Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009A15Rik |
T |
C |
19: 8,867,417 (GRCm39) |
L72P |
probably benign |
Het |
4930407I10Rik |
C |
A |
15: 81,948,306 (GRCm39) |
H734Q |
probably benign |
Het |
Acadl |
A |
G |
1: 66,877,522 (GRCm39) |
V343A |
possibly damaging |
Het |
Acot4 |
A |
T |
12: 84,090,011 (GRCm39) |
D236V |
probably damaging |
Het |
App |
T |
A |
16: 84,837,197 (GRCm39) |
|
probably null |
Het |
Arfgef1 |
G |
A |
1: 10,264,636 (GRCm39) |
T470I |
possibly damaging |
Het |
Arhgef5 |
T |
C |
6: 43,251,691 (GRCm39) |
I814T |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,028,321 (GRCm39) |
N2329K |
possibly damaging |
Het |
Bltp1 |
C |
T |
3: 37,080,303 (GRCm39) |
S267L |
probably benign |
Het |
Capn7 |
C |
T |
14: 31,074,401 (GRCm39) |
T268I |
probably benign |
Het |
Ccdc192 |
A |
G |
18: 57,696,388 (GRCm39) |
|
probably null |
Het |
Ccn1 |
C |
T |
3: 145,354,447 (GRCm39) |
G155R |
probably damaging |
Het |
Csmd2 |
G |
T |
4: 128,439,549 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
T |
2: 13,352,989 (GRCm39) |
F1916L |
probably benign |
Het |
Cubn |
A |
G |
2: 13,494,728 (GRCm39) |
V107A |
possibly damaging |
Het |
Cyp11b1 |
T |
A |
15: 74,707,691 (GRCm39) |
T473S |
probably damaging |
Het |
Dip2c |
T |
G |
13: 9,709,347 (GRCm39) |
S1396A |
probably benign |
Het |
Dop1b |
T |
G |
16: 93,595,649 (GRCm39) |
|
probably null |
Het |
Dyrk1b |
T |
C |
7: 27,883,737 (GRCm39) |
Y198H |
probably damaging |
Het |
Echdc2 |
G |
T |
4: 108,031,274 (GRCm39) |
R206L |
probably benign |
Het |
Ep400 |
C |
T |
5: 110,843,898 (GRCm39) |
R1594Q |
unknown |
Het |
Esyt1 |
T |
A |
10: 128,351,723 (GRCm39) |
|
probably benign |
Het |
Fmnl2 |
G |
A |
2: 52,926,520 (GRCm39) |
R69Q |
|
Het |
Fry |
T |
A |
5: 150,328,792 (GRCm39) |
H1308Q |
probably damaging |
Het |
Fyb2 |
T |
A |
4: 104,867,651 (GRCm39) |
D667E |
probably benign |
Het |
Gimap7 |
T |
A |
6: 48,700,791 (GRCm39) |
Y126N |
possibly damaging |
Het |
Gm1979 |
A |
T |
5: 26,205,178 (GRCm39) |
W266R |
probably damaging |
Het |
Gm28042 |
T |
A |
2: 119,870,197 (GRCm39) |
M712K |
possibly damaging |
Het |
Gm3238 |
A |
G |
10: 77,606,469 (GRCm39) |
*231R |
probably null |
Het |
Gm5592 |
C |
A |
7: 40,935,831 (GRCm39) |
A111E |
probably damaging |
Het |
Gm7694 |
A |
G |
1: 170,128,717 (GRCm39) |
*271Q |
probably null |
Het |
Gm9195 |
A |
C |
14: 72,693,342 (GRCm39) |
|
probably null |
Het |
Ift81 |
T |
C |
5: 122,732,623 (GRCm39) |
M304V |
possibly damaging |
Het |
Igfals |
T |
C |
17: 25,099,548 (GRCm39) |
L213P |
probably damaging |
Het |
Ints3 |
G |
A |
3: 90,329,111 (GRCm39) |
P83S |
probably benign |
Het |
Kcna10 |
T |
G |
3: 107,102,856 (GRCm39) |
S496A |
probably damaging |
Het |
Kmt2d |
G |
A |
15: 98,741,600 (GRCm39) |
A4520V |
unknown |
Het |
Lemd3 |
A |
T |
10: 120,813,995 (GRCm39) |
Y413N |
probably damaging |
Het |
Lgr6 |
T |
C |
1: 134,923,770 (GRCm39) |
N453S |
probably damaging |
Het |
Lmtk3 |
A |
C |
7: 45,441,998 (GRCm39) |
D352A |
probably damaging |
Het |
Lrrc4c |
T |
C |
2: 97,461,024 (GRCm39) |
M550T |
possibly damaging |
Het |
Maml2 |
A |
T |
9: 13,532,385 (GRCm39) |
Q533L |
|
Het |
Mdn1 |
T |
A |
4: 32,741,344 (GRCm39) |
D3815E |
probably damaging |
Het |
Megf8 |
C |
T |
7: 25,029,353 (GRCm39) |
A299V |
possibly damaging |
Het |
Meis3 |
G |
T |
7: 15,911,481 (GRCm39) |
E59D |
probably benign |
Het |
Mppe1 |
A |
G |
18: 67,358,775 (GRCm39) |
*398R |
probably null |
Het |
Mtmr7 |
G |
A |
8: 41,059,927 (GRCm39) |
A62V |
possibly damaging |
Het |
Mtus1 |
T |
A |
8: 41,537,006 (GRCm39) |
T237S |
possibly damaging |
Het |
Ndfip2 |
T |
A |
14: 105,525,193 (GRCm39) |
V158E |
possibly damaging |
Het |
Nrbp2 |
T |
G |
15: 75,962,746 (GRCm39) |
T53P |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,097,094 (GRCm39) |
P902L |
probably benign |
Het |
Or10ab5 |
T |
A |
7: 108,244,879 (GRCm39) |
K301N |
probably damaging |
Het |
Or11g24 |
T |
A |
14: 50,662,792 (GRCm39) |
M272K |
probably benign |
Het |
Or2y13 |
A |
G |
11: 49,415,381 (GRCm39) |
Y277C |
probably damaging |
Het |
Or6c202 |
T |
C |
10: 128,995,924 (GRCm39) |
M310V |
probably benign |
Het |
Pcdha1 |
A |
G |
18: 37,064,115 (GRCm39) |
T260A |
probably damaging |
Het |
Pdlim1 |
T |
G |
19: 40,238,102 (GRCm39) |
K98N |
probably damaging |
Het |
Pdxk |
A |
T |
10: 78,279,764 (GRCm39) |
|
probably null |
Het |
Phrf1 |
G |
A |
7: 140,834,842 (GRCm39) |
G207R |
unknown |
Het |
Pik3r6 |
A |
G |
11: 68,419,389 (GRCm39) |
K124R |
probably damaging |
Het |
Polr2b |
T |
A |
5: 77,488,268 (GRCm39) |
F823I |
probably benign |
Het |
Prss58 |
T |
C |
6: 40,872,322 (GRCm39) |
I234V |
probably damaging |
Het |
Ptpn14 |
A |
T |
1: 189,597,608 (GRCm39) |
N766I |
probably benign |
Het |
Qrfprl |
T |
A |
6: 65,429,940 (GRCm39) |
I212N |
probably benign |
Het |
Repin1 |
T |
A |
6: 48,574,756 (GRCm39) |
S562T |
probably damaging |
Het |
Rgr |
C |
T |
14: 36,766,552 (GRCm39) |
D165N |
probably damaging |
Het |
Rho |
T |
C |
6: 115,912,200 (GRCm39) |
F221L |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rnase2a |
A |
G |
14: 51,493,248 (GRCm39) |
I39T |
probably damaging |
Het |
Rpl13a |
T |
G |
7: 44,776,660 (GRCm39) |
I43L |
probably benign |
Het |
Rpp30 |
T |
C |
19: 36,066,558 (GRCm39) |
V97A |
probably benign |
Het |
Scube3 |
T |
C |
17: 28,386,023 (GRCm39) |
Y755H |
probably damaging |
Het |
Sec24a |
A |
T |
11: 51,603,084 (GRCm39) |
V788E |
probably damaging |
Het |
Spns2 |
A |
T |
11: 72,380,443 (GRCm39) |
L60* |
probably null |
Het |
Strc |
T |
C |
2: 121,202,229 (GRCm39) |
N1213S |
possibly damaging |
Het |
Tec |
A |
T |
5: 72,943,367 (GRCm39) |
I116N |
possibly damaging |
Het |
Tll1 |
A |
T |
8: 64,546,988 (GRCm39) |
D319E |
probably benign |
Het |
Tmem121b |
T |
C |
6: 120,470,388 (GRCm39) |
T110A |
unknown |
Het |
Tmem232 |
T |
A |
17: 65,572,213 (GRCm39) |
I593F |
probably damaging |
Het |
Tpp2 |
A |
G |
1: 44,009,626 (GRCm39) |
I487V |
probably benign |
Het |
Ubr4 |
C |
A |
4: 139,136,178 (GRCm39) |
C934* |
probably null |
Het |
Vmn1r68 |
A |
G |
7: 10,261,559 (GRCm39) |
Y180H |
probably benign |
Het |
Vmn2r25 |
T |
C |
6: 123,816,882 (GRCm39) |
D233G |
possibly damaging |
Het |
Wdr6 |
A |
G |
9: 108,453,560 (GRCm39) |
W108R |
possibly damaging |
Het |
Zng1 |
A |
G |
19: 24,920,045 (GRCm39) |
|
probably null |
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 |
|
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 |
|
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 |
|