Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
T |
A |
13: 81,652,097 (GRCm39) |
|
probably null |
Het |
Adh7 |
A |
C |
3: 137,929,716 (GRCm39) |
T131P |
possibly damaging |
Het |
Agxt |
G |
A |
1: 93,065,701 (GRCm39) |
G190D |
probably damaging |
Het |
AI182371 |
A |
G |
2: 34,978,815 (GRCm39) |
I193T |
probably damaging |
Het |
Akna |
T |
A |
4: 63,297,547 (GRCm39) |
T836S |
probably benign |
Het |
Alox12 |
T |
C |
11: 70,144,069 (GRCm39) |
|
probably null |
Het |
Anapc2 |
C |
A |
2: 25,163,075 (GRCm39) |
T104K |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,583,935 (GRCm39) |
L346P |
probably damaging |
Het |
Ankfn1 |
A |
T |
11: 89,332,217 (GRCm39) |
I443N |
probably damaging |
Het |
Arhgef17 |
G |
A |
7: 100,539,680 (GRCm39) |
T1066I |
probably damaging |
Het |
Atg2a |
C |
A |
19: 6,296,801 (GRCm39) |
|
probably null |
Het |
Bpifb5 |
T |
A |
2: 154,065,776 (GRCm39) |
H24Q |
probably benign |
Het |
Brd9 |
A |
G |
13: 74,092,862 (GRCm39) |
E283G |
probably damaging |
Het |
Cadm2 |
C |
A |
16: 66,581,727 (GRCm39) |
V184F |
probably damaging |
Het |
Casr |
A |
G |
16: 36,315,499 (GRCm39) |
V857A |
probably benign |
Het |
Ccdc18 |
A |
T |
5: 108,339,843 (GRCm39) |
Q796L |
probably damaging |
Het |
Cep290 |
T |
C |
10: 100,332,690 (GRCm39) |
V263A |
probably benign |
Het |
Clec10a |
A |
T |
11: 70,060,645 (GRCm39) |
N167Y |
probably damaging |
Het |
Cog1 |
A |
G |
11: 113,543,058 (GRCm39) |
I189V |
possibly damaging |
Het |
Commd2 |
A |
G |
3: 57,554,269 (GRCm39) |
I144T |
probably benign |
Het |
Cse1l |
A |
G |
2: 166,768,292 (GRCm39) |
T197A |
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,683,794 (GRCm39) |
S1783R |
probably benign |
Het |
Cxxc1 |
T |
C |
18: 74,352,278 (GRCm39) |
V334A |
possibly damaging |
Het |
Dennd2d |
A |
G |
3: 106,394,236 (GRCm39) |
I39V |
probably benign |
Het |
Dgkz |
G |
A |
2: 91,768,405 (GRCm39) |
P734S |
probably damaging |
Het |
Diaph3 |
T |
C |
14: 86,893,916 (GRCm39) |
D31G |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,956,518 (GRCm39) |
S731P |
probably benign |
Het |
Dmac2l |
G |
A |
12: 69,787,845 (GRCm39) |
D94N |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,894,991 (GRCm39) |
R3619G |
probably benign |
Het |
Doc2b |
A |
G |
11: 75,662,783 (GRCm39) |
L405P |
probably damaging |
Het |
Dock3 |
A |
T |
9: 106,829,563 (GRCm39) |
I1117N |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,874,112 (GRCm39) |
A453V |
probably benign |
Het |
Ece2 |
T |
A |
16: 20,461,263 (GRCm39) |
I474N |
probably damaging |
Het |
Etv4 |
A |
T |
11: 101,662,513 (GRCm39) |
|
probably null |
Het |
Fam171b |
A |
T |
2: 83,710,442 (GRCm39) |
M705L |
probably benign |
Het |
Fyn |
T |
C |
10: 39,408,066 (GRCm39) |
M251T |
possibly damaging |
Het |
Galnt13 |
G |
A |
2: 54,747,869 (GRCm39) |
G250E |
probably damaging |
Het |
Ggh |
T |
C |
4: 20,054,204 (GRCm39) |
|
probably null |
Het |
Glcci1 |
A |
G |
6: 8,591,620 (GRCm39) |
E222G |
probably damaging |
Het |
Gm1968 |
G |
A |
16: 29,777,659 (GRCm39) |
|
noncoding transcript |
Het |
Gm3604 |
T |
A |
13: 62,519,414 (GRCm39) |
I52F |
possibly damaging |
Het |
Gm43302 |
T |
C |
5: 105,422,635 (GRCm39) |
I466V |
probably benign |
Het |
Gm9789 |
T |
C |
16: 88,955,034 (GRCm39) |
S48P |
unknown |
Het |
Gpat3 |
A |
T |
5: 101,031,254 (GRCm39) |
Y136F |
probably benign |
Het |
Gpr171 |
T |
C |
3: 59,005,142 (GRCm39) |
D211G |
possibly damaging |
Het |
Grep1 |
T |
A |
17: 23,936,118 (GRCm39) |
|
probably benign |
Het |
Hs3st1 |
T |
C |
5: 39,771,791 (GRCm39) |
K284R |
probably benign |
Het |
Htr2a |
C |
T |
14: 74,882,608 (GRCm39) |
A198V |
possibly damaging |
Het |
Ice1 |
C |
A |
13: 70,754,023 (GRCm39) |
D688Y |
probably damaging |
Het |
Jade1 |
T |
C |
3: 41,559,431 (GRCm39) |
M504T |
probably benign |
Het |
Lrp1 |
T |
C |
10: 127,420,250 (GRCm39) |
|
probably null |
Het |
Lsr |
A |
T |
7: 30,671,517 (GRCm39) |
I72N |
possibly damaging |
Het |
Magel2 |
G |
A |
7: 62,028,557 (GRCm39) |
R487H |
possibly damaging |
Het |
Mertk |
A |
G |
2: 128,624,446 (GRCm39) |
D619G |
probably benign |
Het |
Myo1b |
A |
T |
1: 51,838,722 (GRCm39) |
V245E |
probably damaging |
Het |
Myrip |
T |
A |
9: 120,253,689 (GRCm39) |
L254Q |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,603,031 (GRCm39) |
S1173P |
probably damaging |
Het |
Ncoa7 |
T |
C |
10: 30,647,725 (GRCm39) |
Y17C |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,187,003 (GRCm39) |
E7G |
probably benign |
Het |
Ninl |
A |
G |
2: 150,817,867 (GRCm39) |
V99A |
probably damaging |
Het |
Noct |
G |
T |
3: 51,155,333 (GRCm39) |
E34* |
probably null |
Het |
Notch1 |
A |
T |
2: 26,362,125 (GRCm39) |
Y1043* |
probably null |
Het |
Or10v1 |
T |
C |
19: 11,873,855 (GRCm39) |
S157P |
possibly damaging |
Het |
Or13a21 |
T |
A |
7: 139,999,326 (GRCm39) |
Y120F |
probably benign |
Het |
Or2d3 |
A |
G |
7: 106,490,483 (GRCm39) |
Y278H |
probably damaging |
Het |
Or6c88 |
G |
A |
10: 129,406,640 (GRCm39) |
G39R |
probably damaging |
Het |
Pde7b |
C |
A |
10: 20,355,432 (GRCm39) |
R104L |
possibly damaging |
Het |
Pkn1 |
C |
A |
8: 84,396,966 (GRCm39) |
R890L |
possibly damaging |
Het |
Podn |
A |
T |
4: 107,878,764 (GRCm39) |
Y368N |
probably damaging |
Het |
Polr1b |
G |
A |
2: 128,960,019 (GRCm39) |
|
probably null |
Het |
Ppp1r3c |
A |
T |
19: 36,711,361 (GRCm39) |
F136L |
probably benign |
Het |
Ppp2ca |
T |
A |
11: 52,011,800 (GRCm39) |
F260Y |
probably damaging |
Het |
Prss39 |
A |
G |
1: 34,537,616 (GRCm39) |
S27G |
possibly damaging |
Het |
Ptch1 |
A |
G |
13: 63,689,101 (GRCm39) |
V340A |
probably benign |
Het |
Ranbp17 |
T |
C |
11: 33,247,394 (GRCm39) |
I246V |
probably damaging |
Het |
Rilpl1 |
T |
A |
5: 124,653,618 (GRCm39) |
D181V |
probably damaging |
Het |
Sdk1 |
T |
A |
5: 142,080,354 (GRCm39) |
V1282D |
probably damaging |
Het |
Sh3rf2 |
T |
C |
18: 42,282,887 (GRCm39) |
S514P |
probably damaging |
Het |
Slc35f2 |
A |
T |
9: 53,716,992 (GRCm39) |
I252F |
possibly damaging |
Het |
Slc7a1 |
A |
G |
5: 148,272,403 (GRCm39) |
Y425H |
possibly damaging |
Het |
Spaca4 |
G |
T |
7: 45,374,984 (GRCm39) |
|
probably benign |
Het |
Spata31d1b |
T |
C |
13: 59,863,733 (GRCm39) |
S294P |
possibly damaging |
Het |
Ssh1 |
T |
G |
5: 114,090,064 (GRCm39) |
T342P |
probably damaging |
Het |
Stk10 |
T |
A |
11: 32,483,440 (GRCm39) |
S13T |
possibly damaging |
Het |
Tbx1 |
G |
T |
16: 18,402,843 (GRCm39) |
D214E |
probably benign |
Het |
Tdp1 |
A |
G |
12: 99,878,571 (GRCm39) |
E453G |
probably damaging |
Het |
Tlr1 |
T |
C |
5: 65,084,319 (GRCm39) |
Y86C |
probably damaging |
Het |
Tmem241 |
A |
T |
18: 12,176,297 (GRCm39) |
C124S |
possibly damaging |
Het |
Trp63 |
A |
G |
16: 25,703,599 (GRCm39) |
M516V |
probably benign |
Het |
Ttc28 |
T |
C |
5: 111,248,677 (GRCm39) |
V210A |
possibly damaging |
Het |
Tut1 |
C |
T |
19: 8,942,850 (GRCm39) |
R646W |
probably benign |
Het |
Ubald1 |
C |
T |
16: 4,694,261 (GRCm39) |
E49K |
possibly damaging |
Het |
Usp28 |
T |
C |
9: 48,949,096 (GRCm39) |
Y897H |
probably benign |
Het |
Vmn2r27 |
A |
C |
6: 124,168,730 (GRCm39) |
F800C |
probably damaging |
Het |
Vmn2r83 |
T |
A |
10: 79,327,759 (GRCm39) |
M789K |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,300,002 (GRCm39) |
D945G |
probably benign |
Het |
Wdhd1 |
T |
A |
14: 47,482,507 (GRCm39) |
K947N |
possibly damaging |
Het |
Wdr12 |
A |
T |
1: 60,123,007 (GRCm39) |
|
probably null |
Het |
Xrra1 |
A |
T |
7: 99,520,564 (GRCm39) |
E57V |
probably damaging |
Het |
|
Other mutations in Frem2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00895:Frem2
|
APN |
3 |
53,493,016 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00911:Frem2
|
APN |
3 |
53,479,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01322:Frem2
|
APN |
3 |
53,448,459 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01330:Frem2
|
APN |
3 |
53,562,662 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01406:Frem2
|
APN |
3 |
53,433,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01556:Frem2
|
APN |
3 |
53,442,702 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01580:Frem2
|
APN |
3 |
53,562,596 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01606:Frem2
|
APN |
3 |
53,561,012 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01611:Frem2
|
APN |
3 |
53,563,130 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01648:Frem2
|
APN |
3 |
53,443,153 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01663:Frem2
|
APN |
3 |
53,424,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01665:Frem2
|
APN |
3 |
53,457,083 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01670:Frem2
|
APN |
3 |
53,564,358 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01960:Frem2
|
APN |
3 |
53,429,725 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02175:Frem2
|
APN |
3 |
53,563,020 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02201:Frem2
|
APN |
3 |
53,427,061 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02202:Frem2
|
APN |
3 |
53,562,220 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02427:Frem2
|
APN |
3 |
53,443,184 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02457:Frem2
|
APN |
3 |
53,428,470 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02638:Frem2
|
APN |
3 |
53,458,767 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02801:Frem2
|
APN |
3 |
53,559,596 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03023:Frem2
|
APN |
3 |
53,563,049 (GRCm39) |
missense |
probably benign |
0.40 |
IGL03169:Frem2
|
APN |
3 |
53,429,713 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03238:Frem2
|
APN |
3 |
53,563,682 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03251:Frem2
|
APN |
3 |
53,479,729 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03273:Frem2
|
APN |
3 |
53,444,930 (GRCm39) |
nonsense |
probably null |
|
IGL03343:Frem2
|
APN |
3 |
53,559,674 (GRCm39) |
missense |
probably damaging |
1.00 |
Biosimilar
|
UTSW |
3 |
53,561,744 (GRCm39) |
missense |
probably benign |
0.01 |
Fruit_stripe
|
UTSW |
3 |
53,444,910 (GRCm39) |
missense |
probably benign |
0.21 |
PIT4366001:Frem2
|
UTSW |
3 |
53,560,622 (GRCm39) |
missense |
probably damaging |
0.98 |
R0019:Frem2
|
UTSW |
3 |
53,431,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R0092:Frem2
|
UTSW |
3 |
53,497,217 (GRCm39) |
missense |
probably benign |
0.03 |
R0108:Frem2
|
UTSW |
3 |
53,555,382 (GRCm39) |
missense |
probably benign |
0.03 |
R0115:Frem2
|
UTSW |
3 |
53,563,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R0118:Frem2
|
UTSW |
3 |
53,442,664 (GRCm39) |
nonsense |
probably null |
|
R0374:Frem2
|
UTSW |
3 |
53,561,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Frem2
|
UTSW |
3 |
53,560,436 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0531:Frem2
|
UTSW |
3 |
53,427,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Frem2
|
UTSW |
3 |
53,424,281 (GRCm39) |
missense |
probably damaging |
0.97 |
R0564:Frem2
|
UTSW |
3 |
53,563,530 (GRCm39) |
missense |
probably damaging |
0.97 |
R0586:Frem2
|
UTSW |
3 |
53,555,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R0726:Frem2
|
UTSW |
3 |
53,427,047 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0925:Frem2
|
UTSW |
3 |
53,561,394 (GRCm39) |
missense |
probably benign |
|
R1233:Frem2
|
UTSW |
3 |
53,455,199 (GRCm39) |
missense |
probably damaging |
0.98 |
R1302:Frem2
|
UTSW |
3 |
53,562,959 (GRCm39) |
missense |
probably benign |
0.00 |
R1333:Frem2
|
UTSW |
3 |
53,457,152 (GRCm39) |
missense |
probably benign |
0.26 |
R1446:Frem2
|
UTSW |
3 |
53,562,017 (GRCm39) |
missense |
probably benign |
0.31 |
R1523:Frem2
|
UTSW |
3 |
53,562,828 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1543:Frem2
|
UTSW |
3 |
53,479,876 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1597:Frem2
|
UTSW |
3 |
53,561,940 (GRCm39) |
missense |
probably benign |
0.19 |
R1600:Frem2
|
UTSW |
3 |
53,455,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Frem2
|
UTSW |
3 |
53,427,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Frem2
|
UTSW |
3 |
53,561,373 (GRCm39) |
missense |
probably benign |
|
R1696:Frem2
|
UTSW |
3 |
53,563,463 (GRCm39) |
nonsense |
probably null |
|
R1758:Frem2
|
UTSW |
3 |
53,560,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1857:Frem2
|
UTSW |
3 |
53,562,294 (GRCm39) |
missense |
probably benign |
0.10 |
R1869:Frem2
|
UTSW |
3 |
53,442,617 (GRCm39) |
missense |
probably benign |
0.04 |
R1921:Frem2
|
UTSW |
3 |
53,560,916 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1973:Frem2
|
UTSW |
3 |
53,559,653 (GRCm39) |
missense |
probably benign |
0.01 |
R2045:Frem2
|
UTSW |
3 |
53,443,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Frem2
|
UTSW |
3 |
53,560,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Frem2
|
UTSW |
3 |
53,424,450 (GRCm39) |
nonsense |
probably null |
|
R2164:Frem2
|
UTSW |
3 |
53,444,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R2181:Frem2
|
UTSW |
3 |
53,482,008 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2201:Frem2
|
UTSW |
3 |
53,423,994 (GRCm39) |
missense |
probably benign |
|
R2221:Frem2
|
UTSW |
3 |
53,424,278 (GRCm39) |
missense |
probably benign |
0.00 |
R2255:Frem2
|
UTSW |
3 |
53,559,935 (GRCm39) |
missense |
probably damaging |
0.96 |
R2280:Frem2
|
UTSW |
3 |
53,479,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R3196:Frem2
|
UTSW |
3 |
53,444,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Frem2
|
UTSW |
3 |
53,479,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Frem2
|
UTSW |
3 |
53,560,870 (GRCm39) |
missense |
probably benign |
0.22 |
R3820:Frem2
|
UTSW |
3 |
53,424,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R3821:Frem2
|
UTSW |
3 |
53,559,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R3977:Frem2
|
UTSW |
3 |
53,559,491 (GRCm39) |
missense |
probably benign |
0.00 |
R3979:Frem2
|
UTSW |
3 |
53,559,491 (GRCm39) |
missense |
probably benign |
0.00 |
R4014:Frem2
|
UTSW |
3 |
53,559,774 (GRCm39) |
missense |
probably benign |
0.01 |
R4127:Frem2
|
UTSW |
3 |
53,433,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4195:Frem2
|
UTSW |
3 |
53,446,689 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4196:Frem2
|
UTSW |
3 |
53,446,689 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4374:Frem2
|
UTSW |
3 |
53,452,923 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4427:Frem2
|
UTSW |
3 |
53,446,583 (GRCm39) |
critical splice donor site |
probably null |
|
R4428:Frem2
|
UTSW |
3 |
53,561,759 (GRCm39) |
missense |
probably benign |
0.40 |
R4559:Frem2
|
UTSW |
3 |
53,561,742 (GRCm39) |
missense |
probably benign |
0.01 |
R4600:Frem2
|
UTSW |
3 |
53,455,228 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4602:Frem2
|
UTSW |
3 |
53,455,228 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4610:Frem2
|
UTSW |
3 |
53,455,228 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4611:Frem2
|
UTSW |
3 |
53,455,228 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4661:Frem2
|
UTSW |
3 |
53,562,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Frem2
|
UTSW |
3 |
53,451,792 (GRCm39) |
missense |
probably benign |
0.00 |
R4689:Frem2
|
UTSW |
3 |
53,455,056 (GRCm39) |
missense |
probably benign |
0.43 |
R4740:Frem2
|
UTSW |
3 |
53,443,240 (GRCm39) |
missense |
probably benign |
0.04 |
R4748:Frem2
|
UTSW |
3 |
53,448,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Frem2
|
UTSW |
3 |
53,424,162 (GRCm39) |
missense |
probably benign |
|
R4809:Frem2
|
UTSW |
3 |
53,561,316 (GRCm39) |
missense |
probably benign |
0.01 |
R4930:Frem2
|
UTSW |
3 |
53,563,736 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4971:Frem2
|
UTSW |
3 |
53,446,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Frem2
|
UTSW |
3 |
53,442,617 (GRCm39) |
missense |
probably benign |
0.37 |
R5202:Frem2
|
UTSW |
3 |
53,458,767 (GRCm39) |
missense |
probably benign |
0.41 |
R5221:Frem2
|
UTSW |
3 |
53,493,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Frem2
|
UTSW |
3 |
53,429,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5268:Frem2
|
UTSW |
3 |
53,560,575 (GRCm39) |
missense |
probably damaging |
0.96 |
R5480:Frem2
|
UTSW |
3 |
53,563,928 (GRCm39) |
nonsense |
probably null |
|
R5637:Frem2
|
UTSW |
3 |
53,560,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R5664:Frem2
|
UTSW |
3 |
53,559,911 (GRCm39) |
missense |
probably benign |
0.33 |
R5698:Frem2
|
UTSW |
3 |
53,559,926 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5744:Frem2
|
UTSW |
3 |
53,563,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Frem2
|
UTSW |
3 |
53,444,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5808:Frem2
|
UTSW |
3 |
53,559,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R5840:Frem2
|
UTSW |
3 |
53,555,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R5874:Frem2
|
UTSW |
3 |
53,444,910 (GRCm39) |
missense |
probably benign |
0.21 |
R6050:Frem2
|
UTSW |
3 |
53,560,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R6103:Frem2
|
UTSW |
3 |
53,457,209 (GRCm39) |
missense |
probably benign |
0.00 |
R6149:Frem2
|
UTSW |
3 |
53,458,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R6182:Frem2
|
UTSW |
3 |
53,555,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Frem2
|
UTSW |
3 |
53,562,701 (GRCm39) |
missense |
probably benign |
0.10 |
R6245:Frem2
|
UTSW |
3 |
53,563,245 (GRCm39) |
missense |
probably benign |
0.00 |
R6252:Frem2
|
UTSW |
3 |
53,479,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Frem2
|
UTSW |
3 |
53,493,061 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6416:Frem2
|
UTSW |
3 |
53,479,799 (GRCm39) |
missense |
probably benign |
0.01 |
R6595:Frem2
|
UTSW |
3 |
53,457,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6665:Frem2
|
UTSW |
3 |
53,562,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Frem2
|
UTSW |
3 |
53,492,922 (GRCm39) |
missense |
probably benign |
0.00 |
R6751:Frem2
|
UTSW |
3 |
53,561,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:Frem2
|
UTSW |
3 |
53,561,744 (GRCm39) |
missense |
probably benign |
0.01 |
R6913:Frem2
|
UTSW |
3 |
53,424,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6916:Frem2
|
UTSW |
3 |
53,455,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Frem2
|
UTSW |
3 |
53,427,023 (GRCm39) |
missense |
probably benign |
0.02 |
R7083:Frem2
|
UTSW |
3 |
53,444,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R7108:Frem2
|
UTSW |
3 |
53,560,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Frem2
|
UTSW |
3 |
53,479,760 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7326:Frem2
|
UTSW |
3 |
53,562,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R7341:Frem2
|
UTSW |
3 |
53,561,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Frem2
|
UTSW |
3 |
53,479,701 (GRCm39) |
splice site |
probably null |
|
R7487:Frem2
|
UTSW |
3 |
53,561,970 (GRCm39) |
missense |
probably benign |
0.40 |
R7495:Frem2
|
UTSW |
3 |
53,424,258 (GRCm39) |
missense |
probably benign |
0.13 |
R7542:Frem2
|
UTSW |
3 |
53,560,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7636:Frem2
|
UTSW |
3 |
53,560,668 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Frem2
|
UTSW |
3 |
53,429,589 (GRCm39) |
missense |
probably benign |
0.01 |
R7750:Frem2
|
UTSW |
3 |
53,431,103 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7849:Frem2
|
UTSW |
3 |
53,479,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Frem2
|
UTSW |
3 |
53,560,725 (GRCm39) |
missense |
probably damaging |
0.98 |
R8008:Frem2
|
UTSW |
3 |
53,560,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8051:Frem2
|
UTSW |
3 |
53,442,776 (GRCm39) |
missense |
probably benign |
0.04 |
R8052:Frem2
|
UTSW |
3 |
53,457,064 (GRCm39) |
missense |
probably benign |
0.02 |
R8176:Frem2
|
UTSW |
3 |
53,562,761 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8220:Frem2
|
UTSW |
3 |
53,563,928 (GRCm39) |
nonsense |
probably null |
|
R8397:Frem2
|
UTSW |
3 |
53,560,562 (GRCm39) |
missense |
probably benign |
0.00 |
R8410:Frem2
|
UTSW |
3 |
53,446,598 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8697:Frem2
|
UTSW |
3 |
53,433,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R9134:Frem2
|
UTSW |
3 |
53,562,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9183:Frem2
|
UTSW |
3 |
53,427,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Frem2
|
UTSW |
3 |
53,560,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Frem2
|
UTSW |
3 |
53,564,504 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R9299:Frem2
|
UTSW |
3 |
53,563,980 (GRCm39) |
missense |
probably benign |
0.37 |
R9378:Frem2
|
UTSW |
3 |
53,559,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R9444:Frem2
|
UTSW |
3 |
53,560,265 (GRCm39) |
missense |
probably benign |
0.10 |
R9459:Frem2
|
UTSW |
3 |
53,560,907 (GRCm39) |
missense |
probably benign |
|
R9487:Frem2
|
UTSW |
3 |
53,560,905 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9728:Frem2
|
UTSW |
3 |
53,564,052 (GRCm39) |
missense |
probably benign |
0.00 |
R9759:Frem2
|
UTSW |
3 |
53,562,918 (GRCm39) |
missense |
possibly damaging |
0.76 |
Z1177:Frem2
|
UTSW |
3 |
53,563,028 (GRCm39) |
missense |
probably benign |
0.31 |
Z1177:Frem2
|
UTSW |
3 |
53,442,587 (GRCm39) |
missense |
probably null |
1.00 |
|