Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
C |
10: 100,430,498 (GRCm39) |
F52L |
possibly damaging |
Het |
Abca16 |
T |
C |
7: 120,126,308 (GRCm39) |
C1156R |
possibly damaging |
Het |
Abcg3 |
A |
C |
5: 105,084,483 (GRCm39) |
S571A |
probably benign |
Het |
Abi3 |
C |
A |
11: 95,724,503 (GRCm39) |
L259F |
unknown |
Het |
Adam19 |
A |
T |
11: 46,027,149 (GRCm39) |
D594V |
probably damaging |
Het |
Adam34 |
C |
T |
8: 44,104,076 (GRCm39) |
S523N |
probably damaging |
Het |
Adam6b |
G |
T |
12: 113,454,176 (GRCm39) |
C331F |
probably benign |
Het |
Adamts14 |
A |
T |
10: 61,106,829 (GRCm39) |
V97E |
probably damaging |
Het |
Adipor1 |
T |
C |
1: 134,355,878 (GRCm39) |
Y226H |
probably damaging |
Het |
Alox12e |
T |
C |
11: 70,212,261 (GRCm39) |
Y139C |
probably damaging |
Het |
Ankrd53 |
A |
G |
6: 83,740,692 (GRCm39) |
D160G |
possibly damaging |
Het |
Ap1m1 |
A |
T |
8: 73,003,606 (GRCm39) |
Y94F |
probably damaging |
Het |
Arhgef28 |
A |
C |
13: 98,078,983 (GRCm39) |
D1314E |
probably benign |
Het |
Bicc1 |
A |
G |
10: 70,863,772 (GRCm39) |
I90T |
probably benign |
Het |
Celf6 |
A |
G |
9: 59,485,833 (GRCm39) |
D58G |
probably damaging |
Het |
Cfap74 |
T |
C |
4: 155,549,054 (GRCm39) |
S38P |
unknown |
Het |
Cps1 |
A |
G |
1: 67,234,342 (GRCm39) |
I910V |
probably benign |
Het |
Cracdl |
C |
T |
1: 37,663,592 (GRCm39) |
A769T |
possibly damaging |
Het |
Crybg2 |
C |
T |
4: 133,816,620 (GRCm39) |
Q1353* |
probably null |
Het |
Cyp4f39 |
T |
C |
17: 32,705,982 (GRCm39) |
Y358H |
probably damaging |
Het |
Dcp1a |
T |
A |
14: 30,241,132 (GRCm39) |
I314N |
probably damaging |
Het |
Dgki |
A |
C |
6: 37,126,489 (GRCm39) |
W164G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,932,029 (GRCm39) |
I1466V |
probably benign |
Het |
Efcab6 |
T |
A |
15: 83,763,676 (GRCm39) |
R1219W |
probably damaging |
Het |
Faap24 |
A |
T |
7: 35,094,494 (GRCm39) |
F102Y |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,838,244 (GRCm39) |
T2667A |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,816,047 (GRCm39) |
T1347A |
probably benign |
Het |
Hipk3 |
A |
T |
2: 104,267,376 (GRCm39) |
H620Q |
probably benign |
Het |
Hpd |
A |
G |
5: 123,310,052 (GRCm39) |
S391P |
probably benign |
Het |
Ino80 |
A |
G |
2: 119,275,965 (GRCm39) |
V437A |
probably benign |
Het |
Itgax |
G |
T |
7: 127,741,152 (GRCm39) |
G785C |
probably damaging |
Het |
Kcnk18 |
C |
T |
19: 59,223,266 (GRCm39) |
T137I |
probably damaging |
Het |
Kif16b |
A |
G |
2: 142,542,589 (GRCm39) |
F236L |
probably benign |
Het |
Lamb1 |
T |
C |
12: 31,337,457 (GRCm39) |
M396T |
probably damaging |
Het |
Lrfn5 |
C |
A |
12: 61,886,540 (GRCm39) |
N109K |
probably damaging |
Het |
Lrrc15 |
T |
A |
16: 30,093,006 (GRCm39) |
N111I |
probably damaging |
Het |
Lrrk2 |
A |
T |
15: 91,671,251 (GRCm39) |
I2011F |
possibly damaging |
Het |
Lsr |
A |
G |
7: 30,658,285 (GRCm39) |
I336T |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,250,351 (GRCm39) |
R18S |
probably benign |
Het |
Mrpl22 |
T |
C |
11: 58,068,047 (GRCm39) |
L115P |
probably damaging |
Het |
N4bp2 |
T |
A |
5: 65,948,035 (GRCm39) |
S222T |
probably benign |
Het |
Nat2 |
A |
G |
8: 67,954,522 (GRCm39) |
T211A |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,350,247 (GRCm39) |
I2432N |
probably damaging |
Het |
Neb |
A |
G |
2: 52,112,783 (GRCm39) |
I1158T |
|
Het |
Nrip3 |
C |
T |
7: 109,362,793 (GRCm39) |
E164K |
probably damaging |
Het |
Obox6 |
G |
A |
7: 15,568,742 (GRCm39) |
Q45* |
probably null |
Het |
Ola1 |
T |
C |
2: 73,033,784 (GRCm39) |
N44D |
probably benign |
Het |
Or1x6 |
C |
T |
11: 50,939,207 (GRCm39) |
T91M |
probably benign |
Het |
Or2y1c |
T |
C |
11: 49,361,509 (GRCm39) |
F177S |
probably damaging |
Het |
Or5b111 |
A |
T |
19: 13,291,100 (GRCm39) |
M183K |
probably damaging |
Het |
Or5d39 |
A |
T |
2: 87,980,255 (GRCm39) |
I36N |
possibly damaging |
Het |
Or5p81 |
A |
T |
7: 108,267,516 (GRCm39) |
N298Y |
probably damaging |
Het |
Or6ae1 |
A |
G |
7: 139,742,771 (GRCm39) |
F31L |
probably benign |
Het |
Or8b51 |
T |
A |
9: 38,568,915 (GRCm39) |
M258L |
probably benign |
Het |
Pde10a |
A |
G |
17: 9,197,816 (GRCm39) |
K753R |
|
Het |
Phldb1 |
T |
C |
9: 44,627,839 (GRCm39) |
D202G |
probably damaging |
Het |
Pik3cb |
T |
C |
9: 98,955,789 (GRCm39) |
N376S |
probably benign |
Het |
Plekhh2 |
A |
G |
17: 84,874,130 (GRCm39) |
N472D |
probably damaging |
Het |
Ppp4r4 |
T |
A |
12: 103,567,811 (GRCm39) |
F708Y |
probably benign |
Het |
Rnf157 |
A |
G |
11: 116,303,576 (GRCm39) |
V12A |
probably benign |
Het |
Saa3 |
T |
C |
7: 46,364,494 (GRCm39) |
I11V |
probably benign |
Het |
Sall2 |
T |
C |
14: 52,550,882 (GRCm39) |
E771G |
probably damaging |
Het |
Sar1b |
C |
T |
11: 51,670,573 (GRCm39) |
T39I |
probably damaging |
Het |
Scn10a |
A |
T |
9: 119,445,869 (GRCm39) |
L1428Q |
possibly damaging |
Het |
Sema3f |
A |
G |
9: 107,565,454 (GRCm39) |
I213T |
unknown |
Het |
Serpina3m |
C |
T |
12: 104,360,085 (GRCm39) |
Q386* |
probably null |
Het |
Sh3gl3 |
G |
A |
7: 81,909,370 (GRCm39) |
G26R |
probably damaging |
Het |
Shq1 |
T |
C |
6: 100,550,633 (GRCm39) |
E435G |
probably damaging |
Het |
Sidt2 |
G |
T |
9: 45,864,495 (GRCm39) |
A78E |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,477,187 (GRCm39) |
Y818C |
probably damaging |
Het |
Smarca2 |
C |
T |
19: 26,656,498 (GRCm39) |
L825F |
possibly damaging |
Het |
Srgn |
T |
A |
10: 62,330,884 (GRCm39) |
M74L |
probably benign |
Het |
Tbc1d22b |
A |
C |
17: 29,813,747 (GRCm39) |
D360A |
possibly damaging |
Het |
Tbx4 |
A |
G |
11: 85,803,128 (GRCm39) |
R335G |
probably damaging |
Het |
Tmem144 |
T |
C |
3: 79,734,200 (GRCm39) |
N168D |
probably benign |
Het |
Trip11 |
G |
A |
12: 101,859,957 (GRCm39) |
Q307* |
probably null |
Het |
Ttyh2 |
T |
C |
11: 114,598,516 (GRCm39) |
Y296H |
probably damaging |
Het |
Vmn1r236 |
G |
T |
17: 21,507,043 (GRCm39) |
V54F |
probably benign |
Het |
Xrra1 |
A |
C |
7: 99,561,088 (GRCm39) |
H443P |
probably benign |
Het |
Zc3h12a |
T |
C |
4: 125,014,852 (GRCm39) |
T211A |
probably damaging |
Het |
Zfp386 |
T |
G |
12: 116,023,330 (GRCm39) |
D349E |
probably benign |
Het |
Zkscan16 |
T |
A |
4: 58,956,577 (GRCm39) |
H286Q |
probably benign |
Het |
Znrf2 |
C |
T |
6: 54,861,788 (GRCm39) |
P233L |
probably damaging |
Het |
|
Other mutations in Frem1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Frem1
|
APN |
4 |
82,877,626 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01069:Frem1
|
APN |
4 |
82,932,104 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01106:Frem1
|
APN |
4 |
82,840,494 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01398:Frem1
|
APN |
4 |
82,868,599 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01617:Frem1
|
APN |
4 |
82,854,376 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01647:Frem1
|
APN |
4 |
82,868,593 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01690:Frem1
|
APN |
4 |
82,877,533 (GRCm39) |
splice site |
probably benign |
|
IGL02006:Frem1
|
APN |
4 |
82,911,037 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02069:Frem1
|
APN |
4 |
82,821,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02131:Frem1
|
APN |
4 |
82,843,091 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02225:Frem1
|
APN |
4 |
82,858,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Frem1
|
APN |
4 |
82,874,582 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02567:Frem1
|
APN |
4 |
82,918,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02647:Frem1
|
APN |
4 |
82,919,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Frem1
|
APN |
4 |
82,877,571 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02831:Frem1
|
APN |
4 |
82,874,395 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02997:Frem1
|
APN |
4 |
82,853,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03005:Frem1
|
APN |
4 |
82,912,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03036:Frem1
|
APN |
4 |
82,877,576 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03193:Frem1
|
APN |
4 |
82,912,263 (GRCm39) |
splice site |
probably benign |
|
IGL03218:Frem1
|
APN |
4 |
82,832,883 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03235:Frem1
|
APN |
4 |
82,938,992 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03243:Frem1
|
APN |
4 |
82,932,206 (GRCm39) |
missense |
probably damaging |
1.00 |
bat
|
UTSW |
4 |
82,983,060 (GRCm38) |
intron |
probably benign |
|
blister
|
UTSW |
4 |
82,939,007 (GRCm39) |
missense |
probably benign |
0.28 |
boy
|
UTSW |
4 |
82,874,492 (GRCm39) |
missense |
probably benign |
0.16 |
Bubblie
|
UTSW |
4 |
82,888,870 (GRCm39) |
critical splice donor site |
probably null |
|
magicbear
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
major
|
UTSW |
4 |
82,907,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324_Frem1_643
|
UTSW |
4 |
82,901,574 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Frem1
|
UTSW |
4 |
82,924,045 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4466001:Frem1
|
UTSW |
4 |
82,890,374 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4472001:Frem1
|
UTSW |
4 |
82,890,374 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4515001:Frem1
|
UTSW |
4 |
82,818,663 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4531001:Frem1
|
UTSW |
4 |
82,868,517 (GRCm39) |
missense |
probably benign |
0.12 |
R0010:Frem1
|
UTSW |
4 |
82,918,335 (GRCm39) |
missense |
probably benign |
0.41 |
R0010:Frem1
|
UTSW |
4 |
82,918,335 (GRCm39) |
missense |
probably benign |
0.41 |
R0115:Frem1
|
UTSW |
4 |
82,854,406 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0125:Frem1
|
UTSW |
4 |
82,930,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0280:Frem1
|
UTSW |
4 |
82,887,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Frem1
|
UTSW |
4 |
82,830,874 (GRCm39) |
missense |
probably benign |
0.26 |
R0519:Frem1
|
UTSW |
4 |
82,888,870 (GRCm39) |
critical splice donor site |
probably null |
|
R0631:Frem1
|
UTSW |
4 |
82,890,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Frem1
|
UTSW |
4 |
82,907,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Frem1
|
UTSW |
4 |
82,868,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1110:Frem1
|
UTSW |
4 |
82,868,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1115:Frem1
|
UTSW |
4 |
82,939,007 (GRCm39) |
missense |
probably benign |
0.28 |
R1130:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably null |
|
R1173:Frem1
|
UTSW |
4 |
82,868,589 (GRCm39) |
missense |
probably benign |
0.16 |
R1349:Frem1
|
UTSW |
4 |
82,840,542 (GRCm39) |
splice site |
probably benign |
|
R1464:Frem1
|
UTSW |
4 |
82,930,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Frem1
|
UTSW |
4 |
82,930,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Frem1
|
UTSW |
4 |
82,920,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Frem1
|
UTSW |
4 |
82,917,128 (GRCm39) |
missense |
probably benign |
0.09 |
R1831:Frem1
|
UTSW |
4 |
82,939,074 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1851:Frem1
|
UTSW |
4 |
82,868,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R2014:Frem1
|
UTSW |
4 |
82,924,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2022:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2023:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2183:Frem1
|
UTSW |
4 |
82,909,732 (GRCm39) |
missense |
probably benign |
0.00 |
R2437:Frem1
|
UTSW |
4 |
82,918,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R2520:Frem1
|
UTSW |
4 |
82,868,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R3195:Frem1
|
UTSW |
4 |
82,932,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R3196:Frem1
|
UTSW |
4 |
82,932,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R3408:Frem1
|
UTSW |
4 |
82,930,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Frem1
|
UTSW |
4 |
82,881,416 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3742:Frem1
|
UTSW |
4 |
82,930,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Frem1
|
UTSW |
4 |
82,917,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Frem1
|
UTSW |
4 |
82,831,844 (GRCm39) |
missense |
probably benign |
0.41 |
R4329:Frem1
|
UTSW |
4 |
82,904,774 (GRCm39) |
missense |
probably benign |
0.01 |
R4364:Frem1
|
UTSW |
4 |
82,831,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4411:Frem1
|
UTSW |
4 |
82,881,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Frem1
|
UTSW |
4 |
82,907,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Frem1
|
UTSW |
4 |
82,938,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Frem1
|
UTSW |
4 |
82,907,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably benign |
|
R4802:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably benign |
|
R4854:Frem1
|
UTSW |
4 |
82,834,995 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4872:Frem1
|
UTSW |
4 |
82,881,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Frem1
|
UTSW |
4 |
82,884,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R5007:Frem1
|
UTSW |
4 |
82,859,049 (GRCm39) |
intron |
probably benign |
|
R5103:Frem1
|
UTSW |
4 |
82,909,849 (GRCm39) |
missense |
probably benign |
|
R5369:Frem1
|
UTSW |
4 |
82,919,976 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5494:Frem1
|
UTSW |
4 |
82,858,990 (GRCm39) |
makesense |
probably null |
|
R5694:Frem1
|
UTSW |
4 |
82,912,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Frem1
|
UTSW |
4 |
82,868,652 (GRCm39) |
missense |
probably benign |
0.12 |
R5813:Frem1
|
UTSW |
4 |
82,918,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Frem1
|
UTSW |
4 |
82,854,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Frem1
|
UTSW |
4 |
82,920,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R5985:Frem1
|
UTSW |
4 |
82,884,287 (GRCm39) |
missense |
probably benign |
|
R6091:Frem1
|
UTSW |
4 |
82,818,796 (GRCm39) |
missense |
probably benign |
0.01 |
R6165:Frem1
|
UTSW |
4 |
82,874,492 (GRCm39) |
missense |
probably benign |
0.16 |
R6324:Frem1
|
UTSW |
4 |
82,901,574 (GRCm39) |
missense |
probably benign |
0.00 |
R6369:Frem1
|
UTSW |
4 |
82,832,029 (GRCm39) |
splice site |
probably null |
|
R6414:Frem1
|
UTSW |
4 |
82,858,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R6421:Frem1
|
UTSW |
4 |
82,912,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Frem1
|
UTSW |
4 |
82,884,253 (GRCm39) |
missense |
probably benign |
0.03 |
R6453:Frem1
|
UTSW |
4 |
82,833,062 (GRCm39) |
nonsense |
probably null |
|
R6598:Frem1
|
UTSW |
4 |
82,932,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R6720:Frem1
|
UTSW |
4 |
82,932,069 (GRCm39) |
missense |
probably damaging |
0.98 |
R6862:Frem1
|
UTSW |
4 |
82,930,251 (GRCm39) |
nonsense |
probably null |
|
R6922:Frem1
|
UTSW |
4 |
82,840,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R6931:Frem1
|
UTSW |
4 |
82,888,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Frem1
|
UTSW |
4 |
82,858,599 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6995:Frem1
|
UTSW |
4 |
82,904,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:Frem1
|
UTSW |
4 |
82,904,798 (GRCm39) |
missense |
probably benign |
0.44 |
R7104:Frem1
|
UTSW |
4 |
82,858,918 (GRCm39) |
missense |
probably benign |
0.30 |
R7146:Frem1
|
UTSW |
4 |
82,840,532 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7174:Frem1
|
UTSW |
4 |
82,840,493 (GRCm39) |
missense |
probably benign |
0.00 |
R7327:Frem1
|
UTSW |
4 |
82,938,992 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7343:Frem1
|
UTSW |
4 |
82,912,359 (GRCm39) |
missense |
probably damaging |
0.99 |
R7368:Frem1
|
UTSW |
4 |
82,884,381 (GRCm39) |
missense |
probably benign |
0.19 |
R7392:Frem1
|
UTSW |
4 |
82,932,064 (GRCm39) |
missense |
probably benign |
0.06 |
R7465:Frem1
|
UTSW |
4 |
82,833,072 (GRCm39) |
missense |
probably benign |
0.11 |
R7499:Frem1
|
UTSW |
4 |
82,924,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7536:Frem1
|
UTSW |
4 |
82,874,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7752:Frem1
|
UTSW |
4 |
82,877,614 (GRCm39) |
missense |
probably benign |
0.02 |
R7753:Frem1
|
UTSW |
4 |
82,832,217 (GRCm39) |
missense |
probably benign |
0.03 |
R7790:Frem1
|
UTSW |
4 |
82,907,401 (GRCm39) |
missense |
probably benign |
0.02 |
R7818:Frem1
|
UTSW |
4 |
82,932,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Frem1
|
UTSW |
4 |
82,932,049 (GRCm39) |
critical splice donor site |
probably null |
|
R7878:Frem1
|
UTSW |
4 |
82,938,917 (GRCm39) |
missense |
probably benign |
0.00 |
R7886:Frem1
|
UTSW |
4 |
82,934,643 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7901:Frem1
|
UTSW |
4 |
82,877,614 (GRCm39) |
missense |
probably benign |
0.02 |
R7976:Frem1
|
UTSW |
4 |
82,919,946 (GRCm39) |
missense |
probably damaging |
0.97 |
R8240:Frem1
|
UTSW |
4 |
82,874,485 (GRCm39) |
missense |
probably benign |
0.21 |
R8305:Frem1
|
UTSW |
4 |
82,918,226 (GRCm39) |
missense |
probably benign |
0.06 |
R8415:Frem1
|
UTSW |
4 |
82,918,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Frem1
|
UTSW |
4 |
82,889,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8819:Frem1
|
UTSW |
4 |
82,821,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8820:Frem1
|
UTSW |
4 |
82,821,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8829:Frem1
|
UTSW |
4 |
82,918,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Frem1
|
UTSW |
4 |
82,922,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Frem1
|
UTSW |
4 |
82,922,280 (GRCm39) |
intron |
probably benign |
|
R8910:Frem1
|
UTSW |
4 |
82,868,694 (GRCm39) |
missense |
probably benign |
0.09 |
R9036:Frem1
|
UTSW |
4 |
82,831,785 (GRCm39) |
missense |
probably benign |
|
R9228:Frem1
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Frem1
|
UTSW |
4 |
82,901,622 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9441:Frem1
|
UTSW |
4 |
82,924,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Frem1
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Frem1
|
UTSW |
4 |
82,901,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R9640:Frem1
|
UTSW |
4 |
82,831,896 (GRCm39) |
missense |
probably benign |
|
X0013:Frem1
|
UTSW |
4 |
82,833,045 (GRCm39) |
missense |
probably benign |
0.38 |
X0017:Frem1
|
UTSW |
4 |
82,909,870 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1088:Frem1
|
UTSW |
4 |
82,890,504 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Frem1
|
UTSW |
4 |
82,918,220 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Frem1
|
UTSW |
4 |
82,918,506 (GRCm39) |
missense |
probably benign |
0.39 |
Z1177:Frem1
|
UTSW |
4 |
82,858,552 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Frem1
|
UTSW |
4 |
82,934,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|