Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l1 |
G |
A |
18: 61,876,432 (GRCm39) |
T395M |
probably damaging |
Het |
Akap8l |
T |
C |
17: 32,557,783 (GRCm39) |
N35D |
probably damaging |
Het |
B3gnt9 |
G |
T |
8: 105,981,129 (GRCm39) |
F86L |
probably damaging |
Het |
Bmp1 |
T |
C |
14: 70,715,360 (GRCm39) |
D925G |
probably damaging |
Het |
Camkmt |
A |
T |
17: 85,759,713 (GRCm39) |
R284S |
probably benign |
Het |
Cavin3 |
G |
T |
7: 105,131,304 (GRCm39) |
H21Q |
probably damaging |
Het |
Ccp110 |
A |
G |
7: 118,334,553 (GRCm39) |
H180R |
|
Het |
Cdh23 |
A |
T |
10: 60,167,135 (GRCm39) |
V1837E |
probably damaging |
Het |
Ces3b |
G |
T |
8: 105,812,257 (GRCm39) |
A169S |
probably damaging |
Het |
Chpt1 |
T |
C |
10: 88,325,499 (GRCm39) |
N122S |
probably benign |
Het |
Cramp1 |
C |
A |
17: 25,201,783 (GRCm39) |
K566N |
probably damaging |
Het |
Ctbp2 |
C |
G |
7: 132,615,933 (GRCm39) |
R334P |
probably damaging |
Het |
Cwh43 |
T |
C |
5: 73,572,340 (GRCm39) |
S193P |
probably benign |
Het |
Dcstamp |
A |
T |
15: 39,623,792 (GRCm39) |
D469V |
probably benign |
Het |
Dst |
T |
A |
1: 34,219,458 (GRCm39) |
I1966N |
probably benign |
Het |
Eif3i |
G |
T |
4: 129,489,094 (GRCm39) |
F121L |
probably benign |
Het |
Erbb2 |
T |
C |
11: 98,326,812 (GRCm39) |
S1074P |
probably damaging |
Het |
Fam186b |
G |
A |
15: 99,177,616 (GRCm39) |
A570V |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,146,722 (GRCm39) |
|
probably null |
Het |
Foxo3 |
C |
T |
10: 42,073,021 (GRCm39) |
V499M |
probably damaging |
Het |
Gm2a |
T |
C |
11: 54,999,764 (GRCm39) |
V95A |
probably benign |
Het |
Gp5 |
A |
C |
16: 30,128,393 (GRCm39) |
F94V |
probably damaging |
Het |
Gramd4 |
G |
A |
15: 86,016,160 (GRCm39) |
E504K |
probably damaging |
Het |
Gusb |
A |
G |
5: 130,026,652 (GRCm39) |
S450P |
probably damaging |
Het |
Htr5a |
A |
G |
5: 28,047,838 (GRCm39) |
N131S |
possibly damaging |
Het |
Itga2 |
G |
A |
13: 115,020,991 (GRCm39) |
P120L |
probably benign |
Het |
Itpkb |
G |
T |
1: 180,160,056 (GRCm39) |
E61* |
probably null |
Het |
Katnbl1 |
T |
A |
2: 112,239,497 (GRCm39) |
V232D |
probably damaging |
Het |
Kifap3 |
T |
C |
1: 163,689,657 (GRCm39) |
L547P |
probably damaging |
Het |
Krt6a |
C |
T |
15: 101,599,120 (GRCm39) |
V482M |
probably benign |
Het |
Lrfn5 |
T |
A |
12: 61,890,418 (GRCm39) |
V569D |
probably damaging |
Het |
Luzp2 |
A |
G |
7: 54,702,580 (GRCm39) |
T48A |
probably damaging |
Het |
Mical2 |
G |
T |
7: 111,945,996 (GRCm39) |
R986L |
probably damaging |
Het |
Mroh8 |
G |
A |
2: 157,094,970 (GRCm39) |
Q339* |
probably null |
Het |
Msln |
A |
T |
17: 25,968,042 (GRCm39) |
V541E |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,498,178 (GRCm39) |
M6590L |
probably benign |
Het |
Nhsl3 |
T |
C |
4: 129,117,962 (GRCm39) |
E279G |
possibly damaging |
Het |
Nisch |
A |
T |
14: 30,893,628 (GRCm39) |
V1315E |
probably damaging |
Het |
Nubp2 |
G |
A |
17: 25,103,382 (GRCm39) |
T165I |
probably damaging |
Het |
Oog3 |
T |
G |
4: 143,884,489 (GRCm39) |
R482S |
probably benign |
Het |
Or2a7 |
A |
G |
6: 43,150,991 (GRCm39) |
M24V |
probably benign |
Het |
Or56a42-ps1 |
A |
T |
7: 104,775,985 (GRCm39) |
N164K |
probably benign |
Het |
Or6c33 |
T |
C |
10: 129,853,809 (GRCm39) |
I193T |
possibly damaging |
Het |
Or7a41 |
T |
C |
10: 78,871,230 (GRCm39) |
I200T |
probably benign |
Het |
Or8k39 |
A |
T |
2: 86,563,636 (GRCm39) |
F107I |
probably damaging |
Het |
P3h4 |
A |
T |
11: 100,304,499 (GRCm39) |
C247* |
probably null |
Het |
Pakap |
G |
A |
4: 57,710,125 (GRCm39) |
A357T |
possibly damaging |
Het |
Plch2 |
T |
A |
4: 155,082,942 (GRCm39) |
M569L |
probably benign |
Het |
Plcl1 |
A |
G |
1: 55,735,450 (GRCm39) |
T264A |
probably benign |
Het |
Rad51ap1 |
G |
T |
6: 126,904,526 (GRCm39) |
N178K |
probably benign |
Het |
Rasa4 |
T |
C |
5: 136,130,494 (GRCm39) |
L340P |
probably damaging |
Het |
Rassf10 |
A |
G |
7: 112,554,784 (GRCm39) |
T462A |
probably benign |
Het |
Rlf |
G |
C |
4: 121,007,865 (GRCm39) |
L482V |
probably damaging |
Het |
Robo1 |
T |
G |
16: 72,821,330 (GRCm39) |
S1357A |
possibly damaging |
Het |
Rp1l1 |
T |
C |
14: 64,269,714 (GRCm39) |
S1767P |
probably damaging |
Het |
Rpl3l |
T |
A |
17: 24,947,328 (GRCm39) |
L14Q |
probably damaging |
Het |
Ryr3 |
T |
A |
2: 112,635,047 (GRCm39) |
T2024S |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 110,040,702 (GRCm39) |
Q375R |
possibly damaging |
Het |
Sema6a |
T |
C |
18: 47,382,252 (GRCm39) |
Q765R |
probably damaging |
Het |
Senp6 |
T |
A |
9: 80,021,228 (GRCm39) |
Y303N |
probably damaging |
Het |
Sertad4 |
C |
T |
1: 192,528,836 (GRCm39) |
D327N |
probably damaging |
Het |
Slc22a15 |
T |
A |
3: 101,790,848 (GRCm39) |
Y219F |
possibly damaging |
Het |
Slco1b2 |
T |
G |
6: 141,594,358 (GRCm39) |
|
probably null |
Het |
Snrnp200 |
G |
T |
2: 127,067,959 (GRCm39) |
V819L |
probably damaging |
Het |
Ssb |
C |
A |
2: 69,700,784 (GRCm39) |
A288E |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,101,620 (GRCm39) |
H638R |
probably benign |
Het |
Tm7sf3 |
A |
G |
6: 146,527,698 (GRCm39) |
S43P |
probably benign |
Het |
Tmem200c |
A |
G |
17: 69,149,181 (GRCm39) |
H588R |
probably benign |
Het |
Tnpo3 |
G |
A |
6: 29,560,173 (GRCm39) |
R657* |
probably null |
Het |
Traf6 |
T |
C |
2: 101,518,927 (GRCm39) |
C139R |
probably damaging |
Het |
Txnrd1 |
C |
A |
10: 82,720,390 (GRCm39) |
N424K |
possibly damaging |
Het |
Ubqln3 |
T |
C |
7: 103,791,962 (GRCm39) |
I43V |
probably damaging |
Het |
Usp32 |
A |
G |
11: 84,921,317 (GRCm39) |
V699A |
probably damaging |
Het |
Vmn2r103 |
T |
C |
17: 20,014,027 (GRCm39) |
V273A |
probably benign |
Het |
Vmn2r8 |
A |
G |
5: 108,951,107 (GRCm39) |
S113P |
probably benign |
Het |
Wdr7 |
T |
A |
18: 63,860,826 (GRCm39) |
I161N |
probably damaging |
Het |
Zfp474 |
A |
T |
18: 52,772,015 (GRCm39) |
I223F |
probably damaging |
Het |
Zfp583 |
A |
G |
7: 6,320,328 (GRCm39) |
L228P |
probably damaging |
Het |
Zfyve27 |
A |
G |
19: 42,165,856 (GRCm39) |
T76A |
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 |
|
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 |
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 |
|