Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
A |
C |
9: 55,909,807 (GRCm39) |
D144E |
possibly damaging |
Het |
Amigo2 |
T |
A |
15: 97,143,419 (GRCm39) |
K334N |
probably benign |
Het |
Ano6 |
T |
C |
15: 95,846,380 (GRCm39) |
|
probably null |
Het |
Ap1m2 |
C |
A |
9: 21,210,601 (GRCm39) |
V343F |
probably benign |
Het |
Apol6 |
T |
C |
15: 76,940,098 (GRCm39) |
V307A |
probably benign |
Het |
Arsi |
C |
A |
18: 61,045,544 (GRCm39) |
A78E |
probably damaging |
Het |
B2m |
A |
T |
2: 121,981,396 (GRCm39) |
N37I |
possibly damaging |
Het |
Bltp3b |
G |
T |
10: 89,641,180 (GRCm39) |
G784C |
possibly damaging |
Het |
C8a |
T |
C |
4: 104,703,100 (GRCm39) |
K363R |
probably benign |
Het |
Ccdc117 |
C |
A |
11: 5,484,242 (GRCm39) |
|
probably null |
Het |
Ccdc154 |
C |
A |
17: 25,386,945 (GRCm39) |
Q325K |
probably damaging |
Het |
Cd300e |
A |
T |
11: 114,945,359 (GRCm39) |
V145E |
possibly damaging |
Het |
Col19a1 |
G |
T |
1: 24,356,474 (GRCm39) |
P673Q |
probably damaging |
Het |
Csn2 |
A |
G |
5: 87,843,885 (GRCm39) |
|
probably null |
Het |
Ctnna1 |
T |
C |
18: 35,307,408 (GRCm39) |
V135A |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 118,154,632 (GRCm39) |
D216V |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,431,412 (GRCm39) |
H410R |
probably benign |
Het |
Dock2 |
C |
T |
11: 34,181,652 (GRCm39) |
R1637H |
possibly damaging |
Het |
Dspp |
A |
G |
5: 104,325,214 (GRCm39) |
N526D |
unknown |
Het |
Galc |
A |
T |
12: 98,218,293 (GRCm39) |
H186Q |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,218 (GRCm39) |
V262A |
probably damaging |
Het |
Gse1 |
G |
A |
8: 121,280,542 (GRCm39) |
|
probably null |
Het |
H2-Oa |
C |
A |
17: 34,312,842 (GRCm39) |
Q40K |
probably damaging |
Het |
Hfm1 |
C |
A |
5: 107,034,419 (GRCm39) |
D763Y |
possibly damaging |
Het |
Hmcn2 |
T |
A |
2: 31,348,758 (GRCm39) |
Y4925N |
probably damaging |
Het |
Hs3st3b1 |
C |
A |
11: 63,780,029 (GRCm39) |
R366L |
probably benign |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Iqank1 |
T |
C |
15: 75,918,218 (GRCm39) |
|
probably null |
Het |
Itpr2 |
A |
G |
6: 146,229,833 (GRCm39) |
V1221A |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,297,584 (GRCm39) |
N285S |
probably benign |
Het |
Klk1b1 |
T |
A |
7: 43,620,081 (GRCm39) |
N181K |
probably damaging |
Het |
Kmt2a |
C |
A |
9: 44,738,125 (GRCm39) |
|
probably benign |
Het |
Lama5 |
T |
C |
2: 179,827,752 (GRCm39) |
D2170G |
probably damaging |
Het |
Lama5 |
T |
A |
2: 179,822,404 (GRCm39) |
T2890S |
probably damaging |
Het |
Lsm2 |
T |
A |
17: 35,201,131 (GRCm39) |
|
probably benign |
Het |
Map3k5 |
G |
T |
10: 19,899,415 (GRCm39) |
C232F |
probably damaging |
Het |
Mapk9 |
T |
G |
11: 49,754,383 (GRCm39) |
D45E |
probably damaging |
Het |
Mpnd |
T |
C |
17: 56,319,482 (GRCm39) |
V315A |
possibly damaging |
Het |
Msh2 |
A |
G |
17: 88,030,900 (GRCm39) |
I926V |
probably benign |
Het |
Mtcl1 |
C |
T |
17: 66,650,521 (GRCm39) |
R1345H |
probably damaging |
Het |
Nbeal2 |
A |
G |
9: 110,457,058 (GRCm39) |
|
probably null |
Het |
Neo1 |
T |
C |
9: 58,796,312 (GRCm39) |
D1205G |
probably damaging |
Het |
Nhlrc2 |
A |
G |
19: 56,559,291 (GRCm39) |
S259G |
probably benign |
Het |
Nkain4 |
G |
A |
2: 180,577,796 (GRCm39) |
P186L |
probably damaging |
Het |
Nkain4 |
G |
A |
2: 180,577,797 (GRCm39) |
P186S |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,109,283 (GRCm39) |
R73* |
probably null |
Het |
Nr5a2 |
T |
C |
1: 136,818,536 (GRCm39) |
D330G |
probably damaging |
Het |
Nup54 |
A |
G |
5: 92,572,153 (GRCm39) |
L299P |
probably damaging |
Het |
Or2v1 |
T |
C |
11: 49,025,877 (GRCm39) |
L286P |
probably damaging |
Het |
Or5aq7 |
A |
G |
2: 86,938,296 (GRCm39) |
V145A |
probably damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,489,279 (GRCm39) |
V319E |
probably benign |
Het |
Pcsk6 |
T |
A |
7: 65,578,875 (GRCm39) |
D129E |
probably benign |
Het |
Pld5 |
G |
A |
1: 175,798,100 (GRCm39) |
T433I |
probably benign |
Het |
Plin1 |
A |
T |
7: 79,371,347 (GRCm39) |
L459H |
probably benign |
Het |
Psd4 |
T |
C |
2: 24,284,499 (GRCm39) |
V121A |
probably damaging |
Het |
Pxdn |
A |
T |
12: 30,032,716 (GRCm39) |
I167F |
possibly damaging |
Het |
R3hdm2 |
T |
C |
10: 127,320,384 (GRCm39) |
S569P |
probably damaging |
Het |
Rfng |
T |
A |
11: 120,673,516 (GRCm39) |
T202S |
probably damaging |
Het |
Robo1 |
T |
C |
16: 72,730,696 (GRCm39) |
S266P |
probably benign |
Het |
Sema3c |
G |
T |
5: 17,858,804 (GRCm39) |
V68L |
probably damaging |
Het |
Slco6c1 |
C |
T |
1: 96,993,808 (GRCm39) |
R645H |
possibly damaging |
Het |
Slfn8 |
A |
G |
11: 82,907,626 (GRCm39) |
Y306H |
possibly damaging |
Het |
Snap91 |
T |
C |
9: 86,720,105 (GRCm39) |
D144G |
probably damaging |
Het |
St7l |
T |
G |
3: 104,775,349 (GRCm39) |
F75C |
probably damaging |
Het |
Stard10 |
A |
G |
7: 100,992,468 (GRCm39) |
I145V |
probably damaging |
Het |
Tekt3 |
C |
T |
11: 62,968,999 (GRCm39) |
A242V |
probably damaging |
Het |
Tex44 |
A |
G |
1: 86,354,306 (GRCm39) |
|
probably benign |
Het |
Thg1l |
T |
C |
11: 45,844,988 (GRCm39) |
Q88R |
probably benign |
Het |
Trav8n-2 |
T |
A |
14: 53,583,744 (GRCm39) |
I67N |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,677,770 (GRCm39) |
|
probably benign |
Het |
Ube4a |
A |
T |
9: 44,861,051 (GRCm39) |
L253* |
probably null |
Het |
Uggt1 |
A |
T |
1: 36,201,289 (GRCm39) |
N1150K |
probably damaging |
Het |
Ush2a |
T |
A |
1: 187,995,298 (GRCm39) |
L23* |
probably null |
Het |
Usp22 |
T |
A |
11: 61,065,602 (GRCm39) |
N37I |
probably benign |
Het |
Usp53 |
T |
A |
3: 122,743,390 (GRCm39) |
K515N |
probably damaging |
Het |
Vmn2r4 |
T |
C |
3: 64,322,702 (GRCm39) |
K6E |
probably benign |
Het |
Vps13d |
C |
T |
4: 144,875,918 (GRCm39) |
V1530M |
probably damaging |
Het |
Vwa3b |
A |
G |
1: 37,153,612 (GRCm39) |
I485V |
possibly damaging |
Het |
Wnk4 |
T |
C |
11: 101,155,156 (GRCm39) |
Y356H |
probably damaging |
Het |
Zcchc2 |
A |
G |
1: 105,917,900 (GRCm39) |
|
probably benign |
Het |
Zfp345 |
A |
C |
2: 150,315,010 (GRCm39) |
Y176D |
probably benign |
Het |
Zfp598 |
T |
C |
17: 24,896,850 (GRCm39) |
F238S |
possibly damaging |
Het |
Zkscan17 |
T |
C |
11: 59,393,820 (GRCm39) |
D10G |
probably damaging |
Het |
Zmat4 |
T |
G |
8: 24,392,083 (GRCm39) |
M13R |
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 |
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 |
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 |
|