Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
C |
5: 8,748,604 (GRCm39) |
Y312H |
probably damaging |
Het |
Abcc10 |
A |
T |
17: 46,633,185 (GRCm39) |
I549N |
probably damaging |
Het |
Agpat2 |
A |
G |
2: 26,486,395 (GRCm39) |
Y134H |
probably damaging |
Het |
Alms1 |
A |
G |
6: 85,596,425 (GRCm39) |
D417G |
probably benign |
Het |
Apol11b |
T |
A |
15: 77,519,475 (GRCm39) |
I202F |
probably benign |
Het |
Arap1 |
C |
A |
7: 101,037,376 (GRCm39) |
Q468K |
probably benign |
Het |
Arhgef4 |
T |
C |
1: 34,832,445 (GRCm39) |
|
probably null |
Het |
Asap3 |
A |
T |
4: 135,961,914 (GRCm39) |
N285I |
probably damaging |
Het |
Aspm |
A |
T |
1: 139,408,375 (GRCm39) |
I2421F |
probably damaging |
Het |
Banp |
C |
A |
8: 122,701,285 (GRCm39) |
D17E |
probably benign |
Het |
Bsx |
T |
G |
9: 40,788,905 (GRCm39) |
V154G |
probably damaging |
Het |
Cacnb1 |
T |
C |
11: 97,900,186 (GRCm39) |
D324G |
probably damaging |
Het |
Ccdc170 |
A |
T |
10: 4,483,957 (GRCm39) |
|
probably null |
Het |
Ccdc187 |
T |
C |
2: 26,171,227 (GRCm39) |
H417R |
probably benign |
Het |
Cct4 |
T |
A |
11: 22,949,070 (GRCm39) |
M272K |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,760,417 (GRCm39) |
E2054G |
possibly damaging |
Het |
Ctnnal1 |
A |
T |
4: 56,844,584 (GRCm39) |
S127T |
possibly damaging |
Het |
Cttnbp2 |
T |
A |
6: 18,376,027 (GRCm39) |
H1504L |
probably benign |
Het |
Cyp4a29 |
T |
A |
4: 115,108,380 (GRCm39) |
M368K |
probably damaging |
Het |
Dhx32 |
A |
G |
7: 133,326,267 (GRCm39) |
F527L |
probably benign |
Het |
Foxk1 |
T |
C |
5: 142,387,739 (GRCm39) |
V154A |
probably damaging |
Het |
Garem2 |
C |
A |
5: 30,319,747 (GRCm39) |
A403E |
probably benign |
Het |
Gemin5 |
G |
A |
11: 58,020,846 (GRCm39) |
Q1114* |
probably null |
Het |
Gm11567 |
C |
T |
11: 99,770,274 (GRCm39) |
R71C |
unknown |
Het |
Gm13272 |
T |
C |
4: 88,698,442 (GRCm39) |
V119A |
probably benign |
Het |
Gpc6 |
T |
A |
14: 117,163,435 (GRCm39) |
C30S |
probably damaging |
Het |
Gprc6a |
A |
C |
10: 51,491,395 (GRCm39) |
F785V |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,494,693 (GRCm39) |
V368A |
probably benign |
Het |
Hsd17b4 |
G |
A |
18: 50,324,907 (GRCm39) |
|
probably null |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Il17ra |
C |
T |
6: 120,459,240 (GRCm39) |
S797F |
probably damaging |
Het |
Jmjd6 |
A |
G |
11: 116,733,438 (GRCm39) |
S80P |
probably benign |
Het |
Klhdc2 |
T |
A |
12: 69,346,995 (GRCm39) |
N53K |
probably benign |
Het |
Klhl30 |
C |
T |
1: 91,282,089 (GRCm39) |
P230L |
probably benign |
Het |
Marchf1 |
C |
A |
8: 66,729,339 (GRCm39) |
A46E |
probably benign |
Het |
Mast4 |
T |
C |
13: 102,890,705 (GRCm39) |
T1050A |
probably benign |
Het |
Mpp7 |
T |
C |
18: 7,355,049 (GRCm39) |
N459S |
probably benign |
Het |
Mtfr1l |
A |
G |
4: 134,258,063 (GRCm39) |
V53A |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,025,992 (GRCm39) |
E1326V |
|
Het |
Myh3 |
A |
G |
11: 66,992,005 (GRCm39) |
E1850G |
probably damaging |
Het |
Myo16 |
A |
G |
8: 10,619,925 (GRCm39) |
D1492G |
unknown |
Het |
Myo3b |
C |
A |
2: 70,180,287 (GRCm39) |
H1219Q |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,646,605 (GRCm39) |
Q1379L |
probably null |
Het |
Or8g30 |
C |
T |
9: 39,230,815 (GRCm39) |
V32I |
probably benign |
Het |
Or9q1 |
A |
G |
19: 13,804,914 (GRCm39) |
I282T |
probably benign |
Het |
Osbpl6 |
T |
G |
2: 76,385,361 (GRCm39) |
L265R |
probably damaging |
Het |
Pld4 |
A |
G |
12: 112,734,862 (GRCm39) |
T440A |
probably damaging |
Het |
Prr14 |
T |
C |
7: 127,071,128 (GRCm39) |
M1T |
probably null |
Het |
Ptger4 |
A |
T |
15: 5,273,178 (GRCm39) |
M1K |
probably null |
Het |
Ptpn22 |
A |
T |
3: 103,795,842 (GRCm39) |
T608S |
possibly damaging |
Het |
S1pr2 |
A |
G |
9: 20,879,319 (GRCm39) |
W170R |
probably damaging |
Het |
Specc1l |
A |
G |
10: 75,066,603 (GRCm39) |
I17M |
probably benign |
Het |
Spmap1 |
T |
A |
11: 97,666,594 (GRCm39) |
I31F |
probably benign |
Het |
Sptbn4 |
C |
G |
7: 27,071,662 (GRCm39) |
G1601R |
probably damaging |
Het |
Sqor |
C |
T |
2: 122,626,912 (GRCm39) |
P11L |
probably benign |
Het |
Stac2 |
T |
C |
11: 97,934,449 (GRCm39) |
D85G |
probably benign |
Het |
Svs5 |
G |
A |
2: 164,078,918 (GRCm39) |
Q330* |
probably null |
Het |
Taar7e |
A |
G |
10: 23,913,554 (GRCm39) |
I15V |
probably benign |
Het |
Tcf4 |
A |
T |
18: 69,770,007 (GRCm39) |
Y275F |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,538,046 (GRCm39) |
N1873S |
probably damaging |
Het |
Tert |
T |
A |
13: 73,775,648 (GRCm39) |
V133D |
probably benign |
Het |
Tfap2a |
T |
A |
13: 40,870,658 (GRCm39) |
N410I |
probably damaging |
Het |
Tjp3 |
A |
T |
10: 81,109,694 (GRCm39) |
D836E |
probably benign |
Het |
Tox3 |
A |
T |
8: 90,975,206 (GRCm39) |
M475K |
unknown |
Het |
Traf4 |
A |
T |
11: 78,050,979 (GRCm39) |
D392E |
probably damaging |
Het |
Vav2 |
A |
G |
2: 27,181,825 (GRCm39) |
L338P |
probably damaging |
Het |
Vmn1r81 |
T |
C |
7: 11,994,113 (GRCm39) |
N165S |
probably benign |
Het |
Vmn2r9 |
A |
T |
5: 108,995,409 (GRCm39) |
V413E |
probably damaging |
Het |
Wdr7 |
A |
T |
18: 63,911,059 (GRCm39) |
D817V |
probably damaging |
Het |
Zbtb38 |
G |
A |
9: 96,570,700 (GRCm39) |
S128L |
probably damaging |
Het |
Zfhx4 |
T |
A |
3: 5,464,922 (GRCm39) |
H1718Q |
probably damaging |
Het |
Zfp945 |
G |
A |
17: 23,071,228 (GRCm39) |
H245Y |
probably benign |
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 |
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 |
|
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 |
|