Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,860,634 (GRCm39) |
|
probably benign |
Het |
Abi3 |
T |
C |
11: 95,724,460 (GRCm39) |
|
probably benign |
Het |
Adam2 |
T |
C |
14: 66,295,095 (GRCm39) |
N250S |
probably damaging |
Het |
Agbl4 |
T |
A |
4: 111,514,585 (GRCm39) |
I532K |
probably benign |
Het |
Agrn |
T |
G |
4: 156,258,910 (GRCm39) |
E905A |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,846,742 (GRCm39) |
|
probably benign |
Het |
Aifm2 |
A |
G |
10: 61,562,231 (GRCm39) |
N89S |
probably benign |
Het |
Arsj |
C |
T |
3: 126,231,833 (GRCm39) |
T193I |
probably damaging |
Het |
Ascc2 |
T |
A |
11: 4,632,933 (GRCm39) |
V702E |
probably damaging |
Het |
Avpr1b |
T |
C |
1: 131,528,019 (GRCm39) |
S181P |
probably damaging |
Het |
Bcl7a |
G |
A |
5: 123,490,003 (GRCm39) |
V56I |
possibly damaging |
Het |
Cd160 |
T |
A |
3: 96,713,102 (GRCm39) |
D54V |
probably damaging |
Het |
Celsr2 |
C |
A |
3: 108,322,293 (GRCm39) |
R173M |
probably damaging |
Het |
Cfap57 |
A |
G |
4: 118,426,924 (GRCm39) |
|
probably benign |
Het |
Cfap69 |
G |
A |
5: 5,713,951 (GRCm39) |
T27I |
probably damaging |
Het |
Chaf1b |
T |
C |
16: 93,696,905 (GRCm39) |
|
probably benign |
Het |
Cldn8 |
C |
T |
16: 88,359,527 (GRCm39) |
V133M |
probably damaging |
Het |
Col2a1 |
A |
T |
15: 97,878,073 (GRCm39) |
V954E |
unknown |
Het |
Col6a4 |
T |
C |
9: 105,905,386 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
T |
C |
9: 105,586,685 (GRCm39) |
M1779V |
probably benign |
Het |
Coq8b |
A |
G |
7: 26,941,674 (GRCm39) |
E253G |
probably benign |
Het |
Ctse |
T |
C |
1: 131,602,516 (GRCm39) |
|
probably benign |
Het |
Cyp2c29 |
T |
A |
19: 39,298,170 (GRCm39) |
N238K |
probably benign |
Het |
Dcaf1 |
T |
A |
9: 106,723,848 (GRCm39) |
|
probably benign |
Het |
Dcc |
A |
T |
18: 71,942,275 (GRCm39) |
|
probably benign |
Het |
Dkk1 |
A |
G |
19: 30,526,745 (GRCm39) |
F12S |
probably benign |
Het |
Dnah6 |
A |
G |
6: 73,106,457 (GRCm39) |
V1760A |
probably benign |
Het |
Fam117b |
G |
A |
1: 59,997,512 (GRCm39) |
S288N |
possibly damaging |
Het |
Fam216a |
A |
T |
5: 122,505,709 (GRCm39) |
M110K |
probably damaging |
Het |
Gab1 |
T |
A |
8: 81,526,745 (GRCm39) |
N118Y |
probably damaging |
Het |
Gda |
T |
A |
19: 21,387,251 (GRCm39) |
I251L |
probably benign |
Het |
Gli2 |
C |
A |
1: 118,772,190 (GRCm39) |
R505L |
probably damaging |
Het |
Gm5093 |
A |
T |
17: 46,750,664 (GRCm39) |
I121N |
possibly damaging |
Het |
Gpnmb |
C |
T |
6: 49,024,949 (GRCm39) |
S327L |
probably benign |
Het |
Gpr156 |
T |
A |
16: 37,812,503 (GRCm39) |
Y280N |
probably damaging |
Het |
Gria4 |
A |
G |
9: 4,427,071 (GRCm39) |
Y790H |
probably damaging |
Het |
Guf1 |
C |
A |
5: 69,723,695 (GRCm39) |
|
probably null |
Het |
H6pd |
T |
C |
4: 150,067,030 (GRCm39) |
E452G |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,294,120 (GRCm39) |
Y487* |
probably null |
Het |
Ifi30 |
T |
A |
8: 71,217,593 (GRCm39) |
|
probably benign |
Het |
Klf13 |
G |
A |
7: 63,587,819 (GRCm39) |
A159V |
possibly damaging |
Het |
Med11 |
T |
A |
11: 70,344,052 (GRCm39) |
M124K |
possibly damaging |
Het |
Myom3 |
A |
G |
4: 135,515,737 (GRCm39) |
|
probably benign |
Het |
Nat2 |
A |
T |
8: 67,954,456 (GRCm39) |
I189F |
probably damaging |
Het |
Nhlrc4 |
C |
G |
17: 26,162,658 (GRCm39) |
G30R |
probably damaging |
Het |
Nkx3-2 |
G |
A |
5: 41,919,470 (GRCm39) |
R173C |
probably damaging |
Het |
Nox3 |
T |
C |
17: 3,745,839 (GRCm39) |
N23S |
probably damaging |
Het |
Npr2 |
A |
T |
4: 43,646,991 (GRCm39) |
Y708F |
probably damaging |
Het |
Nsun2 |
A |
G |
13: 69,777,661 (GRCm39) |
N409S |
probably benign |
Het |
Nucb2 |
T |
C |
7: 116,135,086 (GRCm39) |
|
probably benign |
Het |
Or13a26 |
T |
C |
7: 140,284,700 (GRCm39) |
F179L |
possibly damaging |
Het |
Or5be3 |
A |
G |
2: 86,864,226 (GRCm39) |
F113S |
probably damaging |
Het |
Or8b12 |
T |
C |
9: 37,657,513 (GRCm39) |
F28L |
probably benign |
Het |
Orai2 |
A |
T |
5: 136,190,453 (GRCm39) |
V52D |
probably damaging |
Het |
Pcyox1 |
A |
T |
6: 86,371,424 (GRCm39) |
M154K |
probably damaging |
Het |
Pik3r4 |
C |
A |
9: 105,531,175 (GRCm39) |
T492K |
possibly damaging |
Het |
Pmpca |
T |
A |
2: 26,281,109 (GRCm39) |
Y150N |
probably damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,803,820 (GRCm39) |
S446R |
probably damaging |
Het |
Ptpdc1 |
A |
G |
13: 48,740,381 (GRCm39) |
I289T |
probably benign |
Het |
Pyroxd2 |
A |
G |
19: 42,716,081 (GRCm39) |
|
probably benign |
Het |
Qrfpr |
G |
A |
3: 36,243,708 (GRCm39) |
T131M |
probably damaging |
Het |
Rab33b |
A |
G |
3: 51,400,838 (GRCm39) |
Y104C |
probably damaging |
Het |
Rad54l |
G |
T |
4: 115,956,947 (GRCm39) |
|
probably benign |
Het |
Rad9a |
A |
T |
19: 4,247,359 (GRCm39) |
|
probably null |
Het |
Slc1a5 |
A |
T |
7: 16,520,829 (GRCm39) |
M233L |
probably benign |
Het |
Slc47a2 |
C |
T |
11: 61,233,330 (GRCm39) |
V67I |
possibly damaging |
Het |
Slco1a5 |
T |
A |
6: 142,214,004 (GRCm39) |
Y39F |
probably benign |
Het |
Slfn5 |
T |
C |
11: 82,852,229 (GRCm39) |
V785A |
probably damaging |
Het |
Sp6 |
C |
T |
11: 96,912,370 (GRCm39) |
P28S |
possibly damaging |
Het |
Sptbn5 |
A |
G |
2: 119,893,156 (GRCm39) |
|
probably null |
Het |
Sry |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
ACTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
Y: 2,662,944 (GRCm39) |
|
probably benign |
Het |
St8sia1 |
A |
G |
6: 142,774,980 (GRCm39) |
W200R |
probably damaging |
Het |
Stxbp1 |
C |
A |
2: 32,690,707 (GRCm39) |
|
probably benign |
Het |
Syne1 |
A |
G |
10: 4,983,138 (GRCm39) |
|
probably benign |
Het |
Thbs3 |
T |
A |
3: 89,127,472 (GRCm39) |
I371N |
possibly damaging |
Het |
Tll1 |
C |
T |
8: 64,527,324 (GRCm39) |
S399N |
probably damaging |
Het |
Tmem209 |
A |
C |
6: 30,505,833 (GRCm39) |
C114G |
probably null |
Het |
Tmem25 |
C |
T |
9: 44,706,811 (GRCm39) |
|
probably benign |
Het |
Tmem8b |
T |
C |
4: 43,674,562 (GRCm39) |
I282T |
possibly damaging |
Het |
Trdmt1 |
T |
A |
2: 13,549,391 (GRCm39) |
H18L |
probably benign |
Het |
Trim63 |
A |
G |
4: 134,043,716 (GRCm39) |
T60A |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,475,502 (GRCm39) |
|
probably null |
Het |
Ubr2 |
A |
T |
17: 47,249,579 (GRCm39) |
I1591K |
probably damaging |
Het |
Use1 |
A |
T |
8: 71,819,709 (GRCm39) |
|
probably benign |
Het |
Zfp850 |
A |
T |
7: 27,684,642 (GRCm39) |
C35S |
possibly damaging |
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 |
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 |
R7422:Frem3
|
UTSW |
8 |
81,342,392 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|