Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
T |
G |
4: 144,349,849 (GRCm39) |
W369G |
probably damaging |
Het |
Abhd16b |
C |
T |
2: 181,135,461 (GRCm39) |
T121M |
possibly damaging |
Het |
Adam5 |
A |
T |
8: 25,276,262 (GRCm39) |
C468* |
probably null |
Het |
Aim2 |
C |
T |
1: 173,283,152 (GRCm39) |
A78V |
possibly damaging |
Het |
Alg9 |
G |
A |
9: 50,703,422 (GRCm39) |
W254* |
probably null |
Het |
Ankrd55 |
G |
C |
13: 112,504,834 (GRCm39) |
E499Q |
probably benign |
Het |
Atp6v0a2 |
T |
C |
5: 124,791,209 (GRCm39) |
F546S |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Bpi |
A |
T |
2: 158,100,164 (GRCm39) |
|
probably benign |
Het |
Bves |
A |
G |
10: 45,215,514 (GRCm39) |
H63R |
probably benign |
Het |
Ccdc183 |
T |
C |
2: 25,507,057 (GRCm39) |
M45V |
probably benign |
Het |
Cfhr4 |
T |
A |
1: 139,664,668 (GRCm39) |
I464L |
possibly damaging |
Het |
Cmklr1 |
T |
C |
5: 113,752,983 (GRCm39) |
Y6C |
probably damaging |
Het |
Colgalt1 |
C |
T |
8: 72,076,165 (GRCm39) |
R539C |
probably damaging |
Het |
Ctsm |
T |
A |
13: 61,687,698 (GRCm39) |
E53D |
probably damaging |
Het |
Cyp2a22 |
A |
G |
7: 26,638,606 (GRCm39) |
|
probably null |
Het |
Ddx10 |
A |
G |
9: 53,115,411 (GRCm39) |
V641A |
probably damaging |
Het |
Ddx6 |
T |
C |
9: 44,540,020 (GRCm39) |
V316A |
probably damaging |
Het |
Dhx34 |
T |
C |
7: 15,937,799 (GRCm39) |
D767G |
probably benign |
Het |
Dnaaf6rt |
T |
C |
1: 31,261,990 (GRCm39) |
|
probably benign |
Het |
Dtnbp1 |
T |
A |
13: 45,155,405 (GRCm39) |
D15V |
probably damaging |
Het |
Dtx3l |
C |
T |
16: 35,751,742 (GRCm39) |
|
probably null |
Het |
Entpd8 |
T |
C |
2: 24,973,321 (GRCm39) |
I162T |
probably damaging |
Het |
Fam186a |
G |
T |
15: 99,840,347 (GRCm39) |
Q1966K |
probably benign |
Het |
Fbxo27 |
A |
C |
7: 28,392,785 (GRCm39) |
D22A |
probably damaging |
Het |
Fermt3 |
A |
T |
19: 6,977,095 (GRCm39) |
I577N |
probably damaging |
Het |
Frmd8 |
A |
T |
19: 5,923,209 (GRCm39) |
S81T |
probably damaging |
Het |
Gm5108 |
T |
A |
5: 68,102,012 (GRCm39) |
|
probably benign |
Het |
Gm9195 |
T |
C |
14: 72,718,271 (GRCm39) |
Y135C |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Kcnh8 |
A |
T |
17: 53,284,723 (GRCm39) |
I898F |
probably benign |
Het |
Kri1 |
C |
T |
9: 21,199,083 (GRCm39) |
|
probably benign |
Het |
Krt32 |
T |
A |
11: 99,977,271 (GRCm39) |
I210F |
probably damaging |
Het |
Lamc2 |
G |
A |
1: 153,012,508 (GRCm39) |
T722M |
probably benign |
Het |
Lpin3 |
C |
T |
2: 160,746,803 (GRCm39) |
P766L |
probably damaging |
Het |
Macroh2a1 |
T |
C |
13: 56,237,643 (GRCm39) |
N206D |
probably benign |
Het |
Marf1 |
T |
C |
16: 13,946,721 (GRCm39) |
T1169A |
probably damaging |
Het |
Morc1 |
G |
A |
16: 48,385,984 (GRCm39) |
V536M |
probably benign |
Het |
Morc1 |
A |
T |
16: 48,438,909 (GRCm39) |
H768L |
probably benign |
Het |
Mpped2 |
T |
A |
2: 106,529,878 (GRCm39) |
H42Q |
possibly damaging |
Het |
Nfatc1 |
G |
T |
18: 80,696,779 (GRCm39) |
|
probably null |
Het |
Nfkbid |
G |
A |
7: 30,125,192 (GRCm39) |
S263N |
probably benign |
Het |
Npas3 |
C |
A |
12: 54,115,576 (GRCm39) |
Q802K |
probably damaging |
Het |
Or52s1b |
T |
C |
7: 102,822,119 (GRCm39) |
T242A |
probably damaging |
Het |
Or5ac20 |
T |
G |
16: 59,104,453 (GRCm39) |
M136L |
possibly damaging |
Het |
Or5p67 |
T |
A |
7: 107,922,101 (GRCm39) |
I261F |
possibly damaging |
Het |
Pabpc4l |
C |
A |
3: 46,401,345 (GRCm39) |
V100L |
possibly damaging |
Het |
Pagr1a |
A |
G |
7: 126,615,613 (GRCm39) |
|
probably null |
Het |
Pcdh1 |
A |
T |
18: 38,331,553 (GRCm39) |
N483K |
probably damaging |
Het |
Pikfyve |
C |
A |
1: 65,291,689 (GRCm39) |
P1303T |
probably damaging |
Het |
Plekhh3 |
T |
A |
11: 101,056,519 (GRCm39) |
|
probably null |
Het |
Pnkd |
T |
A |
1: 74,332,335 (GRCm39) |
|
probably null |
Het |
Pparg |
A |
T |
6: 115,428,011 (GRCm39) |
Q166L |
probably benign |
Het |
Psenen |
A |
G |
7: 30,262,932 (GRCm39) |
|
probably null |
Het |
Rab4a |
T |
C |
8: 124,557,105 (GRCm39) |
S142P |
probably damaging |
Het |
Reg3a |
T |
C |
6: 78,358,132 (GRCm39) |
V21A |
probably benign |
Het |
Relt |
A |
C |
7: 100,502,321 (GRCm39) |
|
probably benign |
Het |
Rftn1 |
T |
A |
17: 50,344,019 (GRCm39) |
T90S |
possibly damaging |
Het |
Ripor3 |
T |
G |
2: 167,839,186 (GRCm39) |
D105A |
probably damaging |
Het |
Rnase10 |
T |
A |
14: 51,247,138 (GRCm39) |
I135N |
probably damaging |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Rttn |
A |
G |
18: 89,047,023 (GRCm39) |
E895G |
probably damaging |
Het |
Serpina3a |
G |
A |
12: 104,079,089 (GRCm39) |
|
probably null |
Het |
Slco5a1 |
C |
T |
1: 12,951,617 (GRCm39) |
C562Y |
probably damaging |
Het |
Spen |
T |
C |
4: 141,220,770 (GRCm39) |
T396A |
unknown |
Het |
Tgfbr3 |
A |
G |
5: 107,280,892 (GRCm39) |
S623P |
probably damaging |
Het |
Tmem8b |
A |
G |
4: 43,690,192 (GRCm39) |
I876V |
probably damaging |
Het |
Tmod3 |
T |
C |
9: 75,416,669 (GRCm39) |
K221R |
probably damaging |
Het |
Tomm40 |
G |
T |
7: 19,436,831 (GRCm39) |
D40E |
probably damaging |
Het |
Trav6d-4 |
G |
T |
14: 52,991,048 (GRCm39) |
G28V |
probably damaging |
Het |
Trav8d-2 |
G |
T |
14: 53,279,933 (GRCm39) |
A17S |
probably benign |
Het |
Triml2 |
T |
C |
8: 43,643,115 (GRCm39) |
C158R |
possibly damaging |
Het |
Trip10 |
A |
G |
17: 57,562,331 (GRCm39) |
E283G |
probably damaging |
Het |
Tubb2b |
T |
C |
13: 34,311,518 (GRCm39) |
Y425C |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,794,074 (GRCm39) |
T37A |
probably benign |
Het |
Unc13b |
A |
G |
4: 43,171,403 (GRCm39) |
|
probably benign |
Het |
Unc13b |
A |
G |
4: 43,173,203 (GRCm39) |
|
probably benign |
Het |
Vcan |
A |
T |
13: 89,841,526 (GRCm39) |
D379E |
possibly damaging |
Het |
Vmn1r44 |
T |
A |
6: 89,871,140 (GRCm39) |
H295Q |
probably benign |
Het |
Vmn2r16 |
A |
T |
5: 109,487,969 (GRCm39) |
S281C |
probably damaging |
Het |
Vmn2r84 |
C |
T |
10: 130,226,876 (GRCm39) |
A321T |
possibly damaging |
Het |
Vsig10l |
A |
T |
7: 43,114,491 (GRCm39) |
H271L |
possibly damaging |
Het |
Vwa8 |
A |
T |
14: 79,145,596 (GRCm39) |
H91L |
possibly damaging |
Het |
Zfp957 |
T |
A |
14: 79,451,130 (GRCm39) |
E223V |
probably damaging |
Het |
|
Other mutations in Lama1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Lama1
|
APN |
17 |
68,122,923 (GRCm39) |
missense |
probably benign |
|
IGL00336:Lama1
|
APN |
17 |
68,120,943 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01066:Lama1
|
APN |
17 |
68,050,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01140:Lama1
|
APN |
17 |
68,109,928 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01291:Lama1
|
APN |
17 |
68,045,865 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01296:Lama1
|
APN |
17 |
68,052,046 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01317:Lama1
|
APN |
17 |
68,125,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Lama1
|
APN |
17 |
68,057,579 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01506:Lama1
|
APN |
17 |
68,092,065 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01508:Lama1
|
APN |
17 |
68,116,356 (GRCm39) |
splice site |
probably benign |
|
IGL01522:Lama1
|
APN |
17 |
68,059,769 (GRCm39) |
splice site |
probably benign |
|
IGL01530:Lama1
|
APN |
17 |
68,103,785 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01541:Lama1
|
APN |
17 |
68,092,065 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01677:Lama1
|
APN |
17 |
68,086,143 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01886:Lama1
|
APN |
17 |
68,114,792 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01994:Lama1
|
APN |
17 |
68,059,434 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02017:Lama1
|
APN |
17 |
68,071,720 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02021:Lama1
|
APN |
17 |
68,128,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Lama1
|
APN |
17 |
68,116,287 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02044:Lama1
|
APN |
17 |
68,118,485 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02120:Lama1
|
APN |
17 |
68,023,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Lama1
|
APN |
17 |
68,118,480 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02549:Lama1
|
APN |
17 |
68,097,830 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02642:Lama1
|
APN |
17 |
68,119,361 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02795:Lama1
|
APN |
17 |
68,045,889 (GRCm39) |
splice site |
probably null |
|
IGL02798:Lama1
|
APN |
17 |
68,102,186 (GRCm39) |
splice site |
probably benign |
|
IGL02863:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02870:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02876:Lama1
|
APN |
17 |
68,057,687 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02885:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02891:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02978:Lama1
|
APN |
17 |
68,093,076 (GRCm39) |
nonsense |
probably null |
|
IGL03064:Lama1
|
APN |
17 |
68,086,099 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03076:Lama1
|
APN |
17 |
68,023,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03110:Lama1
|
APN |
17 |
68,105,981 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03143:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03159:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03268:Lama1
|
APN |
17 |
68,111,531 (GRCm39) |
missense |
probably damaging |
0.99 |
ANU05:Lama1
|
UTSW |
17 |
68,045,865 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Lama1
|
UTSW |
17 |
68,071,699 (GRCm39) |
missense |
|
|
R0047:Lama1
|
UTSW |
17 |
68,102,181 (GRCm39) |
splice site |
probably benign |
|
R0047:Lama1
|
UTSW |
17 |
68,102,181 (GRCm39) |
splice site |
probably benign |
|
R0050:Lama1
|
UTSW |
17 |
68,089,051 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0096:Lama1
|
UTSW |
17 |
68,112,408 (GRCm39) |
missense |
probably benign |
0.12 |
R0096:Lama1
|
UTSW |
17 |
68,112,408 (GRCm39) |
missense |
probably benign |
0.12 |
R0111:Lama1
|
UTSW |
17 |
68,044,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Lama1
|
UTSW |
17 |
68,083,918 (GRCm39) |
missense |
probably benign |
0.10 |
R0121:Lama1
|
UTSW |
17 |
68,105,508 (GRCm39) |
splice site |
probably benign |
|
R0278:Lama1
|
UTSW |
17 |
68,117,178 (GRCm39) |
missense |
probably null |
0.98 |
R0281:Lama1
|
UTSW |
17 |
68,124,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Lama1
|
UTSW |
17 |
68,082,846 (GRCm39) |
missense |
possibly damaging |
0.45 |
R0419:Lama1
|
UTSW |
17 |
68,098,605 (GRCm39) |
critical splice donor site |
probably null |
|
R0512:Lama1
|
UTSW |
17 |
68,086,129 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0514:Lama1
|
UTSW |
17 |
68,071,693 (GRCm39) |
missense |
probably benign |
0.40 |
R0562:Lama1
|
UTSW |
17 |
68,122,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0632:Lama1
|
UTSW |
17 |
68,059,363 (GRCm39) |
splice site |
probably benign |
|
R0645:Lama1
|
UTSW |
17 |
68,080,707 (GRCm39) |
missense |
probably benign |
0.01 |
R0712:Lama1
|
UTSW |
17 |
68,086,037 (GRCm39) |
splice site |
probably null |
|
R0763:Lama1
|
UTSW |
17 |
68,079,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R0941:Lama1
|
UTSW |
17 |
68,082,860 (GRCm39) |
missense |
probably benign |
0.10 |
R1025:Lama1
|
UTSW |
17 |
68,059,893 (GRCm39) |
missense |
probably benign |
0.00 |
R1084:Lama1
|
UTSW |
17 |
68,111,464 (GRCm39) |
missense |
probably benign |
0.12 |
R1103:Lama1
|
UTSW |
17 |
68,097,942 (GRCm39) |
missense |
probably damaging |
0.98 |
R1420:Lama1
|
UTSW |
17 |
68,097,942 (GRCm39) |
missense |
probably damaging |
0.98 |
R1430:Lama1
|
UTSW |
17 |
68,089,150 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1569:Lama1
|
UTSW |
17 |
68,087,613 (GRCm39) |
splice site |
probably null |
|
R1575:Lama1
|
UTSW |
17 |
68,117,404 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1613:Lama1
|
UTSW |
17 |
68,114,918 (GRCm39) |
missense |
probably benign |
0.42 |
R1620:Lama1
|
UTSW |
17 |
68,074,028 (GRCm39) |
missense |
probably benign |
0.01 |
R1629:Lama1
|
UTSW |
17 |
68,112,423 (GRCm39) |
missense |
probably benign |
0.00 |
R1645:Lama1
|
UTSW |
17 |
68,044,677 (GRCm39) |
missense |
probably benign |
0.14 |
R1652:Lama1
|
UTSW |
17 |
68,114,841 (GRCm39) |
missense |
probably damaging |
0.97 |
R1674:Lama1
|
UTSW |
17 |
68,098,239 (GRCm39) |
missense |
probably benign |
|
R1678:Lama1
|
UTSW |
17 |
68,117,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1710:Lama1
|
UTSW |
17 |
68,060,786 (GRCm39) |
missense |
probably benign |
0.00 |
R1712:Lama1
|
UTSW |
17 |
68,024,181 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1737:Lama1
|
UTSW |
17 |
68,109,916 (GRCm39) |
missense |
probably benign |
0.36 |
R1757:Lama1
|
UTSW |
17 |
68,004,378 (GRCm39) |
missense |
unknown |
|
R1757:Lama1
|
UTSW |
17 |
68,070,831 (GRCm39) |
missense |
probably benign |
0.40 |
R1813:Lama1
|
UTSW |
17 |
68,098,218 (GRCm39) |
missense |
probably benign |
|
R1896:Lama1
|
UTSW |
17 |
68,098,218 (GRCm39) |
missense |
probably benign |
|
R1945:Lama1
|
UTSW |
17 |
68,052,848 (GRCm39) |
missense |
probably benign |
0.14 |
R2086:Lama1
|
UTSW |
17 |
68,124,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Lama1
|
UTSW |
17 |
68,080,860 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2178:Lama1
|
UTSW |
17 |
68,076,510 (GRCm39) |
missense |
probably benign |
0.07 |
R2183:Lama1
|
UTSW |
17 |
68,098,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R2197:Lama1
|
UTSW |
17 |
68,059,936 (GRCm39) |
missense |
probably benign |
0.02 |
R2213:Lama1
|
UTSW |
17 |
68,084,029 (GRCm39) |
nonsense |
probably null |
|
R2260:Lama1
|
UTSW |
17 |
68,044,502 (GRCm39) |
missense |
probably damaging |
0.96 |
R2356:Lama1
|
UTSW |
17 |
68,117,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R2420:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2421:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2422:Lama1
|
UTSW |
17 |
68,057,548 (GRCm39) |
missense |
probably benign |
0.00 |
R2424:Lama1
|
UTSW |
17 |
68,105,660 (GRCm39) |
missense |
probably benign |
0.09 |
R2442:Lama1
|
UTSW |
17 |
68,075,312 (GRCm39) |
missense |
probably benign |
0.04 |
R3147:Lama1
|
UTSW |
17 |
68,044,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R3414:Lama1
|
UTSW |
17 |
68,044,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Lama1
|
UTSW |
17 |
68,075,328 (GRCm39) |
missense |
probably benign |
0.40 |
R3820:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R3821:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R3822:Lama1
|
UTSW |
17 |
68,086,041 (GRCm39) |
splice site |
probably null |
|
R4012:Lama1
|
UTSW |
17 |
68,119,368 (GRCm39) |
nonsense |
probably null |
|
R4113:Lama1
|
UTSW |
17 |
68,071,698 (GRCm39) |
missense |
probably benign |
0.01 |
R4133:Lama1
|
UTSW |
17 |
68,119,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Lama1
|
UTSW |
17 |
68,057,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R4259:Lama1
|
UTSW |
17 |
68,059,413 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4278:Lama1
|
UTSW |
17 |
68,098,512 (GRCm39) |
missense |
probably null |
0.00 |
R4321:Lama1
|
UTSW |
17 |
68,078,078 (GRCm39) |
missense |
probably benign |
0.03 |
R4374:Lama1
|
UTSW |
17 |
68,111,513 (GRCm39) |
missense |
probably benign |
0.00 |
R4386:Lama1
|
UTSW |
17 |
68,080,707 (GRCm39) |
missense |
probably benign |
0.01 |
R4463:Lama1
|
UTSW |
17 |
68,068,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Lama1
|
UTSW |
17 |
68,112,355 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4630:Lama1
|
UTSW |
17 |
68,101,295 (GRCm39) |
missense |
probably benign |
0.00 |
R4633:Lama1
|
UTSW |
17 |
68,105,579 (GRCm39) |
missense |
probably damaging |
0.96 |
R4668:Lama1
|
UTSW |
17 |
68,059,429 (GRCm39) |
missense |
probably benign |
0.27 |
R4684:Lama1
|
UTSW |
17 |
68,080,773 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4745:Lama1
|
UTSW |
17 |
68,045,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Lama1
|
UTSW |
17 |
68,080,854 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4797:Lama1
|
UTSW |
17 |
68,023,770 (GRCm39) |
missense |
probably benign |
0.04 |
R4803:Lama1
|
UTSW |
17 |
68,116,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4925:Lama1
|
UTSW |
17 |
68,101,309 (GRCm39) |
missense |
probably benign |
0.02 |
R4939:Lama1
|
UTSW |
17 |
68,044,470 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4952:Lama1
|
UTSW |
17 |
68,074,561 (GRCm39) |
critical splice donor site |
probably null |
|
R4975:Lama1
|
UTSW |
17 |
68,045,829 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4977:Lama1
|
UTSW |
17 |
68,044,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5039:Lama1
|
UTSW |
17 |
68,052,888 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5047:Lama1
|
UTSW |
17 |
68,050,276 (GRCm39) |
nonsense |
probably null |
|
R5195:Lama1
|
UTSW |
17 |
68,071,795 (GRCm39) |
missense |
probably benign |
0.13 |
R5230:Lama1
|
UTSW |
17 |
68,052,078 (GRCm39) |
nonsense |
probably null |
|
R5236:Lama1
|
UTSW |
17 |
68,111,487 (GRCm39) |
missense |
probably benign |
0.24 |
R5254:Lama1
|
UTSW |
17 |
68,063,711 (GRCm39) |
missense |
probably benign |
0.01 |
R5345:Lama1
|
UTSW |
17 |
68,124,558 (GRCm39) |
missense |
probably benign |
|
R5438:Lama1
|
UTSW |
17 |
68,107,769 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5521:Lama1
|
UTSW |
17 |
68,087,889 (GRCm39) |
nonsense |
probably null |
|
R5568:Lama1
|
UTSW |
17 |
68,075,293 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5645:Lama1
|
UTSW |
17 |
68,109,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Lama1
|
UTSW |
17 |
68,077,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5727:Lama1
|
UTSW |
17 |
68,122,219 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5757:Lama1
|
UTSW |
17 |
68,045,782 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5795:Lama1
|
UTSW |
17 |
68,103,722 (GRCm39) |
missense |
probably benign |
0.02 |
R5857:Lama1
|
UTSW |
17 |
68,114,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R5894:Lama1
|
UTSW |
17 |
68,086,042 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5974:Lama1
|
UTSW |
17 |
68,080,722 (GRCm39) |
missense |
probably benign |
0.31 |
R6032:Lama1
|
UTSW |
17 |
68,057,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6032:Lama1
|
UTSW |
17 |
68,057,638 (GRCm39) |
missense |
probably benign |
0.01 |
R6120:Lama1
|
UTSW |
17 |
68,087,612 (GRCm39) |
critical splice donor site |
probably null |
|
R6219:Lama1
|
UTSW |
17 |
68,097,851 (GRCm39) |
missense |
probably benign |
0.08 |
R6224:Lama1
|
UTSW |
17 |
68,109,982 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6249:Lama1
|
UTSW |
17 |
68,105,599 (GRCm39) |
missense |
probably benign |
|
R6265:Lama1
|
UTSW |
17 |
68,057,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R6276:Lama1
|
UTSW |
17 |
68,091,083 (GRCm39) |
splice site |
probably null |
|
R6284:Lama1
|
UTSW |
17 |
68,117,091 (GRCm39) |
missense |
probably damaging |
0.99 |
R6337:Lama1
|
UTSW |
17 |
68,093,014 (GRCm39) |
missense |
probably benign |
0.27 |
R6414:Lama1
|
UTSW |
17 |
68,053,905 (GRCm39) |
critical splice donor site |
probably null |
|
R6631:Lama1
|
UTSW |
17 |
68,081,477 (GRCm39) |
missense |
probably benign |
0.21 |
R6659:Lama1
|
UTSW |
17 |
68,125,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R6660:Lama1
|
UTSW |
17 |
68,111,495 (GRCm39) |
missense |
probably benign |
0.05 |
R6677:Lama1
|
UTSW |
17 |
68,102,228 (GRCm39) |
missense |
probably benign |
0.14 |
R6763:Lama1
|
UTSW |
17 |
68,053,868 (GRCm39) |
missense |
unknown |
|
R6787:Lama1
|
UTSW |
17 |
68,091,020 (GRCm39) |
missense |
unknown |
|
R6831:Lama1
|
UTSW |
17 |
68,063,749 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6855:Lama1
|
UTSW |
17 |
68,089,150 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6910:Lama1
|
UTSW |
17 |
68,098,459 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6934:Lama1
|
UTSW |
17 |
68,081,538 (GRCm39) |
missense |
probably benign |
0.04 |
R6945:Lama1
|
UTSW |
17 |
68,120,861 (GRCm39) |
missense |
|
|
R6984:Lama1
|
UTSW |
17 |
68,086,107 (GRCm39) |
missense |
|
|
R6989:Lama1
|
UTSW |
17 |
68,060,753 (GRCm39) |
missense |
|
|
R6995:Lama1
|
UTSW |
17 |
68,060,820 (GRCm39) |
missense |
|
|
R7035:Lama1
|
UTSW |
17 |
68,088,044 (GRCm39) |
missense |
|
|
R7133:Lama1
|
UTSW |
17 |
68,089,141 (GRCm39) |
missense |
|
|
R7172:Lama1
|
UTSW |
17 |
68,111,540 (GRCm39) |
missense |
|
|
R7197:Lama1
|
UTSW |
17 |
68,044,700 (GRCm39) |
nonsense |
probably null |
|
R7217:Lama1
|
UTSW |
17 |
68,071,668 (GRCm39) |
missense |
|
|
R7229:Lama1
|
UTSW |
17 |
68,059,441 (GRCm39) |
missense |
|
|
R7264:Lama1
|
UTSW |
17 |
68,050,292 (GRCm39) |
missense |
|
|
R7311:Lama1
|
UTSW |
17 |
68,074,380 (GRCm39) |
missense |
|
|
R7394:Lama1
|
UTSW |
17 |
68,024,256 (GRCm39) |
missense |
|
|
R7419:Lama1
|
UTSW |
17 |
68,024,169 (GRCm39) |
missense |
|
|
R7460:Lama1
|
UTSW |
17 |
68,074,013 (GRCm39) |
missense |
|
|
R7492:Lama1
|
UTSW |
17 |
68,124,646 (GRCm39) |
missense |
|
|
R7494:Lama1
|
UTSW |
17 |
68,118,441 (GRCm39) |
missense |
|
|
R7552:Lama1
|
UTSW |
17 |
68,044,662 (GRCm39) |
missense |
|
|
R7576:Lama1
|
UTSW |
17 |
68,089,036 (GRCm39) |
missense |
|
|
R7583:Lama1
|
UTSW |
17 |
68,068,616 (GRCm39) |
missense |
|
|
R7649:Lama1
|
UTSW |
17 |
68,044,549 (GRCm39) |
missense |
|
|
R7663:Lama1
|
UTSW |
17 |
68,087,875 (GRCm39) |
missense |
|
|
R7667:Lama1
|
UTSW |
17 |
68,087,592 (GRCm39) |
missense |
|
|
R7688:Lama1
|
UTSW |
17 |
68,068,623 (GRCm39) |
missense |
|
|
R7693:Lama1
|
UTSW |
17 |
68,124,026 (GRCm39) |
missense |
|
|
R7748:Lama1
|
UTSW |
17 |
68,057,585 (GRCm39) |
missense |
|
|
R7778:Lama1
|
UTSW |
17 |
68,111,468 (GRCm39) |
missense |
|
|
R7824:Lama1
|
UTSW |
17 |
68,111,468 (GRCm39) |
missense |
|
|
R7861:Lama1
|
UTSW |
17 |
68,116,216 (GRCm39) |
missense |
|
|
R7884:Lama1
|
UTSW |
17 |
68,076,430 (GRCm39) |
missense |
|
|
R8029:Lama1
|
UTSW |
17 |
68,124,589 (GRCm39) |
missense |
|
|
R8078:Lama1
|
UTSW |
17 |
68,098,289 (GRCm39) |
missense |
|
|
R8101:Lama1
|
UTSW |
17 |
68,052,917 (GRCm39) |
missense |
|
|
R8313:Lama1
|
UTSW |
17 |
68,057,515 (GRCm39) |
missense |
|
|
R8356:Lama1
|
UTSW |
17 |
68,044,491 (GRCm39) |
missense |
|
|
R8366:Lama1
|
UTSW |
17 |
68,125,699 (GRCm39) |
missense |
|
|
R8403:Lama1
|
UTSW |
17 |
68,052,918 (GRCm39) |
missense |
|
|
R8456:Lama1
|
UTSW |
17 |
68,044,491 (GRCm39) |
missense |
|
|
R8466:Lama1
|
UTSW |
17 |
68,120,948 (GRCm39) |
missense |
|
|
R8678:Lama1
|
UTSW |
17 |
68,124,098 (GRCm39) |
missense |
|
|
R8728:Lama1
|
UTSW |
17 |
68,125,663 (GRCm39) |
missense |
|
|
R8796:Lama1
|
UTSW |
17 |
68,117,146 (GRCm39) |
missense |
|
|
R8885:Lama1
|
UTSW |
17 |
68,080,779 (GRCm39) |
missense |
|
|
R8893:Lama1
|
UTSW |
17 |
68,112,367 (GRCm39) |
missense |
|
|
R8898:Lama1
|
UTSW |
17 |
68,128,610 (GRCm39) |
missense |
|
|
R8909:Lama1
|
UTSW |
17 |
68,079,736 (GRCm39) |
missense |
|
|
R9025:Lama1
|
UTSW |
17 |
68,119,491 (GRCm39) |
missense |
|
|
R9045:Lama1
|
UTSW |
17 |
68,060,838 (GRCm39) |
missense |
|
|
R9098:Lama1
|
UTSW |
17 |
68,111,508 (GRCm39) |
missense |
|
|
R9114:Lama1
|
UTSW |
17 |
68,128,669 (GRCm39) |
missense |
|
|
R9173:Lama1
|
UTSW |
17 |
68,076,597 (GRCm39) |
missense |
|
|
R9190:Lama1
|
UTSW |
17 |
68,111,514 (GRCm39) |
missense |
|
|
R9381:Lama1
|
UTSW |
17 |
68,044,479 (GRCm39) |
missense |
|
|
R9429:Lama1
|
UTSW |
17 |
68,118,449 (GRCm39) |
missense |
|
|
R9504:Lama1
|
UTSW |
17 |
68,128,661 (GRCm39) |
missense |
|
|
R9558:Lama1
|
UTSW |
17 |
68,124,004 (GRCm39) |
missense |
|
|
R9647:Lama1
|
UTSW |
17 |
68,024,170 (GRCm39) |
missense |
|
|
R9651:Lama1
|
UTSW |
17 |
68,101,215 (GRCm39) |
missense |
|
|
R9654:Lama1
|
UTSW |
17 |
68,101,266 (GRCm39) |
missense |
|
|
R9710:Lama1
|
UTSW |
17 |
68,129,404 (GRCm39) |
missense |
|
|
R9733:Lama1
|
UTSW |
17 |
68,116,940 (GRCm39) |
missense |
|
|
RF001:Lama1
|
UTSW |
17 |
68,059,897 (GRCm39) |
missense |
|
|
RF013:Lama1
|
UTSW |
17 |
68,088,057 (GRCm39) |
missense |
|
|
V8831:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Lama1
|
UTSW |
17 |
68,045,883 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Lama1
|
UTSW |
17 |
68,101,305 (GRCm39) |
missense |
probably benign |
0.06 |
X0028:Lama1
|
UTSW |
17 |
68,074,417 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Lama1
|
UTSW |
17 |
68,118,561 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lama1
|
UTSW |
17 |
68,117,166 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Lama1
|
UTSW |
17 |
68,078,077 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Lama1
|
UTSW |
17 |
68,059,878 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Lama1
|
UTSW |
17 |
68,105,639 (GRCm39) |
missense |
|
|
|