Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
A |
10: 78,902,473 (GRCm39) |
K614N |
probably benign |
Het |
2610008E11Rik |
T |
G |
10: 78,902,474 (GRCm39) |
K614T |
probably benign |
Het |
Ahsa1 |
T |
A |
12: 87,317,116 (GRCm39) |
S120R |
probably benign |
Het |
Anapc16 |
G |
A |
10: 59,832,302 (GRCm39) |
T37I |
possibly damaging |
Het |
Arid2 |
C |
A |
15: 96,276,756 (GRCm39) |
P1606H |
probably damaging |
Het |
Ash1l |
TATCTCCTTTTCCAAAAA |
TA |
3: 88,890,764 (GRCm39) |
|
probably null |
Het |
Asic1 |
T |
A |
15: 99,569,968 (GRCm39) |
N96K |
probably damaging |
Het |
Asph |
A |
T |
4: 9,484,575 (GRCm39) |
D582E |
probably benign |
Het |
Astn1 |
A |
G |
1: 158,400,557 (GRCm39) |
D528G |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,952,871 (GRCm39) |
V164A |
|
Het |
Cbx6 |
C |
T |
15: 79,712,866 (GRCm39) |
G187D |
possibly damaging |
Het |
Cct7 |
A |
G |
6: 85,443,627 (GRCm39) |
T332A |
probably benign |
Het |
Clca4a |
A |
T |
3: 144,667,651 (GRCm39) |
L440* |
probably null |
Het |
Crybg2 |
A |
T |
4: 133,792,754 (GRCm39) |
I130F |
probably benign |
Het |
Crybg3 |
T |
C |
16: 59,357,167 (GRCm39) |
E798G |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,480,995 (GRCm39) |
E81G |
possibly damaging |
Het |
Cwc22 |
C |
T |
2: 77,759,822 (GRCm39) |
R75H |
possibly damaging |
Het |
Cym |
T |
G |
3: 107,121,530 (GRCm39) |
D254A |
probably damaging |
Het |
Dcaf11 |
T |
A |
14: 55,806,383 (GRCm39) |
|
probably null |
Het |
Dctn1 |
A |
T |
6: 83,157,026 (GRCm39) |
|
probably null |
Het |
Dennd5a |
C |
T |
7: 109,495,449 (GRCm39) |
|
probably null |
Het |
Dmpk |
T |
A |
7: 18,821,232 (GRCm39) |
C217S |
probably damaging |
Het |
Dnah1 |
C |
A |
14: 31,008,033 (GRCm39) |
V2125L |
probably benign |
Het |
Exoc4 |
G |
A |
6: 33,415,408 (GRCm39) |
A427T |
probably benign |
Het |
Farp2 |
G |
T |
1: 93,548,956 (GRCm39) |
V1021F |
probably damaging |
Het |
Flg2 |
T |
C |
3: 93,127,069 (GRCm39) |
S1994P |
unknown |
Het |
Fmnl1 |
T |
C |
11: 103,072,610 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
A |
3: 53,479,760 (GRCm39) |
I1978F |
possibly damaging |
Het |
Gan |
T |
A |
8: 117,913,969 (GRCm39) |
C122* |
probably null |
Het |
Gpr25 |
T |
A |
1: 136,188,559 (GRCm39) |
Y18F |
probably damaging |
Het |
Hoxa7 |
C |
T |
6: 52,192,720 (GRCm39) |
E223K |
probably benign |
Het |
Hypk |
A |
G |
2: 121,283,961 (GRCm39) |
|
probably null |
Het |
Ibsp |
A |
T |
5: 104,450,172 (GRCm39) |
K27* |
probably null |
Het |
Ighv6-5 |
T |
A |
12: 114,380,395 (GRCm39) |
T41S |
probably benign |
Het |
Ighv9-4 |
T |
C |
12: 114,263,757 (GRCm39) |
M59V |
probably benign |
Het |
Il17rb |
T |
C |
14: 29,718,828 (GRCm39) |
D418G |
probably damaging |
Het |
Ints5 |
T |
A |
19: 8,872,923 (GRCm39) |
V294E |
probably damaging |
Het |
Irx6 |
G |
A |
8: 93,405,041 (GRCm39) |
C303Y |
probably damaging |
Het |
Itih3 |
T |
A |
14: 30,639,655 (GRCm39) |
I389F |
probably damaging |
Het |
Lama1 |
C |
T |
17: 68,089,141 (GRCm39) |
T1604I |
|
Het |
Lhx1 |
T |
G |
11: 84,410,746 (GRCm39) |
S284R |
probably benign |
Het |
Lrba |
T |
A |
3: 86,302,238 (GRCm39) |
|
probably null |
Het |
Lrg1 |
C |
T |
17: 56,427,592 (GRCm39) |
G127R |
possibly damaging |
Het |
Macir |
G |
A |
1: 97,573,645 (GRCm39) |
P140L |
probably benign |
Het |
Mapre1 |
T |
A |
2: 153,606,883 (GRCm39) |
L205H |
probably benign |
Het |
Meltf |
A |
G |
16: 31,711,617 (GRCm39) |
N581S |
probably damaging |
Het |
Mgat5 |
A |
C |
1: 127,292,926 (GRCm39) |
M149L |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,093,412 (GRCm39) |
T168A |
probably benign |
Het |
Naalad2 |
C |
T |
9: 18,238,673 (GRCm39) |
V681I |
probably benign |
Het |
Or51e2 |
A |
G |
7: 102,391,524 (GRCm39) |
S229P |
probably damaging |
Het |
Or52r1c |
T |
A |
7: 102,735,205 (GRCm39) |
L155Q |
probably damaging |
Het |
Pcnx2 |
T |
C |
8: 126,528,243 (GRCm39) |
T1326A |
probably benign |
Het |
Peg3 |
A |
T |
7: 6,711,944 (GRCm39) |
C1093S |
probably damaging |
Het |
Pidd1 |
T |
C |
7: 141,019,813 (GRCm39) |
S650G |
probably benign |
Het |
Pik3c2b |
T |
C |
1: 133,017,972 (GRCm39) |
S945P |
possibly damaging |
Het |
Plec |
T |
C |
15: 76,060,227 (GRCm39) |
T3237A |
possibly damaging |
Het |
Prpf3 |
A |
T |
3: 95,741,052 (GRCm39) |
|
probably null |
Het |
Prpf4b |
C |
A |
13: 35,085,477 (GRCm39) |
H974Q |
probably benign |
Het |
Ptpn3 |
T |
C |
4: 57,225,863 (GRCm39) |
T451A |
probably benign |
Het |
Ptprs |
A |
G |
17: 56,724,429 (GRCm39) |
Y1577H |
probably damaging |
Het |
Rgr |
C |
T |
14: 36,770,882 (GRCm39) |
M1I |
probably null |
Het |
Rxrg |
A |
T |
1: 167,458,678 (GRCm39) |
N257I |
probably benign |
Het |
Sbno2 |
T |
C |
10: 79,922,146 (GRCm39) |
D9G |
probably damaging |
Het |
Scd1 |
T |
C |
19: 44,395,034 (GRCm39) |
K64E |
probably damaging |
Het |
Serpinb1a |
T |
A |
13: 33,034,308 (GRCm39) |
I28F |
possibly damaging |
Het |
Sfmbt2 |
A |
T |
2: 10,406,818 (GRCm39) |
E39V |
probably damaging |
Het |
Slc29a1 |
A |
G |
17: 45,900,897 (GRCm39) |
M89T |
possibly damaging |
Het |
Slco4a1 |
T |
A |
2: 180,113,856 (GRCm39) |
V431E |
possibly damaging |
Het |
Smg1 |
C |
T |
7: 117,752,131 (GRCm39) |
C2698Y |
unknown |
Het |
Sptlc2 |
C |
T |
12: 87,397,151 (GRCm39) |
D212N |
probably benign |
Het |
St6galnac1 |
T |
C |
11: 116,657,899 (GRCm39) |
T334A |
possibly damaging |
Het |
Stim2 |
A |
T |
5: 54,156,263 (GRCm39) |
D13V |
possibly damaging |
Het |
Syne1 |
A |
G |
10: 5,181,592 (GRCm39) |
W4248R |
probably damaging |
Het |
Tanc1 |
T |
C |
2: 59,627,953 (GRCm39) |
Y584H |
probably benign |
Het |
Thoc6 |
C |
A |
17: 23,892,634 (GRCm39) |
|
probably null |
Het |
Trim30a |
T |
A |
7: 104,078,533 (GRCm39) |
N181I |
possibly damaging |
Het |
Trip11 |
T |
A |
12: 101,850,329 (GRCm39) |
Q1245L |
probably damaging |
Het |
Tshz3 |
A |
G |
7: 36,469,994 (GRCm39) |
D661G |
probably benign |
Het |
Ttll8 |
C |
A |
15: 88,799,630 (GRCm39) |
V604L |
probably damaging |
Het |
Ubtfl1 |
A |
G |
9: 18,320,931 (GRCm39) |
D153G |
probably damaging |
Het |
Ufsp2 |
C |
A |
8: 46,436,661 (GRCm39) |
N137K |
probably benign |
Het |
Ugt2a3 |
A |
G |
5: 87,473,393 (GRCm39) |
I508T |
possibly damaging |
Het |
Uso1 |
G |
A |
5: 92,306,324 (GRCm39) |
E94K |
probably benign |
Het |
Usp54 |
A |
G |
14: 20,611,310 (GRCm39) |
S1169P |
probably benign |
Het |
Vmn1r235 |
C |
T |
17: 21,482,292 (GRCm39) |
P206S |
probably benign |
Het |
Vmn1r69 |
T |
C |
7: 10,314,995 (GRCm39) |
|
probably benign |
Het |
Zfp263 |
T |
A |
16: 3,567,255 (GRCm39) |
C523* |
probably null |
Het |
Zfp799 |
G |
T |
17: 33,039,210 (GRCm39) |
T352K |
probably benign |
Het |
Zfr |
T |
A |
15: 12,180,724 (GRCm39) |
V951E |
probably damaging |
Het |
Zfyve26 |
T |
C |
12: 79,330,926 (GRCm39) |
D431G |
probably benign |
Het |
Zswim9 |
C |
A |
7: 12,993,664 (GRCm39) |
A831S |
probably damaging |
Het |
|
Other mutations in Lama3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Lama3
|
APN |
18 |
12,713,349 (GRCm39) |
missense |
probably benign |
|
IGL00272:Lama3
|
APN |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00335:Lama3
|
APN |
18 |
12,582,645 (GRCm39) |
splice site |
probably benign |
|
IGL00836:Lama3
|
APN |
18 |
12,605,285 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01017:Lama3
|
APN |
18 |
12,574,200 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01025:Lama3
|
APN |
18 |
12,614,094 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01394:Lama3
|
APN |
18 |
12,664,983 (GRCm39) |
missense |
probably null |
0.39 |
IGL01545:Lama3
|
APN |
18 |
12,574,188 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01685:Lama3
|
APN |
18 |
12,586,937 (GRCm39) |
splice site |
probably benign |
|
IGL01863:Lama3
|
APN |
18 |
12,552,993 (GRCm39) |
splice site |
probably benign |
|
IGL01869:Lama3
|
APN |
18 |
12,657,820 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01894:Lama3
|
APN |
18 |
12,705,121 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02027:Lama3
|
APN |
18 |
12,649,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Lama3
|
APN |
18 |
12,601,371 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02307:Lama3
|
APN |
18 |
12,714,840 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02342:Lama3
|
APN |
18 |
12,624,533 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Lama3
|
APN |
18 |
12,689,807 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02401:Lama3
|
APN |
18 |
12,690,784 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02517:Lama3
|
APN |
18 |
12,670,915 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02644:Lama3
|
APN |
18 |
12,658,910 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02733:Lama3
|
APN |
18 |
12,711,184 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02932:Lama3
|
APN |
18 |
12,661,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03006:Lama3
|
APN |
18 |
12,601,425 (GRCm39) |
splice site |
probably benign |
|
IGL03038:Lama3
|
APN |
18 |
12,552,307 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Lama3
|
APN |
18 |
12,572,406 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03146:Lama3
|
APN |
18 |
12,660,681 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03233:Lama3
|
APN |
18 |
12,614,095 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03255:Lama3
|
APN |
18 |
12,672,760 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:Lama3
|
APN |
18 |
12,686,340 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03412:Lama3
|
APN |
18 |
12,552,239 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02980:Lama3
|
UTSW |
18 |
12,686,288 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03014:Lama3
|
UTSW |
18 |
12,673,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0007:Lama3
|
UTSW |
18 |
12,630,938 (GRCm39) |
splice site |
probably benign |
|
R0007:Lama3
|
UTSW |
18 |
12,630,938 (GRCm39) |
splice site |
probably benign |
|
R0050:Lama3
|
UTSW |
18 |
12,537,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Lama3
|
UTSW |
18 |
12,537,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Lama3
|
UTSW |
18 |
12,661,762 (GRCm39) |
splice site |
probably benign |
|
R0063:Lama3
|
UTSW |
18 |
12,661,762 (GRCm39) |
splice site |
probably benign |
|
R0106:Lama3
|
UTSW |
18 |
12,537,039 (GRCm39) |
missense |
probably damaging |
0.96 |
R0148:Lama3
|
UTSW |
18 |
12,581,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0165:Lama3
|
UTSW |
18 |
12,657,867 (GRCm39) |
missense |
probably damaging |
0.99 |
R0240:Lama3
|
UTSW |
18 |
12,672,880 (GRCm39) |
splice site |
probably null |
|
R0240:Lama3
|
UTSW |
18 |
12,672,880 (GRCm39) |
splice site |
probably null |
|
R0316:Lama3
|
UTSW |
18 |
12,652,934 (GRCm39) |
missense |
probably benign |
0.09 |
R0325:Lama3
|
UTSW |
18 |
12,615,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Lama3
|
UTSW |
18 |
12,640,064 (GRCm39) |
missense |
probably damaging |
0.96 |
R0390:Lama3
|
UTSW |
18 |
12,540,620 (GRCm39) |
missense |
probably benign |
0.10 |
R0408:Lama3
|
UTSW |
18 |
12,589,894 (GRCm39) |
missense |
probably benign |
|
R0449:Lama3
|
UTSW |
18 |
12,633,569 (GRCm39) |
splice site |
probably null |
|
R0453:Lama3
|
UTSW |
18 |
12,598,535 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0480:Lama3
|
UTSW |
18 |
12,583,481 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0536:Lama3
|
UTSW |
18 |
12,658,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0545:Lama3
|
UTSW |
18 |
12,694,758 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0567:Lama3
|
UTSW |
18 |
12,682,309 (GRCm39) |
missense |
probably benign |
|
R0605:Lama3
|
UTSW |
18 |
12,640,006 (GRCm39) |
missense |
probably benign |
0.02 |
R0617:Lama3
|
UTSW |
18 |
12,552,315 (GRCm39) |
critical splice donor site |
probably null |
|
R0629:Lama3
|
UTSW |
18 |
12,552,302 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0671:Lama3
|
UTSW |
18 |
12,610,647 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0730:Lama3
|
UTSW |
18 |
12,589,907 (GRCm39) |
splice site |
probably benign |
|
R1216:Lama3
|
UTSW |
18 |
12,554,191 (GRCm39) |
splice site |
probably benign |
|
R1356:Lama3
|
UTSW |
18 |
12,633,634 (GRCm39) |
unclassified |
probably benign |
|
R1386:Lama3
|
UTSW |
18 |
12,610,427 (GRCm39) |
missense |
probably benign |
0.04 |
R1424:Lama3
|
UTSW |
18 |
12,653,048 (GRCm39) |
missense |
probably benign |
0.13 |
R1426:Lama3
|
UTSW |
18 |
12,614,155 (GRCm39) |
critical splice donor site |
probably null |
|
R1437:Lama3
|
UTSW |
18 |
12,682,284 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1468:Lama3
|
UTSW |
18 |
12,574,164 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Lama3
|
UTSW |
18 |
12,574,164 (GRCm39) |
missense |
probably benign |
0.00 |
R1472:Lama3
|
UTSW |
18 |
12,615,102 (GRCm39) |
missense |
probably benign |
0.23 |
R1557:Lama3
|
UTSW |
18 |
12,646,788 (GRCm39) |
splice site |
probably benign |
|
R1571:Lama3
|
UTSW |
18 |
12,672,774 (GRCm39) |
missense |
probably damaging |
0.98 |
R1599:Lama3
|
UTSW |
18 |
12,583,457 (GRCm39) |
nonsense |
probably null |
|
R1631:Lama3
|
UTSW |
18 |
12,540,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Lama3
|
UTSW |
18 |
12,665,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1648:Lama3
|
UTSW |
18 |
12,665,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1719:Lama3
|
UTSW |
18 |
12,612,929 (GRCm39) |
critical splice donor site |
probably null |
|
R1757:Lama3
|
UTSW |
18 |
12,598,556 (GRCm39) |
missense |
probably benign |
0.10 |
R1766:Lama3
|
UTSW |
18 |
12,535,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Lama3
|
UTSW |
18 |
12,646,762 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1856:Lama3
|
UTSW |
18 |
12,670,838 (GRCm39) |
nonsense |
probably null |
|
R1909:Lama3
|
UTSW |
18 |
12,714,855 (GRCm39) |
missense |
probably benign |
0.19 |
R1913:Lama3
|
UTSW |
18 |
12,628,336 (GRCm39) |
missense |
probably benign |
0.15 |
R1975:Lama3
|
UTSW |
18 |
12,586,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Lama3
|
UTSW |
18 |
12,657,778 (GRCm39) |
splice site |
probably benign |
|
R2059:Lama3
|
UTSW |
18 |
12,661,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Lama3
|
UTSW |
18 |
12,661,783 (GRCm39) |
missense |
probably benign |
0.30 |
R2086:Lama3
|
UTSW |
18 |
12,657,887 (GRCm39) |
missense |
probably benign |
0.39 |
R2115:Lama3
|
UTSW |
18 |
12,535,906 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2291:Lama3
|
UTSW |
18 |
12,658,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R2860:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R2862:Lama3
|
UTSW |
18 |
12,586,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3410:Lama3
|
UTSW |
18 |
12,546,915 (GRCm39) |
critical splice donor site |
probably null |
|
R3614:Lama3
|
UTSW |
18 |
12,581,345 (GRCm39) |
missense |
probably benign |
0.03 |
R3696:Lama3
|
UTSW |
18 |
12,572,532 (GRCm39) |
splice site |
probably benign |
|
R3752:Lama3
|
UTSW |
18 |
12,640,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R3967:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3968:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3969:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R3970:Lama3
|
UTSW |
18 |
12,713,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Lama3
|
UTSW |
18 |
12,637,365 (GRCm39) |
nonsense |
probably null |
|
R4118:Lama3
|
UTSW |
18 |
12,583,488 (GRCm39) |
missense |
probably benign |
0.01 |
R4222:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4224:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4225:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R4367:Lama3
|
UTSW |
18 |
12,646,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4404:Lama3
|
UTSW |
18 |
12,715,588 (GRCm39) |
missense |
probably benign |
0.01 |
R4424:Lama3
|
UTSW |
18 |
12,652,929 (GRCm39) |
nonsense |
probably null |
|
R4483:Lama3
|
UTSW |
18 |
12,682,310 (GRCm39) |
missense |
probably benign |
0.32 |
R4484:Lama3
|
UTSW |
18 |
12,614,145 (GRCm39) |
missense |
probably benign |
|
R4516:Lama3
|
UTSW |
18 |
12,628,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R4556:Lama3
|
UTSW |
18 |
12,612,816 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4616:Lama3
|
UTSW |
18 |
12,637,454 (GRCm39) |
critical splice donor site |
probably null |
|
R4702:Lama3
|
UTSW |
18 |
12,711,086 (GRCm39) |
nonsense |
probably null |
|
R4704:Lama3
|
UTSW |
18 |
12,686,280 (GRCm39) |
missense |
probably benign |
0.08 |
R4750:Lama3
|
UTSW |
18 |
12,637,416 (GRCm39) |
missense |
probably benign |
0.25 |
R4753:Lama3
|
UTSW |
18 |
12,615,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R4767:Lama3
|
UTSW |
18 |
12,633,620 (GRCm39) |
missense |
probably benign |
0.32 |
R4777:Lama3
|
UTSW |
18 |
12,546,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Lama3
|
UTSW |
18 |
12,544,627 (GRCm39) |
nonsense |
probably null |
|
R4784:Lama3
|
UTSW |
18 |
12,582,601 (GRCm39) |
missense |
probably benign |
0.20 |
R4816:Lama3
|
UTSW |
18 |
12,610,661 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4833:Lama3
|
UTSW |
18 |
12,574,188 (GRCm39) |
missense |
probably benign |
0.01 |
R4854:Lama3
|
UTSW |
18 |
12,544,599 (GRCm39) |
missense |
probably benign |
0.00 |
R4863:Lama3
|
UTSW |
18 |
12,631,735 (GRCm39) |
intron |
probably benign |
|
R4863:Lama3
|
UTSW |
18 |
12,672,850 (GRCm39) |
missense |
probably damaging |
0.99 |
R4953:Lama3
|
UTSW |
18 |
12,581,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Lama3
|
UTSW |
18 |
12,685,883 (GRCm39) |
missense |
probably damaging |
0.98 |
R4996:Lama3
|
UTSW |
18 |
12,651,800 (GRCm39) |
missense |
probably benign |
0.24 |
R5049:Lama3
|
UTSW |
18 |
12,715,668 (GRCm39) |
missense |
probably benign |
0.19 |
R5057:Lama3
|
UTSW |
18 |
12,665,005 (GRCm39) |
missense |
probably null |
0.82 |
R5090:Lama3
|
UTSW |
18 |
12,675,459 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5122:Lama3
|
UTSW |
18 |
12,672,823 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5215:Lama3
|
UTSW |
18 |
12,710,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5245:Lama3
|
UTSW |
18 |
12,552,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Lama3
|
UTSW |
18 |
12,598,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Lama3
|
UTSW |
18 |
12,685,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R5377:Lama3
|
UTSW |
18 |
12,586,803 (GRCm39) |
missense |
probably damaging |
0.99 |
R5432:Lama3
|
UTSW |
18 |
12,705,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5500:Lama3
|
UTSW |
18 |
12,589,821 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5534:Lama3
|
UTSW |
18 |
12,686,267 (GRCm39) |
missense |
probably benign |
0.00 |
R5589:Lama3
|
UTSW |
18 |
12,605,277 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5604:Lama3
|
UTSW |
18 |
12,572,405 (GRCm39) |
missense |
probably benign |
|
R5617:Lama3
|
UTSW |
18 |
12,631,993 (GRCm39) |
intron |
probably benign |
|
R5709:Lama3
|
UTSW |
18 |
12,672,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Lama3
|
UTSW |
18 |
12,562,944 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6042:Lama3
|
UTSW |
18 |
12,707,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Lama3
|
UTSW |
18 |
12,602,985 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6085:Lama3
|
UTSW |
18 |
12,615,156 (GRCm39) |
missense |
probably benign |
0.01 |
R6212:Lama3
|
UTSW |
18 |
12,646,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6268:Lama3
|
UTSW |
18 |
12,657,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R6276:Lama3
|
UTSW |
18 |
12,640,006 (GRCm39) |
missense |
probably benign |
0.02 |
R6366:Lama3
|
UTSW |
18 |
12,615,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Lama3
|
UTSW |
18 |
12,612,813 (GRCm39) |
missense |
probably benign |
0.44 |
R6493:Lama3
|
UTSW |
18 |
12,615,205 (GRCm39) |
critical splice donor site |
probably null |
|
R6505:Lama3
|
UTSW |
18 |
12,628,405 (GRCm39) |
missense |
probably benign |
0.02 |
R6563:Lama3
|
UTSW |
18 |
12,670,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R6582:Lama3
|
UTSW |
18 |
12,710,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R6585:Lama3
|
UTSW |
18 |
12,552,314 (GRCm39) |
critical splice donor site |
probably null |
|
R6609:Lama3
|
UTSW |
18 |
12,646,735 (GRCm39) |
missense |
probably damaging |
0.99 |
R6656:Lama3
|
UTSW |
18 |
12,682,283 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6833:Lama3
|
UTSW |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R6834:Lama3
|
UTSW |
18 |
12,624,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Lama3
|
UTSW |
18 |
12,661,475 (GRCm39) |
missense |
probably damaging |
0.97 |
R7026:Lama3
|
UTSW |
18 |
12,649,605 (GRCm39) |
missense |
probably damaging |
0.98 |
R7088:Lama3
|
UTSW |
18 |
12,715,602 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7100:Lama3
|
UTSW |
18 |
12,715,701 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7102:Lama3
|
UTSW |
18 |
12,685,870 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7103:Lama3
|
UTSW |
18 |
12,664,936 (GRCm39) |
missense |
probably benign |
0.00 |
R7121:Lama3
|
UTSW |
18 |
12,595,839 (GRCm39) |
missense |
probably benign |
0.06 |
R7150:Lama3
|
UTSW |
18 |
12,601,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R7158:Lama3
|
UTSW |
18 |
12,589,869 (GRCm39) |
missense |
probably benign |
0.20 |
R7170:Lama3
|
UTSW |
18 |
12,537,133 (GRCm39) |
missense |
probably benign |
0.26 |
R7216:Lama3
|
UTSW |
18 |
12,563,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7223:Lama3
|
UTSW |
18 |
12,715,665 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7243:Lama3
|
UTSW |
18 |
12,552,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R7282:Lama3
|
UTSW |
18 |
12,572,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Lama3
|
UTSW |
18 |
12,640,097 (GRCm39) |
splice site |
probably null |
|
R7442:Lama3
|
UTSW |
18 |
12,605,238 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7487:Lama3
|
UTSW |
18 |
12,552,294 (GRCm39) |
missense |
probably benign |
|
R7604:Lama3
|
UTSW |
18 |
12,633,550 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7609:Lama3
|
UTSW |
18 |
12,664,891 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7650:Lama3
|
UTSW |
18 |
12,670,895 (GRCm39) |
missense |
probably benign |
0.01 |
R7894:Lama3
|
UTSW |
18 |
12,595,864 (GRCm39) |
missense |
probably benign |
0.07 |
R7975:Lama3
|
UTSW |
18 |
12,670,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8099:Lama3
|
UTSW |
18 |
12,667,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R8168:Lama3
|
UTSW |
18 |
12,639,999 (GRCm39) |
missense |
probably null |
|
R8219:Lama3
|
UTSW |
18 |
12,572,417 (GRCm39) |
missense |
probably benign |
0.07 |
R8227:Lama3
|
UTSW |
18 |
12,540,608 (GRCm39) |
missense |
probably benign |
|
R8229:Lama3
|
UTSW |
18 |
12,540,608 (GRCm39) |
missense |
probably benign |
|
R8298:Lama3
|
UTSW |
18 |
12,658,910 (GRCm39) |
missense |
probably benign |
0.12 |
R8351:Lama3
|
UTSW |
18 |
12,673,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Lama3
|
UTSW |
18 |
12,661,404 (GRCm39) |
missense |
probably damaging |
0.99 |
R8463:Lama3
|
UTSW |
18 |
12,582,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R8515:Lama3
|
UTSW |
18 |
12,544,688 (GRCm39) |
missense |
probably null |
0.01 |
R8784:Lama3
|
UTSW |
18 |
12,554,212 (GRCm39) |
missense |
probably benign |
|
R8799:Lama3
|
UTSW |
18 |
12,624,000 (GRCm39) |
missense |
probably damaging |
0.96 |
R8874:Lama3
|
UTSW |
18 |
12,582,643 (GRCm39) |
critical splice donor site |
probably null |
|
R8938:Lama3
|
UTSW |
18 |
12,689,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R8967:Lama3
|
UTSW |
18 |
12,665,096 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9039:Lama3
|
UTSW |
18 |
12,614,120 (GRCm39) |
nonsense |
probably null |
|
R9126:Lama3
|
UTSW |
18 |
12,583,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Lama3
|
UTSW |
18 |
12,605,297 (GRCm39) |
missense |
probably benign |
0.00 |
R9203:Lama3
|
UTSW |
18 |
12,595,869 (GRCm39) |
missense |
probably benign |
0.04 |
R9246:Lama3
|
UTSW |
18 |
12,710,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R9284:Lama3
|
UTSW |
18 |
12,583,541 (GRCm39) |
nonsense |
probably null |
|
R9553:Lama3
|
UTSW |
18 |
12,563,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R9716:Lama3
|
UTSW |
18 |
12,583,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R9734:Lama3
|
UTSW |
18 |
12,682,320 (GRCm39) |
missense |
possibly damaging |
0.94 |
X0019:Lama3
|
UTSW |
18 |
12,715,631 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Lama3
|
UTSW |
18 |
12,562,936 (GRCm39) |
critical splice acceptor site |
probably null |
|
|