Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533L02Rik |
T |
C |
7: 124,917,767 (GRCm39) |
M53T |
unknown |
Het |
Abcb11 |
T |
A |
2: 69,089,820 (GRCm39) |
|
probably benign |
Het |
Acap2 |
C |
G |
16: 30,929,763 (GRCm39) |
A432P |
probably damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,146,249 (GRCm39) |
R302G |
probably damaging |
Het |
Aoc1l1 |
A |
G |
6: 48,954,536 (GRCm39) |
E558G |
probably damaging |
Het |
Ap2b1 |
T |
G |
11: 83,241,944 (GRCm39) |
S608A |
possibly damaging |
Het |
Atp13a3 |
T |
A |
16: 30,171,116 (GRCm39) |
T310S |
possibly damaging |
Het |
Atp6v1b1 |
T |
C |
6: 83,734,834 (GRCm39) |
V382A |
probably benign |
Het |
Atp6v1g1 |
T |
A |
4: 63,468,304 (GRCm39) |
F102L |
probably benign |
Het |
B430306N03Rik |
T |
A |
17: 48,623,810 (GRCm39) |
V37D |
probably damaging |
Het |
Cacna1d |
T |
C |
14: 29,769,314 (GRCm39) |
Y1872C |
possibly damaging |
Het |
Carf |
T |
A |
1: 60,148,570 (GRCm39) |
Y54N |
probably damaging |
Het |
Cct5 |
T |
C |
15: 31,594,349 (GRCm39) |
E256G |
probably damaging |
Het |
Cd5 |
A |
G |
19: 10,700,620 (GRCm39) |
S295P |
probably benign |
Het |
Cenpb |
T |
C |
2: 131,020,517 (GRCm39) |
|
probably benign |
Het |
Cntnap3 |
A |
G |
13: 64,942,076 (GRCm39) |
M218T |
possibly damaging |
Het |
Colec11 |
C |
T |
12: 28,644,786 (GRCm39) |
R236H |
probably damaging |
Het |
Crem |
T |
A |
18: 3,288,098 (GRCm39) |
|
probably benign |
Het |
Csnk2a1 |
A |
G |
2: 152,096,201 (GRCm39) |
N58S |
probably benign |
Het |
Cyp2a4 |
T |
G |
7: 26,011,733 (GRCm39) |
M318R |
probably damaging |
Het |
Dhrs1 |
T |
A |
14: 55,981,116 (GRCm39) |
Q98L |
probably null |
Het |
Dnah11 |
G |
T |
12: 118,077,606 (GRCm39) |
Q1296K |
possibly damaging |
Het |
Edc4 |
T |
A |
8: 106,614,634 (GRCm39) |
D105E |
probably damaging |
Het |
Eid2b |
C |
T |
7: 27,977,198 (GRCm39) |
|
probably benign |
Het |
Exoc1 |
A |
T |
5: 76,680,693 (GRCm39) |
K28* |
probably null |
Het |
Fam114a1 |
A |
G |
5: 65,137,402 (GRCm39) |
D115G |
probably benign |
Het |
Fam151a |
A |
T |
4: 106,592,760 (GRCm39) |
|
probably null |
Het |
Gc |
T |
C |
5: 89,586,201 (GRCm39) |
Y313C |
probably damaging |
Het |
Gdpd1 |
A |
G |
11: 86,926,094 (GRCm39) |
Y284H |
probably benign |
Het |
Gm21957 |
T |
A |
7: 124,818,878 (GRCm39) |
|
noncoding transcript |
Het |
Golm1 |
G |
A |
13: 59,792,999 (GRCm39) |
Q169* |
probably null |
Het |
Greb1l |
T |
C |
18: 10,523,281 (GRCm39) |
V813A |
probably damaging |
Het |
Itih1 |
C |
T |
14: 30,659,800 (GRCm39) |
A279T |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lama3 |
T |
A |
18: 12,657,887 (GRCm39) |
N334K |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,472,642 (GRCm39) |
D1053G |
probably damaging |
Het |
Map3k20 |
A |
G |
2: 72,228,729 (GRCm39) |
K316R |
probably benign |
Het |
Mapre3 |
A |
C |
5: 31,020,546 (GRCm39) |
|
probably null |
Het |
Mgam |
T |
A |
6: 40,737,962 (GRCm39) |
|
probably null |
Het |
Mical2 |
A |
C |
7: 111,917,810 (GRCm39) |
H389P |
probably benign |
Het |
Mtmr2 |
A |
G |
9: 13,711,248 (GRCm39) |
D347G |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,463,139 (GRCm39) |
L1309F |
probably benign |
Het |
Nid2 |
G |
A |
14: 19,828,111 (GRCm39) |
G516S |
probably benign |
Het |
Nodal |
A |
T |
10: 61,259,077 (GRCm39) |
E171D |
possibly damaging |
Het |
Notch2 |
T |
C |
3: 98,009,683 (GRCm39) |
S537P |
probably damaging |
Het |
Obox6 |
A |
G |
7: 15,567,532 (GRCm39) |
L305S |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,969,082 (GRCm39) |
D2715G |
probably damaging |
Het |
Or4k1 |
T |
A |
14: 50,377,580 (GRCm39) |
N172I |
probably damaging |
Het |
Or5g26 |
A |
C |
2: 85,494,090 (GRCm39) |
S229R |
probably benign |
Het |
Pcca |
T |
C |
14: 122,923,527 (GRCm39) |
S404P |
probably damaging |
Het |
Pcdh10 |
T |
C |
3: 45,334,906 (GRCm39) |
S407P |
probably damaging |
Het |
Plekha5 |
C |
A |
6: 140,516,044 (GRCm39) |
|
probably null |
Het |
Ptdss1 |
A |
G |
13: 67,101,619 (GRCm39) |
N72S |
probably benign |
Het |
Ptprs |
T |
C |
17: 56,761,984 (GRCm39) |
I43V |
probably null |
Het |
Pygm |
G |
A |
19: 6,441,511 (GRCm39) |
|
probably null |
Het |
Rab7 |
C |
T |
6: 87,989,300 (GRCm39) |
V57I |
probably benign |
Het |
Rasl10a |
A |
G |
11: 5,009,431 (GRCm39) |
|
probably null |
Het |
Rergl |
T |
C |
6: 139,471,832 (GRCm39) |
T106A |
probably benign |
Het |
Rnf17 |
T |
G |
14: 56,720,837 (GRCm39) |
V1023G |
probably damaging |
Het |
Rnf25 |
T |
A |
1: 74,633,126 (GRCm39) |
R409W |
probably damaging |
Het |
Rps6ka1 |
T |
C |
4: 133,600,280 (GRCm39) |
M1V |
probably null |
Het |
Rps6ka5 |
T |
C |
12: 100,585,874 (GRCm39) |
T140A |
possibly damaging |
Het |
Sbno2 |
T |
A |
10: 79,893,690 (GRCm39) |
I1204F |
possibly damaging |
Het |
Serpina16 |
A |
T |
12: 103,641,521 (GRCm39) |
I68N |
probably damaging |
Het |
Slc35a5 |
A |
G |
16: 44,964,628 (GRCm39) |
S202P |
probably damaging |
Het |
Slc35g3 |
G |
C |
11: 69,651,772 (GRCm39) |
S93W |
probably damaging |
Het |
Slc49a3 |
C |
T |
5: 108,593,487 (GRCm39) |
R117H |
probably damaging |
Het |
Smc1b |
A |
G |
15: 85,006,052 (GRCm39) |
|
probably benign |
Het |
Spag1 |
T |
C |
15: 36,227,287 (GRCm39) |
L648P |
probably damaging |
Het |
Tagap1 |
T |
C |
17: 7,224,102 (GRCm39) |
D198G |
probably benign |
Het |
Tedc2 |
T |
C |
17: 24,436,874 (GRCm39) |
E287G |
probably damaging |
Het |
Tjp1 |
C |
A |
7: 64,962,669 (GRCm39) |
R1089S |
probably damaging |
Het |
Tnrc6a |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
CTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTT |
7: 122,761,669 (GRCm39) |
|
probably benign |
Het |
Ttc38 |
T |
A |
15: 85,722,928 (GRCm39) |
D125E |
probably benign |
Het |
Uggt1 |
C |
T |
1: 36,231,495 (GRCm39) |
R490Q |
probably null |
Het |
Uroc1 |
T |
G |
6: 90,321,096 (GRCm39) |
L224R |
probably damaging |
Het |
Vmn1r228 |
A |
T |
17: 20,997,455 (GRCm39) |
I21N |
possibly damaging |
Het |
Vmn2r102 |
T |
G |
17: 19,896,949 (GRCm39) |
L99V |
probably damaging |
Het |
Vps13c |
C |
T |
9: 67,857,571 (GRCm39) |
S2601F |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,010,830 (GRCm39) |
L932P |
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 |
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 |
|
|
|