Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
T |
C |
15: 101,092,722 (GRCm39) |
W122R |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,592,657 (GRCm39) |
R4294H |
probably benign |
Het |
Afdn |
A |
G |
17: 14,024,315 (GRCm39) |
T74A |
probably damaging |
Het |
Aff3 |
T |
A |
1: 38,247,098 (GRCm39) |
D829V |
probably benign |
Het |
Akr1c12 |
T |
C |
13: 4,325,772 (GRCm39) |
Q107R |
probably benign |
Het |
Apc |
T |
A |
18: 34,402,252 (GRCm39) |
F131I |
probably benign |
Het |
Atosb |
A |
T |
4: 43,033,687 (GRCm39) |
F489I |
probably damaging |
Het |
Atp13a1 |
T |
A |
8: 70,259,424 (GRCm39) |
L1036H |
probably damaging |
Het |
BC035044 |
A |
C |
6: 128,867,855 (GRCm39) |
|
probably benign |
Het |
C1rl |
A |
G |
6: 124,485,535 (GRCm39) |
D302G |
probably benign |
Het |
C2cd6 |
A |
C |
1: 59,117,093 (GRCm39) |
D133E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,629,671 (GRCm39) |
Y1061F |
probably damaging |
Het |
Cav1 |
A |
G |
6: 17,308,034 (GRCm39) |
D62G |
probably damaging |
Het |
Ccdc77 |
T |
C |
6: 120,327,242 (GRCm39) |
M68V |
probably damaging |
Het |
Cd55 |
A |
T |
1: 130,375,348 (GRCm39) |
|
probably benign |
Het |
Cdc27 |
C |
A |
11: 104,413,602 (GRCm39) |
A380S |
probably damaging |
Het |
Cenpb |
A |
T |
2: 131,021,477 (GRCm39) |
I107K |
probably damaging |
Het |
Cep135 |
T |
G |
5: 76,769,187 (GRCm39) |
H612Q |
possibly damaging |
Het |
Chd1l |
A |
T |
3: 97,470,849 (GRCm39) |
N815K |
probably damaging |
Het |
Cldn20 |
C |
T |
17: 3,582,992 (GRCm39) |
T55M |
possibly damaging |
Het |
Depdc1a |
A |
T |
3: 159,221,679 (GRCm39) |
I208L |
probably benign |
Het |
Dgkb |
C |
T |
12: 38,134,223 (GRCm39) |
A43V |
possibly damaging |
Het |
Dgkb |
C |
T |
12: 38,654,104 (GRCm39) |
T741I |
probably damaging |
Het |
Dhx16 |
A |
G |
17: 36,197,076 (GRCm39) |
N653S |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,438,329 (GRCm39) |
S3987T |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,906,758 (GRCm39) |
D685G |
probably damaging |
Het |
Dst |
T |
A |
1: 34,334,277 (GRCm39) |
I4835N |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,561,114 (GRCm39) |
I288V |
probably damaging |
Het |
Fnta |
C |
T |
8: 26,497,341 (GRCm39) |
W169* |
probably null |
Het |
Golga4 |
T |
C |
9: 118,365,860 (GRCm39) |
L304P |
probably damaging |
Het |
Hace1 |
A |
G |
10: 45,466,362 (GRCm39) |
|
probably null |
Het |
Ino80b |
G |
T |
6: 83,101,112 (GRCm39) |
|
probably null |
Het |
Kcmf1 |
G |
A |
6: 72,820,082 (GRCm39) |
R306C |
probably damaging |
Het |
Lrrc46 |
G |
A |
11: 96,927,305 (GRCm39) |
T92I |
possibly damaging |
Het |
Man2b1 |
T |
C |
8: 85,824,076 (GRCm39) |
V991A |
possibly damaging |
Het |
Mga |
A |
G |
2: 119,776,776 (GRCm39) |
N1770S |
probably damaging |
Het |
Mgat4e |
T |
C |
1: 134,468,944 (GRCm39) |
T367A |
probably benign |
Het |
Mtr |
A |
G |
13: 12,202,992 (GRCm39) |
S1204P |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,417,487 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,560,585 (GRCm39) |
S74P |
probably damaging |
Het |
Noct |
T |
C |
3: 51,157,508 (GRCm39) |
V282A |
possibly damaging |
Het |
Nol11 |
A |
T |
11: 107,071,912 (GRCm39) |
I227K |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,130,646 (GRCm39) |
S4T |
probably damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,714 (GRCm39) |
Y259* |
probably null |
Het |
Or5p64 |
A |
G |
7: 107,855,109 (GRCm39) |
S79P |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,809,782 (GRCm39) |
L393F |
probably damaging |
Het |
Prex2 |
C |
T |
1: 11,336,259 (GRCm39) |
R1486C |
probably damaging |
Het |
Rc3h2 |
T |
C |
2: 37,272,028 (GRCm39) |
T768A |
probably damaging |
Het |
Rin3 |
A |
T |
12: 102,335,584 (GRCm39) |
E418D |
probably benign |
Het |
Rnf214 |
G |
T |
9: 45,778,886 (GRCm39) |
T586N |
probably damaging |
Het |
Samd4b |
A |
G |
7: 28,101,285 (GRCm39) |
S667P |
probably damaging |
Het |
Sec14l2 |
T |
C |
11: 4,061,161 (GRCm39) |
Y100C |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,914,077 (GRCm39) |
E282G |
probably benign |
Het |
Themis |
A |
C |
10: 28,657,762 (GRCm39) |
N110T |
possibly damaging |
Het |
Tln1 |
C |
A |
4: 43,543,165 (GRCm39) |
S1333I |
probably benign |
Het |
Tmem53 |
T |
C |
4: 117,125,625 (GRCm39) |
V224A |
possibly damaging |
Het |
Tmtc4 |
T |
A |
14: 123,163,391 (GRCm39) |
K664N |
possibly damaging |
Het |
Tnni3k |
T |
C |
3: 154,674,922 (GRCm39) |
D201G |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,912,898 (GRCm39) |
E1681G |
probably damaging |
Het |
Trhde |
A |
T |
10: 114,340,103 (GRCm39) |
D567E |
probably damaging |
Het |
Tsc2 |
T |
C |
17: 24,828,101 (GRCm39) |
M788V |
probably benign |
Het |
Ube3a |
A |
G |
7: 58,926,650 (GRCm39) |
Y476C |
probably damaging |
Het |
Ubiad1 |
T |
C |
4: 148,520,682 (GRCm39) |
N314S |
possibly damaging |
Het |
Vmn2r107 |
A |
T |
17: 20,595,939 (GRCm39) |
I831F |
probably damaging |
Het |
Vwa3b |
T |
A |
1: 37,124,367 (GRCm39) |
C322S |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,939,916 (GRCm39) |
H238Q |
probably benign |
Het |
Wnk2 |
A |
G |
13: 49,300,081 (GRCm39) |
Y210H |
probably damaging |
Het |
Wwc2 |
T |
C |
8: 48,304,943 (GRCm39) |
D894G |
unknown |
Het |
Yes1 |
T |
A |
5: 32,810,381 (GRCm39) |
F180Y |
probably damaging |
Het |
Yju2b |
T |
C |
8: 84,985,318 (GRCm39) |
E317G |
probably benign |
Het |
Zbtb46 |
T |
C |
2: 181,033,062 (GRCm39) |
Y533C |
probably damaging |
Het |
Zfp57 |
T |
C |
17: 37,316,942 (GRCm39) |
S7P |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,802,090 (GRCm39) |
|
probably null |
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 |
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 |
|
|