Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
A |
C |
9: 55,909,807 (GRCm39) |
D144E |
possibly damaging |
Het |
Amigo2 |
T |
A |
15: 97,143,419 (GRCm39) |
K334N |
probably benign |
Het |
Ano6 |
T |
C |
15: 95,846,380 (GRCm39) |
|
probably null |
Het |
Ap1m2 |
C |
A |
9: 21,210,601 (GRCm39) |
V343F |
probably benign |
Het |
Apol6 |
T |
C |
15: 76,940,098 (GRCm39) |
V307A |
probably benign |
Het |
Arsi |
C |
A |
18: 61,045,544 (GRCm39) |
A78E |
probably damaging |
Het |
B2m |
A |
T |
2: 121,981,396 (GRCm39) |
N37I |
possibly damaging |
Het |
Bltp3b |
G |
T |
10: 89,641,180 (GRCm39) |
G784C |
possibly damaging |
Het |
C8a |
T |
C |
4: 104,703,100 (GRCm39) |
K363R |
probably benign |
Het |
Ccdc117 |
C |
A |
11: 5,484,242 (GRCm39) |
|
probably null |
Het |
Ccdc154 |
C |
A |
17: 25,386,945 (GRCm39) |
Q325K |
probably damaging |
Het |
Cd300e |
A |
T |
11: 114,945,359 (GRCm39) |
V145E |
possibly damaging |
Het |
Col19a1 |
G |
T |
1: 24,356,474 (GRCm39) |
P673Q |
probably damaging |
Het |
Csn2 |
A |
G |
5: 87,843,885 (GRCm39) |
|
probably null |
Het |
Ctnna1 |
T |
C |
18: 35,307,408 (GRCm39) |
V135A |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 118,154,632 (GRCm39) |
D216V |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,431,412 (GRCm39) |
H410R |
probably benign |
Het |
Dock2 |
C |
T |
11: 34,181,652 (GRCm39) |
R1637H |
possibly damaging |
Het |
Dspp |
A |
G |
5: 104,325,214 (GRCm39) |
N526D |
unknown |
Het |
Frem2 |
T |
C |
3: 53,562,701 (GRCm39) |
H602R |
probably benign |
Het |
Galc |
A |
T |
12: 98,218,293 (GRCm39) |
H186Q |
probably damaging |
Het |
Grina |
T |
C |
15: 76,133,218 (GRCm39) |
V262A |
probably damaging |
Het |
Gse1 |
G |
A |
8: 121,280,542 (GRCm39) |
|
probably null |
Het |
H2-Oa |
C |
A |
17: 34,312,842 (GRCm39) |
Q40K |
probably damaging |
Het |
Hfm1 |
C |
A |
5: 107,034,419 (GRCm39) |
D763Y |
possibly damaging |
Het |
Hmcn2 |
T |
A |
2: 31,348,758 (GRCm39) |
Y4925N |
probably damaging |
Het |
Hs3st3b1 |
C |
A |
11: 63,780,029 (GRCm39) |
R366L |
probably benign |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Iqank1 |
T |
C |
15: 75,918,218 (GRCm39) |
|
probably null |
Het |
Itpr2 |
A |
G |
6: 146,229,833 (GRCm39) |
V1221A |
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,297,584 (GRCm39) |
N285S |
probably benign |
Het |
Klk1b1 |
T |
A |
7: 43,620,081 (GRCm39) |
N181K |
probably damaging |
Het |
Kmt2a |
C |
A |
9: 44,738,125 (GRCm39) |
|
probably benign |
Het |
Lsm2 |
T |
A |
17: 35,201,131 (GRCm39) |
|
probably benign |
Het |
Map3k5 |
G |
T |
10: 19,899,415 (GRCm39) |
C232F |
probably damaging |
Het |
Mapk9 |
T |
G |
11: 49,754,383 (GRCm39) |
D45E |
probably damaging |
Het |
Mpnd |
T |
C |
17: 56,319,482 (GRCm39) |
V315A |
possibly damaging |
Het |
Msh2 |
A |
G |
17: 88,030,900 (GRCm39) |
I926V |
probably benign |
Het |
Mtcl1 |
C |
T |
17: 66,650,521 (GRCm39) |
R1345H |
probably damaging |
Het |
Nbeal2 |
A |
G |
9: 110,457,058 (GRCm39) |
|
probably null |
Het |
Neo1 |
T |
C |
9: 58,796,312 (GRCm39) |
D1205G |
probably damaging |
Het |
Nhlrc2 |
A |
G |
19: 56,559,291 (GRCm39) |
S259G |
probably benign |
Het |
Nkain4 |
G |
A |
2: 180,577,796 (GRCm39) |
P186L |
probably damaging |
Het |
Nkain4 |
G |
A |
2: 180,577,797 (GRCm39) |
P186S |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,109,283 (GRCm39) |
R73* |
probably null |
Het |
Nr5a2 |
T |
C |
1: 136,818,536 (GRCm39) |
D330G |
probably damaging |
Het |
Nup54 |
A |
G |
5: 92,572,153 (GRCm39) |
L299P |
probably damaging |
Het |
Or2v1 |
T |
C |
11: 49,025,877 (GRCm39) |
L286P |
probably damaging |
Het |
Or5aq7 |
A |
G |
2: 86,938,296 (GRCm39) |
V145A |
probably damaging |
Het |
Pcdhb8 |
T |
A |
18: 37,489,279 (GRCm39) |
V319E |
probably benign |
Het |
Pcsk6 |
T |
A |
7: 65,578,875 (GRCm39) |
D129E |
probably benign |
Het |
Pld5 |
G |
A |
1: 175,798,100 (GRCm39) |
T433I |
probably benign |
Het |
Plin1 |
A |
T |
7: 79,371,347 (GRCm39) |
L459H |
probably benign |
Het |
Psd4 |
T |
C |
2: 24,284,499 (GRCm39) |
V121A |
probably damaging |
Het |
Pxdn |
A |
T |
12: 30,032,716 (GRCm39) |
I167F |
possibly damaging |
Het |
R3hdm2 |
T |
C |
10: 127,320,384 (GRCm39) |
S569P |
probably damaging |
Het |
Rfng |
T |
A |
11: 120,673,516 (GRCm39) |
T202S |
probably damaging |
Het |
Robo1 |
T |
C |
16: 72,730,696 (GRCm39) |
S266P |
probably benign |
Het |
Sema3c |
G |
T |
5: 17,858,804 (GRCm39) |
V68L |
probably damaging |
Het |
Slco6c1 |
C |
T |
1: 96,993,808 (GRCm39) |
R645H |
possibly damaging |
Het |
Slfn8 |
A |
G |
11: 82,907,626 (GRCm39) |
Y306H |
possibly damaging |
Het |
Snap91 |
T |
C |
9: 86,720,105 (GRCm39) |
D144G |
probably damaging |
Het |
St7l |
T |
G |
3: 104,775,349 (GRCm39) |
F75C |
probably damaging |
Het |
Stard10 |
A |
G |
7: 100,992,468 (GRCm39) |
I145V |
probably damaging |
Het |
Tekt3 |
C |
T |
11: 62,968,999 (GRCm39) |
A242V |
probably damaging |
Het |
Tex44 |
A |
G |
1: 86,354,306 (GRCm39) |
|
probably benign |
Het |
Thg1l |
T |
C |
11: 45,844,988 (GRCm39) |
Q88R |
probably benign |
Het |
Trav8n-2 |
T |
A |
14: 53,583,744 (GRCm39) |
I67N |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,677,770 (GRCm39) |
|
probably benign |
Het |
Ube4a |
A |
T |
9: 44,861,051 (GRCm39) |
L253* |
probably null |
Het |
Uggt1 |
A |
T |
1: 36,201,289 (GRCm39) |
N1150K |
probably damaging |
Het |
Ush2a |
T |
A |
1: 187,995,298 (GRCm39) |
L23* |
probably null |
Het |
Usp22 |
T |
A |
11: 61,065,602 (GRCm39) |
N37I |
probably benign |
Het |
Usp53 |
T |
A |
3: 122,743,390 (GRCm39) |
K515N |
probably damaging |
Het |
Vmn2r4 |
T |
C |
3: 64,322,702 (GRCm39) |
K6E |
probably benign |
Het |
Vps13d |
C |
T |
4: 144,875,918 (GRCm39) |
V1530M |
probably damaging |
Het |
Vwa3b |
A |
G |
1: 37,153,612 (GRCm39) |
I485V |
possibly damaging |
Het |
Wnk4 |
T |
C |
11: 101,155,156 (GRCm39) |
Y356H |
probably damaging |
Het |
Zcchc2 |
A |
G |
1: 105,917,900 (GRCm39) |
|
probably benign |
Het |
Zfp345 |
A |
C |
2: 150,315,010 (GRCm39) |
Y176D |
probably benign |
Het |
Zfp598 |
T |
C |
17: 24,896,850 (GRCm39) |
F238S |
possibly damaging |
Het |
Zkscan17 |
T |
C |
11: 59,393,820 (GRCm39) |
D10G |
probably damaging |
Het |
Zmat4 |
T |
G |
8: 24,392,083 (GRCm39) |
M13R |
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 |
179,822,404 (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 |
|