Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406C07Rik |
A |
T |
9: 15,202,066 (GRCm39) |
V152E |
probably damaging |
Het |
Abca5 |
T |
G |
11: 110,167,331 (GRCm39) |
E1495A |
probably damaging |
Het |
Abcc12 |
G |
A |
8: 87,261,627 (GRCm39) |
S668F |
probably benign |
Het |
Adgrl4 |
A |
T |
3: 151,223,247 (GRCm39) |
T608S |
probably benign |
Het |
Angel2 |
G |
A |
1: 190,673,187 (GRCm39) |
D255N |
probably benign |
Het |
Apob |
T |
A |
12: 8,039,113 (GRCm39) |
|
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,715,603 (GRCm39) |
R1349S |
probably damaging |
Het |
Atp2b2 |
C |
T |
6: 113,770,656 (GRCm39) |
V418I |
probably damaging |
Het |
Birc6 |
C |
A |
17: 74,930,741 (GRCm39) |
|
probably benign |
Het |
Capn13 |
T |
A |
17: 73,658,519 (GRCm39) |
Y183F |
probably damaging |
Het |
Cngb1 |
A |
G |
8: 95,987,266 (GRCm39) |
S352P |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,741,273 (GRCm39) |
S720P |
probably damaging |
Het |
Cpa4 |
C |
T |
6: 30,579,657 (GRCm39) |
R155W |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,908,914 (GRCm39) |
I1176V |
probably benign |
Het |
Dnah17 |
T |
C |
11: 117,949,132 (GRCm39) |
E2959G |
probably benign |
Het |
Dnah7b |
T |
A |
1: 46,252,520 (GRCm39) |
I1734N |
possibly damaging |
Het |
Dnajb7 |
A |
G |
15: 81,291,555 (GRCm39) |
Y261H |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,579,392 (GRCm39) |
|
probably benign |
Het |
Dyrk3 |
A |
T |
1: 131,057,576 (GRCm39) |
V199E |
probably damaging |
Het |
F2r |
G |
T |
13: 95,740,994 (GRCm39) |
C180* |
probably null |
Het |
F5 |
A |
G |
1: 164,012,483 (GRCm39) |
S466G |
probably benign |
Het |
Fbn2 |
A |
T |
18: 58,235,445 (GRCm39) |
C677* |
probably null |
Het |
Fbxo41 |
A |
G |
6: 85,454,890 (GRCm39) |
S673P |
probably damaging |
Het |
Fhad1 |
G |
T |
4: 141,667,406 (GRCm39) |
H639N |
probably benign |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Foxa2 |
A |
G |
2: 147,885,481 (GRCm39) |
S270P |
probably damaging |
Het |
Fxyd7 |
C |
T |
7: 30,746,793 (GRCm39) |
|
probably null |
Het |
Gm5225 |
A |
G |
17: 24,243,032 (GRCm39) |
D67G |
probably benign |
Het |
Grik3 |
G |
A |
4: 125,564,349 (GRCm39) |
E444K |
probably benign |
Het |
Gsdma2 |
A |
G |
11: 98,540,009 (GRCm39) |
K44E |
probably damaging |
Het |
Haus1 |
T |
A |
18: 77,849,770 (GRCm39) |
K130* |
probably null |
Het |
Heg1 |
A |
G |
16: 33,556,028 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
A |
G |
11: 4,362,206 (GRCm39) |
|
probably benign |
Het |
Hsd17b3 |
G |
A |
13: 64,206,403 (GRCm39) |
R300C |
possibly damaging |
Het |
Irf5 |
T |
C |
6: 29,536,108 (GRCm39) |
F374S |
probably damaging |
Het |
Itch |
A |
G |
2: 155,059,903 (GRCm39) |
|
probably benign |
Het |
Jade2 |
A |
T |
11: 51,722,136 (GRCm39) |
L139Q |
probably damaging |
Het |
Kif5c |
G |
A |
2: 49,642,251 (GRCm39) |
|
probably benign |
Het |
Larp4b |
A |
G |
13: 9,220,724 (GRCm39) |
R658G |
probably damaging |
Het |
Mcph1 |
C |
T |
8: 18,838,264 (GRCm39) |
L729F |
probably benign |
Het |
Me1 |
A |
T |
9: 86,536,720 (GRCm39) |
N118K |
probably benign |
Het |
Med13 |
A |
G |
11: 86,210,723 (GRCm39) |
L473S |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,635,921 (GRCm39) |
Y359N |
probably damaging |
Het |
Morc2b |
A |
G |
17: 33,356,015 (GRCm39) |
S586P |
probably damaging |
Het |
Mthfr |
A |
G |
4: 148,135,980 (GRCm39) |
D310G |
probably benign |
Het |
Mtmr7 |
A |
T |
8: 41,034,447 (GRCm39) |
|
probably benign |
Het |
Mtus1 |
A |
G |
8: 41,451,514 (GRCm39) |
|
probably benign |
Het |
Mus81 |
G |
T |
19: 5,536,552 (GRCm39) |
A138D |
probably damaging |
Het |
Myom2 |
A |
T |
8: 15,167,633 (GRCm39) |
I1073F |
probably damaging |
Het |
Nhsl1 |
A |
T |
10: 18,400,990 (GRCm39) |
K739* |
probably null |
Het |
Nlrp4d |
T |
A |
7: 10,108,818 (GRCm39) |
K762N |
probably benign |
Het |
Nrap |
T |
C |
19: 56,343,978 (GRCm39) |
Y724C |
probably damaging |
Het |
Ogn |
A |
T |
13: 49,774,514 (GRCm39) |
Y219F |
possibly damaging |
Het |
Or6c212 |
T |
A |
10: 129,558,846 (GRCm39) |
D189V |
probably damaging |
Het |
Or8b56 |
T |
C |
9: 38,739,860 (GRCm39) |
L291P |
probably damaging |
Het |
Or8g30 |
A |
T |
9: 39,230,160 (GRCm39) |
I250N |
probably damaging |
Het |
Padi2 |
T |
C |
4: 140,653,550 (GRCm39) |
V180A |
probably benign |
Het |
Papss2 |
C |
T |
19: 32,615,768 (GRCm39) |
R167* |
probably null |
Het |
Pcbp2 |
T |
C |
15: 102,382,670 (GRCm39) |
|
probably benign |
Het |
Per1 |
T |
A |
11: 68,992,706 (GRCm39) |
|
probably benign |
Het |
Pik3ca |
T |
C |
3: 32,514,094 (GRCm39) |
I860T |
probably damaging |
Het |
Pkdrej |
G |
A |
15: 85,701,746 (GRCm39) |
Q1397* |
probably null |
Het |
Plce1 |
T |
C |
19: 38,710,265 (GRCm39) |
V1133A |
probably benign |
Het |
Pnma8a |
T |
G |
7: 16,694,625 (GRCm39) |
V160G |
probably damaging |
Het |
Prss12 |
T |
C |
3: 123,276,423 (GRCm39) |
C351R |
probably damaging |
Het |
Qprt |
A |
T |
7: 126,708,269 (GRCm39) |
L54Q |
probably damaging |
Het |
Raf1 |
C |
T |
6: 115,603,344 (GRCm39) |
S165N |
probably damaging |
Het |
Rere |
A |
G |
4: 150,701,433 (GRCm39) |
N1271S |
probably benign |
Het |
Rnasel |
T |
A |
1: 153,630,258 (GRCm39) |
L258H |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,724,807 (GRCm39) |
D2502G |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,633,510 (GRCm39) |
S2081L |
probably damaging |
Het |
Sc5d |
G |
T |
9: 42,171,155 (GRCm39) |
Y11* |
probably null |
Het |
Slc25a29 |
A |
C |
12: 108,793,017 (GRCm39) |
L187R |
possibly damaging |
Het |
Slc2a7 |
G |
A |
4: 150,252,721 (GRCm39) |
V454M |
probably benign |
Het |
Slco1b2 |
A |
T |
6: 141,615,114 (GRCm39) |
T340S |
probably benign |
Het |
Smarcc1 |
A |
G |
9: 109,976,172 (GRCm39) |
N153S |
possibly damaging |
Het |
Snx1 |
C |
A |
9: 65,995,821 (GRCm39) |
E516* |
probably null |
Het |
Sptlc2 |
T |
C |
12: 87,403,454 (GRCm39) |
D115G |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,464,736 (GRCm39) |
N67S |
probably damaging |
Het |
Styxl2 |
A |
C |
1: 165,927,270 (GRCm39) |
S781A |
probably benign |
Het |
Swap70 |
G |
A |
7: 109,872,489 (GRCm39) |
R368H |
probably benign |
Het |
Tcaf3 |
T |
C |
6: 42,568,284 (GRCm39) |
K691E |
probably benign |
Het |
Tmco4 |
T |
C |
4: 138,781,231 (GRCm39) |
F465S |
probably damaging |
Het |
Tmem245 |
A |
G |
4: 56,926,213 (GRCm39) |
S290P |
probably benign |
Het |
Top2a |
T |
C |
11: 98,894,416 (GRCm39) |
T972A |
probably benign |
Het |
Tpr |
T |
A |
1: 150,285,898 (GRCm39) |
S527R |
probably damaging |
Het |
Traf2 |
T |
C |
2: 25,409,621 (GRCm39) |
D443G |
probably damaging |
Het |
Trim40 |
A |
T |
17: 37,194,039 (GRCm39) |
|
probably null |
Het |
Trim42 |
A |
T |
9: 97,245,456 (GRCm39) |
I448N |
possibly damaging |
Het |
Ttll9 |
G |
A |
2: 152,825,054 (GRCm39) |
V78M |
probably damaging |
Het |
Vav1 |
C |
T |
17: 57,603,039 (GRCm39) |
L88F |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,423,301 (GRCm39) |
D207G |
probably damaging |
Het |
Wdsub1 |
A |
G |
2: 59,707,009 (GRCm39) |
|
probably null |
Het |
Zfp799 |
A |
G |
17: 33,040,009 (GRCm39) |
W85R |
possibly damaging |
Het |
Zfp839 |
A |
T |
12: 110,825,203 (GRCm39) |
|
probably benign |
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 |
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 |
|
|
R6994:Lama1
|
UTSW |
17 |
68,060,820 (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 |
|
|
|