Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,771,885 (GRCm39) |
C456S |
probably damaging |
Het |
4930524J08Rik |
T |
C |
5: 100,127,068 (GRCm39) |
|
probably benign |
Het |
Adam28 |
T |
G |
14: 68,864,326 (GRCm39) |
R492S |
probably damaging |
Het |
Adarb2 |
G |
A |
13: 8,807,313 (GRCm39) |
A705T |
possibly damaging |
Het |
Adprhl1 |
T |
C |
8: 13,272,873 (GRCm39) |
D1295G |
probably benign |
Het |
Aldh3b3 |
A |
G |
19: 4,016,476 (GRCm39) |
I365V |
probably benign |
Het |
Aldh8a1 |
T |
C |
10: 21,264,996 (GRCm39) |
F208L |
possibly damaging |
Het |
Ap3b1 |
G |
A |
13: 94,664,673 (GRCm39) |
V871I |
unknown |
Het |
Apol7e |
A |
T |
15: 77,598,552 (GRCm39) |
R6* |
probably null |
Het |
Arfgap3 |
T |
C |
15: 83,191,150 (GRCm39) |
E456G |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,615,461 (GRCm39) |
L285P |
probably benign |
Het |
Arhgef7 |
T |
A |
8: 11,850,861 (GRCm39) |
C315S |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,490,513 (GRCm39) |
L829Q |
probably damaging |
Het |
Babam2 |
T |
A |
5: 31,888,393 (GRCm39) |
|
probably null |
Het |
Bptf |
C |
T |
11: 106,951,384 (GRCm39) |
R2185H |
probably damaging |
Het |
Brd9 |
A |
C |
13: 74,102,697 (GRCm39) |
M473L |
probably benign |
Het |
C7 |
T |
C |
15: 5,041,538 (GRCm39) |
H456R |
probably benign |
Het |
Cabp7 |
C |
A |
11: 4,688,856 (GRCm39) |
A205S |
probably damaging |
Het |
Catsperb |
A |
G |
12: 101,554,293 (GRCm39) |
I662M |
probably damaging |
Het |
Ccl21a |
T |
C |
4: 42,773,906 (GRCm39) |
M5V |
probably benign |
Het |
Cdyl |
G |
T |
13: 36,042,177 (GRCm39) |
R405L |
possibly damaging |
Het |
Cep89 |
T |
C |
7: 35,127,672 (GRCm39) |
L538P |
probably damaging |
Het |
Cercam |
A |
G |
2: 29,762,892 (GRCm39) |
M209V |
possibly damaging |
Het |
Chfr |
T |
A |
5: 110,310,571 (GRCm39) |
|
probably null |
Het |
Cntnap5c |
T |
A |
17: 58,717,226 (GRCm39) |
Y1269* |
probably null |
Het |
Col6a2 |
G |
T |
10: 76,439,170 (GRCm39) |
C833* |
probably null |
Het |
Cpeb3 |
T |
A |
19: 37,151,900 (GRCm39) |
I159F |
probably benign |
Het |
Cplx2 |
G |
A |
13: 54,526,663 (GRCm39) |
E24K |
possibly damaging |
Het |
Ctsb |
A |
G |
14: 63,379,752 (GRCm39) |
T332A |
probably benign |
Het |
Cyp2j12 |
T |
A |
4: 96,029,222 (GRCm39) |
T20S |
probably benign |
Het |
Dcst2 |
T |
A |
3: 89,273,993 (GRCm39) |
H181Q |
probably damaging |
Het |
Dnm1l |
T |
C |
16: 16,136,338 (GRCm39) |
I411V |
probably benign |
Het |
Dock5 |
T |
A |
14: 68,046,479 (GRCm39) |
I768F |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,077,334 (GRCm39) |
Y625H |
probably damaging |
Het |
Efl1 |
T |
G |
7: 82,330,587 (GRCm39) |
S253R |
probably damaging |
Het |
Elmod1 |
T |
A |
9: 53,820,127 (GRCm39) |
D287V |
probably damaging |
Het |
Fam171a2 |
T |
C |
11: 102,329,491 (GRCm39) |
S423G |
probably benign |
Het |
Fbxo8 |
A |
T |
8: 57,022,317 (GRCm39) |
|
probably null |
Het |
Flnc |
G |
T |
6: 29,455,470 (GRCm39) |
G2040W |
probably damaging |
Het |
Fras1 |
C |
T |
5: 96,821,458 (GRCm39) |
A1405V |
probably benign |
Het |
Fxr1 |
C |
T |
3: 34,103,369 (GRCm39) |
A233V |
probably damaging |
Het |
H1f9 |
A |
G |
11: 94,859,184 (GRCm39) |
R160G |
possibly damaging |
Het |
Helb |
A |
G |
10: 119,944,799 (GRCm39) |
F246L |
probably damaging |
Het |
Hoxb6 |
G |
T |
11: 96,183,510 (GRCm39) |
|
probably benign |
Het |
Hspa2 |
A |
G |
12: 76,452,884 (GRCm39) |
E526G |
probably damaging |
Het |
Hyal5 |
A |
T |
6: 24,875,983 (GRCm39) |
|
probably benign |
Het |
Ints6 |
A |
T |
14: 62,942,224 (GRCm39) |
V503E |
probably benign |
Het |
Ints9 |
C |
T |
14: 65,269,747 (GRCm39) |
T479I |
possibly damaging |
Het |
Jag1 |
C |
T |
2: 136,926,975 (GRCm39) |
R928H |
probably benign |
Het |
Lman2 |
A |
T |
13: 55,499,338 (GRCm39) |
I179N |
probably damaging |
Het |
Lta |
T |
C |
17: 35,422,805 (GRCm39) |
S173G |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,300,099 (GRCm39) |
P1645L |
probably damaging |
Het |
Mrc2 |
A |
T |
11: 105,183,609 (GRCm39) |
|
probably benign |
Het |
Muc4 |
T |
A |
16: 32,754,689 (GRCm38) |
M1521K |
probably benign |
Het |
Mucl3 |
T |
A |
17: 35,949,312 (GRCm39) |
T96S |
probably benign |
Het |
Mylk3 |
T |
G |
8: 86,081,873 (GRCm39) |
D438A |
probably benign |
Het |
Myo7a |
T |
A |
7: 97,700,833 (GRCm39) |
|
probably null |
Het |
Nsmce4a |
G |
T |
7: 130,135,547 (GRCm39) |
Q342K |
probably benign |
Het |
Or10ac1 |
A |
G |
6: 42,515,053 (GRCm39) |
I301T |
possibly damaging |
Het |
Or4c124 |
T |
A |
2: 89,156,423 (GRCm39) |
I34F |
probably benign |
Het |
Or5p60 |
A |
G |
7: 107,724,068 (GRCm39) |
L134P |
probably damaging |
Het |
Or6c65 |
A |
T |
10: 129,604,136 (GRCm39) |
Y257F |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,423,730 (GRCm39) |
F864L |
probably damaging |
Het |
Pla2g4a |
A |
G |
1: 149,808,438 (GRCm39) |
S2P |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,640,329 (GRCm39) |
L525P |
probably damaging |
Het |
Por |
A |
T |
5: 135,763,773 (GRCm39) |
M667L |
probably benign |
Het |
Psma4 |
T |
C |
9: 54,862,166 (GRCm39) |
Y97H |
probably benign |
Het |
Qtrt1 |
A |
T |
9: 21,323,753 (GRCm39) |
H126L |
probably benign |
Het |
Rab3a |
A |
T |
8: 71,209,170 (GRCm39) |
Y102F |
possibly damaging |
Het |
Rnf212 |
T |
A |
5: 108,879,555 (GRCm39) |
H87L |
probably benign |
Het |
Rnf216 |
A |
G |
5: 143,076,591 (GRCm39) |
S98P |
probably benign |
Het |
Ryr1 |
G |
T |
7: 28,785,295 (GRCm39) |
R1806S |
probably benign |
Het |
Scgb1b3 |
A |
T |
7: 31,075,262 (GRCm39) |
L37F |
probably benign |
Het |
Sds |
T |
C |
5: 120,617,254 (GRCm39) |
S37P |
probably damaging |
Het |
Senp6 |
A |
G |
9: 80,021,159 (GRCm39) |
R280G |
probably damaging |
Het |
She |
T |
A |
3: 89,761,864 (GRCm39) |
I441K |
possibly damaging |
Het |
Slc6a20b |
A |
G |
9: 123,436,682 (GRCm39) |
S244P |
possibly damaging |
Het |
Slc9a3 |
A |
T |
13: 74,299,004 (GRCm39) |
Y141F |
probably damaging |
Het |
Slco6c1 |
A |
T |
1: 97,009,207 (GRCm39) |
H426Q |
probably benign |
Het |
Smc2 |
C |
A |
4: 52,440,301 (GRCm39) |
Q16K |
probably benign |
Het |
Sphkap |
A |
C |
1: 83,241,547 (GRCm39) |
V1535G |
probably benign |
Het |
Stard9 |
C |
A |
2: 120,532,633 (GRCm39) |
N2963K |
probably benign |
Het |
Sycp2 |
C |
T |
2: 178,035,944 (GRCm39) |
A248T |
probably damaging |
Het |
Taar8a |
T |
C |
10: 23,952,762 (GRCm39) |
L122P |
probably damaging |
Het |
Tab1 |
T |
A |
15: 80,044,445 (GRCm39) |
V491E |
probably benign |
Het |
Tanc1 |
T |
C |
2: 59,636,688 (GRCm39) |
M857T |
probably benign |
Het |
Tcirg1 |
C |
A |
19: 3,949,008 (GRCm39) |
R427L |
possibly damaging |
Het |
Tmem109 |
A |
C |
19: 10,849,124 (GRCm39) |
*244G |
probably null |
Het |
Tox2 |
A |
G |
2: 163,163,435 (GRCm39) |
Y136C |
|
Het |
Tubb1 |
T |
C |
2: 174,298,825 (GRCm39) |
V169A |
possibly damaging |
Het |
Ubr3 |
T |
C |
2: 69,783,886 (GRCm39) |
|
probably null |
Het |
Vmn1r225 |
T |
A |
17: 20,723,059 (GRCm39) |
F167I |
probably benign |
Het |
Vmn2r65 |
A |
C |
7: 84,595,569 (GRCm39) |
W372G |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,727,537 (GRCm39) |
D188E |
probably damaging |
Het |
Vsnl1 |
G |
T |
12: 11,376,439 (GRCm39) |
Q149K |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,054,105 (GRCm39) |
N466S |
probably benign |
Het |
Ywhae |
T |
A |
11: 75,650,169 (GRCm39) |
S210R |
probably damaging |
Het |
Zfp28 |
T |
A |
7: 6,397,748 (GRCm39) |
S728T |
probably damaging |
Het |
Zfpm1 |
A |
G |
8: 123,063,698 (GRCm39) |
D919G |
unknown |
Het |
|
Other mutations in Frem3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Frem3
|
APN |
8 |
81,395,439 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01019:Frem3
|
APN |
8 |
81,341,763 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01470:Frem3
|
APN |
8 |
81,340,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Frem3
|
APN |
8 |
81,339,333 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01622:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01623:Frem3
|
APN |
8 |
81,340,544 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01751:Frem3
|
APN |
8 |
81,342,372 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02037:Frem3
|
APN |
8 |
81,338,118 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02039:Frem3
|
APN |
8 |
81,339,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Frem3
|
APN |
8 |
81,339,072 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02124:Frem3
|
APN |
8 |
81,339,723 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Frem3
|
APN |
8 |
81,340,736 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02836:Frem3
|
APN |
8 |
81,341,010 (GRCm39) |
missense |
probably benign |
|
IGL03090:Frem3
|
APN |
8 |
81,344,858 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03102:Frem3
|
APN |
8 |
81,339,661 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03116:Frem3
|
APN |
8 |
81,339,435 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03165:Frem3
|
APN |
8 |
81,339,158 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03224:Frem3
|
APN |
8 |
81,340,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Frem3
|
APN |
8 |
81,341,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03403:Frem3
|
APN |
8 |
81,337,719 (GRCm39) |
missense |
probably benign |
0.04 |
FR4340:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Frem3
|
UTSW |
8 |
81,341,870 (GRCm39) |
small insertion |
probably benign |
|
IGL02991:Frem3
|
UTSW |
8 |
81,395,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03052:Frem3
|
UTSW |
8 |
81,341,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Frem3
|
UTSW |
8 |
81,342,507 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0647:Frem3
|
UTSW |
8 |
81,341,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R0690:Frem3
|
UTSW |
8 |
81,340,581 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0766:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R0834:Frem3
|
UTSW |
8 |
81,413,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0909:Frem3
|
UTSW |
8 |
81,390,035 (GRCm39) |
missense |
probably benign |
0.45 |
R1033:Frem3
|
UTSW |
8 |
81,421,786 (GRCm39) |
missense |
probably benign |
0.00 |
R1144:Frem3
|
UTSW |
8 |
81,338,513 (GRCm39) |
missense |
probably benign |
0.01 |
R1312:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R1330:Frem3
|
UTSW |
8 |
81,395,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R1355:Frem3
|
UTSW |
8 |
81,417,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1390:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R1413:Frem3
|
UTSW |
8 |
81,395,430 (GRCm39) |
missense |
probably benign |
|
R1470:Frem3
|
UTSW |
8 |
81,337,820 (GRCm39) |
missense |
probably benign |
0.05 |
R1470:Frem3
|
UTSW |
8 |
81,337,820 (GRCm39) |
missense |
probably benign |
0.05 |
R1503:Frem3
|
UTSW |
8 |
81,413,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R1538:Frem3
|
UTSW |
8 |
81,339,764 (GRCm39) |
missense |
probably benign |
0.00 |
R1538:Frem3
|
UTSW |
8 |
81,339,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Frem3
|
UTSW |
8 |
81,341,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Frem3
|
UTSW |
8 |
81,339,741 (GRCm39) |
missense |
probably benign |
0.03 |
R1872:Frem3
|
UTSW |
8 |
81,339,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Frem3
|
UTSW |
8 |
81,338,567 (GRCm39) |
nonsense |
probably null |
|
R1886:Frem3
|
UTSW |
8 |
81,340,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Frem3
|
UTSW |
8 |
81,339,519 (GRCm39) |
missense |
probably benign |
0.00 |
R2027:Frem3
|
UTSW |
8 |
81,421,966 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2040:Frem3
|
UTSW |
8 |
81,342,455 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2050:Frem3
|
UTSW |
8 |
81,341,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Frem3
|
UTSW |
8 |
81,341,732 (GRCm39) |
missense |
probably benign |
0.03 |
R2099:Frem3
|
UTSW |
8 |
81,342,488 (GRCm39) |
missense |
probably benign |
0.06 |
R2120:Frem3
|
UTSW |
8 |
81,342,086 (GRCm39) |
missense |
probably benign |
0.20 |
R2842:Frem3
|
UTSW |
8 |
81,395,978 (GRCm39) |
splice site |
probably null |
|
R2845:Frem3
|
UTSW |
8 |
81,339,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R3015:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R3442:Frem3
|
UTSW |
8 |
81,339,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R3724:Frem3
|
UTSW |
8 |
81,341,900 (GRCm39) |
missense |
probably benign |
0.06 |
R3730:Frem3
|
UTSW |
8 |
81,342,545 (GRCm39) |
missense |
probably damaging |
0.99 |
R3939:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3940:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3941:Frem3
|
UTSW |
8 |
81,341,649 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4089:Frem3
|
UTSW |
8 |
81,341,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Frem3
|
UTSW |
8 |
81,340,770 (GRCm39) |
missense |
probably benign |
0.00 |
R4437:Frem3
|
UTSW |
8 |
81,339,236 (GRCm39) |
missense |
probably benign |
0.30 |
R4480:Frem3
|
UTSW |
8 |
81,337,986 (GRCm39) |
missense |
probably benign |
0.10 |
R4575:Frem3
|
UTSW |
8 |
81,342,704 (GRCm39) |
missense |
probably benign |
0.17 |
R4583:Frem3
|
UTSW |
8 |
81,340,143 (GRCm39) |
missense |
probably benign |
0.03 |
R4620:Frem3
|
UTSW |
8 |
81,395,586 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4621:Frem3
|
UTSW |
8 |
81,395,820 (GRCm39) |
splice site |
probably null |
|
R4644:Frem3
|
UTSW |
8 |
81,340,356 (GRCm39) |
missense |
probably benign |
0.33 |
R4667:Frem3
|
UTSW |
8 |
81,390,049 (GRCm39) |
missense |
probably damaging |
0.97 |
R4748:Frem3
|
UTSW |
8 |
81,338,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Frem3
|
UTSW |
8 |
81,340,587 (GRCm39) |
missense |
probably benign |
0.25 |
R4836:Frem3
|
UTSW |
8 |
81,390,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4867:Frem3
|
UTSW |
8 |
81,339,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Frem3
|
UTSW |
8 |
81,339,765 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5030:Frem3
|
UTSW |
8 |
81,339,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5035:Frem3
|
UTSW |
8 |
81,342,543 (GRCm39) |
missense |
probably damaging |
0.97 |
R5172:Frem3
|
UTSW |
8 |
81,339,195 (GRCm39) |
missense |
probably benign |
0.44 |
R5289:Frem3
|
UTSW |
8 |
81,338,948 (GRCm39) |
missense |
probably benign |
0.00 |
R5492:Frem3
|
UTSW |
8 |
81,339,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Frem3
|
UTSW |
8 |
81,339,323 (GRCm39) |
missense |
probably benign |
0.00 |
R5685:Frem3
|
UTSW |
8 |
81,421,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Frem3
|
UTSW |
8 |
81,340,026 (GRCm39) |
missense |
probably benign |
0.02 |
R5743:Frem3
|
UTSW |
8 |
81,342,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R5889:Frem3
|
UTSW |
8 |
81,340,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Frem3
|
UTSW |
8 |
81,340,062 (GRCm39) |
missense |
probably benign |
0.03 |
R6057:Frem3
|
UTSW |
8 |
81,342,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R6137:Frem3
|
UTSW |
8 |
81,341,676 (GRCm39) |
missense |
probably benign |
|
R6264:Frem3
|
UTSW |
8 |
81,341,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Frem3
|
UTSW |
8 |
81,339,644 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6418:Frem3
|
UTSW |
8 |
81,337,781 (GRCm39) |
missense |
probably benign |
0.08 |
R6680:Frem3
|
UTSW |
8 |
81,395,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6773:Frem3
|
UTSW |
8 |
81,338,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6928:Frem3
|
UTSW |
8 |
81,337,911 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6939:Frem3
|
UTSW |
8 |
81,341,774 (GRCm39) |
missense |
probably benign |
0.23 |
R6995:Frem3
|
UTSW |
8 |
81,339,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R7112:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Frem3
|
UTSW |
8 |
81,342,668 (GRCm39) |
missense |
probably benign |
0.01 |
R7235:Frem3
|
UTSW |
8 |
81,417,354 (GRCm39) |
missense |
probably benign |
0.00 |
R7282:Frem3
|
UTSW |
8 |
81,338,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R7403:Frem3
|
UTSW |
8 |
81,342,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Frem3
|
UTSW |
8 |
81,339,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Frem3
|
UTSW |
8 |
81,338,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R7858:Frem3
|
UTSW |
8 |
81,338,350 (GRCm39) |
nonsense |
probably null |
|
R7976:Frem3
|
UTSW |
8 |
81,338,231 (GRCm39) |
nonsense |
probably null |
|
R8171:Frem3
|
UTSW |
8 |
81,341,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8185:Frem3
|
UTSW |
8 |
81,338,933 (GRCm39) |
nonsense |
probably null |
|
R8306:Frem3
|
UTSW |
8 |
81,338,840 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8478:Frem3
|
UTSW |
8 |
81,338,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Frem3
|
UTSW |
8 |
81,339,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:Frem3
|
UTSW |
8 |
81,342,851 (GRCm39) |
missense |
probably benign |
0.02 |
R8794:Frem3
|
UTSW |
8 |
81,338,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R8806:Frem3
|
UTSW |
8 |
81,390,064 (GRCm39) |
missense |
probably benign |
0.30 |
R8833:Frem3
|
UTSW |
8 |
81,339,401 (GRCm39) |
missense |
probably benign |
0.29 |
R8879:Frem3
|
UTSW |
8 |
81,339,777 (GRCm39) |
missense |
probably damaging |
0.98 |
R8897:Frem3
|
UTSW |
8 |
81,339,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Frem3
|
UTSW |
8 |
81,395,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R9207:Frem3
|
UTSW |
8 |
81,340,071 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9277:Frem3
|
UTSW |
8 |
81,417,402 (GRCm39) |
missense |
probably damaging |
0.96 |
R9536:Frem3
|
UTSW |
8 |
81,342,048 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Frem3
|
UTSW |
8 |
81,341,951 (GRCm39) |
missense |
probably benign |
|
R9649:Frem3
|
UTSW |
8 |
81,341,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R9671:Frem3
|
UTSW |
8 |
81,339,134 (GRCm39) |
missense |
probably benign |
0.00 |
R9723:Frem3
|
UTSW |
8 |
81,341,352 (GRCm39) |
missense |
probably benign |
|
R9790:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
R9791:Frem3
|
UTSW |
8 |
81,339,890 (GRCm39) |
missense |
probably benign |
0.01 |
RF030:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF034:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
RF042:Frem3
|
UTSW |
8 |
81,341,867 (GRCm39) |
small insertion |
probably benign |
|
X0024:Frem3
|
UTSW |
8 |
81,339,710 (GRCm39) |
missense |
possibly damaging |
0.76 |
X0027:Frem3
|
UTSW |
8 |
81,339,017 (GRCm39) |
nonsense |
probably null |
|
Z1088:Frem3
|
UTSW |
8 |
81,342,055 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Frem3
|
UTSW |
8 |
81,342,060 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Frem3
|
UTSW |
8 |
81,338,132 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Frem3
|
UTSW |
8 |
81,342,758 (GRCm39) |
missense |
possibly damaging |
0.81 |
|