Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
C |
17: 48,348,357 (GRCm39) |
I27V |
probably benign |
Het |
A2ml1 |
T |
A |
6: 128,537,632 (GRCm39) |
H693L |
probably benign |
Het |
Acacb |
A |
G |
5: 114,354,744 (GRCm39) |
E1206G |
probably benign |
Het |
Acoxl |
A |
G |
2: 127,726,432 (GRCm39) |
T269A |
probably benign |
Het |
Ak9 |
A |
G |
10: 41,309,235 (GRCm39) |
K1879R |
unknown |
Het |
Amot |
A |
T |
X: 144,244,745 (GRCm39) |
L435H |
|
Het |
Bnc2 |
A |
T |
4: 84,329,731 (GRCm39) |
L95Q |
|
Het |
Bpifa2 |
G |
T |
2: 153,851,741 (GRCm39) |
W59L |
probably benign |
Het |
Cd209a |
T |
A |
8: 3,795,602 (GRCm39) |
Q156H |
probably damaging |
Het |
Cep104 |
T |
A |
4: 154,078,971 (GRCm39) |
|
probably null |
Het |
Cpt1c |
A |
G |
7: 44,608,925 (GRCm39) |
*799R |
probably null |
Het |
Csn2 |
A |
T |
5: 87,842,418 (GRCm39) |
M203K |
possibly damaging |
Het |
Dclre1a |
C |
G |
19: 56,526,801 (GRCm39) |
A872P |
probably damaging |
Het |
Dlg5 |
C |
A |
14: 24,196,309 (GRCm39) |
L1629F |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,011,992 (GRCm39) |
D1383G |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,121,924 (GRCm39) |
V1381A |
probably damaging |
Het |
Dnttip2 |
G |
T |
3: 122,070,355 (GRCm39) |
E523D |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,114,883 (GRCm39) |
V2425D |
probably damaging |
Het |
Eif1ad11 |
A |
G |
12: 87,994,077 (GRCm39) |
S102G |
possibly damaging |
Het |
Eif2a |
G |
A |
3: 58,452,695 (GRCm39) |
R199Q |
probably damaging |
Het |
F10 |
T |
C |
8: 13,089,564 (GRCm39) |
F60L |
probably benign |
Het |
Faf2 |
A |
G |
13: 54,799,951 (GRCm39) |
I253V |
probably benign |
Het |
Flt1 |
T |
A |
5: 147,552,047 (GRCm39) |
S715C |
probably damaging |
Het |
Garin4 |
A |
G |
1: 190,895,258 (GRCm39) |
S462P |
probably benign |
Het |
Gm5150 |
G |
T |
3: 16,045,060 (GRCm39) |
T55K |
probably damaging |
Het |
Gria1 |
T |
C |
11: 57,076,759 (GRCm39) |
F121L |
possibly damaging |
Het |
Gucy2d |
A |
G |
7: 98,103,271 (GRCm39) |
Q505R |
probably benign |
Het |
Gzma |
A |
T |
13: 113,237,455 (GRCm39) |
S11T |
probably benign |
Het |
Hoxa6 |
G |
A |
6: 52,185,535 (GRCm39) |
Q24* |
probably null |
Het |
Kcnj14 |
T |
A |
7: 45,469,068 (GRCm39) |
I146L |
possibly damaging |
Het |
Kiss1r |
G |
A |
10: 79,756,605 (GRCm39) |
R149H |
probably damaging |
Het |
Lama2 |
A |
G |
10: 26,929,022 (GRCm39) |
|
probably null |
Het |
Lca5l |
T |
A |
16: 95,977,218 (GRCm39) |
N196I |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,022,394 (GRCm39) |
L462S |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,912,289 (GRCm39) |
V1166E |
probably benign |
Het |
Nr2c1 |
T |
A |
10: 94,017,465 (GRCm39) |
F401Y |
probably benign |
Het |
Or10ak12 |
T |
A |
4: 118,666,195 (GRCm39) |
R289* |
probably null |
Het |
Or14c43 |
A |
T |
7: 86,114,825 (GRCm39) |
M69L |
probably benign |
Het |
Or4e5 |
A |
G |
14: 52,727,830 (GRCm39) |
I197T |
possibly damaging |
Het |
Or5an9 |
A |
T |
19: 12,187,286 (GRCm39) |
M119L |
probably damaging |
Het |
Otop3 |
A |
C |
11: 115,235,424 (GRCm39) |
Y352S |
possibly damaging |
Het |
Plekha6 |
T |
G |
1: 133,200,375 (GRCm39) |
L318R |
probably damaging |
Het |
Pm20d1 |
G |
T |
1: 131,743,825 (GRCm39) |
V497F |
possibly damaging |
Het |
Pnma2 |
G |
A |
14: 67,154,572 (GRCm39) |
R332H |
probably damaging |
Het |
Ppip5k1 |
C |
A |
2: 121,162,045 (GRCm39) |
G1013C |
probably damaging |
Het |
Prdm13 |
C |
G |
4: 21,679,659 (GRCm39) |
R277P |
unknown |
Het |
Prdm2 |
A |
G |
4: 142,858,674 (GRCm39) |
S1539P |
possibly damaging |
Het |
Ptger2 |
A |
G |
14: 45,227,235 (GRCm39) |
T272A |
probably damaging |
Het |
Qser1 |
T |
C |
2: 104,618,815 (GRCm39) |
T576A |
probably benign |
Het |
Rest |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
GGGGGCCTGCCCCTCCCACGGGGCCTGCCCCTCCCACGGAGCCTGCCCCTCCCACGGGGC |
5: 77,429,651 (GRCm39) |
|
probably benign |
Het |
Sacm1l |
G |
T |
9: 123,398,021 (GRCm39) |
V238L |
probably damaging |
Het |
Sanbr |
T |
C |
11: 23,565,244 (GRCm39) |
I248V |
probably benign |
Het |
Sec16a |
C |
T |
2: 26,313,645 (GRCm39) |
G454D |
|
Het |
Sil1 |
A |
G |
18: 35,450,899 (GRCm39) |
S259P |
possibly damaging |
Het |
Sirpb1b |
A |
G |
3: 15,639,964 (GRCm39) |
L16P |
probably damaging |
Het |
Slc22a20 |
A |
T |
19: 6,032,879 (GRCm39) |
V262D |
probably damaging |
Het |
Slc4a9 |
G |
T |
18: 36,666,676 (GRCm39) |
R580L |
probably benign |
Het |
Ssr3 |
A |
G |
3: 65,290,521 (GRCm39) |
V128A |
probably damaging |
Het |
Stpg2 |
G |
T |
3: 139,014,993 (GRCm39) |
S386I |
possibly damaging |
Het |
Taar8c |
C |
A |
10: 23,977,500 (GRCm39) |
C104F |
probably damaging |
Het |
Tex2 |
T |
C |
11: 106,458,095 (GRCm39) |
E445G |
unknown |
Het |
Tmem253 |
A |
C |
14: 52,256,099 (GRCm39) |
D126A |
probably benign |
Het |
Tox4 |
A |
G |
14: 52,523,247 (GRCm39) |
Q69R |
possibly damaging |
Het |
Tpi1 |
T |
A |
6: 124,788,501 (GRCm39) |
S254C |
probably benign |
Het |
Trmt12 |
T |
G |
15: 58,745,594 (GRCm39) |
S331A |
probably benign |
Het |
Ttn |
A |
G |
2: 76,543,350 (GRCm39) |
V33212A |
probably damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,734 (GRCm39) |
E431K |
unknown |
Het |
Ugt1a10 |
A |
T |
1: 87,983,509 (GRCm39) |
E102D |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,589,000 (GRCm39) |
E1055V |
probably null |
Het |
Vav1 |
C |
A |
17: 57,618,895 (GRCm39) |
S708R |
probably damaging |
Het |
Vmn1r20 |
A |
G |
6: 57,409,246 (GRCm39) |
M191V |
probably damaging |
Het |
Vmn1r37 |
A |
T |
6: 66,709,054 (GRCm39) |
T227S |
probably damaging |
Het |
Vmn1r72 |
C |
A |
7: 11,412,951 (GRCm39) |
|
probably benign |
Het |
Vps33b |
G |
A |
7: 79,924,434 (GRCm39) |
|
probably null |
Het |
Vrtn |
T |
A |
12: 84,697,251 (GRCm39) |
L667Q |
probably benign |
Het |
Xirp1 |
G |
A |
9: 119,847,302 (GRCm39) |
T527M |
probably benign |
Het |
Ylpm1 |
T |
A |
12: 85,077,342 (GRCm39) |
Y1356N |
probably damaging |
Het |
Zfp980 |
A |
T |
4: 145,428,024 (GRCm39) |
Y251F |
possibly damaging |
Het |
Zmym2 |
A |
T |
14: 57,185,464 (GRCm39) |
Y1032F |
probably 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 |
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 |
|
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 |
|