Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
A |
T |
5: 144,981,624 (GRCm39) |
Y153F |
probably damaging |
Het |
Abcb1b |
T |
A |
5: 8,862,656 (GRCm39) |
Y113N |
probably damaging |
Het |
Albfm1 |
A |
G |
5: 90,727,474 (GRCm39) |
H364R |
probably damaging |
Het |
Anapc1 |
C |
G |
2: 128,501,657 (GRCm39) |
R795T |
probably null |
Het |
Arhgap18 |
T |
A |
10: 26,725,917 (GRCm39) |
N47K |
possibly damaging |
Het |
Arhgap26 |
A |
G |
18: 39,232,660 (GRCm39) |
N96D |
probably damaging |
Het |
Asxl3 |
G |
T |
18: 22,598,457 (GRCm39) |
E191* |
probably null |
Het |
Cc2d2b |
A |
G |
19: 40,779,652 (GRCm39) |
E697G |
possibly damaging |
Het |
Chaf1a |
A |
T |
17: 56,354,059 (GRCm39) |
I110F |
unknown |
Het |
Clca4b |
A |
T |
3: 144,621,388 (GRCm39) |
|
probably null |
Het |
Dagla |
C |
A |
19: 10,234,214 (GRCm39) |
V366L |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,900,049 (GRCm39) |
N878S |
probably benign |
Het |
Dapk3 |
A |
G |
10: 81,026,096 (GRCm39) |
Y129C |
probably damaging |
Het |
Dhx38 |
A |
G |
8: 110,279,834 (GRCm39) |
L952P |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,912,623 (GRCm39) |
Y1080* |
probably null |
Het |
Dscaml1 |
G |
A |
9: 45,361,881 (GRCm39) |
V214I |
probably benign |
Het |
Dtymk |
A |
G |
1: 93,726,214 (GRCm39) |
L15P |
probably benign |
Het |
E330034G19Rik |
A |
G |
14: 24,346,178 (GRCm39) |
M30V |
probably benign |
Het |
Egfr |
G |
A |
11: 16,846,952 (GRCm39) |
C783Y |
probably damaging |
Het |
Epha8 |
C |
T |
4: 136,672,980 (GRCm39) |
R268Q |
probably benign |
Het |
Fbxw24 |
T |
A |
9: 109,453,998 (GRCm39) |
R49S |
probably damaging |
Het |
Fcsk |
T |
C |
8: 111,620,050 (GRCm39) |
M276V |
probably benign |
Het |
Gm8797 |
A |
T |
3: 5,816,027 (GRCm39) |
T22S |
probably benign |
Het |
Hao1 |
T |
C |
2: 134,372,685 (GRCm39) |
S108G |
probably damaging |
Het |
Hdac4 |
C |
A |
1: 91,929,935 (GRCm39) |
A184S |
probably damaging |
Het |
Hikeshi |
T |
A |
7: 89,579,553 (GRCm39) |
|
probably benign |
Het |
Hivep2 |
C |
T |
10: 14,004,757 (GRCm39) |
R452C |
probably benign |
Het |
Hsdl1 |
T |
C |
8: 120,293,169 (GRCm39) |
S68G |
probably benign |
Het |
Kctd20 |
T |
C |
17: 29,182,351 (GRCm39) |
|
probably null |
Het |
Klf11 |
T |
C |
12: 24,705,638 (GRCm39) |
V364A |
possibly damaging |
Het |
Kpna6 |
A |
G |
4: 129,551,247 (GRCm39) |
L86P |
probably damaging |
Het |
Lpin1 |
T |
A |
12: 16,611,045 (GRCm39) |
N516Y |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,314,248 (GRCm39) |
Y2161C |
probably damaging |
Het |
Lrrtm3 |
A |
T |
10: 63,923,630 (GRCm39) |
C512* |
probably null |
Het |
Mfsd1 |
T |
C |
3: 67,507,314 (GRCm39) |
I405T |
probably damaging |
Het |
Msc |
T |
G |
1: 14,825,491 (GRCm39) |
D161A |
probably damaging |
Het |
Mttp |
T |
C |
3: 137,800,841 (GRCm39) |
I755V |
probably benign |
Het |
Ncam1 |
T |
C |
9: 49,419,911 (GRCm39) |
T803A |
probably damaging |
Het |
Nlrp14 |
A |
G |
7: 106,795,346 (GRCm39) |
I210V |
probably benign |
Het |
Npat |
A |
T |
9: 53,462,930 (GRCm39) |
H108L |
probably benign |
Het |
Nt5dc1 |
A |
G |
10: 34,189,703 (GRCm39) |
I329T |
possibly damaging |
Het |
Or10v5 |
T |
A |
19: 11,806,178 (GRCm39) |
I71F |
possibly damaging |
Het |
Or51q1c |
T |
A |
7: 103,648,006 (GRCm39) |
|
probably null |
Het |
Or8b35 |
T |
C |
9: 37,904,478 (GRCm39) |
L230P |
possibly damaging |
Het |
Parm1 |
C |
T |
5: 91,742,070 (GRCm39) |
T146I |
possibly damaging |
Het |
Parp2 |
T |
C |
14: 51,058,553 (GRCm39) |
Y528H |
probably damaging |
Het |
Pias1 |
G |
T |
9: 62,789,334 (GRCm39) |
S624R |
probably benign |
Het |
Ppif |
A |
G |
14: 25,696,488 (GRCm39) |
H95R |
probably damaging |
Het |
Prrc2c |
TTGCTGCTGCTGCTGCTGCTGCTGCTGC |
TTGCTGCTGCTGCTGCTGCTGCTGC |
1: 162,536,630 (GRCm39) |
|
probably benign |
Het |
Psg20 |
A |
G |
7: 18,418,345 (GRCm39) |
Y141H |
probably benign |
Het |
Pygm |
A |
T |
19: 6,448,157 (GRCm39) |
Y733F |
probably damaging |
Het |
Rcc1l |
A |
T |
5: 134,205,552 (GRCm39) |
M1K |
probably null |
Het |
Rfpl4b |
T |
C |
10: 38,697,341 (GRCm39) |
K87E |
possibly damaging |
Het |
Rnf113a1 |
A |
C |
X: 36,455,840 (GRCm39) |
T266P |
probably benign |
Het |
Scn5a |
A |
C |
9: 119,324,688 (GRCm39) |
I1380S |
possibly damaging |
Het |
Sel1l |
A |
G |
12: 91,781,742 (GRCm39) |
|
probably null |
Het |
Slc18a1 |
T |
A |
8: 69,493,633 (GRCm39) |
I400L |
probably benign |
Het |
Slc30a3 |
A |
G |
5: 31,246,958 (GRCm39) |
S73P |
probably damaging |
Het |
Slc9a5 |
A |
T |
8: 106,090,600 (GRCm39) |
N685I |
possibly damaging |
Het |
Tnc |
C |
T |
4: 63,883,841 (GRCm39) |
R1868H |
probably benign |
Het |
Trdmt1 |
A |
G |
2: 13,520,824 (GRCm39) |
|
probably null |
Het |
Ttyh1 |
G |
T |
7: 4,136,221 (GRCm39) |
|
probably null |
Het |
Tyms |
A |
T |
5: 30,266,069 (GRCm39) |
D283E |
probably benign |
Het |
Vmn2r110 |
T |
A |
17: 20,803,798 (GRCm39) |
Y259F |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r88 |
C |
A |
14: 51,651,426 (GRCm39) |
Q255K |
probably benign |
Het |
Vmn2r95 |
C |
T |
17: 18,659,555 (GRCm39) |
P100S |
probably damaging |
Het |
Zfp128 |
A |
T |
7: 12,624,826 (GRCm39) |
H398L |
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 |
|
R0326:Lama5
|
UTSW |
2 |
179,824,219 (GRCm39) |
missense |
possibly damaging |
0.90 |
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 |
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 |
|