Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
T |
C |
7: 29,260,131 (GRCm39) |
|
noncoding transcript |
Het |
4930568D16Rik |
A |
G |
2: 35,244,995 (GRCm39) |
M119T |
probably damaging |
Het |
Aadacl2 |
A |
G |
3: 59,924,871 (GRCm39) |
|
probably null |
Het |
Abca9 |
C |
T |
11: 110,021,542 (GRCm39) |
W1056* |
probably null |
Het |
Adam20 |
A |
C |
8: 41,249,698 (GRCm39) |
T603P |
possibly damaging |
Het |
Adgrl1 |
T |
C |
8: 84,656,666 (GRCm39) |
L323P |
probably damaging |
Het |
Afap1l2 |
C |
T |
19: 56,904,638 (GRCm39) |
E628K |
possibly damaging |
Het |
Ahctf1 |
A |
T |
1: 179,580,580 (GRCm39) |
L1874Q |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,602,333 (GRCm39) |
E89G |
probably benign |
Het |
Aldh16a1 |
G |
A |
7: 44,796,732 (GRCm39) |
R256C |
probably damaging |
Het |
Anxa5 |
G |
A |
3: 36,519,480 (GRCm39) |
T3M |
probably damaging |
Het |
Arhgef16 |
T |
C |
4: 154,372,443 (GRCm39) |
K210E |
probably benign |
Het |
Baz2b |
T |
C |
2: 59,836,480 (GRCm39) |
T18A |
unknown |
Het |
Bub1 |
A |
C |
2: 127,645,042 (GRCm39) |
I960M |
possibly damaging |
Het |
Cbln2 |
G |
T |
18: 86,731,272 (GRCm39) |
D27Y |
probably benign |
Het |
Ces2h |
C |
A |
8: 105,741,239 (GRCm39) |
P77Q |
possibly damaging |
Het |
Cfap410 |
G |
T |
10: 77,818,778 (GRCm39) |
A150S |
probably benign |
Het |
Chga |
T |
A |
12: 102,527,959 (GRCm39) |
M150K |
probably benign |
Het |
Chmp3 |
A |
G |
6: 71,554,791 (GRCm39) |
E162G |
probably benign |
Het |
Clip3 |
A |
G |
7: 29,996,861 (GRCm39) |
N161S |
probably damaging |
Het |
Col12a1 |
T |
A |
9: 79,511,867 (GRCm39) |
|
probably benign |
Het |
Cuedc2 |
C |
T |
19: 46,320,079 (GRCm39) |
G105D |
probably benign |
Het |
Cyp2j7 |
A |
C |
4: 96,087,627 (GRCm39) |
F428V |
probably damaging |
Het |
Ddx60 |
A |
G |
8: 62,427,210 (GRCm39) |
I762V |
possibly damaging |
Het |
Def6 |
G |
A |
17: 28,439,160 (GRCm39) |
R257Q |
probably benign |
Het |
Dkkl1 |
A |
T |
7: 44,860,819 (GRCm39) |
|
probably null |
Het |
Dnah3 |
A |
G |
7: 119,677,625 (GRCm39) |
L433P |
probably damaging |
Het |
Eif2s3y |
C |
T |
Y: 1,011,287 (GRCm39) |
R33C |
probably benign |
Het |
Elavl2 |
T |
A |
4: 91,141,715 (GRCm39) |
Y269F |
probably damaging |
Het |
Esco2 |
A |
G |
14: 66,068,711 (GRCm39) |
S200P |
possibly damaging |
Het |
Fcrl1 |
T |
A |
3: 87,292,626 (GRCm39) |
|
probably benign |
Het |
Fhod1 |
C |
A |
8: 106,056,309 (GRCm39) |
D1135Y |
probably damaging |
Het |
Fnbp1l |
T |
C |
3: 122,383,796 (GRCm39) |
N41D |
possibly damaging |
Het |
Folh1 |
A |
T |
7: 86,410,907 (GRCm39) |
|
probably null |
Het |
Fpr-rs7 |
T |
C |
17: 20,334,277 (GRCm39) |
D71G |
probably damaging |
Het |
Gm10271 |
A |
G |
10: 116,797,844 (GRCm39) |
|
probably benign |
Het |
Gm4841 |
A |
T |
18: 60,404,020 (GRCm39) |
Y24* |
probably null |
Het |
Greb1 |
G |
A |
12: 16,740,895 (GRCm39) |
R1396C |
probably benign |
Het |
Hectd1 |
C |
T |
12: 51,800,590 (GRCm39) |
C2076Y |
probably damaging |
Het |
Hnrnpu |
A |
G |
1: 178,152,806 (GRCm39) |
|
probably benign |
Het |
Ice2 |
T |
C |
9: 69,322,930 (GRCm39) |
I475T |
probably benign |
Het |
Ifit1bl1 |
T |
A |
19: 34,571,593 (GRCm39) |
Q288L |
probably damaging |
Het |
Ift56 |
T |
A |
6: 38,386,411 (GRCm39) |
D377E |
possibly damaging |
Het |
Ik |
T |
C |
18: 36,889,871 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
C |
T |
12: 25,063,445 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,577,972 (GRCm39) |
D768G |
probably benign |
Het |
Kmt2e |
A |
G |
5: 23,697,362 (GRCm39) |
T87A |
probably damaging |
Het |
Lmbr1l |
A |
G |
15: 98,810,357 (GRCm39) |
S85P |
probably damaging |
Het |
Lrig2 |
A |
G |
3: 104,374,682 (GRCm39) |
|
probably benign |
Het |
Lrig3 |
A |
G |
10: 125,845,944 (GRCm39) |
D791G |
probably damaging |
Het |
Lrrc2 |
G |
A |
9: 110,809,908 (GRCm39) |
V315M |
probably benign |
Het |
Lrrc4b |
A |
G |
7: 44,111,823 (GRCm39) |
D565G |
probably benign |
Het |
Mpped1 |
C |
T |
15: 83,676,191 (GRCm39) |
|
probably benign |
Het |
Msrb2 |
T |
A |
2: 19,388,114 (GRCm39) |
D87E |
probably benign |
Het |
Muc20 |
T |
C |
16: 32,614,511 (GRCm39) |
T289A |
possibly damaging |
Het |
Myo15a |
C |
A |
11: 60,369,238 (GRCm39) |
P666Q |
possibly damaging |
Het |
Nfat5 |
C |
T |
8: 108,088,421 (GRCm39) |
P579L |
probably damaging |
Het |
Nipbl |
A |
C |
15: 8,348,972 (GRCm39) |
M1920R |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,210,738 (GRCm39) |
|
probably null |
Het |
Nup210l |
A |
G |
3: 90,096,793 (GRCm39) |
E1334G |
probably damaging |
Het |
Odad2 |
A |
T |
18: 7,127,388 (GRCm39) |
C942S |
probably damaging |
Het |
Or52e8b |
A |
T |
7: 104,673,370 (GRCm39) |
N272K |
probably benign |
Het |
Or5an1c |
T |
A |
19: 12,218,819 (GRCm39) |
I69F |
probably benign |
Het |
Or6c6c |
T |
C |
10: 129,541,574 (GRCm39) |
Y276H |
probably benign |
Het |
Or9s13 |
G |
A |
1: 92,548,342 (GRCm39) |
G238E |
possibly damaging |
Het |
Or9s14 |
A |
T |
1: 92,535,831 (GRCm39) |
N91Y |
possibly damaging |
Het |
P4ha3 |
A |
T |
7: 99,949,898 (GRCm39) |
|
probably null |
Het |
Pbld2 |
C |
T |
10: 62,890,150 (GRCm39) |
A186V |
probably benign |
Het |
Pcdh18 |
A |
T |
3: 49,710,083 (GRCm39) |
Y411N |
probably benign |
Het |
Pgf |
A |
G |
12: 85,218,541 (GRCm39) |
S70P |
probably benign |
Het |
Phrf1 |
T |
A |
7: 140,812,369 (GRCm39) |
D44E |
probably benign |
Het |
Pla2g4a |
A |
G |
1: 149,778,196 (GRCm39) |
|
probably benign |
Het |
Plce1 |
A |
G |
19: 38,769,234 (GRCm39) |
|
probably benign |
Het |
Plxna2 |
A |
G |
1: 194,493,278 (GRCm39) |
N1851S |
probably benign |
Het |
Prl7a2 |
G |
A |
13: 27,843,254 (GRCm39) |
T183I |
probably damaging |
Het |
Prxl2b |
A |
T |
4: 154,981,814 (GRCm39) |
V151D |
probably damaging |
Het |
Ptger4 |
A |
T |
15: 5,264,576 (GRCm39) |
L335H |
probably damaging |
Het |
Ptgr1 |
A |
G |
4: 58,984,865 (GRCm39) |
|
probably benign |
Het |
Rdh7 |
A |
G |
10: 127,720,590 (GRCm39) |
S261P |
probably benign |
Het |
Reg3a |
A |
G |
6: 78,360,269 (GRCm39) |
T150A |
probably benign |
Het |
Rnf111 |
A |
G |
9: 70,383,394 (GRCm39) |
S180P |
probably benign |
Het |
Rnf17 |
A |
G |
14: 56,759,856 (GRCm39) |
M1554V |
probably damaging |
Het |
Rnf215 |
T |
A |
11: 4,085,873 (GRCm39) |
Y117* |
probably null |
Het |
Rnps1-ps |
A |
T |
6: 7,983,124 (GRCm39) |
|
noncoding transcript |
Het |
Rogdi |
T |
C |
16: 4,828,369 (GRCm39) |
T165A |
probably benign |
Het |
Rpe65 |
A |
G |
3: 159,328,485 (GRCm39) |
Y431C |
probably damaging |
Het |
Scube1 |
A |
G |
15: 83,494,405 (GRCm39) |
F844S |
probably damaging |
Het |
Sdr16c6 |
T |
A |
4: 4,058,814 (GRCm39) |
E257D |
probably benign |
Het |
Sim1 |
C |
A |
10: 50,857,649 (GRCm39) |
C466* |
probably null |
Het |
Spi1 |
T |
A |
2: 90,929,867 (GRCm39) |
H46Q |
probably damaging |
Het |
Sumf2 |
C |
A |
5: 129,873,909 (GRCm39) |
|
probably benign |
Het |
Tbcb |
A |
G |
7: 29,931,037 (GRCm39) |
Y28H |
probably benign |
Het |
Tecta |
C |
T |
9: 42,254,927 (GRCm39) |
C1752Y |
probably damaging |
Het |
Tep1 |
T |
C |
14: 51,067,079 (GRCm39) |
|
probably benign |
Het |
Tmem245 |
A |
T |
4: 56,903,968 (GRCm39) |
W591R |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,902,548 (GRCm39) |
I1134V |
probably benign |
Het |
Trappc14 |
T |
C |
5: 138,260,739 (GRCm39) |
|
probably null |
Het |
Trim13 |
G |
T |
14: 61,843,068 (GRCm39) |
A362S |
probably benign |
Het |
Trim47 |
T |
A |
11: 116,000,646 (GRCm39) |
D134V |
probably damaging |
Het |
Utrn |
C |
A |
10: 12,312,108 (GRCm39) |
D616Y |
probably damaging |
Het |
Vnn1 |
G |
T |
10: 23,775,415 (GRCm39) |
A222S |
possibly damaging |
Het |
Wdr17 |
A |
G |
8: 55,143,249 (GRCm39) |
W110R |
probably damaging |
Het |
Wwp1 |
G |
T |
4: 19,627,892 (GRCm39) |
Y700* |
probably null |
Het |
Zbtb21 |
T |
C |
16: 97,751,785 (GRCm39) |
S661G |
probably benign |
Het |
Zfp955b |
A |
G |
17: 33,521,788 (GRCm39) |
K419R |
probably benign |
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 |
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 |
|