Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
A |
T |
9: 55,898,622 (GRCm39) |
V238E |
possibly damaging |
Het |
Actn3 |
G |
A |
19: 4,917,842 (GRCm39) |
S375L |
possibly damaging |
Het |
Adgrg6 |
T |
C |
10: 14,319,810 (GRCm39) |
T476A |
probably benign |
Het |
Afm |
T |
A |
5: 90,679,486 (GRCm39) |
S327T |
probably damaging |
Het |
Apol7e |
T |
A |
15: 77,602,143 (GRCm39) |
M247K |
probably benign |
Het |
Aqp12 |
T |
A |
1: 92,936,385 (GRCm39) |
L237Q |
probably damaging |
Het |
Arhgef12 |
A |
T |
9: 42,951,848 (GRCm39) |
S63T |
probably damaging |
Het |
Axdnd1 |
T |
A |
1: 156,204,086 (GRCm39) |
E393V |
|
Het |
Cacna1g |
T |
A |
11: 94,352,765 (GRCm39) |
D365V |
possibly damaging |
Het |
Ccdc3 |
T |
A |
2: 5,143,115 (GRCm39) |
V124E |
possibly damaging |
Het |
Ccr7 |
C |
T |
11: 99,036,383 (GRCm39) |
V180M |
possibly damaging |
Het |
Cd47 |
T |
A |
16: 49,704,585 (GRCm39) |
I119K |
|
Het |
Cenpe |
A |
T |
3: 134,947,916 (GRCm39) |
L1158F |
probably damaging |
Het |
Cfi |
A |
G |
3: 129,648,736 (GRCm39) |
R207G |
probably benign |
Het |
Cyp2j6 |
T |
C |
4: 96,423,708 (GRCm39) |
Y220C |
probably benign |
Het |
Ddhd2 |
A |
G |
8: 26,225,087 (GRCm39) |
F577L |
probably benign |
Het |
Dhx40 |
T |
C |
11: 86,667,528 (GRCm39) |
E537G |
probably damaging |
Het |
Disp3 |
A |
T |
4: 148,345,527 (GRCm39) |
C438S |
possibly damaging |
Het |
Dock3 |
A |
G |
9: 106,882,644 (GRCm39) |
S380P |
probably damaging |
Het |
Ehmt2 |
A |
G |
17: 35,118,372 (GRCm39) |
E106G |
possibly damaging |
Het |
Fmnl2 |
A |
T |
2: 52,932,377 (GRCm39) |
I119F |
probably damaging |
Het |
Gm11554 |
A |
C |
11: 99,695,190 (GRCm39) |
S8A |
unknown |
Het |
Grm7 |
A |
G |
6: 111,478,476 (GRCm39) |
I54V |
|
Het |
Hbs1l |
T |
C |
10: 21,234,683 (GRCm39) |
F579L |
possibly damaging |
Het |
Hgf |
C |
A |
5: 16,823,854 (GRCm39) |
Q684K |
probably benign |
Het |
Igsf3 |
T |
C |
3: 101,358,391 (GRCm39) |
Y741H |
possibly damaging |
Het |
Il17rb |
C |
A |
14: 29,719,990 (GRCm39) |
G304W |
probably damaging |
Het |
Ino80c |
C |
T |
18: 24,241,895 (GRCm39) |
W163* |
probably null |
Het |
Kcnt1 |
A |
C |
2: 25,799,845 (GRCm39) |
D997A |
probably damaging |
Het |
Klf7 |
C |
T |
1: 64,081,472 (GRCm39) |
|
probably null |
Het |
Lingo1 |
T |
C |
9: 56,527,908 (GRCm39) |
Y233C |
probably damaging |
Het |
Lmo7 |
C |
A |
14: 102,138,040 (GRCm39) |
T914K |
possibly damaging |
Het |
Mark1 |
G |
T |
1: 184,660,241 (GRCm39) |
Y138* |
probably null |
Het |
Mcm3ap |
C |
A |
10: 76,344,231 (GRCm39) |
T1791K |
probably damaging |
Het |
Mcts2 |
T |
C |
2: 152,529,582 (GRCm39) |
I131T |
probably benign |
Het |
Mipep |
A |
G |
14: 61,040,344 (GRCm39) |
D288G |
probably benign |
Het |
Ms4a8a |
T |
A |
19: 11,053,714 (GRCm39) |
N131Y |
possibly damaging |
Het |
Nalcn |
T |
C |
14: 123,809,456 (GRCm39) |
E232G |
probably benign |
Het |
Nat10 |
C |
T |
2: 103,565,226 (GRCm39) |
A452T |
probably benign |
Het |
Nfatc2 |
G |
A |
2: 168,365,227 (GRCm39) |
Q596* |
probably null |
Het |
Nudt13 |
G |
T |
14: 20,359,791 (GRCm39) |
G173W |
probably damaging |
Het |
Or10n1 |
C |
A |
9: 39,524,998 (GRCm39) |
T45K |
probably benign |
Het |
Or1e16 |
T |
A |
11: 73,286,714 (GRCm39) |
I45F |
probably damaging |
Het |
Or5l14 |
A |
T |
2: 87,792,793 (GRCm39) |
C148S |
possibly damaging |
Het |
Or8b4 |
T |
A |
9: 37,830,592 (GRCm39) |
I213N |
probably damaging |
Het |
Otud4 |
T |
C |
8: 80,399,989 (GRCm39) |
V901A |
probably benign |
Het |
Pah |
G |
A |
10: 87,399,286 (GRCm39) |
R155Q |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,365,008 (GRCm39) |
H1130R |
probably benign |
Het |
Pnliprp1 |
A |
G |
19: 58,720,457 (GRCm39) |
N111S |
possibly damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,869,649 (GRCm39) |
Y401H |
probably damaging |
Het |
Prr14 |
A |
G |
7: 127,074,997 (GRCm39) |
K466R |
probably null |
Het |
Ralgapa2 |
A |
G |
2: 146,266,587 (GRCm39) |
L663P |
probably damaging |
Het |
Reg3d |
A |
T |
6: 78,353,071 (GRCm39) |
C171S |
possibly damaging |
Het |
Reln |
G |
T |
5: 22,147,739 (GRCm39) |
L2404I |
probably damaging |
Het |
Rnasel |
A |
C |
1: 153,629,777 (GRCm39) |
I98L |
probably benign |
Het |
Rnf216 |
T |
C |
5: 142,978,480 (GRCm39) |
D886G |
possibly damaging |
Het |
Rp1l1 |
A |
G |
14: 64,266,015 (GRCm39) |
R534G |
probably benign |
Het |
Selenon |
A |
C |
4: 134,267,061 (GRCm39) |
S514A |
probably benign |
Het |
Sema3d |
T |
A |
5: 12,558,152 (GRCm39) |
I228N |
probably damaging |
Het |
Serpinb9g |
T |
A |
13: 33,670,617 (GRCm39) |
I35N |
probably damaging |
Het |
Siglec1 |
A |
C |
2: 130,917,744 (GRCm39) |
H1044Q |
probably benign |
Het |
Skint5 |
T |
A |
4: 113,614,128 (GRCm39) |
I693F |
unknown |
Het |
Skint5 |
G |
T |
4: 113,743,000 (GRCm39) |
L370M |
unknown |
Het |
Slc12a1 |
G |
A |
2: 125,059,815 (GRCm39) |
W905* |
probably null |
Het |
Slc26a9 |
G |
C |
1: 131,691,781 (GRCm39) |
V675L |
probably benign |
Het |
Slc5a7 |
A |
T |
17: 54,583,990 (GRCm39) |
Y433* |
probably null |
Het |
Slc7a4 |
A |
G |
16: 17,392,977 (GRCm39) |
I274T |
probably benign |
Het |
Slmap |
A |
G |
14: 26,148,575 (GRCm39) |
V612A |
probably benign |
Het |
Spen |
T |
C |
4: 141,206,605 (GRCm39) |
D674G |
unknown |
Het |
Ssh1 |
T |
C |
5: 114,080,488 (GRCm39) |
T981A |
possibly damaging |
Het |
Sycp2l |
T |
C |
13: 41,316,580 (GRCm39) |
S180P |
probably benign |
Het |
Tdrd7 |
C |
A |
4: 45,990,144 (GRCm39) |
S181R |
probably benign |
Het |
Thada |
T |
C |
17: 84,533,469 (GRCm39) |
N1661D |
probably benign |
Het |
Tsga13 |
C |
A |
6: 30,876,981 (GRCm39) |
D179Y |
possibly damaging |
Het |
Ttf2 |
T |
G |
3: 100,870,478 (GRCm39) |
Q198H |
possibly damaging |
Het |
Ugt2b37 |
T |
G |
5: 87,401,971 (GRCm39) |
Y220S |
probably benign |
Het |
Unc80 |
T |
A |
1: 66,661,621 (GRCm39) |
M1682K |
probably benign |
Het |
Vcp |
A |
G |
4: 42,982,891 (GRCm39) |
S652P |
probably damaging |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,697,310 (GRCm39) |
M789K |
probably damaging |
Het |
Wrnip1 |
T |
A |
13: 33,000,310 (GRCm39) |
L439* |
probably null |
Het |
Zfhx2 |
A |
G |
14: 55,304,207 (GRCm39) |
I1259T |
possibly damaging |
Het |
Zfp369 |
A |
T |
13: 65,439,960 (GRCm39) |
T215S |
probably benign |
Het |
Zfp64 |
A |
T |
2: 168,767,731 (GRCm39) |
V627E |
probably damaging |
Het |
Zfp873 |
T |
C |
10: 81,895,773 (GRCm39) |
I168T |
probably benign |
Het |
|
Other mutations in Unc79 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00718:Unc79
|
APN |
12 |
103,135,906 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00835:Unc79
|
APN |
12 |
103,108,149 (GRCm39) |
splice site |
probably benign |
|
IGL00917:Unc79
|
APN |
12 |
103,054,766 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01012:Unc79
|
APN |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01121:Unc79
|
APN |
12 |
103,131,890 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01303:Unc79
|
APN |
12 |
103,128,126 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01305:Unc79
|
APN |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01315:Unc79
|
APN |
12 |
103,054,780 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01388:Unc79
|
APN |
12 |
103,136,018 (GRCm39) |
splice site |
probably benign |
|
IGL01415:Unc79
|
APN |
12 |
103,074,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01447:Unc79
|
APN |
12 |
103,045,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01655:Unc79
|
APN |
12 |
103,134,546 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Unc79
|
APN |
12 |
103,115,279 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01728:Unc79
|
APN |
12 |
103,131,943 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01767:Unc79
|
APN |
12 |
103,108,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02080:Unc79
|
APN |
12 |
102,968,234 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Unc79
|
APN |
12 |
102,964,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Unc79
|
APN |
12 |
102,965,006 (GRCm39) |
splice site |
probably null |
|
IGL02186:Unc79
|
APN |
12 |
102,977,542 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02205:Unc79
|
APN |
12 |
103,045,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Unc79
|
APN |
12 |
103,122,705 (GRCm39) |
splice site |
probably benign |
|
IGL02498:Unc79
|
APN |
12 |
103,137,837 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Unc79
|
APN |
12 |
103,078,535 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02508:Unc79
|
APN |
12 |
103,078,277 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Unc79
|
APN |
12 |
103,148,418 (GRCm39) |
splice site |
probably benign |
|
IGL02589:Unc79
|
APN |
12 |
103,139,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02611:Unc79
|
APN |
12 |
103,131,967 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02728:Unc79
|
APN |
12 |
103,088,688 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02827:Unc79
|
APN |
12 |
103,041,105 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03028:Unc79
|
APN |
12 |
103,139,785 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03144:Unc79
|
APN |
12 |
103,008,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03229:Unc79
|
APN |
12 |
103,100,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03269:Unc79
|
APN |
12 |
103,054,936 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03325:Unc79
|
APN |
12 |
103,135,869 (GRCm39) |
missense |
probably damaging |
0.98 |
pencil-thin
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
sweetpea
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Unc79
|
UTSW |
12 |
103,039,009 (GRCm39) |
nonsense |
probably null |
|
ANU22:Unc79
|
UTSW |
12 |
102,968,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Unc79
|
UTSW |
12 |
103,091,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0067:Unc79
|
UTSW |
12 |
103,025,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R0107:Unc79
|
UTSW |
12 |
103,100,784 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0110:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0128:Unc79
|
UTSW |
12 |
103,054,693 (GRCm39) |
splice site |
probably benign |
|
R0166:Unc79
|
UTSW |
12 |
103,122,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Unc79
|
UTSW |
12 |
103,058,286 (GRCm39) |
missense |
probably benign |
0.00 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0211:Unc79
|
UTSW |
12 |
103,039,051 (GRCm39) |
missense |
probably benign |
0.01 |
R0218:Unc79
|
UTSW |
12 |
103,075,040 (GRCm39) |
splice site |
probably null |
|
R0244:Unc79
|
UTSW |
12 |
103,079,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0305:Unc79
|
UTSW |
12 |
103,079,459 (GRCm39) |
missense |
probably benign |
0.18 |
R0310:Unc79
|
UTSW |
12 |
103,027,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Unc79
|
UTSW |
12 |
103,137,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R0369:Unc79
|
UTSW |
12 |
103,055,031 (GRCm39) |
critical splice donor site |
probably null |
|
R0450:Unc79
|
UTSW |
12 |
103,045,329 (GRCm39) |
critical splice donor site |
probably null |
|
R0503:Unc79
|
UTSW |
12 |
103,045,127 (GRCm39) |
missense |
probably benign |
0.01 |
R0542:Unc79
|
UTSW |
12 |
103,060,437 (GRCm39) |
splice site |
probably benign |
|
R0845:Unc79
|
UTSW |
12 |
103,139,703 (GRCm39) |
splice site |
probably benign |
|
R0893:Unc79
|
UTSW |
12 |
102,957,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Unc79
|
UTSW |
12 |
103,041,112 (GRCm39) |
missense |
probably benign |
0.03 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Unc79
|
UTSW |
12 |
103,078,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Unc79
|
UTSW |
12 |
103,013,311 (GRCm39) |
splice site |
probably benign |
|
R1191:Unc79
|
UTSW |
12 |
103,013,271 (GRCm39) |
nonsense |
probably null |
|
R1307:Unc79
|
UTSW |
12 |
103,036,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R1368:Unc79
|
UTSW |
12 |
103,122,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Unc79
|
UTSW |
12 |
103,149,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Unc79
|
UTSW |
12 |
103,079,052 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1777:Unc79
|
UTSW |
12 |
103,078,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Unc79
|
UTSW |
12 |
103,109,005 (GRCm39) |
missense |
probably damaging |
0.99 |
R1824:Unc79
|
UTSW |
12 |
103,025,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Unc79
|
UTSW |
12 |
103,100,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Unc79
|
UTSW |
12 |
103,135,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Unc79
|
UTSW |
12 |
103,041,178 (GRCm39) |
missense |
probably benign |
0.19 |
R1958:Unc79
|
UTSW |
12 |
102,957,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Unc79
|
UTSW |
12 |
102,977,538 (GRCm39) |
nonsense |
probably null |
|
R2019:Unc79
|
UTSW |
12 |
103,137,830 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2290:Unc79
|
UTSW |
12 |
103,112,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2939:Unc79
|
UTSW |
12 |
102,957,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R2962:Unc79
|
UTSW |
12 |
103,061,378 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3176:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Unc79
|
UTSW |
12 |
103,079,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3684:Unc79
|
UTSW |
12 |
103,041,062 (GRCm39) |
missense |
probably benign |
0.00 |
R3686:Unc79
|
UTSW |
12 |
103,054,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R3760:Unc79
|
UTSW |
12 |
103,058,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Unc79
|
UTSW |
12 |
103,039,018 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4039:Unc79
|
UTSW |
12 |
103,041,208 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4110:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4113:Unc79
|
UTSW |
12 |
103,025,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4159:Unc79
|
UTSW |
12 |
103,036,512 (GRCm39) |
intron |
probably benign |
|
R4273:Unc79
|
UTSW |
12 |
103,088,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R4292:Unc79
|
UTSW |
12 |
103,149,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R4334:Unc79
|
UTSW |
12 |
103,045,233 (GRCm39) |
missense |
probably benign |
|
R4513:Unc79
|
UTSW |
12 |
102,988,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Unc79
|
UTSW |
12 |
102,957,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Unc79
|
UTSW |
12 |
102,968,062 (GRCm39) |
splice site |
probably benign |
|
R4645:Unc79
|
UTSW |
12 |
103,079,081 (GRCm39) |
missense |
probably benign |
|
R4758:Unc79
|
UTSW |
12 |
103,128,080 (GRCm39) |
nonsense |
probably null |
|
R4787:Unc79
|
UTSW |
12 |
103,013,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Unc79
|
UTSW |
12 |
103,139,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R4883:Unc79
|
UTSW |
12 |
103,060,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4898:Unc79
|
UTSW |
12 |
103,128,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R4979:Unc79
|
UTSW |
12 |
103,078,691 (GRCm39) |
missense |
probably benign |
|
R5044:Unc79
|
UTSW |
12 |
103,078,962 (GRCm39) |
missense |
probably benign |
0.32 |
R5053:Unc79
|
UTSW |
12 |
103,071,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5061:Unc79
|
UTSW |
12 |
103,134,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5075:Unc79
|
UTSW |
12 |
103,041,213 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5101:Unc79
|
UTSW |
12 |
103,078,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5236:Unc79
|
UTSW |
12 |
103,060,654 (GRCm39) |
critical splice donor site |
probably null |
|
R5240:Unc79
|
UTSW |
12 |
103,037,010 (GRCm39) |
missense |
probably damaging |
0.99 |
R5383:Unc79
|
UTSW |
12 |
103,070,886 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5461:Unc79
|
UTSW |
12 |
103,078,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R5535:Unc79
|
UTSW |
12 |
103,135,962 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5609:Unc79
|
UTSW |
12 |
103,094,527 (GRCm39) |
missense |
probably benign |
|
R5639:Unc79
|
UTSW |
12 |
103,137,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Unc79
|
UTSW |
12 |
102,968,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5923:Unc79
|
UTSW |
12 |
103,078,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5925:Unc79
|
UTSW |
12 |
103,091,989 (GRCm39) |
splice site |
probably null |
|
R5975:Unc79
|
UTSW |
12 |
103,091,885 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6047:Unc79
|
UTSW |
12 |
103,027,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Unc79
|
UTSW |
12 |
103,027,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Unc79
|
UTSW |
12 |
103,149,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R6292:Unc79
|
UTSW |
12 |
103,108,991 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6313:Unc79
|
UTSW |
12 |
103,078,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R6391:Unc79
|
UTSW |
12 |
102,987,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6405:Unc79
|
UTSW |
12 |
103,134,595 (GRCm39) |
missense |
probably damaging |
0.97 |
R6416:Unc79
|
UTSW |
12 |
103,097,905 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6467:Unc79
|
UTSW |
12 |
103,139,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6573:Unc79
|
UTSW |
12 |
103,027,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R6614:Unc79
|
UTSW |
12 |
102,957,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Unc79
|
UTSW |
12 |
103,045,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R6700:Unc79
|
UTSW |
12 |
103,091,962 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6724:Unc79
|
UTSW |
12 |
103,071,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Unc79
|
UTSW |
12 |
103,108,267 (GRCm39) |
missense |
probably benign |
0.12 |
R6869:Unc79
|
UTSW |
12 |
103,079,331 (GRCm39) |
missense |
probably benign |
0.33 |
R6879:Unc79
|
UTSW |
12 |
103,115,046 (GRCm39) |
splice site |
probably null |
|
R6942:Unc79
|
UTSW |
12 |
103,088,704 (GRCm39) |
critical splice donor site |
probably null |
|
R6961:Unc79
|
UTSW |
12 |
103,079,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Unc79
|
UTSW |
12 |
102,964,699 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6980:Unc79
|
UTSW |
12 |
103,025,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Unc79
|
UTSW |
12 |
103,027,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Unc79
|
UTSW |
12 |
103,108,885 (GRCm39) |
missense |
probably benign |
0.06 |
R7197:Unc79
|
UTSW |
12 |
103,078,765 (GRCm39) |
missense |
probably benign |
|
R7209:Unc79
|
UTSW |
12 |
103,091,883 (GRCm39) |
missense |
probably benign |
|
R7232:Unc79
|
UTSW |
12 |
103,100,734 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7304:Unc79
|
UTSW |
12 |
103,029,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7354:Unc79
|
UTSW |
12 |
103,108,961 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7384:Unc79
|
UTSW |
12 |
103,137,837 (GRCm39) |
missense |
probably benign |
0.11 |
R7400:Unc79
|
UTSW |
12 |
103,070,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Unc79
|
UTSW |
12 |
103,055,017 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7842:Unc79
|
UTSW |
12 |
103,058,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8037:Unc79
|
UTSW |
12 |
103,016,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R8041:Unc79
|
UTSW |
12 |
103,054,726 (GRCm39) |
missense |
probably benign |
0.06 |
R8146:Unc79
|
UTSW |
12 |
103,036,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R8276:Unc79
|
UTSW |
12 |
102,968,122 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8427:Unc79
|
UTSW |
12 |
103,045,297 (GRCm39) |
missense |
probably benign |
0.24 |
R8501:Unc79
|
UTSW |
12 |
103,058,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Unc79
|
UTSW |
12 |
103,070,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,013,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Unc79
|
UTSW |
12 |
103,049,855 (GRCm39) |
missense |
probably benign |
0.13 |
R8795:Unc79
|
UTSW |
12 |
103,074,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R9017:Unc79
|
UTSW |
12 |
103,074,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9121:Unc79
|
UTSW |
12 |
102,968,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Unc79
|
UTSW |
12 |
103,078,613 (GRCm39) |
missense |
probably benign |
|
R9443:Unc79
|
UTSW |
12 |
103,037,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R9548:Unc79
|
UTSW |
12 |
102,977,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Unc79
|
UTSW |
12 |
103,135,972 (GRCm39) |
missense |
probably benign |
0.07 |
R9767:Unc79
|
UTSW |
12 |
103,079,234 (GRCm39) |
missense |
probably benign |
|
R9787:Unc79
|
UTSW |
12 |
103,112,620 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Unc79
|
UTSW |
12 |
103,079,046 (GRCm39) |
missense |
probably benign |
0.17 |
X0017:Unc79
|
UTSW |
12 |
103,074,520 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Unc79
|
UTSW |
12 |
102,957,662 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Unc79
|
UTSW |
12 |
102,987,271 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Unc79
|
UTSW |
12 |
103,108,312 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Unc79
|
UTSW |
12 |
103,054,937 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Unc79
|
UTSW |
12 |
103,131,948 (GRCm39) |
missense |
probably benign |
|
|