Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,323,323 (GRCm39) |
F3387I |
possibly damaging |
Het |
Acacb |
T |
A |
5: 114,304,088 (GRCm39) |
S170R |
probably benign |
Het |
Adamtsl4 |
A |
G |
3: 95,588,960 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
G |
13: 81,637,050 (GRCm39) |
C3464R |
probably benign |
Het |
Apbb1 |
A |
T |
7: 105,214,889 (GRCm39) |
|
probably benign |
Het |
Cad |
A |
G |
5: 31,212,365 (GRCm39) |
T23A |
probably benign |
Het |
Cdca7 |
A |
G |
2: 72,313,759 (GRCm39) |
R183G |
probably benign |
Het |
Cdpf1 |
T |
C |
15: 85,693,513 (GRCm39) |
T5A |
probably benign |
Het |
Cep85 |
T |
C |
4: 133,883,490 (GRCm39) |
D133G |
probably damaging |
Het |
Chrna9 |
T |
C |
5: 66,128,359 (GRCm39) |
L189P |
probably damaging |
Het |
Clca3a1 |
A |
C |
3: 144,713,689 (GRCm39) |
|
probably null |
Het |
Cntn1 |
G |
T |
15: 92,140,876 (GRCm39) |
V201F |
probably damaging |
Het |
Col4a3 |
A |
G |
1: 82,644,267 (GRCm39) |
E352G |
unknown |
Het |
Ddhd2 |
T |
C |
8: 26,242,164 (GRCm39) |
Y237C |
probably damaging |
Het |
Dnah6 |
A |
C |
6: 73,014,605 (GRCm39) |
F3609V |
probably benign |
Het |
Epha3 |
T |
C |
16: 63,422,650 (GRCm39) |
K580R |
possibly damaging |
Het |
Fam135b |
T |
C |
15: 71,334,560 (GRCm39) |
N878S |
probably benign |
Het |
Fbn1 |
T |
G |
2: 125,171,022 (GRCm39) |
T1938P |
probably damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,969 (GRCm39) |
V234A |
probably damaging |
Het |
Garin5b |
T |
C |
7: 4,761,660 (GRCm39) |
N351D |
probably benign |
Het |
Glt1d1 |
A |
T |
5: 127,721,478 (GRCm39) |
N55I |
probably benign |
Het |
Gm17641 |
C |
A |
3: 68,776,807 (GRCm39) |
|
probably benign |
Het |
Gm7665 |
A |
G |
18: 16,407,788 (GRCm39) |
|
noncoding transcript |
Het |
Hgf |
A |
C |
5: 16,819,892 (GRCm39) |
N541T |
probably benign |
Het |
Hipk2 |
G |
A |
6: 38,795,814 (GRCm39) |
P152S |
probably benign |
Het |
Jarid2 |
C |
T |
13: 45,060,041 (GRCm39) |
L720F |
probably damaging |
Het |
Kifc5b |
A |
G |
17: 27,143,761 (GRCm39) |
E511G |
probably damaging |
Het |
Ldlr |
G |
A |
9: 21,646,538 (GRCm39) |
A235T |
probably benign |
Het |
Lmln |
A |
G |
16: 32,894,550 (GRCm39) |
D231G |
possibly damaging |
Het |
Lrp1 |
A |
G |
10: 127,403,364 (GRCm39) |
C2070R |
probably damaging |
Het |
Mbl1 |
A |
G |
14: 40,880,681 (GRCm39) |
T190A |
possibly damaging |
Het |
Mpdz |
A |
T |
4: 81,299,934 (GRCm39) |
S355T |
probably benign |
Het |
Muc19 |
C |
T |
15: 91,772,332 (GRCm39) |
|
noncoding transcript |
Het |
Mycbp2 |
A |
C |
14: 103,376,671 (GRCm39) |
|
probably null |
Het |
Naa20 |
T |
C |
2: 145,757,762 (GRCm39) |
S164P |
probably damaging |
Het |
Nme4 |
A |
T |
17: 26,312,807 (GRCm39) |
|
probably benign |
Het |
Npas2 |
A |
T |
1: 39,386,587 (GRCm39) |
R619* |
probably null |
Het |
Nudt19 |
G |
A |
7: 35,255,171 (GRCm39) |
T20I |
possibly damaging |
Het |
Or4c119 |
T |
A |
2: 88,987,283 (GRCm39) |
K79* |
probably null |
Het |
Or5b97 |
A |
G |
19: 12,878,365 (GRCm39) |
Y260H |
probably damaging |
Het |
Pitpnc1 |
A |
G |
11: 107,187,054 (GRCm39) |
Y90H |
possibly damaging |
Het |
Rcor2 |
A |
G |
19: 7,247,150 (GRCm39) |
T6A |
probably benign |
Het |
Rif1 |
T |
A |
2: 51,999,940 (GRCm39) |
S1131R |
probably damaging |
Het |
Rtkn |
T |
A |
6: 83,127,972 (GRCm39) |
D377E |
probably benign |
Het |
Rtn4rl2 |
T |
A |
2: 84,702,846 (GRCm39) |
N242I |
probably damaging |
Het |
Sbno2 |
G |
A |
10: 79,898,022 (GRCm39) |
L719F |
probably benign |
Het |
Scn11a |
G |
T |
9: 119,648,897 (GRCm39) |
D55E |
probably damaging |
Het |
Setd1b |
T |
A |
5: 123,289,929 (GRCm39) |
I632N |
unknown |
Het |
Spaca6 |
A |
G |
17: 18,051,458 (GRCm39) |
T45A |
probably benign |
Het |
Srpk2 |
A |
T |
5: 23,729,390 (GRCm39) |
D416E |
possibly damaging |
Het |
Sspo |
A |
T |
6: 48,443,889 (GRCm39) |
|
probably null |
Het |
Sycp1 |
A |
T |
3: 102,752,370 (GRCm39) |
I804N |
probably benign |
Het |
Tdp2 |
G |
A |
13: 25,015,809 (GRCm39) |
R32Q |
probably benign |
Het |
Tgfbr3 |
A |
G |
5: 107,284,795 (GRCm39) |
V618A |
possibly damaging |
Het |
Tmc3 |
C |
T |
7: 83,258,326 (GRCm39) |
P439S |
probably benign |
Het |
Tnxb |
A |
T |
17: 34,936,457 (GRCm39) |
D2740V |
probably damaging |
Het |
Tspyl4 |
A |
G |
10: 34,173,933 (GRCm39) |
T142A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,710,785 (GRCm39) |
|
probably benign |
Het |
Tubgcp4 |
T |
C |
2: 121,004,061 (GRCm39) |
L34P |
probably damaging |
Het |
Tubgcp6 |
G |
T |
15: 88,983,748 (GRCm39) |
|
probably benign |
Het |
Vps4b |
T |
C |
1: 106,724,148 (GRCm39) |
|
probably null |
Het |
Wtap |
A |
G |
17: 13,186,525 (GRCm39) |
S341P |
possibly damaging |
Het |
Wwc1 |
T |
C |
11: 35,774,172 (GRCm39) |
T363A |
probably benign |
Het |
Zbtb8a |
G |
A |
4: 129,254,293 (GRCm39) |
T67M |
probably damaging |
Het |
Zfp865 |
T |
C |
7: 5,037,668 (GRCm39) |
|
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 |
|
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 |
R7470:Unc79
|
UTSW |
12 |
103,061,235 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|