Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acte1 |
A |
G |
7: 143,425,498 (GRCm39) |
D49G |
probably damaging |
Het |
Alg12 |
T |
C |
15: 88,690,850 (GRCm39) |
Y256C |
probably damaging |
Het |
Alox15 |
T |
A |
11: 70,241,021 (GRCm39) |
D160V |
probably damaging |
Het |
Aox1 |
T |
C |
1: 58,373,941 (GRCm39) |
|
probably benign |
Het |
Bbs9 |
G |
T |
9: 22,705,119 (GRCm39) |
A729S |
probably damaging |
Het |
Bltp3a |
T |
C |
17: 28,104,463 (GRCm39) |
V503A |
possibly damaging |
Het |
Bmp2k |
T |
A |
5: 97,235,353 (GRCm39) |
|
probably benign |
Het |
Braf |
C |
T |
6: 39,639,082 (GRCm39) |
R223Q |
possibly damaging |
Het |
Cd101 |
A |
T |
3: 100,927,938 (GRCm39) |
S48T |
possibly damaging |
Het |
Cdh9 |
T |
G |
15: 16,831,130 (GRCm39) |
D322E |
probably benign |
Het |
Col28a1 |
C |
T |
6: 8,014,495 (GRCm39) |
|
probably null |
Het |
Cpxm1 |
G |
A |
2: 130,232,859 (GRCm39) |
R712W |
probably damaging |
Het |
Csnk1g1 |
T |
C |
9: 65,939,637 (GRCm39) |
|
probably benign |
Het |
Cyp2d37-ps |
A |
C |
15: 82,574,650 (GRCm39) |
|
noncoding transcript |
Het |
Cyth3 |
T |
C |
5: 143,678,397 (GRCm39) |
V115A |
probably benign |
Het |
Dnah9 |
C |
T |
11: 65,856,507 (GRCm39) |
V2885M |
probably damaging |
Het |
Dock9 |
G |
T |
14: 121,889,180 (GRCm39) |
Y326* |
probably null |
Het |
Espl1 |
T |
C |
15: 102,231,033 (GRCm39) |
I1844T |
probably benign |
Het |
Fam20a |
T |
A |
11: 109,568,020 (GRCm39) |
N357Y |
probably damaging |
Het |
Fancc |
C |
A |
13: 63,471,225 (GRCm39) |
R385L |
probably benign |
Het |
Foxe3 |
A |
T |
4: 114,782,447 (GRCm39) |
L255H |
unknown |
Het |
Gabra6 |
T |
G |
11: 42,205,954 (GRCm39) |
T301P |
probably damaging |
Het |
Ganab |
T |
A |
19: 8,888,477 (GRCm39) |
Y511N |
probably damaging |
Het |
Grm4 |
T |
A |
17: 27,657,412 (GRCm39) |
|
probably benign |
Het |
H1f6 |
G |
T |
13: 23,880,307 (GRCm39) |
K153N |
possibly damaging |
Het |
Kcnj9 |
G |
A |
1: 172,153,488 (GRCm39) |
S212F |
probably damaging |
Het |
Kif15 |
C |
A |
9: 122,788,993 (GRCm39) |
H62N |
probably benign |
Het |
Kptn |
A |
G |
7: 15,854,647 (GRCm39) |
D106G |
probably damaging |
Het |
Krtap13-1 |
T |
A |
16: 88,526,192 (GRCm39) |
S139T |
probably damaging |
Het |
Lepr |
C |
A |
4: 101,622,131 (GRCm39) |
N354K |
probably benign |
Het |
Lypd3 |
G |
T |
7: 24,337,969 (GRCm39) |
E112* |
probably null |
Het |
Med13l |
A |
T |
5: 118,886,749 (GRCm39) |
N1550I |
probably damaging |
Het |
Mettl2 |
C |
T |
11: 105,017,670 (GRCm39) |
P60L |
probably benign |
Het |
Mtcl2 |
G |
T |
2: 156,902,182 (GRCm39) |
R278S |
probably damaging |
Het |
Muc4 |
A |
G |
16: 32,590,201 (GRCm39) |
E850G |
probably damaging |
Het |
Mylk |
G |
C |
16: 34,699,845 (GRCm39) |
E403Q |
possibly damaging |
Het |
Nek1 |
A |
G |
8: 61,542,626 (GRCm39) |
R739G |
probably damaging |
Het |
Nipbl |
A |
T |
15: 8,381,039 (GRCm39) |
D584E |
probably benign |
Het |
Nkain3 |
C |
T |
4: 20,158,388 (GRCm39) |
V162M |
possibly damaging |
Het |
Nmrk1 |
T |
C |
19: 18,618,844 (GRCm39) |
|
probably benign |
Het |
Nsd2 |
T |
C |
5: 34,018,372 (GRCm39) |
|
probably benign |
Het |
Or2n1b |
T |
C |
17: 38,459,515 (GRCm39) |
F12S |
probably damaging |
Het |
Or4b1 |
T |
A |
2: 89,979,627 (GRCm39) |
H241L |
probably damaging |
Het |
Or4p23 |
A |
T |
2: 88,576,352 (GRCm39) |
N293K |
probably benign |
Het |
Or5b24 |
T |
A |
19: 12,912,969 (GRCm39) |
V289D |
probably damaging |
Het |
Or8b44 |
T |
A |
9: 38,410,418 (GRCm39) |
M151K |
possibly damaging |
Het |
Otulinl |
A |
T |
15: 27,657,033 (GRCm39) |
I338N |
probably damaging |
Het |
Phex |
T |
A |
X: 156,155,557 (GRCm39) |
|
probably benign |
Het |
Pip5k1b |
G |
T |
19: 24,356,256 (GRCm39) |
D227E |
probably damaging |
Het |
Prdm13 |
A |
G |
4: 21,683,914 (GRCm39) |
I119T |
unknown |
Het |
Rab19 |
G |
T |
6: 39,360,893 (GRCm39) |
V14L |
probably benign |
Het |
Rasa3 |
A |
G |
8: 13,630,118 (GRCm39) |
|
probably benign |
Het |
Rgsl1 |
C |
T |
1: 153,678,074 (GRCm39) |
S118N |
probably damaging |
Het |
Rif1 |
C |
T |
2: 52,000,365 (GRCm39) |
T1273M |
possibly damaging |
Het |
Scn8a |
A |
G |
15: 100,870,711 (GRCm39) |
N254S |
probably damaging |
Het |
Sema6a |
T |
C |
18: 47,425,048 (GRCm39) |
T188A |
probably damaging |
Het |
Sh3pxd2a |
C |
T |
19: 47,257,201 (GRCm39) |
E506K |
probably damaging |
Het |
Smarca2 |
A |
T |
19: 26,675,803 (GRCm39) |
K1014N |
probably damaging |
Het |
Smarca4 |
T |
G |
9: 21,611,435 (GRCm39) |
|
probably null |
Het |
Sntb1 |
T |
C |
15: 55,539,752 (GRCm39) |
R361G |
probably benign |
Het |
Stx5a |
T |
A |
19: 8,732,275 (GRCm39) |
I208N |
probably damaging |
Het |
Tas2r102 |
T |
A |
6: 132,739,415 (GRCm39) |
W108R |
probably damaging |
Het |
Tcl1 |
A |
G |
12: 105,184,929 (GRCm39) |
Y94H |
probably damaging |
Het |
Tenm3 |
T |
A |
8: 48,689,629 (GRCm39) |
Y1986F |
probably damaging |
Het |
Tet2 |
G |
A |
3: 133,173,945 (GRCm39) |
P1439L |
probably benign |
Het |
Tiam2 |
T |
C |
17: 3,563,108 (GRCm39) |
|
probably benign |
Het |
Ubap2l |
G |
A |
3: 89,928,553 (GRCm39) |
T526M |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ushbp1 |
T |
A |
8: 71,841,391 (GRCm39) |
|
probably benign |
Het |
Usp28 |
C |
T |
9: 48,915,169 (GRCm39) |
R115C |
probably damaging |
Het |
Vldlr |
A |
T |
19: 27,215,786 (GRCm39) |
D261V |
probably damaging |
Het |
Vmn2r5 |
C |
T |
3: 64,411,186 (GRCm39) |
D461N |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,282,265 (GRCm39) |
F784I |
probably damaging |
Het |
Zfp59 |
A |
T |
7: 27,553,513 (GRCm39) |
I322F |
probably damaging |
Het |
Zfp607a |
A |
T |
7: 27,578,574 (GRCm39) |
H548L |
probably benign |
Het |
Zfp626 |
G |
A |
7: 27,518,048 (GRCm39) |
C343Y |
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 |
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 |
R1539:Frem2
|
UTSW |
3 |
53,561,631 (GRCm39) |
missense |
probably benign |
0.19 |
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 |
|