Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
A |
T |
10: 80,421,534 (GRCm39) |
Y145* |
probably null |
Het |
Afdn |
T |
G |
17: 14,108,350 (GRCm39) |
I1291S |
probably benign |
Het |
Arfgap3 |
T |
G |
15: 83,191,127 (GRCm39) |
I16L |
possibly damaging |
Het |
Bbs12 |
T |
A |
3: 37,373,343 (GRCm39) |
H45Q |
possibly damaging |
Het |
Brpf3 |
T |
C |
17: 29,043,022 (GRCm39) |
L1021P |
possibly damaging |
Het |
Cep170 |
A |
G |
1: 176,596,903 (GRCm39) |
S485P |
possibly damaging |
Het |
Cgref1 |
A |
T |
5: 31,090,937 (GRCm39) |
N292K |
probably damaging |
Het |
Chst3 |
A |
T |
10: 60,022,261 (GRCm39) |
Y195* |
probably null |
Het |
Clmn |
T |
C |
12: 104,740,782 (GRCm39) |
Y125C |
probably damaging |
Het |
Col13a1 |
A |
G |
10: 61,729,692 (GRCm39) |
|
probably null |
Het |
Cpeb3 |
A |
T |
19: 37,002,348 (GRCm39) |
I688N |
probably damaging |
Het |
Cpn2 |
A |
T |
16: 30,079,647 (GRCm39) |
L18H |
probably benign |
Het |
Crybg3 |
T |
A |
16: 59,375,542 (GRCm39) |
H1904L |
possibly damaging |
Het |
Csde1 |
C |
T |
3: 102,951,155 (GRCm39) |
P249S |
probably damaging |
Het |
Dcaf1 |
T |
C |
9: 106,721,339 (GRCm39) |
L377P |
probably damaging |
Het |
Dmwd |
A |
T |
7: 18,815,054 (GRCm39) |
K568M |
probably damaging |
Het |
Dsg2 |
T |
C |
18: 20,712,134 (GRCm39) |
I90T |
probably damaging |
Het |
Dytn |
A |
G |
1: 63,680,281 (GRCm39) |
I426T |
probably damaging |
Het |
Edc4 |
G |
A |
8: 106,613,943 (GRCm39) |
|
probably null |
Het |
Elac1 |
G |
T |
18: 73,871,985 (GRCm39) |
Q337K |
probably benign |
Het |
Exd2 |
G |
T |
12: 80,536,185 (GRCm39) |
A272S |
probably damaging |
Het |
F13b |
A |
G |
1: 139,435,853 (GRCm39) |
I220V |
possibly damaging |
Het |
Fblim1 |
G |
T |
4: 141,310,435 (GRCm39) |
R276S |
possibly damaging |
Het |
Fn1 |
A |
C |
1: 71,668,932 (GRCm39) |
L671R |
probably damaging |
Het |
H2-T23 |
T |
A |
17: 36,343,249 (GRCm39) |
I43F |
possibly damaging |
Het |
Hp1bp3 |
G |
A |
4: 137,956,043 (GRCm39) |
G202D |
probably damaging |
Het |
Kdm5b |
A |
G |
1: 134,536,675 (GRCm39) |
M632V |
probably damaging |
Het |
Klra5 |
T |
A |
6: 129,885,830 (GRCm39) |
S20C |
probably damaging |
Het |
Lancl1 |
A |
T |
1: 67,046,074 (GRCm39) |
C276S |
probably damaging |
Het |
Lect2 |
A |
G |
13: 56,690,520 (GRCm39) |
*152Q |
probably null |
Het |
Maff |
C |
A |
15: 79,241,658 (GRCm39) |
S25* |
probably null |
Het |
Mtr |
A |
G |
13: 12,262,263 (GRCm39) |
L171P |
probably damaging |
Het |
Ndufs1 |
A |
T |
1: 63,202,855 (GRCm39) |
Y236* |
probably null |
Het |
Neb |
A |
C |
2: 52,134,165 (GRCm39) |
Y3273D |
probably damaging |
Het |
Nup133 |
A |
T |
8: 124,673,333 (GRCm39) |
I66K |
probably benign |
Het |
Or4c110 |
T |
C |
2: 88,832,459 (GRCm39) |
M58V |
possibly damaging |
Het |
Psmd14 |
A |
G |
2: 61,614,205 (GRCm39) |
Y200C |
probably damaging |
Het |
Ptgds |
T |
C |
2: 25,359,622 (GRCm39) |
T22A |
probably benign |
Het |
Ptk2b |
T |
A |
14: 66,411,344 (GRCm39) |
|
probably benign |
Het |
Pum3 |
G |
A |
19: 27,398,713 (GRCm39) |
T279M |
probably damaging |
Het |
Rabl6 |
C |
T |
2: 25,474,868 (GRCm39) |
G614D |
probably benign |
Het |
Ripk3 |
T |
C |
14: 56,024,796 (GRCm39) |
D128G |
probably benign |
Het |
Serinc4 |
A |
T |
2: 121,270,039 (GRCm39) |
|
probably benign |
Het |
Slco1a8 |
T |
G |
6: 141,954,333 (GRCm39) |
I47L |
possibly damaging |
Het |
Sorbs2 |
T |
C |
8: 46,235,902 (GRCm39) |
S322P |
probably benign |
Het |
Spmap2l |
A |
C |
5: 77,164,197 (GRCm39) |
K67Q |
possibly damaging |
Het |
Srebf1 |
A |
T |
11: 60,111,284 (GRCm39) |
I29N |
possibly damaging |
Het |
Stk38l |
T |
C |
6: 146,670,372 (GRCm39) |
L238S |
probably damaging |
Het |
Supt20 |
T |
A |
3: 54,616,723 (GRCm39) |
C298* |
probably null |
Het |
Tbc1d19 |
A |
G |
5: 54,054,389 (GRCm39) |
D459G |
probably damaging |
Het |
Ulk2 |
A |
T |
11: 61,725,660 (GRCm39) |
L139M |
probably damaging |
Het |
Unc13b |
A |
G |
4: 43,235,249 (GRCm39) |
N3279S |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,596,818 (GRCm39) |
R3853G |
possibly damaging |
Het |
Usp7 |
C |
T |
16: 8,556,078 (GRCm39) |
M24I |
probably benign |
Het |
Vil1 |
A |
G |
1: 74,458,771 (GRCm39) |
T131A |
probably damaging |
Het |
Vmn2r2 |
C |
T |
3: 64,024,321 (GRCm39) |
M753I |
probably benign |
Het |
Vmn2r74 |
A |
T |
7: 85,601,900 (GRCm39) |
Y579* |
probably null |
Het |
Zdhhc3 |
A |
T |
9: 122,929,582 (GRCm39) |
Y18N |
probably damaging |
Het |
Zfp609 |
C |
T |
9: 65,609,927 (GRCm39) |
S1012N |
possibly damaging |
Het |
Zfr2 |
A |
T |
10: 81,077,985 (GRCm39) |
M271L |
probably benign |
Het |
|
Other mutations in Frem1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00155:Frem1
|
APN |
4 |
82,877,626 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01069:Frem1
|
APN |
4 |
82,932,104 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01106:Frem1
|
APN |
4 |
82,840,494 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01398:Frem1
|
APN |
4 |
82,868,599 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01617:Frem1
|
APN |
4 |
82,854,376 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01647:Frem1
|
APN |
4 |
82,868,593 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01690:Frem1
|
APN |
4 |
82,877,533 (GRCm39) |
splice site |
probably benign |
|
IGL02006:Frem1
|
APN |
4 |
82,911,037 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02069:Frem1
|
APN |
4 |
82,821,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02131:Frem1
|
APN |
4 |
82,843,091 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02225:Frem1
|
APN |
4 |
82,858,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Frem1
|
APN |
4 |
82,874,582 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02567:Frem1
|
APN |
4 |
82,918,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02647:Frem1
|
APN |
4 |
82,919,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02653:Frem1
|
APN |
4 |
82,877,571 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02831:Frem1
|
APN |
4 |
82,874,395 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02997:Frem1
|
APN |
4 |
82,853,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03005:Frem1
|
APN |
4 |
82,912,371 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03193:Frem1
|
APN |
4 |
82,912,263 (GRCm39) |
splice site |
probably benign |
|
IGL03218:Frem1
|
APN |
4 |
82,832,883 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03235:Frem1
|
APN |
4 |
82,938,992 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03243:Frem1
|
APN |
4 |
82,932,206 (GRCm39) |
missense |
probably damaging |
1.00 |
bat
|
UTSW |
4 |
82,983,060 (GRCm38) |
intron |
probably benign |
|
blister
|
UTSW |
4 |
82,939,007 (GRCm39) |
missense |
probably benign |
0.28 |
boy
|
UTSW |
4 |
82,874,492 (GRCm39) |
missense |
probably benign |
0.16 |
Bubblie
|
UTSW |
4 |
82,888,870 (GRCm39) |
critical splice donor site |
probably null |
|
magicbear
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
major
|
UTSW |
4 |
82,907,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324_Frem1_643
|
UTSW |
4 |
82,901,574 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Frem1
|
UTSW |
4 |
82,924,045 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4466001:Frem1
|
UTSW |
4 |
82,890,374 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4472001:Frem1
|
UTSW |
4 |
82,890,374 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4515001:Frem1
|
UTSW |
4 |
82,818,663 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4531001:Frem1
|
UTSW |
4 |
82,868,517 (GRCm39) |
missense |
probably benign |
0.12 |
R0010:Frem1
|
UTSW |
4 |
82,918,335 (GRCm39) |
missense |
probably benign |
0.41 |
R0010:Frem1
|
UTSW |
4 |
82,918,335 (GRCm39) |
missense |
probably benign |
0.41 |
R0115:Frem1
|
UTSW |
4 |
82,854,406 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0125:Frem1
|
UTSW |
4 |
82,930,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R0280:Frem1
|
UTSW |
4 |
82,887,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Frem1
|
UTSW |
4 |
82,830,874 (GRCm39) |
missense |
probably benign |
0.26 |
R0519:Frem1
|
UTSW |
4 |
82,888,870 (GRCm39) |
critical splice donor site |
probably null |
|
R0631:Frem1
|
UTSW |
4 |
82,890,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0645:Frem1
|
UTSW |
4 |
82,907,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Frem1
|
UTSW |
4 |
82,868,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1110:Frem1
|
UTSW |
4 |
82,868,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R1115:Frem1
|
UTSW |
4 |
82,939,007 (GRCm39) |
missense |
probably benign |
0.28 |
R1130:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably null |
|
R1173:Frem1
|
UTSW |
4 |
82,868,589 (GRCm39) |
missense |
probably benign |
0.16 |
R1349:Frem1
|
UTSW |
4 |
82,840,542 (GRCm39) |
splice site |
probably benign |
|
R1464:Frem1
|
UTSW |
4 |
82,930,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Frem1
|
UTSW |
4 |
82,930,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Frem1
|
UTSW |
4 |
82,920,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Frem1
|
UTSW |
4 |
82,917,128 (GRCm39) |
missense |
probably benign |
0.09 |
R1831:Frem1
|
UTSW |
4 |
82,939,074 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1851:Frem1
|
UTSW |
4 |
82,868,737 (GRCm39) |
missense |
probably damaging |
0.98 |
R2014:Frem1
|
UTSW |
4 |
82,924,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2022:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2023:Frem1
|
UTSW |
4 |
82,831,795 (GRCm39) |
missense |
probably benign |
0.02 |
R2183:Frem1
|
UTSW |
4 |
82,909,732 (GRCm39) |
missense |
probably benign |
0.00 |
R2437:Frem1
|
UTSW |
4 |
82,918,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R2520:Frem1
|
UTSW |
4 |
82,868,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R3195:Frem1
|
UTSW |
4 |
82,932,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R3196:Frem1
|
UTSW |
4 |
82,932,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R3408:Frem1
|
UTSW |
4 |
82,930,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R3411:Frem1
|
UTSW |
4 |
82,881,416 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3742:Frem1
|
UTSW |
4 |
82,930,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Frem1
|
UTSW |
4 |
82,917,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Frem1
|
UTSW |
4 |
82,831,844 (GRCm39) |
missense |
probably benign |
0.41 |
R4329:Frem1
|
UTSW |
4 |
82,904,774 (GRCm39) |
missense |
probably benign |
0.01 |
R4364:Frem1
|
UTSW |
4 |
82,831,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R4411:Frem1
|
UTSW |
4 |
82,881,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Frem1
|
UTSW |
4 |
82,907,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Frem1
|
UTSW |
4 |
82,938,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:Frem1
|
UTSW |
4 |
82,907,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably benign |
|
R4802:Frem1
|
UTSW |
4 |
82,834,865 (GRCm39) |
splice site |
probably benign |
|
R4854:Frem1
|
UTSW |
4 |
82,834,995 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4872:Frem1
|
UTSW |
4 |
82,881,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Frem1
|
UTSW |
4 |
82,884,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R5007:Frem1
|
UTSW |
4 |
82,859,049 (GRCm39) |
intron |
probably benign |
|
R5103:Frem1
|
UTSW |
4 |
82,909,849 (GRCm39) |
missense |
probably benign |
|
R5369:Frem1
|
UTSW |
4 |
82,919,976 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5494:Frem1
|
UTSW |
4 |
82,858,990 (GRCm39) |
makesense |
probably null |
|
R5694:Frem1
|
UTSW |
4 |
82,912,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Frem1
|
UTSW |
4 |
82,868,652 (GRCm39) |
missense |
probably benign |
0.12 |
R5813:Frem1
|
UTSW |
4 |
82,918,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Frem1
|
UTSW |
4 |
82,854,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Frem1
|
UTSW |
4 |
82,920,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R5985:Frem1
|
UTSW |
4 |
82,884,287 (GRCm39) |
missense |
probably benign |
|
R6091:Frem1
|
UTSW |
4 |
82,818,796 (GRCm39) |
missense |
probably benign |
0.01 |
R6165:Frem1
|
UTSW |
4 |
82,874,492 (GRCm39) |
missense |
probably benign |
0.16 |
R6324:Frem1
|
UTSW |
4 |
82,901,574 (GRCm39) |
missense |
probably benign |
0.00 |
R6369:Frem1
|
UTSW |
4 |
82,832,029 (GRCm39) |
splice site |
probably null |
|
R6414:Frem1
|
UTSW |
4 |
82,858,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R6421:Frem1
|
UTSW |
4 |
82,912,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Frem1
|
UTSW |
4 |
82,884,253 (GRCm39) |
missense |
probably benign |
0.03 |
R6453:Frem1
|
UTSW |
4 |
82,833,062 (GRCm39) |
nonsense |
probably null |
|
R6598:Frem1
|
UTSW |
4 |
82,932,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R6720:Frem1
|
UTSW |
4 |
82,932,069 (GRCm39) |
missense |
probably damaging |
0.98 |
R6862:Frem1
|
UTSW |
4 |
82,930,251 (GRCm39) |
nonsense |
probably null |
|
R6922:Frem1
|
UTSW |
4 |
82,840,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R6931:Frem1
|
UTSW |
4 |
82,888,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R6992:Frem1
|
UTSW |
4 |
82,858,599 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6995:Frem1
|
UTSW |
4 |
82,904,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:Frem1
|
UTSW |
4 |
82,904,798 (GRCm39) |
missense |
probably benign |
0.44 |
R7104:Frem1
|
UTSW |
4 |
82,858,918 (GRCm39) |
missense |
probably benign |
0.30 |
R7146:Frem1
|
UTSW |
4 |
82,840,532 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7174:Frem1
|
UTSW |
4 |
82,840,493 (GRCm39) |
missense |
probably benign |
0.00 |
R7327:Frem1
|
UTSW |
4 |
82,938,992 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7343:Frem1
|
UTSW |
4 |
82,912,359 (GRCm39) |
missense |
probably damaging |
0.99 |
R7368:Frem1
|
UTSW |
4 |
82,884,381 (GRCm39) |
missense |
probably benign |
0.19 |
R7392:Frem1
|
UTSW |
4 |
82,932,064 (GRCm39) |
missense |
probably benign |
0.06 |
R7465:Frem1
|
UTSW |
4 |
82,833,072 (GRCm39) |
missense |
probably benign |
0.11 |
R7499:Frem1
|
UTSW |
4 |
82,924,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7536:Frem1
|
UTSW |
4 |
82,874,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7752:Frem1
|
UTSW |
4 |
82,877,614 (GRCm39) |
missense |
probably benign |
0.02 |
R7753:Frem1
|
UTSW |
4 |
82,832,217 (GRCm39) |
missense |
probably benign |
0.03 |
R7790:Frem1
|
UTSW |
4 |
82,907,401 (GRCm39) |
missense |
probably benign |
0.02 |
R7818:Frem1
|
UTSW |
4 |
82,932,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Frem1
|
UTSW |
4 |
82,932,049 (GRCm39) |
critical splice donor site |
probably null |
|
R7878:Frem1
|
UTSW |
4 |
82,938,917 (GRCm39) |
missense |
probably benign |
0.00 |
R7886:Frem1
|
UTSW |
4 |
82,934,643 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7901:Frem1
|
UTSW |
4 |
82,877,614 (GRCm39) |
missense |
probably benign |
0.02 |
R7976:Frem1
|
UTSW |
4 |
82,919,946 (GRCm39) |
missense |
probably damaging |
0.97 |
R8240:Frem1
|
UTSW |
4 |
82,874,485 (GRCm39) |
missense |
probably benign |
0.21 |
R8305:Frem1
|
UTSW |
4 |
82,918,226 (GRCm39) |
missense |
probably benign |
0.06 |
R8415:Frem1
|
UTSW |
4 |
82,918,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Frem1
|
UTSW |
4 |
82,889,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8819:Frem1
|
UTSW |
4 |
82,821,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8820:Frem1
|
UTSW |
4 |
82,821,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R8829:Frem1
|
UTSW |
4 |
82,918,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Frem1
|
UTSW |
4 |
82,922,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Frem1
|
UTSW |
4 |
82,922,280 (GRCm39) |
intron |
probably benign |
|
R8910:Frem1
|
UTSW |
4 |
82,868,694 (GRCm39) |
missense |
probably benign |
0.09 |
R9036:Frem1
|
UTSW |
4 |
82,831,785 (GRCm39) |
missense |
probably benign |
|
R9228:Frem1
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Frem1
|
UTSW |
4 |
82,901,622 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9441:Frem1
|
UTSW |
4 |
82,924,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Frem1
|
UTSW |
4 |
82,920,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Frem1
|
UTSW |
4 |
82,901,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R9640:Frem1
|
UTSW |
4 |
82,831,896 (GRCm39) |
missense |
probably benign |
|
R9641:Frem1
|
UTSW |
4 |
82,877,653 (GRCm39) |
missense |
probably damaging |
1.00 |
X0013:Frem1
|
UTSW |
4 |
82,833,045 (GRCm39) |
missense |
probably benign |
0.38 |
X0017:Frem1
|
UTSW |
4 |
82,909,870 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1088:Frem1
|
UTSW |
4 |
82,890,504 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Frem1
|
UTSW |
4 |
82,918,220 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Frem1
|
UTSW |
4 |
82,918,506 (GRCm39) |
missense |
probably benign |
0.39 |
Z1177:Frem1
|
UTSW |
4 |
82,858,552 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Frem1
|
UTSW |
4 |
82,934,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|