Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
G |
11: 110,202,236 (GRCm39) |
T390P |
possibly damaging |
Het |
Acss3 |
A |
T |
10: 106,859,563 (GRCm39) |
Y345* |
probably null |
Het |
Adam26b |
A |
T |
8: 43,973,764 (GRCm39) |
S413T |
probably benign |
Het |
Angpt2 |
T |
A |
8: 18,764,098 (GRCm39) |
Q148L |
probably damaging |
Het |
Ank3 |
T |
A |
10: 69,823,981 (GRCm39) |
Y883* |
probably null |
Het |
Ankrd52 |
A |
G |
10: 128,216,814 (GRCm39) |
K190E |
possibly damaging |
Het |
Anks1b |
A |
G |
10: 89,999,137 (GRCm39) |
R415G |
probably damaging |
Het |
Ano3 |
T |
A |
2: 110,715,264 (GRCm39) |
Q58L |
probably benign |
Het |
Aoc1l2 |
T |
A |
6: 48,907,486 (GRCm39) |
I162N |
probably damaging |
Het |
Arhgap39 |
A |
T |
15: 76,610,931 (GRCm39) |
M924K |
possibly damaging |
Het |
AU040320 |
A |
G |
4: 126,741,008 (GRCm39) |
M910V |
possibly damaging |
Het |
BC051019 |
T |
A |
7: 109,315,553 (GRCm39) |
H86L |
probably benign |
Het |
C1qbp |
G |
A |
11: 70,870,856 (GRCm39) |
Q151* |
probably null |
Het |
C4b |
G |
T |
17: 34,953,117 (GRCm39) |
D1069E |
probably benign |
Het |
Casp1 |
C |
T |
9: 5,303,020 (GRCm39) |
T158I |
probably benign |
Het |
Casq1 |
T |
C |
1: 172,044,404 (GRCm39) |
D141G |
probably damaging |
Het |
Ccdc33 |
T |
A |
9: 57,937,240 (GRCm39) |
E653V |
probably damaging |
Het |
Cd180 |
C |
T |
13: 102,839,330 (GRCm39) |
T71M |
probably damaging |
Het |
Cdk4 |
T |
C |
10: 126,900,570 (GRCm39) |
L112P |
probably damaging |
Het |
Celf2 |
A |
G |
2: 6,554,714 (GRCm39) |
F425S |
probably damaging |
Het |
Chrm3 |
A |
T |
13: 9,927,698 (GRCm39) |
V446E |
probably benign |
Het |
Chst9 |
A |
T |
18: 15,586,107 (GRCm39) |
L152H |
probably damaging |
Het |
Cib2 |
A |
G |
9: 54,457,087 (GRCm39) |
|
probably null |
Het |
Clec18a |
T |
C |
8: 111,798,717 (GRCm39) |
S366G |
probably damaging |
Het |
Crebbp |
A |
G |
16: 3,997,983 (GRCm39) |
F34L |
probably damaging |
Het |
Dapk1 |
AT |
A |
13: 60,870,919 (GRCm39) |
|
probably null |
Het |
Ddi1 |
T |
A |
9: 6,265,761 (GRCm39) |
M203L |
probably benign |
Het |
Ddx20 |
G |
T |
3: 105,590,485 (GRCm39) |
S270R |
probably benign |
Het |
Eddm13 |
A |
T |
7: 6,269,317 (GRCm39) |
K31* |
probably null |
Het |
Espnl |
A |
T |
1: 91,272,146 (GRCm39) |
E458V |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,909,780 (GRCm39) |
D2074G |
probably damaging |
Het |
Fcf1 |
A |
G |
12: 85,020,902 (GRCm39) |
T61A |
probably benign |
Het |
Fkbp15 |
T |
C |
4: 62,226,234 (GRCm39) |
R772G |
probably benign |
Het |
Flnb |
T |
C |
14: 7,905,661 (GRCm38) |
V1137A |
probably benign |
Het |
Fosb |
C |
A |
7: 19,043,313 (GRCm39) |
C15F |
probably damaging |
Het |
Gm3248 |
T |
C |
14: 5,945,831 (GRCm38) |
I28V |
probably damaging |
Het |
Gm4922 |
G |
T |
10: 18,659,916 (GRCm39) |
L269I |
possibly damaging |
Het |
Gucy2e |
G |
A |
11: 69,119,274 (GRCm39) |
R627W |
probably damaging |
Het |
Hephl1 |
T |
A |
9: 14,970,467 (GRCm39) |
E1009V |
probably damaging |
Het |
Hsf4 |
A |
T |
8: 105,997,237 (GRCm39) |
Q61L |
probably damaging |
Het |
Itgam |
T |
A |
7: 127,715,445 (GRCm39) |
N1046K |
probably benign |
Het |
Itgav |
G |
A |
2: 83,586,154 (GRCm39) |
C138Y |
probably damaging |
Het |
Itih4 |
A |
T |
14: 30,611,867 (GRCm39) |
Y157F |
probably damaging |
Het |
Kcnt2 |
C |
T |
1: 140,282,254 (GRCm39) |
R80C |
probably damaging |
Het |
Kdm4b |
G |
A |
17: 56,708,618 (GRCm39) |
V986M |
probably damaging |
Het |
Lamb3 |
T |
A |
1: 193,022,194 (GRCm39) |
V1014D |
probably damaging |
Het |
Lrrc74b |
G |
T |
16: 17,367,717 (GRCm39) |
N282K |
probably damaging |
Het |
Map3k20 |
T |
A |
2: 72,272,048 (GRCm39) |
H725Q |
probably benign |
Het |
Mink1 |
A |
G |
11: 70,489,867 (GRCm39) |
N81S |
probably damaging |
Het |
Mmp21 |
A |
G |
7: 133,276,759 (GRCm39) |
Y415H |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,466,873 (GRCm39) |
W1297R |
probably damaging |
Het |
Myh8 |
T |
C |
11: 67,170,789 (GRCm39) |
M95T |
probably damaging |
Het |
Myo7b |
A |
T |
18: 32,133,158 (GRCm39) |
|
probably null |
Het |
Nanog |
A |
G |
6: 122,684,874 (GRCm39) |
M20V |
probably benign |
Het |
Ncapd3 |
A |
G |
9: 26,963,146 (GRCm39) |
I484V |
probably benign |
Het |
Ndufa12 |
A |
T |
10: 94,056,620 (GRCm39) |
N116I |
probably benign |
Het |
Nedd4l |
A |
G |
18: 65,337,016 (GRCm39) |
I668V |
possibly damaging |
Het |
Nhsl3 |
C |
A |
4: 129,117,095 (GRCm39) |
R523L |
probably damaging |
Het |
Nobox |
T |
C |
6: 43,282,480 (GRCm39) |
D309G |
probably benign |
Het |
Npnt |
A |
G |
3: 132,596,523 (GRCm39) |
|
probably benign |
Het |
Nrxn1 |
A |
C |
17: 90,762,477 (GRCm39) |
Y2D |
possibly damaging |
Het |
Obox6 |
G |
T |
7: 15,568,502 (GRCm39) |
P125T |
possibly damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Or14j8 |
T |
C |
17: 38,263,633 (GRCm39) |
Y94C |
probably damaging |
Het |
Or2ag15 |
C |
G |
7: 106,340,998 (GRCm39) |
V48L |
probably benign |
Het |
Or4s2b |
T |
A |
2: 88,508,731 (GRCm39) |
N177K |
possibly damaging |
Het |
Or56a3 |
T |
C |
7: 104,735,844 (GRCm39) |
|
probably benign |
Het |
Or5ac20 |
A |
T |
16: 59,104,821 (GRCm39) |
V13D |
probably damaging |
Het |
Or5an10 |
A |
G |
19: 12,276,305 (GRCm39) |
Y64H |
possibly damaging |
Het |
Or8k32 |
T |
C |
2: 86,369,224 (GRCm39) |
T10A |
possibly damaging |
Het |
Osm |
A |
T |
11: 4,188,435 (GRCm39) |
M21L |
probably benign |
Het |
Otogl |
T |
A |
10: 107,657,894 (GRCm39) |
|
probably null |
Het |
Otud4 |
T |
G |
8: 80,393,402 (GRCm39) |
S493A |
possibly damaging |
Het |
Pars2 |
A |
G |
4: 106,508,308 (GRCm39) |
|
probably benign |
Het |
Phlda3 |
T |
A |
1: 135,694,557 (GRCm39) |
V124E |
possibly damaging |
Het |
Pias4 |
T |
C |
10: 80,993,326 (GRCm39) |
D199G |
probably damaging |
Het |
Pm20d1 |
T |
C |
1: 131,739,777 (GRCm39) |
L375P |
probably benign |
Het |
Pole2 |
T |
C |
12: 69,273,139 (GRCm39) |
I48V |
probably benign |
Het |
Prrc2c |
T |
C |
1: 162,538,050 (GRCm39) |
R527G |
unknown |
Het |
Rasgrf2 |
G |
T |
13: 92,136,135 (GRCm39) |
N592K |
probably damaging |
Het |
Rbm7 |
A |
G |
9: 48,406,474 (GRCm39) |
L26P |
probably damaging |
Het |
Rhag |
A |
G |
17: 41,142,181 (GRCm39) |
H208R |
probably benign |
Het |
Rnf17 |
A |
G |
14: 56,671,812 (GRCm39) |
E268G |
probably damaging |
Het |
Rnf220 |
A |
G |
4: 117,146,252 (GRCm39) |
V23A |
probably benign |
Het |
Rnf7 |
A |
T |
9: 96,360,472 (GRCm39) |
V55D |
probably damaging |
Het |
Sdr9c7 |
C |
A |
10: 127,739,448 (GRCm39) |
R188S |
possibly damaging |
Het |
Senp6 |
T |
A |
9: 79,997,140 (GRCm39) |
N51K |
probably benign |
Het |
Skint3 |
C |
A |
4: 112,113,095 (GRCm39) |
T235K |
possibly damaging |
Het |
Slc10a5 |
A |
G |
3: 10,400,096 (GRCm39) |
F188S |
probably damaging |
Het |
Slc41a1 |
G |
A |
1: 131,758,690 (GRCm39) |
G111R |
probably damaging |
Het |
Smarca1 |
T |
C |
X: 46,972,944 (GRCm39) |
D132G |
probably null |
Het |
Snrnp48 |
C |
T |
13: 38,405,299 (GRCm39) |
R299W |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,437,705 (GRCm39) |
G1413D |
probably benign |
Het |
Star |
T |
A |
8: 26,298,644 (GRCm39) |
H16Q |
probably damaging |
Het |
Strc |
T |
C |
2: 121,206,075 (GRCm39) |
D779G |
probably benign |
Het |
Sulf2 |
T |
C |
2: 165,931,215 (GRCm39) |
Y264C |
probably damaging |
Het |
Supt7l |
A |
G |
5: 31,680,248 (GRCm39) |
S6P |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,067,165 (GRCm39) |
D4289G |
probably benign |
Het |
Szrd1 |
A |
T |
4: 140,867,001 (GRCm39) |
|
probably null |
Het |
Tada1 |
T |
C |
1: 166,219,523 (GRCm39) |
V275A |
possibly damaging |
Het |
Tbr1 |
A |
T |
2: 61,641,932 (GRCm39) |
Y136F |
probably benign |
Het |
Tbx20 |
T |
A |
9: 24,637,010 (GRCm39) |
H359L |
probably benign |
Het |
Thbs4 |
G |
T |
13: 92,899,314 (GRCm39) |
D560E |
probably damaging |
Het |
Tnfsf14 |
T |
C |
17: 57,497,740 (GRCm39) |
H164R |
probably damaging |
Het |
Trmu |
T |
C |
15: 85,767,006 (GRCm39) |
S72P |
probably damaging |
Het |
Tsnaxip1 |
C |
A |
8: 106,560,155 (GRCm39) |
Q36K |
probably benign |
Het |
Ttc28 |
T |
A |
5: 111,372,083 (GRCm39) |
M844K |
possibly damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,579,201 (GRCm39) |
Y695C |
probably damaging |
Het |
Ugt1a10 |
T |
A |
1: 87,984,009 (GRCm39) |
M269K |
probably damaging |
Het |
Urb1 |
A |
T |
16: 90,566,443 (GRCm39) |
L1448* |
probably null |
Het |
Vmn2r124 |
A |
T |
17: 18,269,855 (GRCm39) |
H37L |
probably damaging |
Het |
Vmn2r44 |
T |
C |
7: 8,370,949 (GRCm39) |
N699S |
probably damaging |
Het |
Vps35 |
A |
T |
8: 86,005,486 (GRCm39) |
|
probably null |
Het |
Yipf1 |
G |
T |
4: 107,193,396 (GRCm39) |
|
probably null |
Het |
Zfp395 |
A |
G |
14: 65,623,990 (GRCm39) |
N153S |
possibly damaging |
Het |
Zfp395 |
A |
G |
14: 65,630,656 (GRCm39) |
D402G |
probably damaging |
Het |
Zfp652 |
T |
C |
11: 95,640,435 (GRCm39) |
V120A |
probably damaging |
Het |
Zp3r |
T |
C |
1: 130,510,629 (GRCm39) |
I364M |
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 |
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 |
|