Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadm |
T |
C |
3: 153,644,720 (GRCm39) |
D68G |
probably damaging |
Het |
Amer3 |
A |
G |
1: 34,625,761 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,617,390 (GRCm39) |
L2133P |
probably damaging |
Het |
Bcdin3d |
G |
T |
15: 99,368,673 (GRCm39) |
H175Q |
probably damaging |
Het |
Brd8 |
C |
A |
18: 34,741,117 (GRCm39) |
|
probably benign |
Het |
C1rl |
C |
A |
6: 124,470,806 (GRCm39) |
T38N |
possibly damaging |
Het |
Cd160 |
T |
C |
3: 96,707,927 (GRCm39) |
T140A |
probably benign |
Het |
Cdk16 |
T |
G |
X: 20,563,167 (GRCm39) |
D381E |
probably benign |
Het |
Cpq |
G |
A |
15: 33,381,546 (GRCm39) |
G303D |
probably damaging |
Het |
Dmp1 |
T |
C |
5: 104,359,536 (GRCm39) |
S71P |
probably damaging |
Het |
Enc1 |
A |
C |
13: 97,382,042 (GRCm39) |
D184A |
possibly damaging |
Het |
Enkur |
T |
C |
2: 21,199,198 (GRCm39) |
D112G |
probably benign |
Het |
Esrra |
A |
T |
19: 6,890,218 (GRCm39) |
V59E |
possibly damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,433,058 (GRCm39) |
N47S |
probably benign |
Het |
Fads1 |
T |
A |
19: 10,163,785 (GRCm39) |
V189D |
probably damaging |
Het |
Fam167a |
T |
A |
14: 63,689,721 (GRCm39) |
I6N |
probably damaging |
Het |
Fam98b |
A |
G |
2: 117,090,793 (GRCm39) |
T164A |
probably benign |
Het |
Fhip2a |
A |
G |
19: 57,373,782 (GRCm39) |
N681D |
possibly damaging |
Het |
Fryl |
T |
A |
5: 73,252,809 (GRCm39) |
I953L |
probably benign |
Het |
Gm10610 |
T |
A |
7: 83,198,813 (GRCm39) |
|
noncoding transcript |
Het |
Grik5 |
G |
T |
7: 24,758,408 (GRCm39) |
N338K |
possibly damaging |
Het |
Gstt2 |
A |
G |
10: 75,668,652 (GRCm39) |
I72T |
probably benign |
Het |
Gusb |
T |
C |
5: 130,029,376 (GRCm39) |
|
probably null |
Het |
Hccs |
A |
G |
X: 168,098,588 (GRCm39) |
|
probably benign |
Het |
Hoxb4 |
A |
G |
11: 96,211,050 (GRCm39) |
K217E |
probably damaging |
Het |
Hpd |
C |
T |
5: 123,319,503 (GRCm39) |
V22I |
possibly damaging |
Het |
Ighv1-47 |
A |
G |
12: 114,954,844 (GRCm39) |
Y79H |
probably damaging |
Het |
Il7r |
C |
A |
15: 9,513,133 (GRCm39) |
|
probably benign |
Het |
Lama1 |
A |
T |
17: 68,119,361 (GRCm39) |
M2613L |
probably benign |
Het |
Lce1c |
C |
A |
3: 92,587,845 (GRCm39) |
|
probably benign |
Het |
Lmx1a |
G |
T |
1: 167,672,192 (GRCm39) |
|
probably benign |
Het |
Lrfn1 |
T |
C |
7: 28,158,113 (GRCm39) |
|
probably benign |
Het |
Lrriq1 |
T |
A |
10: 103,057,322 (GRCm39) |
|
probably null |
Het |
Mri1 |
A |
T |
8: 84,983,702 (GRCm39) |
L63Q |
probably damaging |
Het |
Mrps11 |
G |
T |
7: 78,438,522 (GRCm39) |
|
probably null |
Het |
Mtif2 |
C |
A |
11: 29,494,395 (GRCm39) |
Q666K |
probably benign |
Het |
Mtr |
A |
T |
13: 12,210,118 (GRCm39) |
|
probably benign |
Het |
Mug1 |
A |
G |
6: 121,859,544 (GRCm39) |
N1181S |
probably benign |
Het |
Myom1 |
A |
T |
17: 71,408,093 (GRCm39) |
E1209V |
possibly damaging |
Het |
Nhsl1 |
A |
G |
10: 18,284,138 (GRCm39) |
I26M |
possibly damaging |
Het |
Nlrp1a |
T |
A |
11: 71,014,358 (GRCm39) |
K297N |
probably benign |
Het |
Obox5 |
T |
C |
7: 15,491,972 (GRCm39) |
V129A |
probably benign |
Het |
Pex16 |
C |
T |
2: 92,206,981 (GRCm39) |
A53V |
probably damaging |
Het |
Pfpl |
T |
C |
19: 12,407,107 (GRCm39) |
F453L |
probably damaging |
Het |
Pip5k1b |
G |
T |
19: 24,323,731 (GRCm39) |
H406N |
probably benign |
Het |
Pip5k1c |
C |
A |
10: 81,153,155 (GRCm39) |
|
probably null |
Het |
Plcxd3 |
T |
C |
15: 4,546,122 (GRCm39) |
F42S |
possibly damaging |
Het |
Pnpla7 |
T |
C |
2: 24,940,288 (GRCm39) |
F1056L |
probably benign |
Het |
Rapgef1 |
T |
C |
2: 29,590,872 (GRCm39) |
|
probably benign |
Het |
Rdh11 |
G |
A |
12: 79,232,110 (GRCm39) |
|
probably benign |
Het |
Serac1 |
A |
G |
17: 6,096,021 (GRCm39) |
F576S |
possibly damaging |
Het |
Slc45a4 |
A |
T |
15: 73,458,664 (GRCm39) |
M295K |
probably benign |
Het |
Taf1c |
T |
C |
8: 120,325,796 (GRCm39) |
T689A |
probably benign |
Het |
Timm10b |
G |
T |
7: 105,317,645 (GRCm39) |
|
probably benign |
Het |
Tle5 |
A |
T |
10: 81,397,126 (GRCm39) |
Q34L |
possibly damaging |
Het |
Tnc |
A |
T |
4: 63,883,816 (GRCm39) |
|
probably benign |
Het |
Toporsl |
T |
C |
4: 52,611,114 (GRCm39) |
W336R |
probably benign |
Het |
Usp54 |
C |
A |
14: 20,615,140 (GRCm39) |
|
probably benign |
Het |
Vmn1r233 |
T |
C |
17: 21,214,291 (GRCm39) |
R220G |
probably damaging |
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 |
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 |
R6180:Lama2
|
UTSW |
10 |
26,857,495 (GRCm39) |
missense |
probably benign |
0.03 |
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 |
|