Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730018C14Rik |
T |
A |
12: 112,381,489 (GRCm39) |
|
noncoding transcript |
Het |
Acss3 |
A |
G |
10: 106,773,169 (GRCm39) |
S606P |
probably benign |
Het |
Adamts13 |
C |
T |
2: 26,868,327 (GRCm39) |
T146M |
probably damaging |
Het |
Adora2b |
G |
A |
11: 62,156,363 (GRCm39) |
V271M |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,896,739 (GRCm39) |
Y55C |
probably damaging |
Het |
AI987944 |
A |
C |
7: 41,023,772 (GRCm39) |
Y402* |
probably null |
Het |
Angptl4 |
C |
T |
17: 34,000,165 (GRCm39) |
A68T |
possibly damaging |
Het |
Ankmy1 |
T |
C |
1: 92,814,531 (GRCm39) |
I325M |
probably benign |
Het |
Arfgap2 |
A |
G |
2: 91,105,204 (GRCm39) |
K423E |
probably damaging |
Het |
Arfgef3 |
A |
T |
10: 18,522,302 (GRCm39) |
S575T |
probably damaging |
Het |
Arhgap24 |
A |
G |
5: 103,008,198 (GRCm39) |
I40V |
possibly damaging |
Het |
Arhgef7 |
T |
C |
8: 11,869,733 (GRCm39) |
|
probably null |
Het |
Arid1a |
C |
A |
4: 133,448,237 (GRCm39) |
S477I |
unknown |
Het |
Armc7 |
T |
C |
11: 115,367,029 (GRCm39) |
V58A |
probably damaging |
Het |
Arrdc5 |
A |
T |
17: 56,601,222 (GRCm39) |
I301N |
probably damaging |
Het |
Capn15 |
G |
A |
17: 26,183,453 (GRCm39) |
P343S |
probably damaging |
Het |
Catspere2 |
C |
T |
1: 177,843,495 (GRCm39) |
T69I |
possibly damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Cgn |
C |
T |
3: 94,670,535 (GRCm39) |
R1002Q |
probably damaging |
Het |
Clstn3 |
A |
T |
6: 124,414,449 (GRCm39) |
I759N |
possibly damaging |
Het |
Cops5 |
A |
G |
1: 10,104,243 (GRCm39) |
V166A |
possibly damaging |
Het |
Cramp1 |
G |
T |
17: 25,191,323 (GRCm39) |
T1046K |
probably benign |
Het |
Cthrc1 |
T |
G |
15: 38,950,072 (GRCm39) |
V143G |
probably damaging |
Het |
Cyp27b1 |
A |
T |
10: 126,886,957 (GRCm39) |
D391V |
probably damaging |
Het |
Dcun1d2 |
A |
G |
8: 13,331,040 (GRCm39) |
L30S |
probably damaging |
Het |
Dsc3 |
T |
C |
18: 20,120,091 (GRCm39) |
E189G |
probably damaging |
Het |
Dst |
T |
G |
1: 34,193,675 (GRCm39) |
S295A |
probably damaging |
Het |
Dusp22 |
A |
G |
13: 30,892,798 (GRCm39) |
T192A |
probably benign |
Het |
Esp24 |
A |
T |
17: 39,349,176 (GRCm39) |
M1L |
probably null |
Het |
Evc2 |
G |
A |
5: 37,550,541 (GRCm39) |
|
probably null |
Het |
Fgd6 |
A |
G |
10: 93,880,694 (GRCm39) |
N516S |
probably benign |
Het |
Fmn1 |
T |
C |
2: 113,426,714 (GRCm39) |
Y1144H |
probably damaging |
Het |
Fut8 |
T |
A |
12: 77,495,448 (GRCm39) |
I346K |
possibly damaging |
Het |
Gata3 |
A |
C |
2: 9,882,201 (GRCm39) |
V32G |
probably damaging |
Het |
Glrb |
A |
T |
3: 80,819,282 (GRCm39) |
C39S |
possibly damaging |
Het |
Gpr171 |
A |
G |
3: 59,005,016 (GRCm39) |
V253A |
probably benign |
Het |
Hdac5 |
A |
G |
11: 102,092,079 (GRCm39) |
V670A |
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,266,980 (GRCm39) |
S1085G |
probably benign |
Het |
Hspa4l |
A |
G |
3: 40,741,226 (GRCm39) |
N746S |
probably benign |
Het |
Hyal5 |
A |
G |
6: 24,877,902 (GRCm39) |
T333A |
probably benign |
Het |
Ippk |
T |
C |
13: 49,615,069 (GRCm39) |
V484A |
probably benign |
Het |
Jmjd8 |
A |
T |
17: 26,048,266 (GRCm39) |
T33S |
possibly damaging |
Het |
Kctd19 |
T |
A |
8: 106,113,694 (GRCm39) |
I660L |
possibly damaging |
Het |
Lrat |
A |
G |
3: 82,810,649 (GRCm39) |
V124A |
probably benign |
Het |
Madcam1 |
A |
G |
10: 79,502,358 (GRCm39) |
I281V |
probably benign |
Het |
Mast2 |
T |
A |
4: 116,173,688 (GRCm39) |
I455F |
possibly damaging |
Het |
Mroh7 |
A |
G |
4: 106,560,255 (GRCm39) |
L683P |
probably benign |
Het |
Myo15b |
C |
A |
11: 115,777,683 (GRCm39) |
|
probably null |
Het |
Ncam1 |
T |
C |
9: 49,416,849 (GRCm39) |
E814G |
probably benign |
Het |
Ncoa3 |
A |
G |
2: 165,897,182 (GRCm39) |
T658A |
probably benign |
Het |
Or13a20 |
T |
G |
7: 140,232,650 (GRCm39) |
Y253D |
probably damaging |
Het |
Or9a2 |
T |
C |
6: 41,748,456 (GRCm39) |
Y259C |
possibly damaging |
Het |
P2ry13 |
T |
C |
3: 59,116,939 (GRCm39) |
K280E |
probably damaging |
Het |
Paqr8 |
C |
A |
1: 21,005,048 (GRCm39) |
F67L |
probably benign |
Het |
Pfkfb3 |
G |
T |
2: 11,498,747 (GRCm39) |
R37S |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,941,478 (GRCm39) |
D310G |
possibly damaging |
Het |
Phkb |
A |
G |
8: 86,602,286 (GRCm39) |
S26G |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,755,147 (GRCm39) |
I1684F |
probably damaging |
Het |
Plod2 |
T |
C |
9: 92,488,637 (GRCm39) |
V621A |
probably benign |
Het |
Plvap |
T |
C |
8: 71,964,116 (GRCm39) |
N82S |
probably damaging |
Het |
Pomgnt2 |
A |
G |
9: 121,811,326 (GRCm39) |
V485A |
probably damaging |
Het |
Psmd9 |
A |
G |
5: 123,366,410 (GRCm39) |
E14G |
probably benign |
Het |
Pwwp2b |
A |
G |
7: 138,835,879 (GRCm39) |
E440G |
probably damaging |
Het |
Rasgrp1 |
G |
A |
2: 117,113,100 (GRCm39) |
Q771* |
probably null |
Het |
Rft1 |
C |
T |
14: 30,388,744 (GRCm39) |
Q223* |
probably null |
Het |
Rgs22 |
C |
A |
15: 36,093,047 (GRCm39) |
V409F |
probably damaging |
Het |
Rgsl1 |
G |
A |
1: 153,701,672 (GRCm39) |
P261S |
possibly damaging |
Het |
Rpl7a |
A |
G |
2: 26,801,127 (GRCm39) |
N38S |
probably damaging |
Het |
Sh3rf2 |
T |
A |
18: 42,187,004 (GRCm39) |
F41Y |
probably damaging |
Het |
Spata6 |
T |
A |
4: 111,603,388 (GRCm39) |
S34R |
probably damaging |
Het |
Sult2a3 |
A |
T |
7: 13,856,867 (GRCm39) |
Y18N |
probably benign |
Het |
Tapt1 |
A |
G |
5: 44,375,444 (GRCm39) |
|
probably null |
Het |
Tex2 |
A |
T |
11: 106,394,466 (GRCm39) |
C615S |
possibly damaging |
Het |
Trim43b |
T |
C |
9: 88,969,665 (GRCm39) |
K261R |
possibly damaging |
Het |
Unc5c |
T |
A |
3: 141,495,583 (GRCm39) |
M484K |
probably damaging |
Het |
Vezf1 |
T |
A |
11: 87,964,573 (GRCm39) |
S242T |
probably damaging |
Het |
Vmn2r1 |
A |
G |
3: 63,997,034 (GRCm39) |
Y230C |
probably damaging |
Het |
Vmn2r94 |
A |
G |
17: 18,477,965 (GRCm39) |
S149P |
probably damaging |
Het |
Wfdc1 |
T |
A |
8: 120,393,405 (GRCm39) |
|
probably null |
Het |
Zfp975 |
T |
C |
7: 42,312,236 (GRCm39) |
T126A |
probably benign |
Het |
Zmym4 |
T |
C |
4: 126,776,105 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cul9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Cul9
|
APN |
17 |
46,836,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00330:Cul9
|
APN |
17 |
46,821,767 (GRCm39) |
splice site |
probably benign |
|
IGL00726:Cul9
|
APN |
17 |
46,839,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Cul9
|
APN |
17 |
46,849,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01358:Cul9
|
APN |
17 |
46,849,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01410:Cul9
|
APN |
17 |
46,839,572 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01781:Cul9
|
APN |
17 |
46,850,230 (GRCm39) |
missense |
probably benign |
|
IGL01873:Cul9
|
APN |
17 |
46,813,378 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02117:Cul9
|
APN |
17 |
46,851,301 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02300:Cul9
|
APN |
17 |
46,831,958 (GRCm39) |
splice site |
probably benign |
|
IGL02426:Cul9
|
APN |
17 |
46,834,184 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02427:Cul9
|
APN |
17 |
46,813,558 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02496:Cul9
|
APN |
17 |
46,851,302 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03008:Cul9
|
APN |
17 |
46,813,623 (GRCm39) |
splice site |
probably benign |
|
IGL03059:Cul9
|
APN |
17 |
46,849,913 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03302:Cul9
|
APN |
17 |
46,837,566 (GRCm39) |
missense |
probably damaging |
0.98 |
bottlenose
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
flipper
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
orca
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Cul9
|
UTSW |
17 |
46,811,779 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,784 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,772 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,779 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,776 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
R0012:Cul9
|
UTSW |
17 |
46,849,436 (GRCm39) |
missense |
probably benign |
0.26 |
R0079:Cul9
|
UTSW |
17 |
46,848,589 (GRCm39) |
nonsense |
probably null |
|
R0143:Cul9
|
UTSW |
17 |
46,837,336 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0390:Cul9
|
UTSW |
17 |
46,839,515 (GRCm39) |
missense |
probably benign |
0.34 |
R0401:Cul9
|
UTSW |
17 |
46,852,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Cul9
|
UTSW |
17 |
46,831,394 (GRCm39) |
splice site |
probably benign |
|
R0815:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0863:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0972:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1173:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1261:Cul9
|
UTSW |
17 |
46,836,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R1278:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R1281:Cul9
|
UTSW |
17 |
46,822,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1372:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Cul9
|
UTSW |
17 |
46,819,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1618:Cul9
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
R1641:Cul9
|
UTSW |
17 |
46,854,486 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1679:Cul9
|
UTSW |
17 |
46,832,082 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1771:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R1803:Cul9
|
UTSW |
17 |
46,814,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Cul9
|
UTSW |
17 |
46,854,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Cul9
|
UTSW |
17 |
46,854,298 (GRCm39) |
missense |
probably benign |
|
R2088:Cul9
|
UTSW |
17 |
46,837,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2415:Cul9
|
UTSW |
17 |
46,854,364 (GRCm39) |
missense |
probably benign |
|
R2925:Cul9
|
UTSW |
17 |
46,821,907 (GRCm39) |
missense |
probably benign |
0.08 |
R2964:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R2965:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R3690:Cul9
|
UTSW |
17 |
46,814,957 (GRCm39) |
splice site |
probably null |
|
R3847:Cul9
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Cul9
|
UTSW |
17 |
46,813,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Cul9
|
UTSW |
17 |
46,849,262 (GRCm39) |
missense |
probably benign |
0.00 |
R4540:Cul9
|
UTSW |
17 |
46,814,015 (GRCm39) |
missense |
probably null |
0.98 |
R4555:Cul9
|
UTSW |
17 |
46,812,755 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4604:Cul9
|
UTSW |
17 |
46,841,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R4646:Cul9
|
UTSW |
17 |
46,849,943 (GRCm39) |
nonsense |
probably null |
|
R4799:Cul9
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4822:Cul9
|
UTSW |
17 |
46,840,977 (GRCm39) |
missense |
probably benign |
0.01 |
R4964:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5027:Cul9
|
UTSW |
17 |
46,811,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R5185:Cul9
|
UTSW |
17 |
46,836,758 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5237:Cul9
|
UTSW |
17 |
46,854,393 (GRCm39) |
missense |
probably benign |
0.00 |
R5278:Cul9
|
UTSW |
17 |
46,821,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R5455:Cul9
|
UTSW |
17 |
46,821,772 (GRCm39) |
splice site |
probably null |
|
R5592:Cul9
|
UTSW |
17 |
46,831,517 (GRCm39) |
missense |
probably benign |
0.00 |
R5597:Cul9
|
UTSW |
17 |
46,813,591 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5613:Cul9
|
UTSW |
17 |
46,814,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Cul9
|
UTSW |
17 |
46,832,854 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6135:Cul9
|
UTSW |
17 |
46,832,379 (GRCm39) |
missense |
probably benign |
|
R6352:Cul9
|
UTSW |
17 |
46,822,241 (GRCm39) |
missense |
probably benign |
0.00 |
R6376:Cul9
|
UTSW |
17 |
46,819,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Cul9
|
UTSW |
17 |
46,833,109 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6898:Cul9
|
UTSW |
17 |
46,821,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7090:Cul9
|
UTSW |
17 |
46,811,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R7193:Cul9
|
UTSW |
17 |
46,849,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R7221:Cul9
|
UTSW |
17 |
46,839,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R7291:Cul9
|
UTSW |
17 |
46,851,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Cul9
|
UTSW |
17 |
46,821,835 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7348:Cul9
|
UTSW |
17 |
46,821,919 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7463:Cul9
|
UTSW |
17 |
46,831,402 (GRCm39) |
splice site |
probably null |
|
R7480:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R7573:Cul9
|
UTSW |
17 |
46,830,836 (GRCm39) |
missense |
probably benign |
|
R7582:Cul9
|
UTSW |
17 |
46,821,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Cul9
|
UTSW |
17 |
46,852,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R7684:Cul9
|
UTSW |
17 |
46,820,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Cul9
|
UTSW |
17 |
46,851,237 (GRCm39) |
missense |
probably benign |
0.37 |
R7834:Cul9
|
UTSW |
17 |
46,836,630 (GRCm39) |
splice site |
probably null |
|
R8131:Cul9
|
UTSW |
17 |
46,822,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Cul9
|
UTSW |
17 |
46,849,273 (GRCm39) |
missense |
probably benign |
0.01 |
R8231:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Cul9
|
UTSW |
17 |
46,840,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R8504:Cul9
|
UTSW |
17 |
46,814,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R8550:Cul9
|
UTSW |
17 |
46,830,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Cul9
|
UTSW |
17 |
46,838,840 (GRCm39) |
missense |
probably benign |
0.28 |
R8769:Cul9
|
UTSW |
17 |
46,832,828 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8893:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R8904:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8936:Cul9
|
UTSW |
17 |
46,839,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8972:Cul9
|
UTSW |
17 |
46,854,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R9003:Cul9
|
UTSW |
17 |
46,836,001 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9012:Cul9
|
UTSW |
17 |
46,854,447 (GRCm39) |
missense |
probably benign |
|
R9056:Cul9
|
UTSW |
17 |
46,854,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R9071:Cul9
|
UTSW |
17 |
46,837,379 (GRCm39) |
missense |
probably benign |
|
R9162:Cul9
|
UTSW |
17 |
46,837,529 (GRCm39) |
missense |
probably benign |
0.32 |
R9476:Cul9
|
UTSW |
17 |
46,821,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Cul9
|
UTSW |
17 |
46,841,026 (GRCm39) |
missense |
probably benign |
0.41 |
R9563:Cul9
|
UTSW |
17 |
46,820,897 (GRCm39) |
missense |
probably benign |
0.01 |
R9568:Cul9
|
UTSW |
17 |
46,831,044 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9610:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9611:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9705:Cul9
|
UTSW |
17 |
46,854,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Cul9
|
UTSW |
17 |
46,850,224 (GRCm39) |
missense |
probably benign |
0.18 |
RF011:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF016:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
RF026:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
nonsense |
probably null |
|
RF027:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF030:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
small insertion |
probably benign |
|
RF033:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF039:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF041:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
nonsense |
probably null |
|
RF042:Cul9
|
UTSW |
17 |
46,851,541 (GRCm39) |
frame shift |
probably null |
|
RF057:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,511 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,502 (GRCm39) |
nonsense |
probably null |
|
Z1177:Cul9
|
UTSW |
17 |
46,848,723 (GRCm39) |
missense |
probably benign |
0.14 |
|