Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
T |
C |
4: 144,282,081 (GRCm39) |
Y237C |
probably damaging |
Het |
Adcyap1 |
A |
G |
17: 93,510,260 (GRCm39) |
D96G |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,688,134 (GRCm39) |
V1749M |
probably damaging |
Het |
Adnp2 |
A |
T |
18: 80,173,868 (GRCm39) |
N180K |
probably benign |
Het |
Ahdc1 |
G |
T |
4: 132,790,030 (GRCm39) |
A424S |
unknown |
Het |
Alpk3 |
G |
A |
7: 80,717,701 (GRCm39) |
R86H |
possibly damaging |
Het |
Atf7ip |
A |
C |
6: 136,537,987 (GRCm39) |
T49P |
possibly damaging |
Het |
Atp7b |
G |
A |
8: 22,518,467 (GRCm39) |
L124F |
probably benign |
Het |
Bub1 |
A |
T |
2: 127,643,314 (GRCm39) |
L1010* |
probably null |
Het |
Cd300c |
C |
A |
11: 114,850,411 (GRCm39) |
E131* |
probably null |
Het |
Cep135 |
A |
G |
5: 76,763,590 (GRCm39) |
K527E |
probably damaging |
Het |
Cfd |
G |
T |
10: 79,727,592 (GRCm39) |
E89* |
probably null |
Het |
Crb1 |
A |
C |
1: 139,168,904 (GRCm39) |
C871W |
probably damaging |
Het |
D6Ertd527e |
A |
T |
6: 87,088,277 (GRCm39) |
S147C |
unknown |
Het |
Ddx60 |
A |
T |
8: 62,436,889 (GRCm39) |
E946D |
probably benign |
Het |
Dmrt1 |
G |
A |
19: 25,523,371 (GRCm39) |
E241K |
probably benign |
Het |
Dnah11 |
C |
G |
12: 117,976,074 (GRCm39) |
V2782L |
probably benign |
Het |
Dzip1 |
T |
C |
14: 119,146,969 (GRCm39) |
I313M |
probably damaging |
Het |
Egln3 |
T |
C |
12: 54,250,298 (GRCm39) |
E17G |
probably benign |
Het |
Eif3d |
A |
G |
15: 77,852,420 (GRCm39) |
V42A |
probably damaging |
Het |
Elapor1 |
A |
G |
3: 108,368,567 (GRCm39) |
L808P |
probably damaging |
Het |
Eogt |
C |
A |
6: 97,090,916 (GRCm39) |
G408W |
probably damaging |
Het |
Fip1l1 |
T |
A |
5: 74,756,503 (GRCm39) |
N498K |
probably damaging |
Het |
Fmn2 |
T |
A |
1: 174,437,520 (GRCm39) |
|
probably null |
Het |
Fndc3b |
T |
C |
3: 27,521,579 (GRCm39) |
E532G |
probably damaging |
Het |
Gabrb3 |
T |
C |
7: 57,415,278 (GRCm39) |
L116P |
probably damaging |
Het |
Galnt6 |
A |
T |
15: 100,591,352 (GRCm39) |
|
probably null |
Het |
Glmp |
G |
A |
3: 88,232,391 (GRCm39) |
M1I |
probably null |
Het |
Gm5478 |
T |
C |
15: 101,552,761 (GRCm39) |
D79G |
probably damaging |
Het |
Gnb1 |
T |
G |
4: 155,636,140 (GRCm39) |
D153E |
probably benign |
Het |
Grik2 |
T |
C |
10: 49,116,821 (GRCm39) |
I86V |
probably damaging |
Het |
Hdac3 |
C |
T |
18: 38,074,005 (GRCm39) |
|
probably null |
Het |
Hdgfl2 |
G |
A |
17: 56,406,181 (GRCm39) |
R523H |
possibly damaging |
Het |
Ifngr1 |
T |
A |
10: 19,473,180 (GRCm39) |
N43K |
probably damaging |
Het |
Iqgap1 |
A |
G |
7: 80,401,678 (GRCm39) |
W476R |
probably benign |
Het |
Jag1 |
A |
G |
2: 136,937,365 (GRCm39) |
|
probably null |
Het |
Kars1 |
T |
C |
8: 112,734,848 (GRCm39) |
D46G |
probably benign |
Het |
Kcnd2 |
A |
G |
6: 21,216,682 (GRCm39) |
I129V |
probably damaging |
Het |
Lars1 |
A |
T |
18: 42,383,967 (GRCm39) |
V76E |
possibly damaging |
Het |
Lgals9 |
T |
C |
11: 78,854,274 (GRCm39) |
I337V |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,741,723 (GRCm39) |
D3068G |
probably damaging |
Het |
Med12l |
A |
G |
3: 58,984,480 (GRCm39) |
T462A |
possibly damaging |
Het |
Megf9 |
T |
A |
4: 70,374,178 (GRCm39) |
D286V |
probably damaging |
Het |
Meox1 |
T |
A |
11: 101,770,227 (GRCm39) |
S167C |
probably damaging |
Het |
Mier2 |
C |
T |
10: 79,378,430 (GRCm39) |
|
probably null |
Het |
Mrps2 |
C |
A |
2: 28,359,791 (GRCm39) |
T216K |
probably damaging |
Het |
Mto1 |
A |
T |
9: 78,360,286 (GRCm39) |
D258V |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,826,801 (GRCm39) |
H208L |
probably benign |
Het |
Myo15b |
T |
A |
11: 115,775,091 (GRCm39) |
I751N |
probably damaging |
Het |
Napg |
C |
T |
18: 63,120,034 (GRCm39) |
R149C |
probably damaging |
Het |
Ndrg4 |
T |
A |
8: 96,437,563 (GRCm39) |
M17K |
probably damaging |
Het |
Nfrkb |
T |
G |
9: 31,325,476 (GRCm39) |
M973R |
probably benign |
Het |
Nxph4 |
C |
T |
10: 127,362,780 (GRCm39) |
R37H |
probably damaging |
Het |
Oas1e |
A |
G |
5: 120,933,460 (GRCm39) |
I35T |
probably damaging |
Het |
Oc90 |
C |
T |
15: 65,769,514 (GRCm39) |
|
probably null |
Het |
Or4b12 |
A |
T |
2: 90,095,880 (GRCm39) |
M298K |
probably null |
Het |
Or52d3 |
A |
T |
7: 104,229,567 (GRCm39) |
D238V |
probably damaging |
Het |
Or8j3 |
G |
A |
2: 86,029,055 (GRCm39) |
L14F |
possibly damaging |
Het |
Or8k30 |
A |
T |
2: 86,339,549 (GRCm39) |
T249S |
probably benign |
Het |
Or9a7 |
A |
T |
6: 40,521,057 (GRCm39) |
N285K |
possibly damaging |
Het |
Papola |
T |
A |
12: 105,773,452 (GRCm39) |
I157N |
probably damaging |
Het |
Pcyox1l |
G |
C |
18: 61,830,964 (GRCm39) |
P303A |
possibly damaging |
Het |
Pkdrej |
T |
C |
15: 85,703,752 (GRCm39) |
N728S |
probably benign |
Het |
Pkp4 |
A |
G |
2: 59,148,873 (GRCm39) |
D542G |
probably damaging |
Het |
Pla2g5 |
C |
T |
4: 138,527,967 (GRCm39) |
D100N |
probably benign |
Het |
Poln |
C |
T |
5: 34,307,108 (GRCm39) |
R31H |
probably benign |
Het |
Ppp3ca |
G |
A |
3: 136,640,900 (GRCm39) |
A484T |
probably benign |
Het |
Prag1 |
A |
G |
8: 36,570,958 (GRCm39) |
T514A |
probably benign |
Het |
Pramel28 |
A |
T |
4: 143,693,310 (GRCm39) |
V56E |
probably damaging |
Het |
Prex2 |
G |
A |
1: 11,270,281 (GRCm39) |
|
probably null |
Het |
Prrc2b |
G |
T |
2: 32,089,103 (GRCm39) |
W403L |
probably damaging |
Het |
Pter |
A |
T |
2: 13,005,748 (GRCm39) |
K307M |
probably damaging |
Het |
Ptpn5 |
G |
A |
7: 46,740,506 (GRCm39) |
S99L |
probably benign |
Het |
Ptpn5 |
A |
C |
7: 46,740,507 (GRCm39) |
S99A |
probably benign |
Het |
Rpap1 |
A |
C |
2: 119,602,321 (GRCm39) |
H674Q |
probably benign |
Het |
Rph3a |
A |
T |
5: 121,081,127 (GRCm39) |
D623E |
probably benign |
Het |
Sdr9c7 |
G |
T |
10: 127,734,588 (GRCm39) |
E25D |
probably benign |
Het |
Septin9 |
T |
G |
11: 117,247,458 (GRCm39) |
V479G |
probably damaging |
Het |
Sgo2a |
A |
G |
1: 58,055,856 (GRCm39) |
D680G |
probably benign |
Het |
Sgo2b |
A |
T |
8: 64,381,410 (GRCm39) |
I474N |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,436,701 (GRCm39) |
I43N |
probably damaging |
Het |
Shprh |
G |
A |
10: 11,045,853 (GRCm39) |
M891I |
probably benign |
Het |
Skic2 |
A |
T |
17: 35,063,791 (GRCm39) |
Y551N |
possibly damaging |
Het |
Slc12a9 |
A |
G |
5: 137,321,108 (GRCm39) |
M469T |
probably damaging |
Het |
Slc4a2 |
A |
T |
5: 24,640,941 (GRCm39) |
I747F |
probably damaging |
Het |
Slc7a6 |
T |
A |
8: 106,921,149 (GRCm39) |
N373K |
probably damaging |
Het |
Slc7a6os |
T |
C |
8: 106,927,688 (GRCm39) |
D296G |
probably benign |
Het |
Sncaip |
A |
G |
18: 53,038,881 (GRCm39) |
T120A |
probably damaging |
Het |
Sorcs1 |
G |
C |
19: 50,301,480 (GRCm39) |
|
probably null |
Het |
Spata16 |
A |
G |
3: 26,721,605 (GRCm39) |
E42G |
probably damaging |
Het |
Spata31e2 |
G |
T |
1: 26,724,347 (GRCm39) |
Q278K |
possibly damaging |
Het |
Syne2 |
A |
T |
12: 76,009,415 (GRCm39) |
M2440L |
probably benign |
Het |
Taf7l2 |
T |
C |
10: 115,949,474 (GRCm39) |
I17M |
probably damaging |
Het |
Tead2 |
A |
G |
7: 44,875,179 (GRCm39) |
E232G |
probably damaging |
Het |
Tmf1 |
T |
G |
6: 97,153,465 (GRCm39) |
T203P |
possibly damaging |
Het |
Trrap |
C |
A |
5: 144,753,205 (GRCm39) |
H1843Q |
probably benign |
Het |
Unc79 |
C |
A |
12: 103,137,903 (GRCm39) |
Q2314K |
probably damaging |
Het |
Unc80 |
G |
T |
1: 66,550,040 (GRCm39) |
G766V |
probably damaging |
Het |
Vmn1r217 |
A |
G |
13: 23,298,764 (GRCm39) |
L46P |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 78,984,773 (GRCm39) |
I42F |
possibly damaging |
Het |
Vwa5a |
T |
C |
9: 38,639,961 (GRCm39) |
V403A |
probably damaging |
Het |
Zfp42 |
T |
C |
8: 43,748,988 (GRCm39) |
E171G |
probably damaging |
Het |
Zfp64 |
A |
T |
2: 168,767,960 (GRCm39) |
S551T |
probably benign |
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 |
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 |
R7133:Lama3
|
UTSW |
18 |
12,672,843 (GRCm39) |
missense |
probably benign |
0.05 |
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 |
|
|