Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
A |
G |
8: 41,279,610 (GRCm39) |
N667S |
probably benign |
Het |
Ap4e1 |
T |
A |
2: 126,908,508 (GRCm39) |
C1085* |
probably null |
Het |
BC035044 |
A |
T |
6: 128,861,997 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
A |
G |
11: 78,164,084 (GRCm39) |
M1142V |
possibly damaging |
Het |
Capn11 |
T |
C |
17: 45,941,692 (GRCm39) |
D693G |
probably damaging |
Het |
Cavin4 |
A |
T |
4: 48,663,917 (GRCm39) |
H99L |
possibly damaging |
Het |
Ccdc86 |
T |
C |
19: 10,925,945 (GRCm39) |
K218R |
possibly damaging |
Het |
Ccno |
T |
C |
13: 113,126,379 (GRCm39) |
S283P |
probably damaging |
Het |
Ccser2 |
A |
T |
14: 36,662,276 (GRCm39) |
S303T |
probably benign |
Het |
Cd53 |
T |
A |
3: 106,674,680 (GRCm39) |
N129I |
probably damaging |
Het |
Cd63 |
G |
A |
10: 128,747,933 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
G |
C |
4: 96,424,323 (GRCm39) |
L145V |
probably damaging |
Het |
Daam2 |
A |
G |
17: 49,776,694 (GRCm39) |
M797T |
probably damaging |
Het |
Dennd2b |
A |
C |
7: 109,156,095 (GRCm39) |
D218E |
probably benign |
Het |
Dmgdh |
G |
A |
13: 93,888,794 (GRCm39) |
V811I |
possibly damaging |
Het |
Dpysl4 |
A |
T |
7: 138,670,250 (GRCm39) |
T123S |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,814,345 (GRCm39) |
E428G |
possibly damaging |
Het |
Fam124b |
T |
A |
1: 80,177,902 (GRCm39) |
T366S |
possibly damaging |
Het |
Fbxw22 |
T |
C |
9: 109,215,747 (GRCm39) |
D167G |
probably damaging |
Het |
Flrt2 |
C |
T |
12: 95,746,012 (GRCm39) |
Q117* |
probably null |
Het |
Ftsj3 |
A |
T |
11: 106,144,166 (GRCm39) |
|
probably null |
Het |
Ggn |
A |
G |
7: 28,872,474 (GRCm39) |
Y618C |
probably damaging |
Het |
Glis1 |
T |
A |
4: 107,484,710 (GRCm39) |
S402T |
probably benign |
Het |
Gm4781 |
T |
A |
10: 100,232,349 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
T |
A |
17: 14,168,858 (GRCm39) |
I75K |
probably damaging |
Het |
Gm7298 |
C |
T |
6: 121,737,782 (GRCm39) |
H348Y |
probably benign |
Het |
Gria1 |
G |
T |
11: 57,133,618 (GRCm39) |
R499L |
probably damaging |
Het |
Gtf2ird2 |
C |
T |
5: 134,245,389 (GRCm39) |
T549M |
probably damaging |
Het |
H2-M10.6 |
T |
A |
17: 37,125,178 (GRCm39) |
V323E |
probably damaging |
Het |
Hoxb3 |
G |
A |
11: 96,236,929 (GRCm39) |
V336I |
probably benign |
Het |
Il12b |
G |
A |
11: 44,303,453 (GRCm39) |
A327T |
probably benign |
Het |
Inpp4a |
C |
A |
1: 37,419,183 (GRCm39) |
P588T |
probably benign |
Het |
Kctd12 |
C |
A |
14: 103,219,027 (GRCm39) |
D284Y |
probably damaging |
Het |
Kif28 |
C |
A |
1: 179,525,337 (GRCm39) |
|
probably null |
Het |
Krt1c |
T |
C |
15: 101,723,479 (GRCm39) |
N332S |
probably benign |
Het |
Lgi1 |
T |
C |
19: 38,253,404 (GRCm39) |
L25P |
probably damaging |
Het |
Lhx3 |
T |
A |
2: 26,091,503 (GRCm39) |
M269L |
probably benign |
Het |
Lmtk2 |
A |
T |
5: 144,112,160 (GRCm39) |
E960V |
probably damaging |
Het |
Loxl4 |
A |
T |
19: 42,596,791 (GRCm39) |
D60E |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,333,868 (GRCm39) |
N1458Y |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,224,677 (GRCm39) |
S16T |
probably damaging |
Het |
Mllt6 |
G |
A |
11: 97,569,362 (GRCm39) |
A875T |
possibly damaging |
Het |
Mrgprb4 |
A |
T |
7: 47,848,574 (GRCm39) |
I118N |
probably damaging |
Het |
Mrps7 |
A |
G |
11: 115,495,707 (GRCm39) |
T82A |
possibly damaging |
Het |
Mug2 |
A |
G |
6: 122,056,565 (GRCm39) |
E1170G |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,107,915 (GRCm39) |
H647R |
probably benign |
Het |
Nbeal2 |
T |
C |
9: 110,454,215 (GRCm39) |
Y2710C |
probably damaging |
Het |
Ndc1 |
A |
T |
4: 107,268,395 (GRCm39) |
I644L |
possibly damaging |
Het |
Or4c108 |
T |
G |
2: 88,804,226 (GRCm39) |
N3T |
probably damaging |
Het |
Or8g33 |
A |
T |
9: 39,338,008 (GRCm39) |
Y120N |
probably damaging |
Het |
Padi4 |
A |
G |
4: 140,483,784 (GRCm39) |
M352T |
possibly damaging |
Het |
Pals1 |
C |
T |
12: 78,864,084 (GRCm39) |
H216Y |
probably benign |
Het |
Pcdhgc3 |
C |
A |
18: 37,939,990 (GRCm39) |
D130E |
probably damaging |
Het |
Pde6a |
A |
T |
18: 61,417,163 (GRCm39) |
|
probably null |
Het |
Pdpn |
C |
T |
4: 143,025,792 (GRCm39) |
G12R |
probably damaging |
Het |
Pot1a |
A |
T |
6: 25,771,620 (GRCm39) |
D200E |
probably benign |
Het |
Ppa1 |
A |
T |
10: 61,503,431 (GRCm39) |
D236V |
probably benign |
Het |
Ptprn2 |
T |
A |
12: 116,822,739 (GRCm39) |
S273T |
probably benign |
Het |
Rasgrf2 |
T |
C |
13: 92,165,609 (GRCm39) |
E297G |
probably damaging |
Het |
Rgl1 |
T |
C |
1: 152,394,923 (GRCm39) |
N750S |
probably damaging |
Het |
Rinl |
A |
G |
7: 28,496,365 (GRCm39) |
N449D |
probably benign |
Het |
Samd8 |
T |
A |
14: 21,825,093 (GRCm39) |
H79Q |
probably benign |
Het |
Scn11a |
T |
C |
9: 119,583,933 (GRCm39) |
I1561V |
probably benign |
Het |
Slc39a12 |
T |
C |
2: 14,400,938 (GRCm39) |
L105P |
probably benign |
Het |
Slc7a12 |
A |
T |
3: 14,546,200 (GRCm39) |
|
probably null |
Het |
Slco1a4 |
A |
G |
6: 141,763,546 (GRCm39) |
I390T |
possibly damaging |
Het |
Snta1 |
T |
C |
2: 154,219,102 (GRCm39) |
N411S |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,277,279 (GRCm39) |
T323A |
probably benign |
Het |
Ssh2 |
G |
T |
11: 77,344,291 (GRCm39) |
V759L |
probably benign |
Het |
Swap70 |
G |
T |
7: 109,869,188 (GRCm39) |
R327L |
probably damaging |
Het |
Tbc1d4 |
C |
A |
14: 101,696,206 (GRCm39) |
C914F |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,812,132 (GRCm39) |
D144G |
probably damaging |
Het |
Tgfbr2 |
T |
C |
9: 115,939,212 (GRCm39) |
K205R |
possibly damaging |
Het |
Tmem94 |
A |
T |
11: 115,681,857 (GRCm39) |
|
probably null |
Het |
Usf3 |
T |
A |
16: 44,041,468 (GRCm39) |
F1983I |
probably damaging |
Het |
Ush2a |
T |
A |
1: 188,132,068 (GRCm39) |
C763* |
probably null |
Het |
Vmn1r115 |
A |
C |
7: 20,578,640 (GRCm39) |
L91V |
probably damaging |
Het |
Vmn1r201 |
A |
T |
13: 22,659,499 (GRCm39) |
I238F |
possibly damaging |
Het |
Vmn1r28 |
T |
A |
6: 58,242,476 (GRCm39) |
S106R |
probably damaging |
Het |
Vmn1r82 |
T |
C |
7: 12,039,012 (GRCm39) |
V95A |
probably damaging |
Het |
Vrk3 |
A |
T |
7: 44,419,035 (GRCm39) |
N371I |
possibly damaging |
Het |
Wnt8b |
C |
A |
19: 44,500,082 (GRCm39) |
A223E |
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,335,921 (GRCm39) |
|
probably null |
Het |
Xpo7 |
T |
C |
14: 70,920,243 (GRCm39) |
N642S |
probably benign |
Het |
Ythdc1 |
G |
A |
5: 86,975,953 (GRCm39) |
R520H |
possibly damaging |
Het |
Zfp367 |
T |
C |
13: 64,283,204 (GRCm39) |
E316G |
probably damaging |
Het |
Zfp488 |
T |
A |
14: 33,692,751 (GRCm39) |
R137S |
possibly damaging |
Het |
Zfp532 |
G |
T |
18: 65,789,542 (GRCm39) |
V994L |
probably benign |
Het |
|
Other mutations in Lama2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Lama2
|
APN |
10 |
27,064,261 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00467:Lama2
|
APN |
10 |
27,343,193 (GRCm39) |
splice site |
probably benign |
|
IGL00470:Lama2
|
APN |
10 |
27,119,738 (GRCm39) |
missense |
probably benign |
0.22 |
IGL00517:Lama2
|
APN |
10 |
27,073,326 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00541:Lama2
|
APN |
10 |
27,064,302 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00931:Lama2
|
APN |
10 |
26,882,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00951:Lama2
|
APN |
10 |
26,906,281 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00988:Lama2
|
APN |
10 |
27,245,011 (GRCm39) |
nonsense |
probably null |
|
IGL01098:Lama2
|
APN |
10 |
26,907,108 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01152:Lama2
|
APN |
10 |
27,084,425 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01293:Lama2
|
APN |
10 |
27,107,632 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01338:Lama2
|
APN |
10 |
27,064,268 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01609:Lama2
|
APN |
10 |
27,220,417 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01643:Lama2
|
APN |
10 |
26,946,368 (GRCm39) |
splice site |
probably benign |
|
IGL01675:Lama2
|
APN |
10 |
27,064,050 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01681:Lama2
|
APN |
10 |
27,141,041 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01694:Lama2
|
APN |
10 |
26,882,738 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01705:Lama2
|
APN |
10 |
27,065,270 (GRCm39) |
splice site |
probably benign |
|
IGL01885:Lama2
|
APN |
10 |
26,981,135 (GRCm39) |
nonsense |
probably null |
|
IGL01935:Lama2
|
APN |
10 |
27,298,600 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01994:Lama2
|
APN |
10 |
27,343,199 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02041:Lama2
|
APN |
10 |
26,860,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02067:Lama2
|
APN |
10 |
27,052,792 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02097:Lama2
|
APN |
10 |
27,014,956 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02179:Lama2
|
APN |
10 |
26,946,360 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02268:Lama2
|
APN |
10 |
26,877,112 (GRCm39) |
splice site |
probably benign |
|
IGL02302:Lama2
|
APN |
10 |
27,088,039 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02363:Lama2
|
APN |
10 |
27,242,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02378:Lama2
|
APN |
10 |
26,919,652 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02642:Lama2
|
APN |
10 |
27,343,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02676:Lama2
|
APN |
10 |
26,994,489 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02695:Lama2
|
APN |
10 |
26,876,771 (GRCm39) |
missense |
probably benign |
|
IGL02735:Lama2
|
APN |
10 |
26,980,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02794:Lama2
|
APN |
10 |
26,917,227 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02823:Lama2
|
APN |
10 |
26,877,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02869:Lama2
|
APN |
10 |
26,891,534 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02942:Lama2
|
APN |
10 |
26,917,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03201:Lama2
|
APN |
10 |
27,220,566 (GRCm39) |
nonsense |
probably null |
|
IGL03268:Lama2
|
APN |
10 |
27,298,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Lama2
|
APN |
10 |
27,245,047 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03380:Lama2
|
APN |
10 |
26,926,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03407:Lama2
|
APN |
10 |
27,223,017 (GRCm39) |
missense |
probably damaging |
1.00 |
cowboy
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
petri
|
UTSW |
10 |
26,869,394 (GRCm39) |
splice site |
probably null |
|
PIT4362001:Lama2
|
UTSW |
10 |
27,245,132 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Lama2
|
UTSW |
10 |
27,080,901 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Lama2
|
UTSW |
10 |
26,977,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Lama2
|
UTSW |
10 |
26,862,793 (GRCm39) |
missense |
probably benign |
0.02 |
R0038:Lama2
|
UTSW |
10 |
26,862,793 (GRCm39) |
missense |
probably benign |
0.02 |
R0114:Lama2
|
UTSW |
10 |
26,869,064 (GRCm39) |
nonsense |
probably null |
|
R0142:Lama2
|
UTSW |
10 |
27,063,841 (GRCm39) |
missense |
probably benign |
|
R0313:Lama2
|
UTSW |
10 |
26,869,394 (GRCm39) |
splice site |
probably null |
|
R0376:Lama2
|
UTSW |
10 |
26,891,542 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0412:Lama2
|
UTSW |
10 |
27,066,621 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0472:Lama2
|
UTSW |
10 |
26,866,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Lama2
|
UTSW |
10 |
27,065,127 (GRCm39) |
missense |
probably benign |
0.34 |
R0648:Lama2
|
UTSW |
10 |
26,865,372 (GRCm39) |
missense |
probably benign |
0.00 |
R0667:Lama2
|
UTSW |
10 |
27,220,406 (GRCm39) |
splice site |
probably null |
|
R0760:Lama2
|
UTSW |
10 |
26,920,429 (GRCm39) |
critical splice donor site |
probably null |
|
R1240:Lama2
|
UTSW |
10 |
26,917,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1385:Lama2
|
UTSW |
10 |
27,100,039 (GRCm39) |
missense |
probably benign |
0.11 |
R1433:Lama2
|
UTSW |
10 |
27,063,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Lama2
|
UTSW |
10 |
27,084,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Lama2
|
UTSW |
10 |
27,200,750 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1574:Lama2
|
UTSW |
10 |
27,200,750 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1645:Lama2
|
UTSW |
10 |
27,244,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Lama2
|
UTSW |
10 |
27,066,525 (GRCm39) |
missense |
probably benign |
|
R1703:Lama2
|
UTSW |
10 |
27,142,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Lama2
|
UTSW |
10 |
27,084,403 (GRCm39) |
missense |
probably benign |
|
R1769:Lama2
|
UTSW |
10 |
27,084,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Lama2
|
UTSW |
10 |
27,088,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Lama2
|
UTSW |
10 |
26,907,078 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1871:Lama2
|
UTSW |
10 |
26,860,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Lama2
|
UTSW |
10 |
27,064,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R1906:Lama2
|
UTSW |
10 |
26,932,523 (GRCm39) |
critical splice donor site |
probably null |
|
R1958:Lama2
|
UTSW |
10 |
26,857,594 (GRCm39) |
missense |
probably damaging |
0.97 |
R1959:Lama2
|
UTSW |
10 |
27,298,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R1977:Lama2
|
UTSW |
10 |
26,866,796 (GRCm39) |
splice site |
probably null |
|
R2063:Lama2
|
UTSW |
10 |
27,040,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Lama2
|
UTSW |
10 |
27,245,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R2085:Lama2
|
UTSW |
10 |
27,080,837 (GRCm39) |
nonsense |
probably null |
|
R2125:Lama2
|
UTSW |
10 |
26,920,449 (GRCm39) |
nonsense |
probably null |
|
R2140:Lama2
|
UTSW |
10 |
26,930,690 (GRCm39) |
splice site |
probably null |
|
R2219:Lama2
|
UTSW |
10 |
26,919,565 (GRCm39) |
missense |
probably damaging |
0.99 |
R2259:Lama2
|
UTSW |
10 |
26,907,123 (GRCm39) |
missense |
probably benign |
0.00 |
R2265:Lama2
|
UTSW |
10 |
26,868,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R2266:Lama2
|
UTSW |
10 |
26,862,793 (GRCm39) |
missense |
probably benign |
0.02 |
R2267:Lama2
|
UTSW |
10 |
26,868,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Lama2
|
UTSW |
10 |
26,868,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Lama2
|
UTSW |
10 |
26,868,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:Lama2
|
UTSW |
10 |
27,298,608 (GRCm39) |
nonsense |
probably null |
|
R2912:Lama2
|
UTSW |
10 |
26,876,799 (GRCm39) |
missense |
probably benign |
|
R2999:Lama2
|
UTSW |
10 |
26,865,417 (GRCm39) |
missense |
probably benign |
0.18 |
R3034:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3081:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3107:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3109:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3436:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3437:Lama2
|
UTSW |
10 |
26,877,231 (GRCm39) |
missense |
probably benign |
0.11 |
R3706:Lama2
|
UTSW |
10 |
27,014,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Lama2
|
UTSW |
10 |
27,335,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Lama2
|
UTSW |
10 |
27,066,661 (GRCm39) |
frame shift |
probably null |
|
R3919:Lama2
|
UTSW |
10 |
26,994,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4014:Lama2
|
UTSW |
10 |
26,860,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4131:Lama2
|
UTSW |
10 |
26,917,170 (GRCm39) |
missense |
probably benign |
0.00 |
R4190:Lama2
|
UTSW |
10 |
27,142,660 (GRCm39) |
missense |
probably damaging |
0.96 |
R4273:Lama2
|
UTSW |
10 |
27,223,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R4358:Lama2
|
UTSW |
10 |
26,860,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4407:Lama2
|
UTSW |
10 |
27,088,124 (GRCm39) |
small deletion |
probably benign |
|
R4415:Lama2
|
UTSW |
10 |
26,865,340 (GRCm39) |
nonsense |
probably null |
|
R4426:Lama2
|
UTSW |
10 |
27,298,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Lama2
|
UTSW |
10 |
26,865,410 (GRCm39) |
missense |
probably benign |
0.00 |
R4615:Lama2
|
UTSW |
10 |
26,857,520 (GRCm39) |
missense |
probably damaging |
0.99 |
R4736:Lama2
|
UTSW |
10 |
27,080,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R4754:Lama2
|
UTSW |
10 |
26,994,527 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4791:Lama2
|
UTSW |
10 |
27,343,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Lama2
|
UTSW |
10 |
26,882,745 (GRCm39) |
missense |
probably benign |
0.30 |
R4856:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4858:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4859:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4897:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4898:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4899:Lama2
|
UTSW |
10 |
26,919,639 (GRCm39) |
frame shift |
probably null |
|
R4907:Lama2
|
UTSW |
10 |
27,040,942 (GRCm39) |
missense |
probably benign |
0.11 |
R4911:Lama2
|
UTSW |
10 |
27,014,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Lama2
|
UTSW |
10 |
27,245,137 (GRCm39) |
missense |
probably damaging |
0.98 |
R5023:Lama2
|
UTSW |
10 |
27,066,500 (GRCm39) |
missense |
probably damaging |
0.97 |
R5057:Lama2
|
UTSW |
10 |
27,040,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Lama2
|
UTSW |
10 |
27,226,247 (GRCm39) |
critical splice donor site |
probably null |
|
R5116:Lama2
|
UTSW |
10 |
26,994,556 (GRCm39) |
missense |
probably benign |
0.08 |
R5177:Lama2
|
UTSW |
10 |
27,066,699 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5198:Lama2
|
UTSW |
10 |
27,222,999 (GRCm39) |
missense |
probably damaging |
0.96 |
R5289:Lama2
|
UTSW |
10 |
27,088,069 (GRCm39) |
nonsense |
probably null |
|
R5327:Lama2
|
UTSW |
10 |
27,014,942 (GRCm39) |
missense |
probably benign |
|
R5424:Lama2
|
UTSW |
10 |
26,860,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:Lama2
|
UTSW |
10 |
26,917,185 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5620:Lama2
|
UTSW |
10 |
26,866,876 (GRCm39) |
missense |
probably damaging |
0.99 |
R5667:Lama2
|
UTSW |
10 |
27,066,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Lama2
|
UTSW |
10 |
27,066,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5815:Lama2
|
UTSW |
10 |
26,862,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R5917:Lama2
|
UTSW |
10 |
27,066,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Lama2
|
UTSW |
10 |
26,891,494 (GRCm39) |
missense |
probably benign |
|
R5976:Lama2
|
UTSW |
10 |
27,066,672 (GRCm39) |
missense |
probably benign |
0.00 |
R5979:Lama2
|
UTSW |
10 |
27,111,728 (GRCm39) |
missense |
probably damaging |
0.99 |
R6004:Lama2
|
UTSW |
10 |
27,111,781 (GRCm39) |
missense |
probably benign |
0.01 |
R6198:Lama2
|
UTSW |
10 |
27,064,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Lama2
|
UTSW |
10 |
26,862,895 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6271:Lama2
|
UTSW |
10 |
26,899,325 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6322:Lama2
|
UTSW |
10 |
27,066,543 (GRCm39) |
missense |
probably damaging |
0.96 |
R6354:Lama2
|
UTSW |
10 |
27,088,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Lama2
|
UTSW |
10 |
26,929,027 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6499:Lama2
|
UTSW |
10 |
26,907,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6535:Lama2
|
UTSW |
10 |
26,980,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R6545:Lama2
|
UTSW |
10 |
27,052,793 (GRCm39) |
missense |
probably benign |
|
R6636:Lama2
|
UTSW |
10 |
27,000,564 (GRCm39) |
missense |
probably benign |
0.13 |
R6891:Lama2
|
UTSW |
10 |
27,204,078 (GRCm39) |
nonsense |
probably null |
|
R6891:Lama2
|
UTSW |
10 |
27,204,068 (GRCm39) |
nonsense |
probably null |
|
R6902:Lama2
|
UTSW |
10 |
26,857,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Lama2
|
UTSW |
10 |
26,907,192 (GRCm39) |
splice site |
probably null |
|
R7168:Lama2
|
UTSW |
10 |
27,242,148 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7233:Lama2
|
UTSW |
10 |
27,107,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Lama2
|
UTSW |
10 |
27,000,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Lama2
|
UTSW |
10 |
26,995,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R7419:Lama2
|
UTSW |
10 |
27,142,630 (GRCm39) |
missense |
probably benign |
|
R7423:Lama2
|
UTSW |
10 |
27,088,222 (GRCm39) |
missense |
probably benign |
0.00 |
R7554:Lama2
|
UTSW |
10 |
27,031,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7569:Lama2
|
UTSW |
10 |
27,141,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Lama2
|
UTSW |
10 |
26,882,726 (GRCm39) |
missense |
probably benign |
0.03 |
R7584:Lama2
|
UTSW |
10 |
26,980,257 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7586:Lama2
|
UTSW |
10 |
26,977,389 (GRCm39) |
missense |
probably benign |
0.00 |
R7603:Lama2
|
UTSW |
10 |
27,142,676 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7691:Lama2
|
UTSW |
10 |
27,084,389 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7750:Lama2
|
UTSW |
10 |
26,866,920 (GRCm39) |
missense |
probably damaging |
0.97 |
R7841:Lama2
|
UTSW |
10 |
27,031,529 (GRCm39) |
missense |
probably benign |
0.00 |
R7864:Lama2
|
UTSW |
10 |
26,932,611 (GRCm39) |
missense |
probably benign |
0.08 |
R7960:Lama2
|
UTSW |
10 |
26,869,094 (GRCm39) |
missense |
probably benign |
0.04 |
R7964:Lama2
|
UTSW |
10 |
27,099,977 (GRCm39) |
critical splice donor site |
probably null |
|
R7980:Lama2
|
UTSW |
10 |
27,239,609 (GRCm39) |
missense |
probably damaging |
0.98 |
R8013:Lama2
|
UTSW |
10 |
27,220,494 (GRCm39) |
missense |
probably benign |
0.00 |
R8028:Lama2
|
UTSW |
10 |
27,204,145 (GRCm39) |
missense |
probably benign |
0.13 |
R8097:Lama2
|
UTSW |
10 |
27,066,660 (GRCm39) |
nonsense |
probably null |
|
R8100:Lama2
|
UTSW |
10 |
26,917,113 (GRCm39) |
missense |
probably benign |
0.03 |
R8110:Lama2
|
UTSW |
10 |
26,866,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8122:Lama2
|
UTSW |
10 |
26,930,592 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8264:Lama2
|
UTSW |
10 |
27,343,218 (GRCm39) |
missense |
probably benign |
0.07 |
R8315:Lama2
|
UTSW |
10 |
27,298,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8318:Lama2
|
UTSW |
10 |
26,860,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R8419:Lama2
|
UTSW |
10 |
27,298,559 (GRCm39) |
missense |
probably benign |
0.26 |
R8475:Lama2
|
UTSW |
10 |
26,977,369 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8735:Lama2
|
UTSW |
10 |
27,066,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Lama2
|
UTSW |
10 |
26,877,147 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8817:Lama2
|
UTSW |
10 |
27,063,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8851:Lama2
|
UTSW |
10 |
27,242,119 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8859:Lama2
|
UTSW |
10 |
27,335,384 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8886:Lama2
|
UTSW |
10 |
27,245,157 (GRCm39) |
splice site |
probably benign |
|
R8937:Lama2
|
UTSW |
10 |
26,862,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R8993:Lama2
|
UTSW |
10 |
27,298,710 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9025:Lama2
|
UTSW |
10 |
26,860,367 (GRCm39) |
missense |
probably benign |
0.00 |
R9027:Lama2
|
UTSW |
10 |
27,080,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R9047:Lama2
|
UTSW |
10 |
26,882,697 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9075:Lama2
|
UTSW |
10 |
26,857,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Lama2
|
UTSW |
10 |
27,298,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R9165:Lama2
|
UTSW |
10 |
26,929,022 (GRCm39) |
critical splice donor site |
probably null |
|
R9192:Lama2
|
UTSW |
10 |
27,204,181 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9254:Lama2
|
UTSW |
10 |
27,298,685 (GRCm39) |
missense |
probably damaging |
0.96 |
R9326:Lama2
|
UTSW |
10 |
26,906,193 (GRCm39) |
missense |
probably benign |
0.04 |
R9356:Lama2
|
UTSW |
10 |
27,088,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9358:Lama2
|
UTSW |
10 |
27,492,761 (GRCm39) |
missense |
unknown |
|
R9358:Lama2
|
UTSW |
10 |
27,064,378 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9376:Lama2
|
UTSW |
10 |
26,994,620 (GRCm39) |
missense |
probably benign |
0.11 |
R9381:Lama2
|
UTSW |
10 |
27,064,023 (GRCm39) |
nonsense |
probably null |
|
R9397:Lama2
|
UTSW |
10 |
26,981,117 (GRCm39) |
missense |
probably benign |
0.01 |
R9460:Lama2
|
UTSW |
10 |
27,298,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R9478:Lama2
|
UTSW |
10 |
26,891,478 (GRCm39) |
missense |
probably damaging |
0.98 |
R9503:Lama2
|
UTSW |
10 |
26,865,440 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9514:Lama2
|
UTSW |
10 |
27,100,015 (GRCm39) |
missense |
probably benign |
0.00 |
R9515:Lama2
|
UTSW |
10 |
26,877,170 (GRCm39) |
missense |
probably benign |
0.23 |
R9516:Lama2
|
UTSW |
10 |
27,100,015 (GRCm39) |
missense |
probably benign |
0.00 |
R9533:Lama2
|
UTSW |
10 |
26,862,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9619:Lama2
|
UTSW |
10 |
27,064,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R9721:Lama2
|
UTSW |
10 |
27,343,338 (GRCm39) |
missense |
possibly damaging |
0.58 |
|