Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
T |
C |
14: 70,394,096 (GRCm39) |
|
probably benign |
Het |
Adam23 |
T |
C |
1: 63,573,515 (GRCm39) |
L261P |
probably benign |
Het |
Adgra3 |
G |
A |
5: 50,159,194 (GRCm39) |
|
probably benign |
Het |
Agtr1b |
A |
G |
3: 20,369,704 (GRCm39) |
F301L |
probably benign |
Het |
Ahnak2 |
G |
A |
12: 112,748,776 (GRCm39) |
T357I |
probably benign |
Het |
Aldh1a7 |
T |
C |
19: 20,704,430 (GRCm39) |
|
probably benign |
Het |
Apoh |
A |
T |
11: 108,302,899 (GRCm39) |
N288I |
probably damaging |
Het |
Arfgap3 |
A |
G |
15: 83,227,340 (GRCm39) |
V24A |
probably benign |
Het |
Atp6v0a1 |
A |
G |
11: 100,929,677 (GRCm39) |
|
probably null |
Het |
Axl |
A |
T |
7: 25,486,368 (GRCm39) |
M112K |
probably benign |
Het |
Bnc2 |
A |
C |
4: 84,211,169 (GRCm39) |
I425S |
probably damaging |
Het |
Ccn4 |
T |
C |
15: 66,789,194 (GRCm39) |
S227P |
possibly damaging |
Het |
Cdc42bpa |
C |
T |
1: 179,788,763 (GRCm39) |
T30M |
probably damaging |
Het |
Cebpz |
C |
A |
17: 79,227,317 (GRCm39) |
R1051M |
possibly damaging |
Het |
Ces1d |
A |
C |
8: 93,901,810 (GRCm39) |
|
probably benign |
Het |
Chd1l |
T |
C |
3: 97,494,465 (GRCm39) |
N405S |
probably benign |
Het |
Chodl |
G |
T |
16: 78,738,311 (GRCm39) |
G93V |
probably damaging |
Het |
Cpeb2 |
C |
T |
5: 43,395,743 (GRCm39) |
|
probably benign |
Het |
Crebbp |
A |
G |
16: 3,935,105 (GRCm39) |
|
probably benign |
Het |
Crybb3 |
T |
C |
5: 113,227,675 (GRCm39) |
T49A |
possibly damaging |
Het |
Ctps1 |
A |
G |
4: 120,418,722 (GRCm39) |
|
probably benign |
Het |
Cyp26b1 |
A |
G |
6: 84,551,497 (GRCm39) |
Y240H |
probably damaging |
Het |
Cyp2d11 |
A |
C |
15: 82,273,422 (GRCm39) |
V483G |
probably benign |
Het |
Dennd2b |
T |
C |
7: 109,155,545 (GRCm39) |
K402E |
probably benign |
Het |
Dnah14 |
A |
T |
1: 181,579,628 (GRCm39) |
N3054Y |
probably damaging |
Het |
Dspp |
A |
C |
5: 104,325,905 (GRCm39) |
D756A |
unknown |
Het |
Dst |
T |
C |
1: 34,309,984 (GRCm39) |
S1553P |
probably damaging |
Het |
Elp4 |
A |
G |
2: 105,622,559 (GRCm39) |
|
probably null |
Het |
Eml6 |
G |
T |
11: 29,832,088 (GRCm39) |
T194K |
probably benign |
Het |
Evi5 |
A |
G |
5: 107,943,638 (GRCm39) |
I569T |
probably benign |
Het |
Fancm |
C |
T |
12: 65,168,730 (GRCm39) |
P1698S |
possibly damaging |
Het |
Fhdc1 |
T |
C |
3: 84,352,852 (GRCm39) |
D791G |
probably benign |
Het |
Gpn3 |
A |
G |
5: 122,519,481 (GRCm39) |
Y196C |
probably benign |
Het |
Hcls1 |
A |
G |
16: 36,782,525 (GRCm39) |
D398G |
probably benign |
Het |
Hydin |
T |
C |
8: 111,189,163 (GRCm39) |
V1189A |
probably benign |
Het |
Itgb3 |
G |
A |
11: 104,534,789 (GRCm39) |
D549N |
probably damaging |
Het |
Itpr2 |
A |
G |
6: 146,141,951 (GRCm39) |
F1697S |
probably benign |
Het |
Klk1b11 |
A |
G |
7: 43,648,475 (GRCm39) |
T161A |
probably benign |
Het |
Kntc1 |
G |
A |
5: 123,903,120 (GRCm39) |
|
probably benign |
Het |
Map3k19 |
A |
T |
1: 127,750,837 (GRCm39) |
F838Y |
probably benign |
Het |
Map6 |
T |
A |
7: 98,985,187 (GRCm39) |
|
probably null |
Het |
Mcrs1 |
A |
G |
15: 99,142,608 (GRCm39) |
|
probably benign |
Het |
Mdn1 |
A |
T |
4: 32,729,956 (GRCm39) |
Y2766F |
probably damaging |
Het |
Med23 |
C |
T |
10: 24,776,686 (GRCm39) |
H739Y |
probably damaging |
Het |
Mmp17 |
T |
A |
5: 129,671,646 (GRCm39) |
D65E |
possibly damaging |
Het |
Mmp9 |
T |
A |
2: 164,793,177 (GRCm39) |
L442Q |
probably damaging |
Het |
Myo19 |
T |
C |
11: 84,779,001 (GRCm39) |
|
probably benign |
Het |
Nedd1 |
A |
C |
10: 92,527,791 (GRCm39) |
S468A |
possibly damaging |
Het |
Niban2 |
T |
A |
2: 32,813,833 (GRCm39) |
V682D |
probably benign |
Het |
Nlrp4d |
A |
C |
7: 10,116,316 (GRCm39) |
V152G |
probably damaging |
Het |
Nxf1 |
T |
A |
19: 8,740,170 (GRCm39) |
D112E |
probably benign |
Het |
Oas1h |
A |
T |
5: 121,000,626 (GRCm39) |
K79* |
probably null |
Het |
Omg |
T |
A |
11: 79,393,679 (GRCm39) |
I60F |
possibly damaging |
Het |
Or5p69 |
A |
G |
7: 107,967,576 (GRCm39) |
Y293C |
probably damaging |
Het |
Or8b101 |
A |
G |
9: 38,020,815 (GRCm39) |
T278A |
probably benign |
Het |
Or8b1b |
T |
A |
9: 38,375,757 (GRCm39) |
L140* |
probably null |
Het |
Pck1 |
G |
A |
2: 172,997,874 (GRCm39) |
W314* |
probably null |
Het |
Pla2g15 |
T |
C |
8: 106,889,756 (GRCm39) |
Y343H |
probably benign |
Het |
Plcb3 |
T |
C |
19: 6,936,276 (GRCm39) |
E749G |
probably damaging |
Het |
Plgrkt |
A |
G |
19: 29,328,442 (GRCm39) |
|
probably null |
Het |
Pprc1 |
A |
G |
19: 46,057,951 (GRCm39) |
|
probably benign |
Het |
Prkdc |
A |
T |
16: 15,516,871 (GRCm39) |
I1082F |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,516,701 (GRCm39) |
Y172* |
probably null |
Het |
Ros1 |
G |
T |
10: 52,001,885 (GRCm39) |
A1079D |
probably benign |
Het |
Sap30 |
T |
C |
8: 57,938,545 (GRCm39) |
E147G |
probably null |
Het |
Sell |
T |
C |
1: 163,899,674 (GRCm39) |
|
probably benign |
Het |
Senp1 |
A |
T |
15: 97,946,112 (GRCm39) |
D544E |
probably damaging |
Het |
Shpk |
G |
A |
11: 73,105,048 (GRCm39) |
|
probably benign |
Het |
Slc35b1 |
A |
T |
11: 95,277,353 (GRCm39) |
T74S |
probably benign |
Het |
Slc6a3 |
T |
A |
13: 73,718,098 (GRCm39) |
|
probably benign |
Het |
Slf1 |
T |
C |
13: 77,191,864 (GRCm39) |
N990S |
probably benign |
Het |
Smgc |
A |
G |
15: 91,738,746 (GRCm39) |
|
probably benign |
Het |
Snx19 |
T |
A |
9: 30,351,515 (GRCm39) |
V861D |
probably damaging |
Het |
Sprr2e |
C |
T |
3: 92,260,285 (GRCm39) |
P39S |
unknown |
Het |
Sstr2 |
T |
A |
11: 113,515,303 (GRCm39) |
M74K |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,099,937 (GRCm39) |
|
probably benign |
Het |
Tas2r143 |
A |
G |
6: 42,377,889 (GRCm39) |
I240V |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,563,937 (GRCm39) |
I233V |
probably benign |
Het |
Tecpr1 |
G |
T |
5: 144,134,717 (GRCm39) |
D1055E |
probably damaging |
Het |
Thap2 |
A |
T |
10: 115,212,277 (GRCm39) |
|
probably null |
Het |
Tinagl1 |
A |
G |
4: 130,060,101 (GRCm39) |
Y388H |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,585,896 (GRCm39) |
Y21945F |
probably damaging |
Het |
Ugt2b1 |
A |
T |
5: 87,073,961 (GRCm39) |
W133R |
probably benign |
Het |
Usp24 |
C |
T |
4: 106,254,496 (GRCm39) |
P1491L |
possibly damaging |
Het |
Utp15 |
A |
G |
13: 98,387,390 (GRCm39) |
S395P |
possibly damaging |
Het |
Vav1 |
T |
A |
17: 57,606,847 (GRCm39) |
L254Q |
probably damaging |
Het |
Vmn2r104 |
T |
C |
17: 20,250,069 (GRCm39) |
Y734C |
probably damaging |
Het |
Vps8 |
T |
A |
16: 21,288,904 (GRCm39) |
V421E |
probably benign |
Het |
Xkr7 |
G |
T |
2: 152,874,346 (GRCm39) |
A138S |
probably benign |
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 |
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 |
|
R9641:Frem1
|
UTSW |
4 |
82,877,653 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|