Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,383,749 (GRCm39) |
S739P |
possibly damaging |
Het |
Acacb |
T |
C |
5: 114,384,089 (GRCm39) |
I2206T |
possibly damaging |
Het |
Actn2 |
A |
G |
13: 12,303,408 (GRCm39) |
I464T |
possibly damaging |
Het |
AI987944 |
C |
T |
7: 41,024,748 (GRCm39) |
G77D |
probably benign |
Het |
Ankar |
T |
C |
1: 72,719,369 (GRCm39) |
|
probably null |
Het |
Armc9 |
A |
T |
1: 86,184,959 (GRCm39) |
H670L |
probably benign |
Het |
Arvcf |
A |
G |
16: 18,217,736 (GRCm39) |
Y412C |
probably damaging |
Het |
Baiap3 |
A |
T |
17: 25,468,082 (GRCm39) |
C283S |
probably damaging |
Het |
Bend3 |
A |
T |
10: 43,369,681 (GRCm39) |
E11D |
probably damaging |
Het |
Birc6 |
C |
T |
17: 74,872,967 (GRCm39) |
R409C |
probably damaging |
Het |
Cds2 |
T |
A |
2: 132,144,008 (GRCm39) |
Y4* |
probably null |
Het |
Celsr1 |
G |
T |
15: 85,823,335 (GRCm39) |
P1691Q |
possibly damaging |
Het |
Chmp1a |
A |
T |
8: 123,933,054 (GRCm39) |
V133E |
probably benign |
Het |
Cnbd2 |
T |
C |
2: 156,177,318 (GRCm39) |
V92A |
probably damaging |
Het |
Comp |
G |
A |
8: 70,829,145 (GRCm39) |
G272S |
probably benign |
Het |
Csnk1a1 |
T |
A |
18: 61,688,852 (GRCm39) |
F11I |
probably benign |
Het |
Ctse |
A |
G |
1: 131,595,917 (GRCm39) |
D203G |
probably damaging |
Het |
Cyp1b1 |
T |
A |
17: 80,018,040 (GRCm39) |
M372L |
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,151,914 (GRCm39) |
S210T |
probably benign |
Het |
Dnah1 |
G |
A |
14: 31,004,375 (GRCm39) |
P2385S |
probably benign |
Het |
Dsp |
A |
C |
13: 38,381,099 (GRCm39) |
T2615P |
possibly damaging |
Het |
Eif4g3 |
A |
G |
4: 137,873,610 (GRCm39) |
T682A |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,727,450 (GRCm39) |
Y513C |
probably damaging |
Het |
Ercc6 |
T |
C |
14: 32,292,020 (GRCm39) |
V1128A |
probably benign |
Het |
Fam136b-ps |
C |
T |
15: 31,276,862 (GRCm39) |
|
probably benign |
Het |
Fbxl7 |
T |
A |
15: 26,789,640 (GRCm39) |
H29L |
probably benign |
Het |
Fbxw22 |
A |
G |
9: 109,214,183 (GRCm39) |
V211A |
probably benign |
Het |
Frk |
A |
T |
10: 34,360,280 (GRCm39) |
K94* |
probably null |
Het |
G0s2 |
T |
A |
1: 192,954,870 (GRCm39) |
E71D |
probably damaging |
Het |
Gfpt1 |
A |
G |
6: 87,030,727 (GRCm39) |
|
probably null |
Het |
Gga1 |
A |
G |
15: 78,776,217 (GRCm39) |
D420G |
possibly damaging |
Het |
Gldc |
T |
C |
19: 30,095,998 (GRCm39) |
Q671R |
possibly damaging |
Het |
Gpc6 |
A |
G |
14: 117,424,181 (GRCm39) |
T90A |
probably benign |
Het |
Gucy2g |
C |
A |
19: 55,218,219 (GRCm39) |
V410F |
probably damaging |
Het |
Ifnlr1 |
T |
C |
4: 135,431,509 (GRCm39) |
S233P |
probably benign |
Het |
Ighv1-9 |
A |
T |
12: 114,547,377 (GRCm39) |
W55R |
probably damaging |
Het |
Igsf10 |
T |
A |
3: 59,235,714 (GRCm39) |
H1489L |
probably benign |
Het |
Il17re |
T |
C |
6: 113,435,971 (GRCm39) |
L39P |
probably damaging |
Het |
Irag1 |
A |
G |
7: 110,524,519 (GRCm39) |
S208P |
probably benign |
Het |
Kcna2 |
T |
A |
3: 107,011,953 (GRCm39) |
V178D |
probably damaging |
Het |
Kcnk3 |
A |
G |
5: 30,779,730 (GRCm39) |
H260R |
possibly damaging |
Het |
Kctd19 |
T |
C |
8: 106,118,631 (GRCm39) |
Y287C |
probably damaging |
Het |
Klhl28 |
A |
T |
12: 65,004,486 (GRCm39) |
M9K |
probably benign |
Het |
Lrrc27 |
A |
T |
7: 138,794,715 (GRCm39) |
D26V |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,443,434 (GRCm39) |
S830P |
probably damaging |
Het |
Mei1 |
T |
A |
15: 81,961,804 (GRCm39) |
C188S |
possibly damaging |
Het |
Mettl13 |
C |
T |
1: 162,373,468 (GRCm39) |
R261H |
possibly damaging |
Het |
Mex3a |
A |
T |
3: 88,443,694 (GRCm39) |
I257F |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,793,002 (GRCm39) |
E646G |
probably damaging |
Het |
Mier2 |
T |
C |
10: 79,385,411 (GRCm39) |
D139G |
probably benign |
Het |
Mmp14 |
T |
A |
14: 54,676,570 (GRCm39) |
Y372N |
probably damaging |
Het |
Myh14 |
A |
G |
7: 44,265,672 (GRCm39) |
V1569A |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,909,212 (GRCm39) |
E1977G |
probably damaging |
Het |
Myo3b |
T |
C |
2: 70,083,456 (GRCm39) |
L675P |
probably damaging |
Het |
N4bp1 |
A |
G |
8: 87,587,165 (GRCm39) |
V591A |
probably damaging |
Het |
Nedd9 |
C |
A |
13: 41,470,074 (GRCm39) |
V360L |
probably benign |
Het |
Oit3 |
C |
T |
10: 59,259,849 (GRCm39) |
R518H |
probably damaging |
Het |
Or10ag57 |
T |
G |
2: 87,218,507 (GRCm39) |
C153G |
probably damaging |
Het |
Or11g2 |
A |
G |
14: 50,855,931 (GRCm39) |
N84S |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,197 (GRCm39) |
C173S |
probably damaging |
Het |
Or11h4 |
C |
A |
14: 50,974,531 (GRCm39) |
L29F |
probably benign |
Het |
Or1j14 |
T |
A |
2: 36,417,778 (GRCm39) |
M118K |
probably damaging |
Het |
Or2aj6 |
A |
G |
16: 19,443,742 (GRCm39) |
I36T |
possibly damaging |
Het |
Or2j6 |
A |
G |
7: 139,980,482 (GRCm39) |
V159A |
probably benign |
Het |
Or9s23 |
T |
A |
1: 92,501,135 (GRCm39) |
S81T |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pask |
A |
T |
1: 93,258,596 (GRCm39) |
C251S |
probably damaging |
Het |
Pdzk1 |
A |
T |
3: 96,757,637 (GRCm39) |
D31V |
probably benign |
Het |
Pmfbp1 |
A |
T |
8: 110,256,787 (GRCm39) |
Q497L |
probably damaging |
Het |
Pofut1 |
T |
C |
2: 153,103,486 (GRCm39) |
|
probably benign |
Het |
Polr2h |
A |
G |
16: 20,540,716 (GRCm39) |
N95S |
probably damaging |
Het |
Pou2f3 |
A |
G |
9: 43,056,578 (GRCm39) |
V93A |
possibly damaging |
Het |
Ppfia1 |
G |
A |
7: 144,068,210 (GRCm39) |
Q446* |
probably null |
Het |
Prkd1 |
A |
T |
12: 50,441,405 (GRCm39) |
L327* |
probably null |
Het |
Prrt4 |
T |
C |
6: 29,177,511 (GRCm39) |
E86G |
probably benign |
Het |
Psen2 |
T |
C |
1: 180,056,422 (GRCm39) |
I393V |
probably benign |
Het |
Psma2 |
G |
A |
13: 14,790,613 (GRCm39) |
V20I |
probably benign |
Het |
Qser1 |
C |
T |
2: 104,617,627 (GRCm39) |
V1062I |
possibly damaging |
Het |
Rab11b |
G |
T |
17: 33,967,855 (GRCm39) |
A114D |
probably damaging |
Het |
Rag1 |
A |
T |
2: 101,472,656 (GRCm39) |
W829R |
probably damaging |
Het |
Rgl3 |
A |
G |
9: 21,899,340 (GRCm39) |
|
probably null |
Het |
Rgs8 |
C |
T |
1: 153,541,650 (GRCm39) |
T3I |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,743,385 (GRCm39) |
V1317A |
probably damaging |
Het |
Rps6kb2 |
A |
T |
19: 4,213,227 (GRCm39) |
D6E |
probably damaging |
Het |
Shisal1 |
G |
T |
15: 84,304,364 (GRCm39) |
A14E |
possibly damaging |
Het |
Skint5 |
T |
A |
4: 113,652,735 (GRCm39) |
I630F |
unknown |
Het |
Skint7 |
T |
C |
4: 111,841,331 (GRCm39) |
L257P |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,424,343 (GRCm39) |
A434T |
probably damaging |
Het |
Slc5a8 |
A |
T |
10: 88,722,460 (GRCm39) |
I98F |
possibly damaging |
Het |
Sorl1 |
T |
C |
9: 41,943,114 (GRCm39) |
K921E |
possibly damaging |
Het |
Stub1 |
A |
G |
17: 26,051,112 (GRCm39) |
L90P |
probably damaging |
Het |
Sycp1 |
A |
T |
3: 102,827,881 (GRCm39) |
S289T |
probably damaging |
Het |
Taar7b |
T |
G |
10: 23,876,359 (GRCm39) |
S175A |
probably benign |
Het |
Tead3 |
T |
C |
17: 28,560,451 (GRCm39) |
K51R |
probably benign |
Het |
Tmed11 |
T |
A |
5: 108,943,089 (GRCm39) |
I30L |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,893,986 (GRCm39) |
I139T |
probably damaging |
Het |
Tmem191 |
A |
G |
16: 17,095,559 (GRCm39) |
Q206R |
probably null |
Het |
Tph2 |
T |
A |
10: 114,987,079 (GRCm39) |
Y237F |
probably benign |
Het |
Trim35 |
C |
T |
14: 66,546,421 (GRCm39) |
|
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,655,750 (GRCm39) |
I661T |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,106,337 (GRCm39) |
H541Q |
probably damaging |
Het |
Uqcrq |
A |
G |
11: 53,320,954 (GRCm39) |
|
probably null |
Het |
Vmn1r215 |
T |
A |
13: 23,260,666 (GRCm39) |
S235R |
probably benign |
Het |
Vmn1r70 |
T |
C |
7: 10,368,325 (GRCm39) |
V271A |
probably benign |
Het |
Vps13a |
G |
A |
19: 16,631,848 (GRCm39) |
R2596C |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,243,166 (GRCm39) |
V615I |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,307 (GRCm39) |
T1650A |
probably damaging |
Het |
Zbtb32 |
T |
A |
7: 30,290,891 (GRCm39) |
M135L |
probably benign |
Het |
Zc2hc1c |
A |
G |
12: 85,337,288 (GRCm39) |
D315G |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,254,688 (GRCm39) |
C1427* |
probably null |
Het |
Zfp30 |
A |
G |
7: 29,485,691 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
T |
A |
7: 24,214,550 (GRCm39) |
D55E |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,302,135 (GRCm39) |
N1820K |
probably damaging |
Het |
Zw10 |
C |
A |
9: 48,988,759 (GRCm39) |
S675* |
probably null |
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 |
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 |
|