Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630095N17Rik |
T |
A |
1: 75,208,683 (GRCm39) |
R12S |
unknown |
Het |
Ankrd10 |
C |
T |
8: 11,665,707 (GRCm39) |
V298I |
probably benign |
Het |
Atg4d |
T |
A |
9: 21,178,335 (GRCm39) |
M151K |
probably damaging |
Het |
Calhm5 |
C |
A |
10: 33,972,192 (GRCm39) |
C81F |
probably damaging |
Het |
Casp8ap2 |
T |
A |
4: 32,644,072 (GRCm39) |
H1048Q |
probably damaging |
Het |
Cd300ld2 |
A |
G |
11: 114,903,192 (GRCm39) |
S218P |
unknown |
Het |
Clec3a |
T |
C |
8: 115,152,369 (GRCm39) |
V125A |
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,573,002 (GRCm39) |
Y241N |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,015,134 (GRCm39) |
F1686Y |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,613,421 (GRCm39) |
K1285E |
noncoding transcript |
Het |
Dop1b |
T |
C |
16: 93,559,083 (GRCm39) |
S610P |
possibly damaging |
Het |
Ehhadh |
A |
T |
16: 21,592,295 (GRCm39) |
L136H |
probably damaging |
Het |
Epha7 |
A |
G |
4: 28,821,149 (GRCm39) |
T105A |
probably damaging |
Het |
Etl4 |
A |
T |
2: 20,748,965 (GRCm39) |
E434D |
probably benign |
Het |
Fastkd2 |
T |
C |
1: 63,770,968 (GRCm39) |
V108A |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,174,962 (GRCm39) |
T1917I |
probably benign |
Het |
Fbxo45 |
A |
G |
16: 32,065,533 (GRCm39) |
S33P |
unknown |
Het |
Fig4 |
A |
T |
10: 41,143,711 (GRCm39) |
Y249* |
probably null |
Het |
G530012D18Rik |
C |
G |
1: 85,504,935 (GRCm39) |
D113E |
unknown |
Het |
Glod4 |
T |
C |
11: 76,125,318 (GRCm39) |
D147G |
possibly damaging |
Het |
Gm12695 |
T |
G |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
Gm5422 |
A |
G |
10: 31,125,099 (GRCm39) |
T313A |
noncoding transcript |
Het |
Hydin |
C |
A |
8: 111,178,705 (GRCm39) |
A1100D |
probably benign |
Het |
Ift172 |
G |
A |
5: 31,422,681 (GRCm39) |
A923V |
possibly damaging |
Het |
Irgc |
G |
A |
7: 24,132,107 (GRCm39) |
H237Y |
probably damaging |
Het |
Itga11 |
T |
C |
9: 62,604,262 (GRCm39) |
I50T |
possibly damaging |
Het |
Itpr3 |
C |
T |
17: 27,334,887 (GRCm39) |
Q2134* |
probably null |
Het |
Kat8 |
A |
T |
7: 127,523,653 (GRCm39) |
D292V |
possibly damaging |
Het |
Kdm2a |
A |
G |
19: 4,374,392 (GRCm39) |
M913T |
possibly damaging |
Het |
Larp4 |
T |
C |
15: 99,883,961 (GRCm39) |
V66A |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,462,858 (GRCm39) |
D899G |
probably damaging |
Het |
Lrrc47 |
G |
T |
4: 154,100,486 (GRCm39) |
R354L |
probably damaging |
Het |
Lss |
C |
T |
10: 76,367,739 (GRCm39) |
R24C |
probably damaging |
Het |
Mmp14 |
C |
T |
14: 54,673,244 (GRCm39) |
R51C |
probably damaging |
Het |
Mon1a |
C |
T |
9: 107,775,993 (GRCm39) |
T37I |
probably benign |
Het |
Mtcl2 |
A |
G |
2: 156,869,510 (GRCm39) |
W1042R |
possibly damaging |
Het |
Nacc2 |
A |
C |
2: 25,952,240 (GRCm39) |
V372G |
probably damaging |
Het |
Ncapg |
T |
C |
5: 45,849,134 (GRCm39) |
V690A |
probably benign |
Het |
Nhej1 |
A |
G |
1: 75,006,896 (GRCm39) |
L152P |
probably damaging |
Het |
Nol4l |
A |
T |
2: 153,259,337 (GRCm39) |
S522R |
probably damaging |
Het |
Nr0b2 |
A |
G |
4: 133,281,241 (GRCm39) |
Y169C |
probably damaging |
Het |
Numa1 |
A |
G |
7: 101,648,491 (GRCm39) |
M741V |
probably benign |
Het |
Or10d1b |
A |
G |
9: 39,613,453 (GRCm39) |
M204T |
possibly damaging |
Het |
Or8g28 |
A |
G |
9: 39,169,899 (GRCm39) |
L26P |
probably damaging |
Het |
Pebp1 |
C |
A |
5: 117,425,473 (GRCm39) |
|
probably null |
Het |
Pik3ip1 |
A |
T |
11: 3,291,581 (GRCm39) |
I217F |
probably damaging |
Het |
Plekhg1 |
T |
A |
10: 3,907,651 (GRCm39) |
I911N |
|
Het |
Pnpla8 |
T |
C |
12: 44,342,846 (GRCm39) |
I534T |
probably damaging |
Het |
Ppp2r2a |
A |
T |
14: 67,261,205 (GRCm39) |
F172I |
probably damaging |
Het |
Rab7 |
C |
T |
6: 87,989,292 (GRCm39) |
M59I |
probably benign |
Het |
Rbm34 |
T |
C |
8: 127,692,139 (GRCm39) |
N201S |
probably benign |
Het |
Rfx1 |
G |
T |
8: 84,821,483 (GRCm39) |
R764L |
probably damaging |
Het |
Rnase12 |
T |
A |
14: 51,294,580 (GRCm39) |
D33V |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,684,532 (GRCm39) |
L127P |
probably damaging |
Het |
Rtl1 |
C |
A |
12: 109,560,180 (GRCm39) |
R553L |
probably damaging |
Het |
Scn8a |
T |
C |
15: 100,881,736 (GRCm39) |
L601P |
probably damaging |
Het |
Scyl2 |
G |
T |
10: 89,476,525 (GRCm39) |
Q867K |
possibly damaging |
Het |
Sgtb |
T |
C |
13: 104,268,692 (GRCm39) |
F213L |
probably benign |
Het |
Slc35f4 |
A |
G |
14: 49,551,084 (GRCm39) |
V260A |
probably damaging |
Het |
Slfn14 |
A |
G |
11: 83,174,299 (GRCm39) |
Y231H |
possibly damaging |
Het |
Sppl2b |
TGTCACAGGT |
TGT |
10: 80,701,903 (GRCm39) |
|
probably null |
Het |
Stard13 |
G |
A |
5: 151,157,106 (GRCm39) |
A25V |
possibly damaging |
Het |
Stk38 |
C |
T |
17: 29,203,161 (GRCm39) |
R135H |
probably damaging |
Het |
Svil |
A |
G |
18: 5,108,679 (GRCm39) |
D1939G |
probably damaging |
Het |
Tasor2 |
C |
T |
13: 3,625,286 (GRCm39) |
V1555I |
possibly damaging |
Het |
Tasor2 |
G |
T |
13: 3,640,016 (GRCm39) |
P374T |
probably benign |
Het |
Tbc1d7 |
A |
G |
13: 43,323,340 (GRCm39) |
V17A |
possibly damaging |
Het |
Trpc4 |
T |
C |
3: 54,129,756 (GRCm39) |
V174A |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,619,028 (GRCm39) |
T16117K |
probably damaging |
Het |
Tubb3 |
T |
A |
8: 124,147,868 (GRCm39) |
M267K |
possibly damaging |
Het |
Upk1b |
T |
C |
16: 38,604,585 (GRCm39) |
T147A |
probably damaging |
Het |
Vmn2r107 |
G |
T |
17: 20,580,614 (GRCm39) |
C517F |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,824,140 (GRCm39) |
D465G |
probably damaging |
Het |
Vmn2r73 |
A |
T |
7: 85,507,619 (GRCm39) |
H564Q |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,686,726 (GRCm39) |
I702M |
possibly damaging |
Het |
Vmn2r84 |
A |
G |
10: 130,227,037 (GRCm39) |
V267A |
probably damaging |
Het |
Zfp445 |
T |
C |
9: 122,681,878 (GRCm39) |
I688V |
probably benign |
Het |
Zfp955a |
C |
T |
17: 33,463,087 (GRCm39) |
V15M |
probably damaging |
Het |
Zfp960 |
T |
A |
17: 17,308,202 (GRCm39) |
C305* |
probably null |
Het |
Zfp964 |
A |
G |
8: 70,116,345 (GRCm39) |
D315G |
possibly damaging |
Het |
Zmynd10 |
T |
A |
9: 107,426,516 (GRCm39) |
I183K |
possibly 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 |
73,267,614 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|
|