Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930486L24Rik |
A |
T |
13: 60,853,600 (GRCm38) |
H104Q |
probably benign |
Het |
4933405L10Rik |
A |
G |
8: 105,709,569 (GRCm38) |
T158A |
possibly damaging |
Het |
A1cf |
T |
C |
19: 31,917,985 (GRCm38) |
M156T |
probably benign |
Het |
Abca15 |
A |
G |
7: 120,406,975 (GRCm38) |
Y1620C |
probably damaging |
Het |
Abca3 |
C |
T |
17: 24,374,300 (GRCm38) |
R224C |
probably damaging |
Het |
Ablim1 |
A |
G |
19: 57,073,853 (GRCm38) |
|
probably null |
Het |
Acox2 |
A |
T |
14: 8,241,374 (GRCm38) |
Y579* |
probably null |
Het |
Adnp |
A |
T |
2: 168,183,001 (GRCm38) |
S791R |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,421,917 (GRCm38) |
E329G |
probably damaging |
Het |
Alx3 |
G |
T |
3: 107,604,793 (GRCm38) |
S249I |
possibly damaging |
Het |
Apob |
A |
G |
12: 8,008,714 (GRCm38) |
T2366A |
probably benign |
Het |
Apool |
C |
T |
X: 112,349,843 (GRCm38) |
Q60* |
probably null |
Het |
Arid4a |
T |
C |
12: 71,045,079 (GRCm38) |
V213A |
probably benign |
Het |
Atp7a |
A |
G |
X: 106,109,768 (GRCm38) |
D1092G |
probably benign |
Het |
Bpifa5 |
A |
T |
2: 154,165,972 (GRCm38) |
E178V |
probably damaging |
Het |
Car4 |
G |
A |
11: 84,963,367 (GRCm38) |
E47K |
probably benign |
Het |
Catsper1 |
T |
C |
19: 5,340,046 (GRCm38) |
|
probably null |
Het |
Ccdc63 |
T |
A |
5: 122,121,055 (GRCm38) |
Q260L |
probably benign |
Het |
Ccdc83 |
A |
T |
7: 90,250,529 (GRCm38) |
F45Y |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,516,883 (GRCm38) |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,651,689 (GRCm38) |
V7L |
unknown |
Het |
Ces5a |
C |
T |
8: 93,534,668 (GRCm38) |
V44M |
probably damaging |
Het |
Cltc |
A |
G |
11: 86,717,968 (GRCm38) |
I741T |
possibly damaging |
Het |
Cnst |
C |
A |
1: 179,622,886 (GRCm38) |
D638E |
possibly damaging |
Het |
Col13a1 |
A |
G |
10: 61,874,018 (GRCm38) |
|
silent |
Het |
Cyp2a22 |
A |
T |
7: 26,932,481 (GRCm38) |
F450Y |
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,403,753 (GRCm38) |
R383H |
probably benign |
Het |
Cyp4a29 |
A |
G |
4: 115,247,663 (GRCm38) |
T123A |
probably benign |
Het |
Ddx20 |
A |
G |
3: 105,682,875 (GRCm38) |
|
probably null |
Het |
Dnaja3 |
A |
T |
16: 4,696,425 (GRCm38) |
T274S |
probably damaging |
Het |
Dot1l |
A |
G |
10: 80,784,646 (GRCm38) |
D514G |
possibly damaging |
Het |
Dysf |
A |
T |
6: 84,137,272 (GRCm38) |
K1226M |
probably damaging |
Het |
Epha4 |
T |
C |
1: 77,445,002 (GRCm38) |
Y281C |
probably damaging |
Het |
Fbxo42 |
T |
C |
4: 141,198,945 (GRCm38) |
W313R |
probably damaging |
Het |
Fign |
A |
T |
2: 63,979,693 (GRCm38) |
L411* |
probably null |
Het |
Flt1 |
C |
A |
5: 147,683,939 (GRCm38) |
A132S |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,430,958 (GRCm38) |
|
probably benign |
Het |
Gprasp2 |
C |
T |
X: 135,842,597 (GRCm38) |
T235I |
possibly damaging |
Het |
Gtf2ird1 |
G |
T |
5: 134,390,933 (GRCm38) |
|
probably null |
Het |
H2afb3 |
T |
C |
X: 120,312,846 (GRCm38) |
T84A |
probably damaging |
Het |
Hal |
A |
T |
10: 93,514,042 (GRCm38) |
I555F |
probably damaging |
Het |
Hdac6 |
A |
G |
X: 7,944,797 (GRCm38) |
F104L |
probably damaging |
Homo |
Hist2h2ac |
C |
T |
3: 96,220,783 (GRCm38) |
|
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,540,230 (GRCm38) |
S2050P |
probably damaging |
Het |
Irgc1 |
T |
C |
7: 24,432,771 (GRCm38) |
D207G |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,767,227 (GRCm38) |
M37I |
probably benign |
Het |
Kiss1r |
C |
A |
10: 79,918,762 (GRCm38) |
S30* |
probably null |
Het |
Krtap1-4 |
C |
G |
11: 99,583,616 (GRCm38) |
|
probably benign |
Het |
Lrrfip2 |
A |
G |
9: 111,199,804 (GRCm38) |
E365G |
probably damaging |
Het |
Ly75 |
A |
G |
2: 60,375,963 (GRCm38) |
Y121H |
probably damaging |
Het |
Man2a1 |
G |
A |
17: 64,659,079 (GRCm38) |
|
probably null |
Het |
Mkl1 |
A |
G |
15: 81,022,426 (GRCm38) |
V91A |
probably damaging |
Het |
Mllt10 |
C |
A |
2: 18,109,874 (GRCm38) |
H52N |
possibly damaging |
Het |
Myo1a |
T |
C |
10: 127,707,419 (GRCm38) |
|
probably null |
Het |
Myo3b |
C |
A |
2: 70,095,249 (GRCm38) |
T20K |
possibly damaging |
Het |
Nipsnap2 |
A |
T |
5: 129,739,580 (GRCm38) |
K62N |
probably damaging |
Het |
Nr1i3 |
C |
T |
1: 171,216,813 (GRCm38) |
T169I |
probably benign |
Het |
Numbl |
G |
A |
7: 27,280,990 (GRCm38) |
D466N |
probably damaging |
Het |
Olfr1100 |
A |
T |
2: 86,978,322 (GRCm38) |
V158D |
possibly damaging |
Het |
Olfr310 |
A |
G |
7: 86,269,591 (GRCm38) |
I66T |
probably damaging |
Het |
Olfr420 |
A |
T |
1: 174,158,961 (GRCm38) |
I63F |
probably damaging |
Het |
Olfr639 |
T |
A |
7: 104,012,118 (GRCm38) |
R195W |
probably damaging |
Het |
Oprm1 |
A |
G |
10: 6,832,550 (GRCm38) |
S398G |
probably benign |
Het |
Pebp1 |
G |
T |
5: 117,283,410 (GRCm38) |
D156E |
probably benign |
Het |
Pik3c2g |
T |
A |
6: 139,720,147 (GRCm38) |
C65S |
probably null |
Het |
Pilra |
A |
G |
5: 137,835,412 (GRCm38) |
F131L |
probably damaging |
Het |
Pitrm1 |
T |
C |
13: 6,553,190 (GRCm38) |
F91S |
probably damaging |
Het |
Ppl |
A |
T |
16: 5,088,878 (GRCm38) |
S1184R |
probably benign |
Het |
Prmt2 |
C |
T |
10: 76,222,556 (GRCm38) |
V140I |
probably damaging |
Het |
Psg29 |
T |
A |
7: 17,211,838 (GRCm38) |
D444E |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,251,260 (GRCm38) |
N573I |
probably damaging |
Het |
Pygb |
C |
T |
2: 150,801,578 (GRCm38) |
T95M |
probably damaging |
Het |
Rassf9 |
A |
G |
10: 102,545,905 (GRCm38) |
K383E |
probably damaging |
Het |
Rfk |
T |
A |
19: 17,398,599 (GRCm38) |
F86I |
possibly damaging |
Het |
Rims2 |
T |
C |
15: 39,462,590 (GRCm38) |
F773L |
probably benign |
Het |
Sdcbp |
A |
G |
4: 6,393,019 (GRCm38) |
I218V |
probably benign |
Het |
Slc4a2 |
G |
A |
5: 24,438,762 (GRCm38) |
S855N |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 16,150,583 (GRCm38) |
L626P |
possibly damaging |
Het |
Snrpd3 |
G |
T |
10: 75,519,393 (GRCm38) |
C20F |
possibly damaging |
Het |
Spen |
A |
T |
4: 141,522,302 (GRCm38) |
S58R |
unknown |
Het |
St3gal2 |
T |
C |
8: 110,957,718 (GRCm38) |
C3R |
possibly damaging |
Het |
Stab2 |
A |
T |
10: 86,863,558 (GRCm38) |
I481N |
probably benign |
Het |
Stat5b |
T |
C |
11: 100,808,535 (GRCm38) |
|
probably null |
Het |
Tmco3 |
G |
T |
8: 13,292,860 (GRCm38) |
E199* |
probably null |
Het |
Tmem26 |
A |
G |
10: 68,775,348 (GRCm38) |
T216A |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,720,478 (GRCm38) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,772,365 (GRCm38) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,746,402 (GRCm38) |
V24716I |
probably damaging |
Het |
Uba5 |
T |
C |
9: 104,054,427 (GRCm38) |
E202G |
probably damaging |
Het |
Ufl1 |
A |
G |
4: 25,254,780 (GRCm38) |
Y559H |
probably benign |
Het |
Utrn |
A |
T |
10: 12,384,204 (GRCm38) |
|
probably null |
Het |
Vmn2r111 |
C |
A |
17: 22,548,041 (GRCm38) |
C825F |
probably damaging |
Het |
Vmn2r113 |
T |
A |
17: 22,958,355 (GRCm38) |
C704* |
probably null |
Het |
Vmn2r56 |
A |
G |
7: 12,694,056 (GRCm38) |
I761T |
probably benign |
Het |
Vmn2r98 |
C |
T |
17: 19,066,044 (GRCm38) |
T268I |
probably benign |
Het |
Zfp263 |
A |
G |
16: 3,746,840 (GRCm38) |
R240G |
possibly damaging |
Het |
Zfp473 |
T |
A |
7: 44,732,519 (GRCm38) |
I797F |
probably damaging |
Het |
Zfp68 |
A |
T |
5: 138,606,317 (GRCm38) |
D543E |
probably benign |
Het |
|
Other mutations in Fryl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Fryl
|
APN |
5 |
73,148,108 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL01518:Fryl
|
APN |
5 |
73,086,962 (GRCm38) |
missense |
possibly damaging |
0.76 |
IGL01545:Fryl
|
APN |
5 |
73,054,597 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01646:Fryl
|
APN |
5 |
73,022,501 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01938:Fryl
|
APN |
5 |
73,122,364 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01962:Fryl
|
APN |
5 |
73,032,791 (GRCm38) |
missense |
possibly damaging |
0.62 |
IGL02064:Fryl
|
APN |
5 |
73,124,769 (GRCm38) |
unclassified |
probably benign |
|
IGL02148:Fryl
|
APN |
5 |
73,075,959 (GRCm38) |
missense |
probably benign |
0.35 |
IGL02418:Fryl
|
APN |
5 |
73,110,176 (GRCm38) |
splice site |
probably benign |
|
IGL02431:Fryl
|
APN |
5 |
73,098,308 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02513:Fryl
|
APN |
5 |
73,065,293 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02557:Fryl
|
APN |
5 |
73,098,393 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02625:Fryl
|
APN |
5 |
73,069,877 (GRCm38) |
intron |
probably benign |
|
IGL02642:Fryl
|
APN |
5 |
73,095,466 (GRCm38) |
missense |
probably benign |
|
IGL02657:Fryl
|
APN |
5 |
73,054,860 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02706:Fryl
|
APN |
5 |
73,093,163 (GRCm38) |
missense |
probably benign |
0.45 |
IGL03022:Fryl
|
APN |
5 |
73,059,383 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL03144:Fryl
|
APN |
5 |
73,101,455 (GRCm38) |
missense |
probably null |
0.22 |
IGL03155:Fryl
|
APN |
5 |
73,076,695 (GRCm38) |
missense |
probably benign |
|
IGL03183:Fryl
|
APN |
5 |
73,076,695 (GRCm38) |
missense |
probably benign |
|
IGL03275:Fryl
|
APN |
5 |
73,148,033 (GRCm38) |
missense |
possibly damaging |
0.47 |
IGL03310:Fryl
|
APN |
5 |
73,136,316 (GRCm38) |
splice site |
probably benign |
|
IGL03341:Fryl
|
APN |
5 |
73,076,695 (GRCm38) |
missense |
probably benign |
|
IGL03343:Fryl
|
APN |
5 |
73,076,695 (GRCm38) |
missense |
probably benign |
|
IGL03350:Fryl
|
APN |
5 |
73,133,306 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03357:Fryl
|
APN |
5 |
73,054,059 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03374:Fryl
|
APN |
5 |
73,110,281 (GRCm38) |
splice site |
probably benign |
|
IGL03375:Fryl
|
APN |
5 |
73,088,449 (GRCm38) |
missense |
possibly damaging |
0.91 |
bedeviled
|
UTSW |
5 |
73,059,500 (GRCm38) |
missense |
probably damaging |
1.00 |
Besotted
|
UTSW |
5 |
73,072,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R0062:Fryl
|
UTSW |
5 |
73,022,278 (GRCm38) |
missense |
probably benign |
0.02 |
R0062:Fryl
|
UTSW |
5 |
73,022,278 (GRCm38) |
missense |
probably benign |
0.02 |
R0308:Fryl
|
UTSW |
5 |
73,041,604 (GRCm38) |
splice site |
probably benign |
|
R0312:Fryl
|
UTSW |
5 |
73,072,888 (GRCm38) |
missense |
probably damaging |
1.00 |
R0415:Fryl
|
UTSW |
5 |
73,098,414 (GRCm38) |
missense |
probably damaging |
0.99 |
R0440:Fryl
|
UTSW |
5 |
73,086,972 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0446:Fryl
|
UTSW |
5 |
73,097,417 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0566:Fryl
|
UTSW |
5 |
73,064,497 (GRCm38) |
splice site |
probably benign |
|
R0567:Fryl
|
UTSW |
5 |
73,065,391 (GRCm38) |
missense |
possibly damaging |
0.50 |
R0606:Fryl
|
UTSW |
5 |
73,124,734 (GRCm38) |
missense |
probably benign |
0.15 |
R0619:Fryl
|
UTSW |
5 |
73,068,731 (GRCm38) |
missense |
probably benign |
0.22 |
R0654:Fryl
|
UTSW |
5 |
73,083,372 (GRCm38) |
missense |
probably benign |
0.17 |
R0658:Fryl
|
UTSW |
5 |
73,065,359 (GRCm38) |
missense |
probably damaging |
1.00 |
R0707:Fryl
|
UTSW |
5 |
73,083,372 (GRCm38) |
missense |
probably benign |
0.17 |
R0744:Fryl
|
UTSW |
5 |
73,089,081 (GRCm38) |
unclassified |
probably benign |
|
R0745:Fryl
|
UTSW |
5 |
73,071,126 (GRCm38) |
missense |
probably damaging |
0.96 |
R0833:Fryl
|
UTSW |
5 |
73,089,081 (GRCm38) |
unclassified |
probably benign |
|
R0885:Fryl
|
UTSW |
5 |
73,089,196 (GRCm38) |
missense |
probably damaging |
0.97 |
R0894:Fryl
|
UTSW |
5 |
73,041,332 (GRCm38) |
splice site |
probably benign |
|
R1076:Fryl
|
UTSW |
5 |
73,124,673 (GRCm38) |
unclassified |
probably benign |
|
R1241:Fryl
|
UTSW |
5 |
73,110,271 (GRCm38) |
missense |
probably damaging |
1.00 |
R1241:Fryl
|
UTSW |
5 |
73,064,925 (GRCm38) |
splice site |
probably benign |
|
R1394:Fryl
|
UTSW |
5 |
73,072,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R1395:Fryl
|
UTSW |
5 |
73,072,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R1608:Fryl
|
UTSW |
5 |
73,074,751 (GRCm38) |
nonsense |
probably null |
|
R1664:Fryl
|
UTSW |
5 |
73,059,435 (GRCm38) |
missense |
probably damaging |
1.00 |
R1745:Fryl
|
UTSW |
5 |
73,032,861 (GRCm38) |
splice site |
probably benign |
|
R1937:Fryl
|
UTSW |
5 |
73,133,367 (GRCm38) |
missense |
probably damaging |
1.00 |
R1969:Fryl
|
UTSW |
5 |
73,098,266 (GRCm38) |
missense |
probably benign |
0.18 |
R1993:Fryl
|
UTSW |
5 |
73,108,493 (GRCm38) |
missense |
probably damaging |
1.00 |
R1994:Fryl
|
UTSW |
5 |
73,108,493 (GRCm38) |
missense |
probably damaging |
1.00 |
R2029:Fryl
|
UTSW |
5 |
73,022,122 (GRCm38) |
nonsense |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,107,962 (GRCm38) |
critical splice donor site |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,022,544 (GRCm38) |
missense |
probably benign |
|
R2088:Fryl
|
UTSW |
5 |
73,065,461 (GRCm38) |
missense |
probably benign |
0.02 |
R2105:Fryl
|
UTSW |
5 |
73,122,299 (GRCm38) |
missense |
probably benign |
|
R2106:Fryl
|
UTSW |
5 |
73,098,331 (GRCm38) |
missense |
probably damaging |
1.00 |
R2186:Fryl
|
UTSW |
5 |
73,064,975 (GRCm38) |
missense |
probably damaging |
1.00 |
R2239:Fryl
|
UTSW |
5 |
73,108,547 (GRCm38) |
missense |
probably damaging |
0.99 |
R2256:Fryl
|
UTSW |
5 |
73,072,844 (GRCm38) |
missense |
possibly damaging |
0.47 |
R2257:Fryl
|
UTSW |
5 |
73,072,844 (GRCm38) |
missense |
possibly damaging |
0.47 |
R2280:Fryl
|
UTSW |
5 |
73,041,364 (GRCm38) |
missense |
possibly damaging |
0.47 |
R2281:Fryl
|
UTSW |
5 |
73,041,364 (GRCm38) |
missense |
possibly damaging |
0.47 |
R2911:Fryl
|
UTSW |
5 |
73,050,456 (GRCm38) |
missense |
probably damaging |
0.99 |
R3019:Fryl
|
UTSW |
5 |
73,082,850 (GRCm38) |
missense |
probably benign |
0.01 |
R3416:Fryl
|
UTSW |
5 |
73,108,074 (GRCm38) |
missense |
possibly damaging |
0.84 |
R3783:Fryl
|
UTSW |
5 |
73,101,476 (GRCm38) |
missense |
probably benign |
|
R3787:Fryl
|
UTSW |
5 |
73,101,476 (GRCm38) |
missense |
probably benign |
|
R3837:Fryl
|
UTSW |
5 |
73,071,265 (GRCm38) |
missense |
probably benign |
0.03 |
R3969:Fryl
|
UTSW |
5 |
73,112,423 (GRCm38) |
missense |
probably damaging |
0.97 |
R4387:Fryl
|
UTSW |
5 |
73,086,560 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4502:Fryl
|
UTSW |
5 |
73,088,397 (GRCm38) |
missense |
probably damaging |
1.00 |
R4658:Fryl
|
UTSW |
5 |
73,081,053 (GRCm38) |
missense |
probably damaging |
1.00 |
R4664:Fryl
|
UTSW |
5 |
73,090,679 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4690:Fryl
|
UTSW |
5 |
73,100,293 (GRCm38) |
missense |
probably benign |
|
R4700:Fryl
|
UTSW |
5 |
73,065,538 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4709:Fryl
|
UTSW |
5 |
73,080,972 (GRCm38) |
missense |
probably benign |
0.03 |
R4807:Fryl
|
UTSW |
5 |
73,041,362 (GRCm38) |
missense |
probably benign |
0.00 |
R4912:Fryl
|
UTSW |
5 |
73,068,782 (GRCm38) |
frame shift |
probably null |
|
R4948:Fryl
|
UTSW |
5 |
73,089,130 (GRCm38) |
missense |
probably benign |
0.08 |
R4959:Fryl
|
UTSW |
5 |
73,035,058 (GRCm38) |
missense |
probably benign |
0.00 |
R5062:Fryl
|
UTSW |
5 |
73,075,893 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5067:Fryl
|
UTSW |
5 |
73,057,755 (GRCm38) |
missense |
probably benign |
0.13 |
R5071:Fryl
|
UTSW |
5 |
73,074,767 (GRCm38) |
missense |
probably damaging |
0.99 |
R5073:Fryl
|
UTSW |
5 |
73,074,767 (GRCm38) |
missense |
probably damaging |
0.99 |
R5074:Fryl
|
UTSW |
5 |
73,074,767 (GRCm38) |
missense |
probably damaging |
0.99 |
R5139:Fryl
|
UTSW |
5 |
73,090,718 (GRCm38) |
missense |
probably damaging |
1.00 |
R5172:Fryl
|
UTSW |
5 |
73,101,673 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5187:Fryl
|
UTSW |
5 |
73,086,600 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5272:Fryl
|
UTSW |
5 |
73,065,136 (GRCm38) |
nonsense |
probably null |
|
R5275:Fryl
|
UTSW |
5 |
73,112,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R5295:Fryl
|
UTSW |
5 |
73,112,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R5344:Fryl
|
UTSW |
5 |
73,104,774 (GRCm38) |
missense |
probably damaging |
1.00 |
R5355:Fryl
|
UTSW |
5 |
73,073,904 (GRCm38) |
missense |
probably damaging |
1.00 |
R5716:Fryl
|
UTSW |
5 |
73,100,465 (GRCm38) |
missense |
probably benign |
|
R5778:Fryl
|
UTSW |
5 |
73,072,778 (GRCm38) |
missense |
probably damaging |
1.00 |
R5810:Fryl
|
UTSW |
5 |
73,090,755 (GRCm38) |
missense |
probably benign |
0.06 |
R5934:Fryl
|
UTSW |
5 |
73,090,717 (GRCm38) |
missense |
probably damaging |
1.00 |
R5948:Fryl
|
UTSW |
5 |
73,097,372 (GRCm38) |
critical splice donor site |
probably null |
|
R6005:Fryl
|
UTSW |
5 |
73,083,295 (GRCm38) |
missense |
probably damaging |
1.00 |
R6026:Fryl
|
UTSW |
5 |
73,099,997 (GRCm38) |
missense |
probably benign |
0.04 |
R6045:Fryl
|
UTSW |
5 |
73,118,551 (GRCm38) |
missense |
probably damaging |
0.99 |
R6185:Fryl
|
UTSW |
5 |
73,112,788 (GRCm38) |
missense |
probably benign |
0.43 |
R6247:Fryl
|
UTSW |
5 |
73,065,481 (GRCm38) |
missense |
probably damaging |
0.98 |
R6294:Fryl
|
UTSW |
5 |
73,191,759 (GRCm38) |
intron |
probably benign |
|
R6310:Fryl
|
UTSW |
5 |
73,191,761 (GRCm38) |
intron |
probably benign |
|
R6429:Fryl
|
UTSW |
5 |
73,090,751 (GRCm38) |
missense |
possibly damaging |
0.84 |
R6568:Fryl
|
UTSW |
5 |
73,059,516 (GRCm38) |
missense |
probably damaging |
1.00 |
R6636:Fryl
|
UTSW |
5 |
73,133,312 (GRCm38) |
missense |
probably benign |
0.01 |
R6664:Fryl
|
UTSW |
5 |
73,132,481 (GRCm38) |
missense |
probably damaging |
1.00 |
R6732:Fryl
|
UTSW |
5 |
73,054,781 (GRCm38) |
missense |
probably damaging |
1.00 |
R6750:Fryl
|
UTSW |
5 |
73,022,232 (GRCm38) |
missense |
probably damaging |
1.00 |
R6805:Fryl
|
UTSW |
5 |
73,065,094 (GRCm38) |
missense |
probably benign |
0.03 |
R6823:Fryl
|
UTSW |
5 |
73,065,217 (GRCm38) |
missense |
probably damaging |
0.99 |
R6855:Fryl
|
UTSW |
5 |
73,059,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R6858:Fryl
|
UTSW |
5 |
73,065,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R6868:Fryl
|
UTSW |
5 |
73,068,803 (GRCm38) |
missense |
probably damaging |
1.00 |
R6898:Fryl
|
UTSW |
5 |
73,022,142 (GRCm38) |
missense |
probably damaging |
0.96 |
R6908:Fryl
|
UTSW |
5 |
73,022,211 (GRCm38) |
missense |
probably damaging |
1.00 |
R6958:Fryl
|
UTSW |
5 |
73,073,929 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6980:Fryl
|
UTSW |
5 |
73,050,430 (GRCm38) |
missense |
probably benign |
0.06 |
R7036:Fryl
|
UTSW |
5 |
73,055,608 (GRCm38) |
missense |
probably benign |
0.03 |
R7065:Fryl
|
UTSW |
5 |
73,090,756 (GRCm38) |
missense |
probably damaging |
0.96 |
R7097:Fryl
|
UTSW |
5 |
73,073,908 (GRCm38) |
missense |
probably benign |
0.31 |
R7171:Fryl
|
UTSW |
5 |
73,122,310 (GRCm38) |
missense |
probably damaging |
0.97 |
R7191:Fryl
|
UTSW |
5 |
73,072,912 (GRCm38) |
missense |
probably damaging |
1.00 |
R7207:Fryl
|
UTSW |
5 |
73,065,095 (GRCm38) |
missense |
probably benign |
|
R7236:Fryl
|
UTSW |
5 |
73,108,478 (GRCm38) |
missense |
possibly damaging |
0.66 |
R7334:Fryl
|
UTSW |
5 |
73,047,496 (GRCm38) |
splice site |
probably null |
|
R7425:Fryl
|
UTSW |
5 |
73,104,748 (GRCm38) |
missense |
probably damaging |
1.00 |
R7452:Fryl
|
UTSW |
5 |
73,023,988 (GRCm38) |
missense |
probably damaging |
1.00 |
R7479:Fryl
|
UTSW |
5 |
73,097,561 (GRCm38) |
missense |
possibly damaging |
0.71 |
R7535:Fryl
|
UTSW |
5 |
73,098,196 (GRCm38) |
missense |
probably benign |
0.15 |
R7538:Fryl
|
UTSW |
5 |
73,022,676 (GRCm38) |
missense |
probably benign |
0.09 |
R7544:Fryl
|
UTSW |
5 |
73,081,039 (GRCm38) |
missense |
probably benign |
|
R7548:Fryl
|
UTSW |
5 |
73,191,762 (GRCm38) |
missense |
unknown |
|
R7565:Fryl
|
UTSW |
5 |
73,033,720 (GRCm38) |
missense |
probably benign |
0.18 |
R7572:Fryl
|
UTSW |
5 |
73,088,396 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7582:Fryl
|
UTSW |
5 |
73,022,500 (GRCm38) |
critical splice donor site |
probably null |
|
R7630:Fryl
|
UTSW |
5 |
73,110,245 (GRCm38) |
missense |
possibly damaging |
0.62 |
R7774:Fryl
|
UTSW |
5 |
73,083,384 (GRCm38) |
missense |
probably benign |
0.12 |
R7777:Fryl
|
UTSW |
5 |
73,071,298 (GRCm38) |
missense |
probably damaging |
0.98 |
R7917:Fryl
|
UTSW |
5 |
73,054,532 (GRCm38) |
missense |
probably damaging |
1.00 |
R7920:Fryl
|
UTSW |
5 |
73,101,807 (GRCm38) |
splice site |
probably null |
|
R8110:Fryl
|
UTSW |
5 |
73,133,277 (GRCm38) |
missense |
probably benign |
0.10 |
R8120:Fryl
|
UTSW |
5 |
73,071,184 (GRCm38) |
missense |
probably benign |
0.01 |
R8143:Fryl
|
UTSW |
5 |
73,050,339 (GRCm38) |
missense |
probably benign |
0.00 |
R8207:Fryl
|
UTSW |
5 |
73,100,500 (GRCm38) |
splice site |
probably null |
|
R8263:Fryl
|
UTSW |
5 |
73,081,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R8350:Fryl
|
UTSW |
5 |
73,068,730 (GRCm38) |
missense |
probably benign |
|
R8359:Fryl
|
UTSW |
5 |
73,075,933 (GRCm38) |
missense |
probably benign |
0.39 |
R8387:Fryl
|
UTSW |
5 |
73,136,320 (GRCm38) |
critical splice donor site |
probably null |
|
R8403:Fryl
|
UTSW |
5 |
73,118,447 (GRCm38) |
makesense |
probably null |
|
R8450:Fryl
|
UTSW |
5 |
73,068,730 (GRCm38) |
missense |
probably benign |
|
R8514:Fryl
|
UTSW |
5 |
73,085,356 (GRCm38) |
missense |
probably benign |
|
R8536:Fryl
|
UTSW |
5 |
73,100,353 (GRCm38) |
missense |
probably damaging |
0.99 |
R8703:Fryl
|
UTSW |
5 |
73,090,654 (GRCm38) |
missense |
probably damaging |
0.99 |
R8708:Fryl
|
UTSW |
5 |
73,132,562 (GRCm38) |
missense |
probably benign |
0.01 |
R8783:Fryl
|
UTSW |
5 |
73,068,842 (GRCm38) |
missense |
probably benign |
0.45 |
R9028:Fryl
|
UTSW |
5 |
73,098,266 (GRCm38) |
missense |
probably benign |
0.18 |
R9045:Fryl
|
UTSW |
5 |
73,024,775 (GRCm38) |
missense |
|
|
R9063:Fryl
|
UTSW |
5 |
73,081,003 (GRCm38) |
missense |
possibly damaging |
0.70 |
R9096:Fryl
|
UTSW |
5 |
73,108,577 (GRCm38) |
missense |
probably benign |
0.01 |
R9244:Fryl
|
UTSW |
5 |
73,191,519 (GRCm38) |
intron |
probably benign |
|
R9345:Fryl
|
UTSW |
5 |
73,050,411 (GRCm38) |
missense |
probably benign |
|
R9381:Fryl
|
UTSW |
5 |
73,083,294 (GRCm38) |
missense |
probably benign |
0.24 |
R9386:Fryl
|
UTSW |
5 |
73,191,809 (GRCm38) |
missense |
unknown |
|
R9401:Fryl
|
UTSW |
5 |
73,065,220 (GRCm38) |
nonsense |
probably null |
|
R9497:Fryl
|
UTSW |
5 |
73,057,791 (GRCm38) |
missense |
|
|
R9514:Fryl
|
UTSW |
5 |
73,104,772 (GRCm38) |
missense |
probably damaging |
1.00 |
R9570:Fryl
|
UTSW |
5 |
73,022,155 (GRCm38) |
missense |
probably benign |
0.02 |
R9654:Fryl
|
UTSW |
5 |
73,118,458 (GRCm38) |
missense |
probably benign |
|
R9665:Fryl
|
UTSW |
5 |
73,064,956 (GRCm38) |
missense |
probably damaging |
1.00 |
R9685:Fryl
|
UTSW |
5 |
73,059,536 (GRCm38) |
missense |
probably damaging |
0.99 |
R9798:Fryl
|
UTSW |
5 |
73,035,059 (GRCm38) |
missense |
probably benign |
|
Z1088:Fryl
|
UTSW |
5 |
73,090,738 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Fryl
|
UTSW |
5 |
73,090,709 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1176:Fryl
|
UTSW |
5 |
73,072,837 (GRCm38) |
missense |
probably benign |
|
Z1177:Fryl
|
UTSW |
5 |
73,041,595 (GRCm38) |
critical splice acceptor site |
probably null |
|
|