damaging |
Het |
Or8k30 |
T |
A |
2: 86,339,369 (GRCm39) |
C189S |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,398,363 (GRCm39) |
F768S |
probably damaging |
Het |
Plekha2 |
A |
G |
8: 25,553,957 (GRCm39) |
F82L |
probably damaging |
Het |
Ppie |
T |
C |
4: 123,028,900 (GRCm39) |
E111G |
probably benign |
Het |
Rps6ka5 |
T |
C |
12: 100,547,679 (GRCm39) |
Y277C |
probably damaging |
Het |
Scgb2b12 |
A |
G |
7: 32,026,102 (GRCm39) |
V30A |
probably benign |
Het |
Serac1 |
A |
T |
17: 6,124,476 (GRCm39) |
S16T |
probably benign |
Het |
Sf3a3 |
T |
C |
4: 124,616,693 (GRCm39) |
Y192H |
probably damaging |
Het |
Slc14a1 |
A |
G |
18: 78,145,626 (GRCm39) |
V436A |
probably benign |
Het |
Smc3 |
T |
A |
19: 53,630,329 (GRCm39) |
M1112K |
probably damaging |
Het |
Tnk2 |
G |
A |
16: 32,499,986 (GRCm39) |
G1017E |
probably damaging |
Het |
Tnn |
T |
A |
1: 159,953,947 (GRCm39) |
K603* |
probably null |
Het |
Trpm6 |
T |
C |
19: 18,815,462 (GRCm39) |
S1183P |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,614,724 (GRCm39) |
V16964E |
possibly damaging |
Het |
Usp17le |
G |
A |
7: 104,417,696 (GRCm39) |
T482I |
probably benign |
Het |
Vmn1r219 |
T |
A |
13: 23,347,525 (GRCm39) |
M238K |
probably damaging |
Het |
Wfs1 |
C |
T |
5: 37,124,516 (GRCm39) |
G792S |
probably benign |
Het |
Xpa |
A |
T |
4: 46,185,612 (GRCm39) |
L122Q |
probably 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 |
|
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 |
|
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 |
|