Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
T |
1: 130,670,635 (GRCm39) |
P286S |
possibly damaging |
Het |
Aagab |
T |
A |
9: 63,526,444 (GRCm39) |
S156T |
probably damaging |
Het |
Abca14 |
T |
G |
7: 119,823,642 (GRCm39) |
Y390D |
probably damaging |
Het |
Abcc2 |
T |
A |
19: 43,814,386 (GRCm39) |
I1122N |
possibly damaging |
Het |
Adamts16 |
T |
C |
13: 70,927,730 (GRCm39) |
E503G |
possibly damaging |
Het |
Adamts9 |
A |
T |
6: 92,835,038 (GRCm39) |
C697* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,623,112 (GRCm39) |
D3837G |
possibly damaging |
Het |
Ahcyl |
T |
A |
16: 45,974,246 (GRCm39) |
D377V |
probably benign |
Het |
Aire |
T |
A |
10: 77,878,433 (GRCm39) |
R128S |
probably damaging |
Het |
Alkbh2 |
A |
C |
5: 114,262,011 (GRCm39) |
*240E |
probably null |
Het |
Als2 |
T |
C |
1: 59,219,742 (GRCm39) |
Y1191C |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,952,667 (GRCm39) |
V186E |
probably benign |
Het |
Apob |
C |
T |
12: 8,040,307 (GRCm39) |
A548V |
probably damaging |
Het |
B3galt4 |
A |
T |
17: 34,169,722 (GRCm39) |
V172E |
probably damaging |
Het |
Bbs7 |
A |
C |
3: 36,646,525 (GRCm39) |
C432G |
possibly damaging |
Het |
Cacna2d3 |
T |
A |
14: 28,767,601 (GRCm39) |
E758V |
probably damaging |
Het |
Cactin |
T |
G |
10: 81,158,496 (GRCm39) |
L154R |
probably benign |
Het |
Ccdc88a |
A |
C |
11: 29,411,021 (GRCm39) |
R502S |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,450,784 (GRCm39) |
I398N |
possibly damaging |
Het |
Chd1 |
A |
T |
17: 15,988,828 (GRCm39) |
D1527V |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,988,830 (GRCm39) |
M1528L |
probably benign |
Het |
Chrac1 |
G |
A |
15: 72,964,675 (GRCm39) |
|
probably null |
Het |
Cln3 |
T |
G |
7: 126,182,217 (GRCm39) |
M1L |
probably damaging |
Het |
Cnot6 |
T |
C |
11: 49,568,263 (GRCm39) |
Y442C |
probably damaging |
Het |
Col19a1 |
A |
T |
1: 24,324,132 (GRCm39) |
|
probably null |
Het |
Col1a2 |
T |
C |
6: 4,537,838 (GRCm39) |
F1116L |
unknown |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cops4 |
T |
G |
5: 100,676,408 (GRCm39) |
V53G |
probably damaging |
Het |
Crnkl1 |
A |
G |
2: 145,761,875 (GRCm39) |
S561P |
probably benign |
Het |
Ctnnb1 |
C |
A |
9: 120,780,778 (GRCm39) |
Q99K |
probably benign |
Het |
Cxcr5 |
T |
C |
9: 44,424,578 (GRCm39) |
S360G |
probably benign |
Het |
Dab2 |
G |
A |
15: 6,447,797 (GRCm39) |
V60M |
probably damaging |
Het |
Ddx3y |
A |
T |
Y: 1,263,321 (GRCm39) |
Y648* |
probably null |
Het |
Dennd2a |
T |
A |
6: 39,474,044 (GRCm39) |
D430V |
probably damaging |
Het |
Dsp |
G |
T |
13: 38,376,846 (GRCm39) |
E1544* |
probably null |
Het |
Efcab7 |
A |
T |
4: 99,719,631 (GRCm39) |
M38L |
possibly damaging |
Het |
Fto |
A |
G |
8: 92,136,155 (GRCm39) |
N141S |
probably damaging |
Het |
Gabrp |
A |
G |
11: 33,504,362 (GRCm39) |
F318L |
probably damaging |
Het |
Gmeb1 |
A |
C |
4: 131,969,663 (GRCm39) |
C103W |
probably damaging |
Het |
Heatr9 |
T |
C |
11: 83,405,365 (GRCm39) |
D365G |
probably damaging |
Het |
Hif3a |
G |
A |
7: 16,778,325 (GRCm39) |
R436W |
probably benign |
Het |
Hint2 |
A |
G |
4: 43,654,378 (GRCm39) |
V145A |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,313,237 (GRCm39) |
L3482* |
probably null |
Het |
Hsd3b1 |
A |
T |
3: 98,760,590 (GRCm39) |
Y134N |
probably damaging |
Het |
Impg2 |
T |
A |
16: 56,080,848 (GRCm39) |
V775E |
probably damaging |
Het |
Ipo5 |
A |
G |
14: 121,159,635 (GRCm39) |
I154M |
probably benign |
Het |
Itgad |
T |
A |
7: 127,797,550 (GRCm39) |
F893Y |
probably benign |
Het |
Itprid1 |
A |
T |
6: 55,875,228 (GRCm39) |
M393L |
possibly damaging |
Het |
Kdm4a |
T |
C |
4: 118,018,903 (GRCm39) |
R438G |
probably benign |
Het |
Klk1b11 |
T |
A |
7: 43,425,943 (GRCm39) |
M1K |
probably null |
Het |
Lrch3 |
T |
C |
16: 32,799,870 (GRCm39) |
S35P |
probably damaging |
Het |
Mfn2 |
A |
G |
4: 147,967,745 (GRCm39) |
L441P |
probably damaging |
Het |
Mgat4c |
A |
T |
10: 102,224,565 (GRCm39) |
I260F |
probably damaging |
Het |
Mon1b |
T |
A |
8: 114,364,375 (GRCm39) |
S51T |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,036,744 (GRCm39) |
D993G |
probably benign |
Het |
Myo1a |
A |
G |
10: 127,552,166 (GRCm39) |
N762D |
probably benign |
Het |
Nacc2 |
A |
T |
2: 25,950,345 (GRCm39) |
Y464N |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,383,714 (GRCm39) |
I150T |
probably benign |
Het |
Ndufv2 |
G |
T |
17: 66,387,816 (GRCm39) |
P119T |
probably damaging |
Het |
Noc4l |
G |
A |
5: 110,800,241 (GRCm39) |
R95* |
probably null |
Het |
Ntng1 |
A |
T |
3: 110,042,819 (GRCm39) |
Y2* |
probably null |
Het |
Oog4 |
T |
C |
4: 143,165,773 (GRCm39) |
N53D |
probably benign |
Het |
Or10ak11 |
A |
T |
4: 118,687,022 (GRCm39) |
V205D |
possibly damaging |
Het |
Or4d11 |
C |
T |
19: 12,013,525 (GRCm39) |
V194I |
probably benign |
Het |
Or6c6c |
A |
G |
10: 129,541,638 (GRCm39) |
E297G |
possibly damaging |
Het |
Or9i1b |
C |
T |
19: 13,896,873 (GRCm39) |
T163I |
probably benign |
Het |
Phkg2 |
T |
G |
7: 127,173,075 (GRCm39) |
L11R |
probably damaging |
Het |
Pogz |
A |
G |
3: 94,777,424 (GRCm39) |
D368G |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,355,289 (GRCm39) |
L1530Q |
probably damaging |
Het |
Prmt1 |
C |
T |
7: 44,628,878 (GRCm39) |
E144K |
probably damaging |
Het |
Prss8 |
T |
A |
7: 127,526,348 (GRCm39) |
I121F |
probably benign |
Het |
Psmd13 |
T |
C |
7: 140,477,624 (GRCm39) |
L314P |
probably damaging |
Het |
Ptch2 |
G |
A |
4: 116,966,081 (GRCm39) |
G467D |
probably damaging |
Het |
Rbm20 |
C |
A |
19: 53,852,596 (GRCm39) |
P1192Q |
probably damaging |
Het |
Rpl19 |
T |
A |
11: 97,919,200 (GRCm39) |
D45E |
probably benign |
Het |
Rsph10b |
C |
T |
5: 143,903,946 (GRCm39) |
A219V |
probably damaging |
Het |
Rtraf |
C |
T |
14: 19,864,600 (GRCm39) |
|
probably null |
Het |
Scaf1 |
T |
A |
7: 44,658,175 (GRCm39) |
T235S |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,968,594 (GRCm39) |
C296S |
unknown |
Het |
Slc39a7 |
A |
T |
17: 34,247,924 (GRCm39) |
V426D |
probably damaging |
Het |
Slc41a2 |
A |
T |
10: 83,119,610 (GRCm39) |
V384D |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,505,499 (GRCm39) |
L475P |
probably benign |
Het |
Slco6d1 |
A |
C |
1: 98,418,359 (GRCm39) |
K515T |
probably benign |
Het |
Sos2 |
T |
C |
12: 69,682,459 (GRCm39) |
E253G |
probably damaging |
Het |
Sp6 |
G |
T |
11: 96,912,361 (GRCm39) |
D25Y |
possibly damaging |
Het |
Syt11 |
A |
C |
3: 88,669,855 (GRCm39) |
D12E |
possibly damaging |
Het |
Taf2 |
A |
G |
15: 54,910,856 (GRCm39) |
L606P |
probably damaging |
Het |
Tbc1d5 |
A |
G |
17: 51,273,764 (GRCm39) |
Y116H |
probably damaging |
Het |
Tnfrsf8 |
A |
G |
4: 145,015,029 (GRCm39) |
I243T |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,917,153 (GRCm39) |
S2183G |
probably benign |
Het |
Trim66 |
T |
C |
7: 109,059,379 (GRCm39) |
Y853C |
probably benign |
Het |
Ttn |
T |
A |
2: 76,567,839 (GRCm39) |
T27685S |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,573,466 (GRCm39) |
E25809G |
probably damaging |
Het |
Uvssa |
G |
A |
5: 33,566,191 (GRCm39) |
G445S |
probably benign |
Het |
Zfp326 |
T |
C |
5: 106,058,141 (GRCm39) |
S427P |
probably damaging |
Het |
Zfp592 |
A |
G |
7: 80,674,637 (GRCm39) |
T534A |
possibly damaging |
Het |
Zfp672 |
A |
G |
11: 58,207,173 (GRCm39) |
S383P |
possibly damaging |
Het |
Zfp799 |
A |
G |
17: 33,039,700 (GRCm39) |
S188P |
possibly damaging |
Het |
Zyg11b |
A |
C |
4: 108,129,450 (GRCm39) |
V54G |
possibly damaging |
Het |
|
Other mutations in Lama5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01067:Lama5
|
APN |
2 |
179,818,336 (GRCm39) |
unclassified |
probably benign |
|
IGL01370:Lama5
|
APN |
2 |
179,839,193 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01474:Lama5
|
APN |
2 |
179,838,363 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01614:Lama5
|
APN |
2 |
179,822,657 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Lama5
|
APN |
2 |
179,834,185 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01953:Lama5
|
APN |
2 |
179,832,497 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02093:Lama5
|
APN |
2 |
179,830,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02197:Lama5
|
APN |
2 |
179,849,012 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02308:Lama5
|
APN |
2 |
179,832,120 (GRCm39) |
splice site |
probably benign |
|
IGL02314:Lama5
|
APN |
2 |
179,836,275 (GRCm39) |
splice site |
probably benign |
|
IGL02317:Lama5
|
APN |
2 |
179,833,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Lama5
|
APN |
2 |
179,835,677 (GRCm39) |
nonsense |
probably null |
|
IGL02361:Lama5
|
APN |
2 |
179,835,677 (GRCm39) |
nonsense |
probably null |
|
IGL02557:Lama5
|
APN |
2 |
179,832,725 (GRCm39) |
nonsense |
probably null |
|
IGL03026:Lama5
|
APN |
2 |
179,837,760 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03160:Lama5
|
APN |
2 |
179,822,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03238:Lama5
|
APN |
2 |
179,830,367 (GRCm39) |
missense |
probably benign |
|
IGL03390:Lama5
|
APN |
2 |
179,849,011 (GRCm39) |
missense |
probably damaging |
1.00 |
blancmange
|
UTSW |
2 |
179,822,404 (GRCm39) |
missense |
probably damaging |
0.98 |
cupcake
|
UTSW |
2 |
179,827,752 (GRCm39) |
missense |
probably damaging |
1.00 |
layercake
|
UTSW |
2 |
179,822,511 (GRCm39) |
missense |
possibly damaging |
0.83 |
poundcake
|
UTSW |
2 |
179,837,401 (GRCm39) |
missense |
probably damaging |
1.00 |
Salty
|
UTSW |
2 |
179,823,444 (GRCm39) |
missense |
possibly damaging |
0.84 |
PIT4378001:Lama5
|
UTSW |
2 |
179,831,238 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0003:Lama5
|
UTSW |
2 |
179,819,872 (GRCm39) |
splice site |
probably null |
|
R0056:Lama5
|
UTSW |
2 |
179,828,899 (GRCm39) |
intron |
probably benign |
|
R0147:Lama5
|
UTSW |
2 |
179,832,199 (GRCm39) |
missense |
probably benign |
|
R0148:Lama5
|
UTSW |
2 |
179,832,199 (GRCm39) |
missense |
probably benign |
|
R0310:Lama5
|
UTSW |
2 |
179,823,359 (GRCm39) |
splice site |
probably benign |
|
R0368:Lama5
|
UTSW |
2 |
179,823,023 (GRCm39) |
nonsense |
probably null |
|
R0479:Lama5
|
UTSW |
2 |
179,826,250 (GRCm39) |
missense |
probably benign |
0.03 |
R0490:Lama5
|
UTSW |
2 |
179,821,962 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0636:Lama5
|
UTSW |
2 |
179,831,124 (GRCm39) |
critical splice donor site |
probably null |
|
R0704:Lama5
|
UTSW |
2 |
179,821,277 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0733:Lama5
|
UTSW |
2 |
179,822,511 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1017:Lama5
|
UTSW |
2 |
179,837,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Lama5
|
UTSW |
2 |
179,821,557 (GRCm39) |
unclassified |
probably benign |
|
R1294:Lama5
|
UTSW |
2 |
179,832,714 (GRCm39) |
missense |
probably benign |
0.00 |
R1423:Lama5
|
UTSW |
2 |
179,837,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Lama5
|
UTSW |
2 |
179,824,593 (GRCm39) |
missense |
probably benign |
0.01 |
R1447:Lama5
|
UTSW |
2 |
179,827,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R1540:Lama5
|
UTSW |
2 |
179,821,944 (GRCm39) |
missense |
probably benign |
|
R1601:Lama5
|
UTSW |
2 |
179,839,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Lama5
|
UTSW |
2 |
179,848,551 (GRCm39) |
missense |
probably benign |
0.02 |
R1674:Lama5
|
UTSW |
2 |
179,843,780 (GRCm39) |
missense |
probably benign |
0.00 |
R1687:Lama5
|
UTSW |
2 |
179,835,859 (GRCm39) |
missense |
probably benign |
0.00 |
R1696:Lama5
|
UTSW |
2 |
179,844,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R1701:Lama5
|
UTSW |
2 |
179,863,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Lama5
|
UTSW |
2 |
179,837,274 (GRCm39) |
splice site |
probably benign |
|
R1936:Lama5
|
UTSW |
2 |
179,832,714 (GRCm39) |
missense |
probably benign |
0.00 |
R1939:Lama5
|
UTSW |
2 |
179,832,714 (GRCm39) |
missense |
probably benign |
0.00 |
R1940:Lama5
|
UTSW |
2 |
179,832,714 (GRCm39) |
missense |
probably benign |
0.00 |
R1953:Lama5
|
UTSW |
2 |
179,832,540 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1966:Lama5
|
UTSW |
2 |
179,830,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R2024:Lama5
|
UTSW |
2 |
179,820,923 (GRCm39) |
missense |
probably benign |
0.00 |
R2079:Lama5
|
UTSW |
2 |
179,867,301 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2115:Lama5
|
UTSW |
2 |
179,828,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Lama5
|
UTSW |
2 |
179,838,035 (GRCm39) |
missense |
probably benign |
0.00 |
R2272:Lama5
|
UTSW |
2 |
179,820,396 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2357:Lama5
|
UTSW |
2 |
179,821,890 (GRCm39) |
missense |
probably benign |
0.01 |
R2860:Lama5
|
UTSW |
2 |
179,829,040 (GRCm39) |
missense |
probably benign |
0.00 |
R2861:Lama5
|
UTSW |
2 |
179,829,040 (GRCm39) |
missense |
probably benign |
0.00 |
R2939:Lama5
|
UTSW |
2 |
179,840,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3053:Lama5
|
UTSW |
2 |
179,824,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R3430:Lama5
|
UTSW |
2 |
179,838,110 (GRCm39) |
missense |
probably benign |
0.00 |
R3752:Lama5
|
UTSW |
2 |
179,829,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R3782:Lama5
|
UTSW |
2 |
179,836,356 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3901:Lama5
|
UTSW |
2 |
179,824,144 (GRCm39) |
splice site |
probably benign |
|
R4248:Lama5
|
UTSW |
2 |
179,822,220 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4626:Lama5
|
UTSW |
2 |
179,826,253 (GRCm39) |
missense |
probably damaging |
0.98 |
R4638:Lama5
|
UTSW |
2 |
179,832,206 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4669:Lama5
|
UTSW |
2 |
179,822,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Lama5
|
UTSW |
2 |
179,841,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Lama5
|
UTSW |
2 |
179,821,159 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4701:Lama5
|
UTSW |
2 |
179,833,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Lama5
|
UTSW |
2 |
179,827,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4880:Lama5
|
UTSW |
2 |
179,818,861 (GRCm39) |
unclassified |
probably benign |
|
R4923:Lama5
|
UTSW |
2 |
179,825,942 (GRCm39) |
missense |
probably benign |
0.18 |
R4960:Lama5
|
UTSW |
2 |
179,850,045 (GRCm39) |
critical splice donor site |
probably null |
|
R4983:Lama5
|
UTSW |
2 |
179,835,242 (GRCm39) |
missense |
probably benign |
0.13 |
R5061:Lama5
|
UTSW |
2 |
179,840,579 (GRCm39) |
nonsense |
probably null |
|
R5080:Lama5
|
UTSW |
2 |
179,848,993 (GRCm39) |
nonsense |
probably null |
|
R5135:Lama5
|
UTSW |
2 |
179,844,013 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5206:Lama5
|
UTSW |
2 |
179,833,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Lama5
|
UTSW |
2 |
179,835,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R5319:Lama5
|
UTSW |
2 |
179,822,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5355:Lama5
|
UTSW |
2 |
179,823,444 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5388:Lama5
|
UTSW |
2 |
179,832,539 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5528:Lama5
|
UTSW |
2 |
179,836,356 (GRCm39) |
missense |
probably benign |
0.21 |
R5536:Lama5
|
UTSW |
2 |
179,831,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R5658:Lama5
|
UTSW |
2 |
179,850,069 (GRCm39) |
nonsense |
probably null |
|
R5823:Lama5
|
UTSW |
2 |
179,834,285 (GRCm39) |
missense |
probably benign |
0.04 |
R5885:Lama5
|
UTSW |
2 |
179,843,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R5889:Lama5
|
UTSW |
2 |
179,835,467 (GRCm39) |
intron |
probably benign |
|
R5912:Lama5
|
UTSW |
2 |
179,837,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Lama5
|
UTSW |
2 |
179,839,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R6015:Lama5
|
UTSW |
2 |
179,827,185 (GRCm39) |
missense |
probably benign |
0.36 |
R6037:Lama5
|
UTSW |
2 |
179,848,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Lama5
|
UTSW |
2 |
179,848,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Lama5
|
UTSW |
2 |
179,827,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Lama5
|
UTSW |
2 |
179,822,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R6359:Lama5
|
UTSW |
2 |
179,837,775 (GRCm39) |
missense |
probably benign |
0.01 |
R6385:Lama5
|
UTSW |
2 |
179,838,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Lama5
|
UTSW |
2 |
179,839,257 (GRCm39) |
nonsense |
probably null |
|
R6552:Lama5
|
UTSW |
2 |
179,822,947 (GRCm39) |
missense |
probably damaging |
0.98 |
R6632:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6633:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6645:Lama5
|
UTSW |
2 |
179,821,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R6731:Lama5
|
UTSW |
2 |
179,830,367 (GRCm39) |
missense |
probably benign |
0.09 |
R6744:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6799:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6801:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6851:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6881:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6882:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R6884:Lama5
|
UTSW |
2 |
179,833,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R7022:Lama5
|
UTSW |
2 |
179,822,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Lama5
|
UTSW |
2 |
179,843,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Lama5
|
UTSW |
2 |
179,848,877 (GRCm39) |
missense |
probably damaging |
0.98 |
R7282:Lama5
|
UTSW |
2 |
179,843,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Lama5
|
UTSW |
2 |
179,834,751 (GRCm39) |
missense |
probably benign |
0.01 |
R7410:Lama5
|
UTSW |
2 |
179,844,183 (GRCm39) |
critical splice donor site |
probably null |
|
R7699:Lama5
|
UTSW |
2 |
179,822,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Lama5
|
UTSW |
2 |
179,843,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7909:Lama5
|
UTSW |
2 |
179,834,069 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7948:Lama5
|
UTSW |
2 |
179,843,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Lama5
|
UTSW |
2 |
179,829,724 (GRCm39) |
missense |
probably benign |
0.37 |
R8317:Lama5
|
UTSW |
2 |
179,848,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8351:Lama5
|
UTSW |
2 |
179,837,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Lama5
|
UTSW |
2 |
179,843,280 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8398:Lama5
|
UTSW |
2 |
179,838,827 (GRCm39) |
critical splice donor site |
probably null |
|
R8401:Lama5
|
UTSW |
2 |
179,840,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R8404:Lama5
|
UTSW |
2 |
179,837,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Lama5
|
UTSW |
2 |
179,837,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Lama5
|
UTSW |
2 |
179,822,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R8705:Lama5
|
UTSW |
2 |
179,820,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Lama5
|
UTSW |
2 |
179,828,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Lama5
|
UTSW |
2 |
179,832,714 (GRCm39) |
missense |
probably benign |
0.00 |
R8786:Lama5
|
UTSW |
2 |
179,838,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R8926:Lama5
|
UTSW |
2 |
179,835,783 (GRCm39) |
missense |
probably benign |
0.08 |
R8928:Lama5
|
UTSW |
2 |
179,843,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Lama5
|
UTSW |
2 |
179,835,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R8958:Lama5
|
UTSW |
2 |
179,835,592 (GRCm39) |
missense |
probably benign |
|
R9002:Lama5
|
UTSW |
2 |
179,838,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R9081:Lama5
|
UTSW |
2 |
179,833,930 (GRCm39) |
nonsense |
probably null |
|
R9165:Lama5
|
UTSW |
2 |
179,821,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R9233:Lama5
|
UTSW |
2 |
179,840,502 (GRCm39) |
nonsense |
probably null |
|
R9264:Lama5
|
UTSW |
2 |
179,838,271 (GRCm39) |
splice site |
probably benign |
|
R9311:Lama5
|
UTSW |
2 |
179,838,275 (GRCm39) |
critical splice donor site |
probably null |
|
R9443:Lama5
|
UTSW |
2 |
179,843,522 (GRCm39) |
missense |
probably benign |
0.00 |
R9488:Lama5
|
UTSW |
2 |
179,823,234 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9674:Lama5
|
UTSW |
2 |
179,840,267 (GRCm39) |
critical splice donor site |
probably null |
|
R9684:Lama5
|
UTSW |
2 |
179,849,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Lama5
|
UTSW |
2 |
179,825,433 (GRCm39) |
missense |
probably benign |
0.00 |
RF020:Lama5
|
UTSW |
2 |
179,837,971 (GRCm39) |
missense |
probably benign |
|
X0065:Lama5
|
UTSW |
2 |
179,823,524 (GRCm39) |
missense |
probably benign |
0.26 |
Z1177:Lama5
|
UTSW |
2 |
179,832,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Lama5
|
UTSW |
2 |
179,831,212 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lama5
|
UTSW |
2 |
179,825,423 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Lama5
|
UTSW |
2 |
179,840,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|