Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
C |
T |
1: 183,765,702 (GRCm39) |
S119N |
probably benign |
Het |
9030619P08Rik |
A |
C |
15: 75,301,846 (GRCm39) |
|
noncoding transcript |
Het |
Aldh1l2 |
T |
C |
10: 83,331,889 (GRCm39) |
I639V |
probably benign |
Het |
Ambra1 |
T |
C |
2: 91,601,241 (GRCm39) |
|
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,455,869 (GRCm39) |
Y299H |
probably damaging |
Het |
Atp6v1b1 |
A |
T |
6: 83,733,526 (GRCm39) |
|
probably benign |
Het |
Atr |
G |
A |
9: 95,832,689 (GRCm39) |
V2574I |
probably benign |
Het |
Atxn1l |
T |
A |
8: 110,459,612 (GRCm39) |
T217S |
probably benign |
Het |
Ccdc85a |
A |
G |
11: 28,346,150 (GRCm39) |
S89P |
probably benign |
Het |
Ccn5 |
T |
A |
2: 163,670,997 (GRCm39) |
M168K |
unknown |
Het |
Cd209e |
A |
T |
8: 3,899,124 (GRCm39) |
I196N |
probably damaging |
Het |
Cdhr4 |
A |
G |
9: 107,872,495 (GRCm39) |
S247G |
probably benign |
Het |
Cntn6 |
A |
T |
6: 104,809,470 (GRCm39) |
I502F |
probably damaging |
Het |
Crisp4 |
T |
C |
1: 18,193,018 (GRCm39) |
Y233C |
probably damaging |
Het |
Ctsb |
C |
A |
14: 63,376,553 (GRCm39) |
T261N |
probably benign |
Het |
Ctsk |
T |
C |
3: 95,408,185 (GRCm39) |
F14L |
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,407,385 (GRCm39) |
I2110V |
probably damaging |
Het |
Dennd5b |
A |
G |
6: 148,969,988 (GRCm39) |
M155T |
probably benign |
Het |
Echdc3 |
T |
C |
2: 6,217,611 (GRCm39) |
D54G |
probably benign |
Het |
Egln3 |
G |
A |
12: 54,228,479 (GRCm39) |
T209I |
probably damaging |
Het |
Fbn1 |
A |
C |
2: 125,214,447 (GRCm39) |
|
probably benign |
Het |
Fkbp15 |
A |
T |
4: 62,222,846 (GRCm39) |
S1018T |
possibly damaging |
Het |
Flnb |
T |
C |
14: 7,896,503 (GRCm38) |
I898T |
probably benign |
Het |
Flt1 |
T |
A |
5: 147,536,456 (GRCm39) |
Y795F |
probably damaging |
Het |
Flt4 |
C |
T |
11: 49,527,166 (GRCm39) |
|
probably benign |
Het |
Gcnt3 |
T |
C |
9: 69,941,615 (GRCm39) |
I318V |
probably benign |
Het |
Gm11437 |
T |
A |
11: 84,055,454 (GRCm39) |
H54L |
possibly damaging |
Het |
Huwe1 |
AGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGA |
X: 150,690,044 (GRCm39) |
|
probably benign |
Het |
Jarid2 |
G |
A |
13: 45,038,368 (GRCm39) |
|
probably benign |
Het |
Kif5b |
A |
T |
18: 6,214,044 (GRCm39) |
V653E |
probably benign |
Het |
Kmt2b |
A |
G |
7: 30,274,365 (GRCm39) |
V2113A |
probably damaging |
Het |
Knl1 |
C |
T |
2: 118,903,054 (GRCm39) |
T1585I |
probably benign |
Het |
Mlxipl |
T |
A |
5: 135,161,572 (GRCm39) |
M497K |
probably benign |
Het |
Mre11a |
T |
A |
9: 14,710,935 (GRCm39) |
W210R |
probably damaging |
Het |
Mrps22 |
A |
G |
9: 98,476,748 (GRCm39) |
V207A |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,390,256 (GRCm39) |
I2111V |
possibly damaging |
Het |
Myo1a |
C |
T |
10: 127,555,148 (GRCm39) |
P838L |
probably benign |
Het |
Nbea |
T |
A |
3: 55,965,461 (GRCm39) |
H484L |
probably damaging |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nlrp2 |
T |
A |
7: 5,331,430 (GRCm39) |
D322V |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,636,947 (GRCm39) |
C1057R |
probably damaging |
Het |
Ntsr1 |
T |
C |
2: 180,142,394 (GRCm39) |
S62P |
probably damaging |
Het |
Nudt18 |
A |
G |
14: 70,816,867 (GRCm39) |
H157R |
probably benign |
Het |
Or10s1 |
C |
A |
9: 39,986,192 (GRCm39) |
N200K |
probably damaging |
Het |
Or5g25 |
T |
A |
2: 85,477,904 (GRCm39) |
T254S |
probably damaging |
Het |
Sidt2 |
T |
C |
9: 45,857,002 (GRCm39) |
T435A |
probably damaging |
Het |
Snx27 |
T |
C |
3: 94,427,540 (GRCm39) |
T312A |
probably benign |
Het |
Srebf2 |
T |
C |
15: 82,061,720 (GRCm39) |
S429P |
probably damaging |
Het |
Suclg2 |
A |
G |
6: 95,474,563 (GRCm39) |
|
probably benign |
Het |
Tchh |
A |
T |
3: 93,352,279 (GRCm39) |
E573V |
unknown |
Het |
Tdrd1 |
A |
G |
19: 56,850,192 (GRCm39) |
T985A |
probably benign |
Het |
Ttc7b |
A |
G |
12: 100,369,698 (GRCm39) |
I357T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,626,008 (GRCm39) |
E13271G |
probably damaging |
Het |
Usp13 |
A |
G |
3: 32,969,857 (GRCm39) |
E661G |
probably damaging |
Het |
Vasp |
T |
G |
7: 18,992,958 (GRCm39) |
|
probably benign |
Het |
Vmn2r109 |
A |
T |
17: 20,775,503 (GRCm39) |
Y75N |
possibly damaging |
Het |
Vmn2r15 |
T |
A |
5: 109,440,770 (GRCm39) |
N363Y |
probably damaging |
Het |
Vmn2r60 |
T |
A |
7: 41,786,476 (GRCm39) |
N426K |
probably benign |
Het |
Znhit2 |
C |
A |
19: 6,112,288 (GRCm39) |
N344K |
probably damaging |
Het |
|
Other mutations in Fryl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Fryl
|
APN |
5 |
73,305,451 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01518:Fryl
|
APN |
5 |
73,244,305 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01545:Fryl
|
APN |
5 |
73,211,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01646:Fryl
|
APN |
5 |
73,179,844 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01938:Fryl
|
APN |
5 |
73,279,707 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01962:Fryl
|
APN |
5 |
73,190,134 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02064:Fryl
|
APN |
5 |
73,282,112 (GRCm39) |
unclassified |
probably benign |
|
IGL02148:Fryl
|
APN |
5 |
73,233,302 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02418:Fryl
|
APN |
5 |
73,267,519 (GRCm39) |
splice site |
probably benign |
|
IGL02431:Fryl
|
APN |
5 |
73,255,651 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02513:Fryl
|
APN |
5 |
73,222,636 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02557:Fryl
|
APN |
5 |
73,255,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02625:Fryl
|
APN |
5 |
73,227,220 (GRCm39) |
intron |
probably benign |
|
IGL02642:Fryl
|
APN |
5 |
73,252,809 (GRCm39) |
missense |
probably benign |
|
IGL02657:Fryl
|
APN |
5 |
73,212,203 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02706:Fryl
|
APN |
5 |
73,250,506 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03022:Fryl
|
APN |
5 |
73,216,726 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03144:Fryl
|
APN |
5 |
73,258,798 (GRCm39) |
missense |
probably null |
0.22 |
IGL03155:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03183:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03275:Fryl
|
APN |
5 |
73,305,376 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03310:Fryl
|
APN |
5 |
73,293,659 (GRCm39) |
splice site |
probably benign |
|
IGL03341:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03343:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03350:Fryl
|
APN |
5 |
73,290,649 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03357:Fryl
|
APN |
5 |
73,211,402 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03374:Fryl
|
APN |
5 |
73,267,624 (GRCm39) |
splice site |
probably benign |
|
IGL03375:Fryl
|
APN |
5 |
73,245,792 (GRCm39) |
missense |
possibly damaging |
0.91 |
bedeviled
|
UTSW |
5 |
73,216,843 (GRCm39) |
missense |
probably damaging |
1.00 |
Besotted
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Fryl
|
UTSW |
5 |
73,179,621 (GRCm39) |
missense |
probably benign |
0.02 |
R0062:Fryl
|
UTSW |
5 |
73,179,621 (GRCm39) |
missense |
probably benign |
0.02 |
R0308:Fryl
|
UTSW |
5 |
73,198,947 (GRCm39) |
splice site |
probably benign |
|
R0312:Fryl
|
UTSW |
5 |
73,230,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Fryl
|
UTSW |
5 |
73,255,757 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Fryl
|
UTSW |
5 |
73,244,315 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0446:Fryl
|
UTSW |
5 |
73,254,760 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0566:Fryl
|
UTSW |
5 |
73,221,840 (GRCm39) |
splice site |
probably benign |
|
R0567:Fryl
|
UTSW |
5 |
73,222,734 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0606:Fryl
|
UTSW |
5 |
73,282,077 (GRCm39) |
missense |
probably benign |
0.15 |
R0619:Fryl
|
UTSW |
5 |
73,226,074 (GRCm39) |
missense |
probably benign |
0.22 |
R0654:Fryl
|
UTSW |
5 |
73,240,715 (GRCm39) |
missense |
probably benign |
0.17 |
R0658:Fryl
|
UTSW |
5 |
73,222,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Fryl
|
UTSW |
5 |
73,240,715 (GRCm39) |
missense |
probably benign |
0.17 |
R0744:Fryl
|
UTSW |
5 |
73,246,424 (GRCm39) |
unclassified |
probably benign |
|
R0745:Fryl
|
UTSW |
5 |
73,228,469 (GRCm39) |
missense |
probably damaging |
0.96 |
R0833:Fryl
|
UTSW |
5 |
73,246,424 (GRCm39) |
unclassified |
probably benign |
|
R0885:Fryl
|
UTSW |
5 |
73,246,539 (GRCm39) |
missense |
probably damaging |
0.97 |
R0894:Fryl
|
UTSW |
5 |
73,198,675 (GRCm39) |
splice site |
probably benign |
|
R1076:Fryl
|
UTSW |
5 |
73,282,016 (GRCm39) |
unclassified |
probably benign |
|
R1241:Fryl
|
UTSW |
5 |
73,222,268 (GRCm39) |
splice site |
probably benign |
|
R1394:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Fryl
|
UTSW |
5 |
73,232,094 (GRCm39) |
nonsense |
probably null |
|
R1664:Fryl
|
UTSW |
5 |
73,216,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Fryl
|
UTSW |
5 |
73,190,204 (GRCm39) |
splice site |
probably benign |
|
R1937:Fryl
|
UTSW |
5 |
73,290,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Fryl
|
UTSW |
5 |
73,255,609 (GRCm39) |
missense |
probably benign |
0.18 |
R1993:Fryl
|
UTSW |
5 |
73,265,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Fryl
|
UTSW |
5 |
73,265,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Fryl
|
UTSW |
5 |
73,179,465 (GRCm39) |
nonsense |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,265,305 (GRCm39) |
critical splice donor site |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,179,887 (GRCm39) |
missense |
probably benign |
|
R2088:Fryl
|
UTSW |
5 |
73,222,804 (GRCm39) |
missense |
probably benign |
0.02 |
R2105:Fryl
|
UTSW |
5 |
73,279,642 (GRCm39) |
missense |
probably benign |
|
R2106:Fryl
|
UTSW |
5 |
73,255,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Fryl
|
UTSW |
5 |
73,222,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Fryl
|
UTSW |
5 |
73,265,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R2256:Fryl
|
UTSW |
5 |
73,230,187 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2257:Fryl
|
UTSW |
5 |
73,230,187 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2280:Fryl
|
UTSW |
5 |
73,198,707 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2281:Fryl
|
UTSW |
5 |
73,198,707 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2911:Fryl
|
UTSW |
5 |
73,207,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R3019:Fryl
|
UTSW |
5 |
73,240,193 (GRCm39) |
missense |
probably benign |
0.01 |
R3416:Fryl
|
UTSW |
5 |
73,265,417 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3783:Fryl
|
UTSW |
5 |
73,258,819 (GRCm39) |
missense |
probably benign |
|
R3787:Fryl
|
UTSW |
5 |
73,258,819 (GRCm39) |
missense |
probably benign |
|
R3837:Fryl
|
UTSW |
5 |
73,228,608 (GRCm39) |
missense |
probably benign |
0.03 |
R3969:Fryl
|
UTSW |
5 |
73,269,766 (GRCm39) |
missense |
probably damaging |
0.97 |
R4387:Fryl
|
UTSW |
5 |
73,243,903 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4502:Fryl
|
UTSW |
5 |
73,245,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Fryl
|
UTSW |
5 |
73,238,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Fryl
|
UTSW |
5 |
73,248,022 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4690:Fryl
|
UTSW |
5 |
73,257,636 (GRCm39) |
missense |
probably benign |
|
R4700:Fryl
|
UTSW |
5 |
73,222,881 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4709:Fryl
|
UTSW |
5 |
73,238,315 (GRCm39) |
missense |
probably benign |
0.03 |
R4807:Fryl
|
UTSW |
5 |
73,198,705 (GRCm39) |
missense |
probably benign |
0.00 |
R4912:Fryl
|
UTSW |
5 |
73,226,125 (GRCm39) |
frame shift |
probably null |
|
R4948:Fryl
|
UTSW |
5 |
73,246,473 (GRCm39) |
missense |
probably benign |
0.08 |
R4959:Fryl
|
UTSW |
5 |
73,192,401 (GRCm39) |
missense |
probably benign |
0.00 |
R5062:Fryl
|
UTSW |
5 |
73,233,236 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5067:Fryl
|
UTSW |
5 |
73,215,098 (GRCm39) |
missense |
probably benign |
0.13 |
R5071:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5072:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5073:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5074:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5139:Fryl
|
UTSW |
5 |
73,248,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R5172:Fryl
|
UTSW |
5 |
73,259,016 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5187:Fryl
|
UTSW |
5 |
73,243,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5272:Fryl
|
UTSW |
5 |
73,222,479 (GRCm39) |
nonsense |
probably null |
|
R5275:Fryl
|
UTSW |
5 |
73,270,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5295:Fryl
|
UTSW |
5 |
73,270,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Fryl
|
UTSW |
5 |
73,262,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R5355:Fryl
|
UTSW |
5 |
73,231,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Fryl
|
UTSW |
5 |
73,257,808 (GRCm39) |
missense |
probably benign |
|
R5778:Fryl
|
UTSW |
5 |
73,230,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Fryl
|
UTSW |
5 |
73,248,098 (GRCm39) |
missense |
probably benign |
0.06 |
R5934:Fryl
|
UTSW |
5 |
73,248,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Fryl
|
UTSW |
5 |
73,254,715 (GRCm39) |
critical splice donor site |
probably null |
|
R6005:Fryl
|
UTSW |
5 |
73,240,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Fryl
|
UTSW |
5 |
73,257,340 (GRCm39) |
missense |
probably benign |
0.04 |
R6045:Fryl
|
UTSW |
5 |
73,275,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R6185:Fryl
|
UTSW |
5 |
73,270,131 (GRCm39) |
missense |
probably benign |
0.43 |
R6247:Fryl
|
UTSW |
5 |
73,222,824 (GRCm39) |
missense |
probably damaging |
0.98 |
R6294:Fryl
|
UTSW |
5 |
73,349,102 (GRCm39) |
intron |
probably benign |
|
R6310:Fryl
|
UTSW |
5 |
73,349,104 (GRCm39) |
intron |
probably benign |
|
R6429:Fryl
|
UTSW |
5 |
73,248,094 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6568:Fryl
|
UTSW |
5 |
73,216,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6636:Fryl
|
UTSW |
5 |
73,290,655 (GRCm39) |
missense |
probably benign |
0.01 |
R6664:Fryl
|
UTSW |
5 |
73,289,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6732:Fryl
|
UTSW |
5 |
73,212,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Fryl
|
UTSW |
5 |
73,179,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Fryl
|
UTSW |
5 |
73,222,437 (GRCm39) |
missense |
probably benign |
0.03 |
R6823:Fryl
|
UTSW |
5 |
73,222,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R6855:Fryl
|
UTSW |
5 |
73,216,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Fryl
|
UTSW |
5 |
73,222,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Fryl
|
UTSW |
5 |
73,226,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Fryl
|
UTSW |
5 |
73,179,485 (GRCm39) |
missense |
probably damaging |
0.96 |
R6908:Fryl
|
UTSW |
5 |
73,179,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6958:Fryl
|
UTSW |
5 |
73,231,272 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6980:Fryl
|
UTSW |
5 |
73,207,773 (GRCm39) |
missense |
probably benign |
0.06 |
R7036:Fryl
|
UTSW |
5 |
73,212,951 (GRCm39) |
missense |
probably benign |
0.03 |
R7065:Fryl
|
UTSW |
5 |
73,248,099 (GRCm39) |
missense |
probably damaging |
0.96 |
R7097:Fryl
|
UTSW |
5 |
73,231,251 (GRCm39) |
missense |
probably benign |
0.31 |
R7171:Fryl
|
UTSW |
5 |
73,279,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R7191:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Fryl
|
UTSW |
5 |
73,222,438 (GRCm39) |
missense |
probably benign |
|
R7236:Fryl
|
UTSW |
5 |
73,265,821 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7334:Fryl
|
UTSW |
5 |
73,204,839 (GRCm39) |
splice site |
probably null |
|
R7425:Fryl
|
UTSW |
5 |
73,262,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Fryl
|
UTSW |
5 |
73,181,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Fryl
|
UTSW |
5 |
73,254,904 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7535:Fryl
|
UTSW |
5 |
73,255,539 (GRCm39) |
missense |
probably benign |
0.15 |
R7538:Fryl
|
UTSW |
5 |
73,180,019 (GRCm39) |
missense |
probably benign |
0.09 |
R7544:Fryl
|
UTSW |
5 |
73,238,382 (GRCm39) |
missense |
probably benign |
|
R7548:Fryl
|
UTSW |
5 |
73,349,105 (GRCm39) |
missense |
unknown |
|
R7565:Fryl
|
UTSW |
5 |
73,191,063 (GRCm39) |
missense |
probably benign |
0.18 |
R7572:Fryl
|
UTSW |
5 |
73,245,739 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7582:Fryl
|
UTSW |
5 |
73,179,843 (GRCm39) |
critical splice donor site |
probably null |
|
R7630:Fryl
|
UTSW |
5 |
73,267,588 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7774:Fryl
|
UTSW |
5 |
73,240,727 (GRCm39) |
missense |
probably benign |
0.12 |
R7777:Fryl
|
UTSW |
5 |
73,228,641 (GRCm39) |
missense |
probably damaging |
0.98 |
R7917:Fryl
|
UTSW |
5 |
73,211,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Fryl
|
UTSW |
5 |
73,259,150 (GRCm39) |
splice site |
probably null |
|
R8110:Fryl
|
UTSW |
5 |
73,290,620 (GRCm39) |
missense |
probably benign |
0.10 |
R8120:Fryl
|
UTSW |
5 |
73,228,527 (GRCm39) |
missense |
probably benign |
0.01 |
R8143:Fryl
|
UTSW |
5 |
73,207,682 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Fryl
|
UTSW |
5 |
73,257,843 (GRCm39) |
splice site |
probably null |
|
R8263:Fryl
|
UTSW |
5 |
73,238,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Fryl
|
UTSW |
5 |
73,226,073 (GRCm39) |
missense |
probably benign |
|
R8359:Fryl
|
UTSW |
5 |
73,233,276 (GRCm39) |
missense |
probably benign |
0.39 |
R8387:Fryl
|
UTSW |
5 |
73,293,663 (GRCm39) |
critical splice donor site |
probably null |
|
R8403:Fryl
|
UTSW |
5 |
73,275,790 (GRCm39) |
makesense |
probably null |
|
R8450:Fryl
|
UTSW |
5 |
73,226,073 (GRCm39) |
missense |
probably benign |
|
R8514:Fryl
|
UTSW |
5 |
73,242,699 (GRCm39) |
missense |
probably benign |
|
R8536:Fryl
|
UTSW |
5 |
73,257,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R8703:Fryl
|
UTSW |
5 |
73,247,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R8708:Fryl
|
UTSW |
5 |
73,289,905 (GRCm39) |
missense |
probably benign |
0.01 |
R8783:Fryl
|
UTSW |
5 |
73,226,185 (GRCm39) |
missense |
probably benign |
0.45 |
R9028:Fryl
|
UTSW |
5 |
73,255,609 (GRCm39) |
missense |
probably benign |
0.18 |
R9045:Fryl
|
UTSW |
5 |
73,182,118 (GRCm39) |
missense |
|
|
R9063:Fryl
|
UTSW |
5 |
73,238,346 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9096:Fryl
|
UTSW |
5 |
73,265,920 (GRCm39) |
missense |
probably benign |
0.01 |
R9244:Fryl
|
UTSW |
5 |
73,348,862 (GRCm39) |
intron |
probably benign |
|
R9345:Fryl
|
UTSW |
5 |
73,207,754 (GRCm39) |
missense |
probably benign |
|
R9381:Fryl
|
UTSW |
5 |
73,240,637 (GRCm39) |
missense |
probably benign |
0.24 |
R9386:Fryl
|
UTSW |
5 |
73,349,152 (GRCm39) |
missense |
unknown |
|
R9401:Fryl
|
UTSW |
5 |
73,222,563 (GRCm39) |
nonsense |
probably null |
|
R9497:Fryl
|
UTSW |
5 |
73,215,134 (GRCm39) |
missense |
|
|
R9514:Fryl
|
UTSW |
5 |
73,262,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Fryl
|
UTSW |
5 |
73,179,498 (GRCm39) |
missense |
probably benign |
0.02 |
R9654:Fryl
|
UTSW |
5 |
73,275,801 (GRCm39) |
missense |
probably benign |
|
R9665:Fryl
|
UTSW |
5 |
73,222,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9685:Fryl
|
UTSW |
5 |
73,216,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R9798:Fryl
|
UTSW |
5 |
73,192,402 (GRCm39) |
missense |
probably benign |
|
Z1088:Fryl
|
UTSW |
5 |
73,248,081 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Fryl
|
UTSW |
5 |
73,248,052 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Fryl
|
UTSW |
5 |
73,230,180 (GRCm39) |
missense |
probably benign |
|
Z1177:Fryl
|
UTSW |
5 |
73,198,938 (GRCm39) |
critical splice acceptor site |
probably null |
|
|