Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810037I17Rik |
G |
A |
3: 122,718,274 (GRCm39) |
A56T |
probably benign |
Het |
4930438A08Rik |
A |
T |
11: 58,178,296 (GRCm39) |
I119F |
|
Het |
Abca12 |
A |
T |
1: 71,332,599 (GRCm39) |
I1254N |
probably damaging |
Het |
Abcb11 |
G |
T |
2: 69,138,809 (GRCm39) |
Y157* |
probably null |
Het |
Adcy7 |
G |
A |
8: 89,044,675 (GRCm39) |
|
probably null |
Het |
Adnp |
A |
G |
2: 168,026,798 (GRCm39) |
Y166H |
probably damaging |
Het |
Adprhl1 |
A |
G |
8: 13,275,279 (GRCm39) |
V493A |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,611,685 (GRCm39) |
T562A |
probably benign |
Het |
Amotl1 |
T |
A |
9: 14,504,320 (GRCm39) |
N296I |
possibly damaging |
Het |
Ankar |
A |
G |
1: 72,713,210 (GRCm39) |
V693A |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,786,318 (GRCm39) |
V189A |
probably benign |
Het |
Bmp1 |
A |
G |
14: 70,757,338 (GRCm39) |
L47P |
probably benign |
Het |
Cacna2d4 |
A |
G |
6: 119,248,476 (GRCm39) |
D429G |
probably benign |
Het |
Cadps2 |
T |
A |
6: 23,688,927 (GRCm39) |
E127D |
probably benign |
Het |
Cd109 |
A |
T |
9: 78,577,042 (GRCm39) |
I580F |
possibly damaging |
Het |
Cdrt4 |
T |
A |
11: 62,842,124 (GRCm39) |
I2N |
unknown |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Chuk |
A |
T |
19: 44,095,789 (GRCm39) |
W15R |
probably damaging |
Het |
Cpvl |
C |
T |
6: 53,951,779 (GRCm39) |
M1I |
probably null |
Het |
Cyfip1 |
A |
G |
7: 55,549,758 (GRCm39) |
M642V |
probably damaging |
Het |
Dhh |
T |
A |
15: 98,795,757 (GRCm39) |
R133* |
probably null |
Het |
Dnmt3b |
G |
A |
2: 153,507,980 (GRCm39) |
V212M |
probably benign |
Het |
Dync2li1 |
A |
G |
17: 84,957,137 (GRCm39) |
S301G |
probably benign |
Het |
Epas1 |
A |
C |
17: 87,133,990 (GRCm39) |
I500L |
possibly damaging |
Het |
Ephb4 |
A |
T |
5: 137,352,824 (GRCm39) |
I136F |
possibly damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,320 (GRCm39) |
F18L |
unknown |
Het |
Gpld1 |
A |
T |
13: 25,136,900 (GRCm39) |
S73C |
probably damaging |
Het |
Hddc3 |
A |
G |
7: 79,993,328 (GRCm39) |
I52V |
probably benign |
Het |
Hmgcll1 |
A |
T |
9: 75,991,732 (GRCm39) |
T252S |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,243,843 (GRCm39) |
R164W |
probably damaging |
Het |
Jph2 |
A |
G |
2: 163,180,606 (GRCm39) |
V675A |
probably benign |
Het |
Kifap3 |
T |
C |
1: 163,689,666 (GRCm39) |
F550S |
probably benign |
Het |
Klk15 |
C |
T |
7: 43,587,790 (GRCm39) |
H73Y |
possibly damaging |
Het |
Kplce |
C |
T |
3: 92,775,951 (GRCm39) |
G244D |
probably benign |
Het |
L1td1 |
T |
C |
4: 98,625,932 (GRCm39) |
V643A |
possibly damaging |
Het |
L3mbtl3 |
C |
T |
10: 26,212,155 (GRCm39) |
M255I |
unknown |
Het |
Layn |
T |
A |
9: 50,968,837 (GRCm39) |
D302V |
probably damaging |
Het |
Lpcat4 |
A |
G |
2: 112,072,418 (GRCm39) |
I136V |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,382,807 (GRCm39) |
D3658V |
probably damaging |
Het |
Metap1d |
T |
C |
2: 71,352,900 (GRCm39) |
L243S |
possibly damaging |
Het |
Midn |
T |
A |
10: 79,990,275 (GRCm39) |
H315Q |
probably damaging |
Het |
Mtrex |
A |
T |
13: 113,050,888 (GRCm39) |
|
probably null |
Het |
Myb |
C |
T |
10: 21,030,612 (GRCm39) |
D62N |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,077,522 (GRCm39) |
S886P |
probably benign |
Het |
Nemf |
T |
C |
12: 69,388,093 (GRCm39) |
I396V |
probably damaging |
Het |
Nemp1 |
T |
G |
10: 127,525,227 (GRCm39) |
V127G |
possibly damaging |
Het |
Nkx3-1 |
C |
T |
14: 69,428,227 (GRCm39) |
T25M |
possibly damaging |
Het |
Nmral1 |
A |
C |
16: 4,531,631 (GRCm39) |
L208R |
probably damaging |
Het |
Nol6 |
A |
T |
4: 41,116,422 (GRCm39) |
I989N |
probably benign |
Het |
Or12e7 |
T |
A |
2: 87,287,907 (GRCm39) |
C133S |
possibly damaging |
Het |
Palld |
A |
T |
8: 62,173,571 (GRCm39) |
S363T |
probably damaging |
Het |
Pcdha11 |
A |
G |
18: 37,144,512 (GRCm39) |
D201G |
probably damaging |
Het |
Per2 |
A |
G |
1: 91,366,081 (GRCm39) |
C339R |
probably damaging |
Het |
Phactr4 |
T |
C |
4: 132,097,874 (GRCm39) |
T455A |
possibly damaging |
Het |
Phc2 |
T |
C |
4: 128,617,062 (GRCm39) |
I445T |
probably damaging |
Het |
Pmepa1 |
T |
C |
2: 173,117,962 (GRCm39) |
T6A |
probably benign |
Het |
Polr1a |
T |
C |
6: 71,931,755 (GRCm39) |
F945L |
probably damaging |
Het |
Ppp2r5e |
T |
A |
12: 75,640,063 (GRCm39) |
K13* |
probably null |
Het |
Ptafr |
T |
C |
4: 132,306,613 (GRCm39) |
M1T |
probably null |
Het |
Rbms1 |
G |
A |
2: 60,610,087 (GRCm39) |
P208S |
probably benign |
Het |
Scg3 |
T |
A |
9: 75,558,955 (GRCm39) |
I419F |
probably damaging |
Het |
Scn1a |
T |
C |
2: 66,130,099 (GRCm39) |
T219A |
probably benign |
Het |
Sec14l4 |
A |
G |
11: 3,989,977 (GRCm39) |
D92G |
probably damaging |
Het |
Senp3 |
G |
T |
11: 69,569,085 (GRCm39) |
Q359K |
probably damaging |
Het |
Sirt1 |
T |
C |
10: 63,172,857 (GRCm39) |
D142G |
probably damaging |
Het |
Skint2 |
T |
C |
4: 112,483,039 (GRCm39) |
M148T |
possibly damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,391 (GRCm39) |
M44K |
probably damaging |
Het |
Snai2 |
T |
A |
16: 14,524,792 (GRCm39) |
D99E |
probably damaging |
Het |
Spg7 |
A |
G |
8: 123,807,408 (GRCm39) |
K395E |
possibly damaging |
Het |
Sphk2 |
G |
A |
7: 45,360,337 (GRCm39) |
H556Y |
possibly damaging |
Het |
Supt6 |
A |
C |
11: 78,116,612 (GRCm39) |
F637L |
probably benign |
Het |
Tcam1 |
A |
G |
11: 106,177,292 (GRCm39) |
N428S |
probably damaging |
Het |
Tctn3 |
C |
T |
19: 40,596,692 (GRCm39) |
R276K |
probably benign |
Het |
Timm29 |
G |
A |
9: 21,504,656 (GRCm39) |
R108H |
probably damaging |
Het |
Tlr9 |
A |
T |
9: 106,102,752 (GRCm39) |
E681V |
possibly damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tns3 |
T |
C |
11: 8,400,094 (GRCm39) |
K1169E |
probably damaging |
Het |
Trim72 |
A |
C |
7: 127,608,315 (GRCm39) |
D271A |
possibly damaging |
Het |
Trpv4 |
A |
T |
5: 114,772,622 (GRCm39) |
D369E |
probably benign |
Het |
Ttn |
A |
G |
2: 76,583,192 (GRCm39) |
L22567P |
probably damaging |
Het |
Uimc1 |
G |
A |
13: 55,223,652 (GRCm39) |
P207S |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,165,448 (GRCm39) |
V781E |
probably damaging |
Het |
Upk3bl |
C |
T |
5: 136,086,076 (GRCm39) |
P4L |
unknown |
Het |
Vmn1r201 |
A |
G |
13: 22,659,670 (GRCm39) |
N295D |
probably benign |
Het |
Vmn2r69 |
A |
G |
7: 85,064,697 (GRCm39) |
I63T |
probably benign |
Het |
Zfyve28 |
T |
C |
5: 34,374,788 (GRCm39) |
T409A |
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 |
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 |
|
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 |
|