Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
G |
A |
13: 119,606,631 (GRCm39) |
R291K |
probably benign |
Het |
Abca2 |
T |
C |
2: 25,332,857 (GRCm39) |
S1519P |
probably damaging |
Het |
Abcb11 |
G |
A |
2: 69,087,639 (GRCm39) |
A1042V |
probably damaging |
Het |
Abcc10 |
A |
T |
17: 46,623,845 (GRCm39) |
|
probably null |
Het |
Abcc10 |
G |
T |
17: 46,623,846 (GRCm39) |
|
probably benign |
Het |
Alkbh3 |
A |
C |
2: 93,811,914 (GRCm39) |
L240V |
probably damaging |
Het |
Apol10b |
T |
C |
15: 77,469,608 (GRCm39) |
S190G |
probably benign |
Het |
Atp1a3 |
C |
A |
7: 24,698,392 (GRCm39) |
C135F |
probably benign |
Het |
Atp4a |
C |
G |
7: 30,419,526 (GRCm39) |
R659G |
probably benign |
Het |
Bicra |
A |
G |
7: 15,722,687 (GRCm39) |
S277P |
possibly damaging |
Het |
Bltp1 |
A |
T |
3: 37,043,953 (GRCm39) |
H2820L |
possibly damaging |
Het |
Bmp8a |
T |
C |
4: 123,210,690 (GRCm39) |
E275G |
probably benign |
Het |
Ccdc102a |
T |
C |
8: 95,640,054 (GRCm39) |
E80G |
probably damaging |
Het |
Cdh23 |
T |
C |
10: 60,246,576 (GRCm39) |
D954G |
probably damaging |
Het |
Chrm4 |
A |
G |
2: 91,758,788 (GRCm39) |
T399A |
possibly damaging |
Het |
Clcn3 |
A |
G |
8: 61,387,571 (GRCm39) |
V199A |
possibly damaging |
Het |
Crlf1 |
T |
C |
8: 70,952,164 (GRCm39) |
|
probably null |
Het |
Crx |
G |
T |
7: 15,605,071 (GRCm39) |
S57* |
probably null |
Het |
Cstpp1 |
A |
G |
2: 91,252,298 (GRCm39) |
L21P |
probably damaging |
Het |
Cyp4f16 |
A |
G |
17: 32,756,072 (GRCm39) |
I34V |
possibly damaging |
Het |
Daxx |
T |
C |
17: 34,132,598 (GRCm39) |
V576A |
probably benign |
Het |
Ddx17 |
C |
T |
15: 79,421,672 (GRCm39) |
R351H |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 110,285,261 (GRCm39) |
|
probably benign |
Het |
Dnd1 |
T |
C |
18: 36,897,552 (GRCm39) |
|
probably benign |
Het |
Dync1i2 |
A |
T |
2: 71,058,169 (GRCm39) |
|
probably null |
Het |
E2f6 |
T |
C |
12: 16,866,446 (GRCm39) |
S52P |
probably benign |
Het |
Epb41l4a |
A |
G |
18: 34,013,326 (GRCm39) |
F116S |
probably damaging |
Het |
Ext1 |
T |
C |
15: 52,969,502 (GRCm39) |
N362S |
probably damaging |
Het |
Fam227a |
C |
A |
15: 79,528,189 (GRCm39) |
K79N |
possibly damaging |
Het |
Fam228a |
T |
A |
12: 4,782,759 (GRCm39) |
L111F |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,173,625 (GRCm39) |
T2363A |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,228 (GRCm39) |
N2591K |
probably damaging |
Het |
Frmd4b |
A |
T |
6: 97,400,424 (GRCm39) |
V29D |
probably damaging |
Het |
G930045G22Rik |
A |
G |
6: 50,823,918 (GRCm39) |
|
noncoding transcript |
Het |
Galnt3 |
A |
G |
2: 65,937,573 (GRCm39) |
S46P |
possibly damaging |
Het |
Gmeb2 |
A |
G |
2: 180,895,766 (GRCm39) |
V468A |
possibly damaging |
Het |
Herc2 |
C |
T |
7: 55,869,563 (GRCm39) |
R4271* |
probably null |
Het |
Il5 |
C |
A |
11: 53,614,733 (GRCm39) |
|
probably benign |
Het |
Ints9 |
G |
A |
14: 65,223,818 (GRCm39) |
|
probably benign |
Het |
Itga10 |
T |
C |
3: 96,556,453 (GRCm39) |
F196S |
probably damaging |
Het |
Itgb3bp |
T |
C |
4: 99,670,126 (GRCm39) |
T138A |
probably damaging |
Het |
Kcnd1 |
G |
A |
X: 7,690,922 (GRCm39) |
V281M |
probably benign |
Het |
Lcp2 |
T |
C |
11: 34,037,229 (GRCm39) |
L391P |
probably benign |
Het |
Lrrc66 |
T |
C |
5: 73,765,030 (GRCm39) |
Y671C |
probably benign |
Het |
Mettl23 |
T |
C |
11: 116,740,120 (GRCm39) |
V197A |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 96,097,400 (GRCm39) |
D456E |
probably benign |
Het |
Mospd4 |
T |
C |
18: 46,598,848 (GRCm39) |
|
noncoding transcript |
Het |
Mov10l1 |
C |
A |
15: 88,889,515 (GRCm39) |
H484N |
probably damaging |
Het |
Mphosph9 |
T |
C |
5: 124,453,631 (GRCm39) |
Q197R |
probably benign |
Het |
Ms4a1 |
T |
A |
19: 11,233,933 (GRCm39) |
|
probably null |
Het |
Mybbp1a |
T |
C |
11: 72,339,674 (GRCm39) |
V919A |
possibly damaging |
Het |
Mycbpap |
A |
T |
11: 94,404,338 (GRCm39) |
|
probably benign |
Het |
Naip6 |
G |
A |
13: 100,433,432 (GRCm39) |
S1135F |
possibly damaging |
Het |
Ndufc2 |
T |
A |
7: 97,049,544 (GRCm39) |
M50K |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,648,082 (GRCm39) |
V842A |
probably damaging |
Het |
Ntsr2 |
G |
T |
12: 16,703,696 (GRCm39) |
G66W |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,885,914 (GRCm39) |
|
probably benign |
Het |
Optn |
C |
T |
2: 5,028,926 (GRCm39) |
G526R |
probably damaging |
Het |
Or4c11 |
T |
A |
2: 88,695,229 (GRCm39) |
N93K |
probably benign |
Het |
Or4c114 |
T |
A |
2: 88,904,956 (GRCm39) |
I160F |
probably benign |
Het |
Or6c33 |
T |
C |
10: 129,853,965 (GRCm39) |
V245A |
probably damaging |
Het |
Or6k14 |
G |
A |
1: 173,927,965 (GRCm39) |
G314R |
probably benign |
Het |
Otud4 |
T |
A |
8: 80,396,626 (GRCm39) |
H628Q |
probably benign |
Het |
Padi6 |
T |
C |
4: 140,456,240 (GRCm39) |
T585A |
probably benign |
Het |
Pex16 |
G |
T |
2: 92,205,937 (GRCm39) |
R10L |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,269,152 (GRCm39) |
|
probably benign |
Het |
Pom121l2 |
A |
G |
13: 22,167,375 (GRCm39) |
T549A |
possibly damaging |
Het |
Prdm15 |
A |
T |
16: 97,613,759 (GRCm39) |
M470K |
probably benign |
Het |
Prkag2 |
T |
A |
5: 25,233,503 (GRCm39) |
D49V |
possibly damaging |
Het |
Prl3c1 |
A |
G |
13: 27,383,447 (GRCm39) |
M38V |
probably benign |
Het |
Prpf18 |
T |
A |
2: 4,648,572 (GRCm39) |
I85F |
possibly damaging |
Het |
Psg27 |
A |
G |
7: 18,294,636 (GRCm39) |
|
probably benign |
Het |
Relt |
A |
G |
7: 100,497,991 (GRCm39) |
|
probably benign |
Het |
Rskr |
T |
C |
11: 78,182,362 (GRCm39) |
L57P |
probably benign |
Het |
Serpina3b |
A |
T |
12: 104,096,929 (GRCm39) |
N70I |
probably damaging |
Het |
Slc19a3 |
T |
C |
1: 83,000,286 (GRCm39) |
S244G |
probably benign |
Het |
Slc39a5 |
T |
C |
10: 128,235,716 (GRCm39) |
T81A |
possibly damaging |
Het |
Slc7a2 |
G |
A |
8: 41,357,563 (GRCm39) |
G277D |
probably damaging |
Het |
Slc9c1 |
C |
T |
16: 45,420,250 (GRCm39) |
|
probably benign |
Het |
Slx1b |
A |
G |
7: 126,291,753 (GRCm39) |
F104L |
probably benign |
Het |
Smg6 |
G |
A |
11: 74,820,527 (GRCm39) |
S266N |
probably damaging |
Het |
Spata9 |
T |
C |
13: 76,146,614 (GRCm39) |
V162A |
possibly damaging |
Het |
Szrd1 |
T |
C |
4: 140,846,055 (GRCm39) |
I47V |
probably benign |
Het |
Tha1 |
G |
T |
11: 117,759,401 (GRCm39) |
L363M |
probably benign |
Het |
Tmc6 |
G |
A |
11: 117,669,087 (GRCm39) |
T89I |
possibly damaging |
Het |
Tmem132d |
C |
T |
5: 127,866,849 (GRCm39) |
G684R |
probably damaging |
Het |
Trim55 |
G |
A |
3: 19,725,142 (GRCm39) |
G220S |
probably benign |
Het |
Ttn |
A |
G |
2: 76,600,874 (GRCm39) |
L18836P |
probably damaging |
Het |
Ubn1 |
G |
T |
16: 4,890,048 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,643,228 (GRCm39) |
W4197G |
probably benign |
Het |
Vmn1r189 |
A |
T |
13: 22,286,231 (GRCm39) |
V202E |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,990,526 (GRCm39) |
I55V |
probably benign |
Het |
Vmn2r86 |
A |
T |
10: 130,282,412 (GRCm39) |
C735S |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,543,281 (GRCm39) |
D174V |
probably damaging |
Het |
Zfp438 |
T |
C |
18: 5,214,910 (GRCm39) |
N16S |
probably damaging |
Het |
Zfp444 |
C |
T |
7: 6,192,408 (GRCm39) |
T142I |
probably benign |
Het |
Zfp804a |
A |
G |
2: 81,884,135 (GRCm39) |
M1V |
probably null |
Het |
Zfp936 |
T |
G |
7: 42,838,734 (GRCm39) |
I67S |
probably benign |
Het |
Zfp948 |
A |
T |
17: 21,807,260 (GRCm39) |
N151Y |
unknown |
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 |
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 |
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 |
|