Other mutations in this stock |
Total: 145 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921517D22Rik |
T |
C |
13: 59,839,406 (GRCm39) |
D13G |
probably benign |
Het |
4930442H23Rik |
C |
T |
10: 81,018,978 (GRCm39) |
|
probably benign |
Het |
Adamts13 |
T |
A |
2: 26,873,054 (GRCm39) |
S341T |
probably damaging |
Het |
Adamts2 |
A |
G |
11: 50,683,549 (GRCm39) |
I944V |
probably benign |
Het |
Adcy3 |
A |
G |
12: 4,256,542 (GRCm39) |
T783A |
probably benign |
Het |
Ago3 |
A |
T |
4: 126,262,296 (GRCm39) |
M418K |
probably benign |
Het |
Alpk1 |
G |
T |
3: 127,481,241 (GRCm39) |
N175K |
possibly damaging |
Het |
Anapc13 |
T |
C |
9: 102,507,020 (GRCm39) |
I11T |
probably benign |
Het |
Ankrd12 |
T |
A |
17: 66,289,994 (GRCm39) |
N1813I |
probably damaging |
Het |
Anks1b |
A |
T |
10: 90,750,612 (GRCm39) |
I176F |
probably null |
Het |
Ap3d1 |
TTCTCTCTCTCTCTCTCT |
TTCTCTCTCTCTCTCT |
10: 80,548,612 (GRCm39) |
|
probably null |
Het |
Arhgap32 |
T |
C |
9: 32,172,076 (GRCm39) |
C1619R |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,040,949 (GRCm39) |
D67G |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,081,677 (GRCm39) |
Y158* |
probably null |
Het |
Atp8b5 |
A |
T |
4: 43,356,980 (GRCm39) |
D576V |
probably damaging |
Het |
Atrnl1 |
A |
G |
19: 57,617,590 (GRCm39) |
I122V |
probably damaging |
Het |
B430203G13Rik |
A |
T |
12: 17,974,520 (GRCm39) |
|
noncoding transcript |
Het |
Baz1b |
T |
G |
5: 135,246,267 (GRCm39) |
L572R |
possibly damaging |
Het |
Ccn3 |
A |
T |
15: 54,615,603 (GRCm39) |
|
probably null |
Het |
Ccnd2 |
T |
C |
6: 127,125,761 (GRCm39) |
T92A |
possibly damaging |
Het |
Ccndbp1 |
A |
T |
2: 120,839,003 (GRCm39) |
T5S |
probably benign |
Het |
Ccr2 |
G |
A |
9: 123,906,409 (GRCm39) |
V230I |
probably benign |
Het |
Cct4 |
T |
A |
11: 22,952,866 (GRCm39) |
V514E |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,428,249 (GRCm39) |
|
probably null |
Het |
Cflar |
C |
T |
1: 58,791,726 (GRCm39) |
T343M |
probably benign |
Het |
Chrm5 |
A |
C |
2: 112,309,930 (GRCm39) |
N395K |
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,762,426 (GRCm39) |
P255S |
possibly damaging |
Het |
Chrna6 |
T |
A |
8: 27,897,134 (GRCm39) |
I248F |
probably damaging |
Het |
Clip1 |
T |
C |
5: 123,717,356 (GRCm39) |
D1387G |
probably damaging |
Het |
Clstn3 |
T |
C |
6: 124,414,331 (GRCm39) |
|
probably null |
Het |
Cntnap5a |
C |
T |
1: 116,029,295 (GRCm39) |
R250W |
probably benign |
Het |
Col12a1 |
C |
A |
9: 79,585,776 (GRCm39) |
V1228F |
possibly damaging |
Het |
Cxcr5 |
T |
C |
9: 44,424,638 (GRCm39) |
T340A |
probably benign |
Het |
Cyp2a4 |
G |
A |
7: 26,012,300 (GRCm39) |
R361K |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 30,985,436 (GRCm39) |
K3818N |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,567,047 (GRCm39) |
K2393M |
probably benign |
Het |
Dpy19l1 |
A |
T |
9: 24,336,119 (GRCm39) |
L529Q |
probably damaging |
Het |
Eif4g2 |
C |
T |
7: 110,676,003 (GRCm39) |
R399H |
probably damaging |
Het |
Elapor1 |
A |
T |
3: 108,365,543 (GRCm39) |
|
probably benign |
Het |
Fam76a |
A |
T |
4: 132,629,428 (GRCm39) |
|
probably null |
Het |
Fam76a |
A |
G |
4: 132,643,501 (GRCm39) |
Y78H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,166,839 (GRCm39) |
C2026S |
probably damaging |
Het |
Fbxo4 |
T |
C |
15: 3,998,523 (GRCm39) |
T312A |
probably benign |
Het |
Fbxw26 |
A |
G |
9: 109,553,868 (GRCm39) |
V257A |
possibly damaging |
Het |
Fhip1a |
G |
T |
3: 85,595,877 (GRCm39) |
T115K |
probably damaging |
Het |
Flnb |
A |
T |
14: 7,905,701 (GRCm38) |
E1150D |
probably benign |
Het |
Fndc3c1 |
A |
T |
X: 105,481,308 (GRCm39) |
S661R |
possibly damaging |
Het |
Gba2 |
A |
C |
4: 43,568,315 (GRCm39) |
L684R |
probably damaging |
Het |
Gbf1 |
G |
T |
19: 46,256,834 (GRCm39) |
C812F |
possibly damaging |
Het |
Glt8d2 |
A |
T |
10: 82,496,583 (GRCm39) |
D158E |
probably damaging |
Het |
Golga2 |
T |
A |
2: 32,187,168 (GRCm39) |
N89K |
probably damaging |
Het |
Got1 |
A |
G |
19: 43,491,376 (GRCm39) |
I358T |
possibly damaging |
Het |
Gpx6 |
C |
T |
13: 21,496,434 (GRCm39) |
Q3* |
probably null |
Het |
Grin1 |
T |
A |
2: 25,182,393 (GRCm39) |
H956L |
possibly damaging |
Het |
Grin2d |
A |
G |
7: 45,506,205 (GRCm39) |
V562A |
probably damaging |
Het |
Grm6 |
A |
G |
11: 50,748,104 (GRCm39) |
I405V |
probably benign |
Het |
Hcar2 |
C |
G |
5: 124,002,513 (GRCm39) |
G330A |
probably benign |
Het |
Hcfc1 |
T |
C |
X: 73,009,552 (GRCm39) |
K20E |
probably damaging |
Het |
Iars1 |
T |
A |
13: 49,878,139 (GRCm39) |
Y888N |
probably damaging |
Het |
Ifi206 |
A |
T |
1: 173,308,432 (GRCm39) |
H521Q |
probably benign |
Het |
Impg1 |
A |
G |
9: 80,305,732 (GRCm39) |
S112P |
probably benign |
Het |
Incenp |
C |
A |
19: 9,855,054 (GRCm39) |
R619M |
unknown |
Het |
Incenp |
T |
A |
19: 9,855,055 (GRCm39) |
R619W |
unknown |
Het |
Kat2b |
A |
G |
17: 53,960,231 (GRCm39) |
E513G |
possibly damaging |
Het |
Kbtbd12 |
G |
T |
6: 88,595,003 (GRCm39) |
L276I |
probably damaging |
Het |
Kctd9 |
T |
A |
14: 67,971,613 (GRCm39) |
D229E |
probably damaging |
Het |
Kdm1b |
C |
T |
13: 47,216,553 (GRCm39) |
R308W |
probably damaging |
Het |
Kif2b |
G |
A |
11: 91,467,254 (GRCm39) |
P343L |
probably benign |
Het |
Kntc1 |
T |
G |
5: 123,954,825 (GRCm39) |
M2081R |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,107,486 (GRCm39) |
N1231S |
probably damaging |
Het |
Lclat1 |
T |
A |
17: 73,547,065 (GRCm39) |
Y327* |
probably null |
Het |
Lgals3bp |
G |
A |
11: 118,284,340 (GRCm39) |
T413I |
probably damaging |
Het |
Lin54 |
A |
G |
5: 100,607,597 (GRCm39) |
I250T |
probably damaging |
Het |
Lrp1 |
T |
C |
10: 127,394,002 (GRCm39) |
N2621S |
probably benign |
Het |
Lrrtm3 |
T |
A |
10: 63,923,781 (GRCm39) |
H462L |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,042,297 (GRCm39) |
Y57C |
probably damaging |
Het |
Mccc1 |
C |
A |
3: 36,030,022 (GRCm39) |
M429I |
probably damaging |
Het |
Metrnl |
A |
G |
11: 121,598,750 (GRCm39) |
E40G |
probably benign |
Het |
Mios |
T |
A |
6: 8,222,464 (GRCm39) |
M466K |
probably benign |
Het |
Mrgpra1 |
A |
G |
7: 46,985,218 (GRCm39) |
S154P |
probably damaging |
Het |
Mrpl24 |
T |
C |
3: 87,829,357 (GRCm39) |
|
probably null |
Het |
Myo1f |
A |
G |
17: 33,817,165 (GRCm39) |
N736S |
possibly damaging |
Het |
Myo1h |
A |
G |
5: 114,498,660 (GRCm39) |
I919V |
possibly damaging |
Het |
Nampt |
T |
C |
12: 32,898,713 (GRCm39) |
L443P |
possibly damaging |
Het |
Ndufaf2 |
C |
G |
13: 108,189,314 (GRCm39) |
A145P |
probably damaging |
Het |
Nek10 |
A |
T |
14: 14,855,714 (GRCm38) |
T403S |
probably benign |
Het |
Nme8 |
C |
A |
13: 19,842,100 (GRCm39) |
V219L |
probably damaging |
Het |
Nps |
T |
A |
7: 134,870,517 (GRCm39) |
L13Q |
probably damaging |
Het |
Nutm1 |
G |
A |
2: 112,079,281 (GRCm39) |
A878V |
probably benign |
Het |
Ogdh |
T |
C |
11: 6,299,875 (GRCm39) |
F794L |
probably damaging |
Het |
Or14a259 |
C |
A |
7: 86,012,943 (GRCm39) |
G201C |
probably damaging |
Het |
Or14c39 |
T |
C |
7: 86,343,736 (GRCm39) |
L24P |
probably damaging |
Het |
Or2t35 |
A |
C |
14: 14,407,729 (GRCm38) |
Y167S |
possibly damaging |
Het |
Or4f56 |
A |
T |
2: 111,703,395 (GRCm39) |
D268E |
possibly damaging |
Het |
Or5a3 |
A |
T |
19: 12,400,341 (GRCm39) |
I223F |
probably damaging |
Het |
Or5g29 |
A |
G |
2: 85,421,282 (GRCm39) |
T133A |
probably benign |
Het |
Pik3cg |
T |
C |
12: 32,255,198 (GRCm39) |
E263G |
probably damaging |
Het |
Pikfyve |
A |
G |
1: 65,307,005 (GRCm39) |
T1798A |
probably benign |
Het |
Poldip3 |
T |
C |
15: 83,015,702 (GRCm39) |
Y305C |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,466,840 (GRCm39) |
I107T |
probably benign |
Het |
Prmt2 |
A |
G |
10: 76,062,055 (GRCm39) |
I50T |
probably damaging |
Het |
Ptprd |
T |
C |
4: 76,058,790 (GRCm39) |
T168A |
probably benign |
Het |
Pudp |
A |
G |
18: 50,701,136 (GRCm39) |
V199A |
probably damaging |
Het |
Rab3c |
T |
C |
13: 110,198,434 (GRCm39) |
E198G |
probably benign |
Het |
Rasl12 |
A |
G |
9: 65,320,730 (GRCm39) |
Y156C |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,484 (GRCm39) |
D596G |
possibly damaging |
Het |
Rbm6 |
T |
C |
9: 107,664,551 (GRCm39) |
E694G |
probably benign |
Het |
Rif1 |
T |
C |
2: 52,002,759 (GRCm39) |
V2071A |
probably damaging |
Het |
Ripply2 |
A |
T |
9: 86,901,849 (GRCm39) |
N125I |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,482,385 (GRCm39) |
H284Q |
probably benign |
Het |
Scara3 |
A |
T |
14: 66,190,950 (GRCm39) |
M1K |
probably null |
Het |
Sfswap |
A |
G |
5: 129,590,147 (GRCm39) |
T215A |
probably damaging |
Het |
Shroom2 |
A |
C |
X: 151,443,903 (GRCm39) |
F421V |
probably benign |
Het |
Sipa1l3 |
A |
G |
7: 29,077,066 (GRCm39) |
V902A |
probably damaging |
Het |
Slamf8 |
G |
T |
1: 172,411,781 (GRCm39) |
P238Q |
probably damaging |
Het |
Slc44a3 |
T |
C |
3: 121,320,723 (GRCm39) |
T93A |
possibly damaging |
Het |
Slc5a7 |
A |
T |
17: 54,585,728 (GRCm39) |
I363N |
probably damaging |
Het |
Slc66a1 |
G |
T |
4: 139,027,312 (GRCm39) |
H343Q |
probably benign |
Het |
Slc7a2 |
T |
A |
8: 41,364,095 (GRCm39) |
M436K |
probably benign |
Het |
Spindoc |
A |
G |
19: 7,351,456 (GRCm39) |
S223P |
probably benign |
Het |
Stk11ip |
T |
C |
1: 75,506,925 (GRCm39) |
F669L |
possibly damaging |
Het |
Sun3 |
G |
A |
11: 8,988,266 (GRCm39) |
L19F |
probably benign |
Het |
Sycp1 |
C |
A |
3: 102,760,805 (GRCm39) |
A703S |
possibly damaging |
Het |
Tas2r139 |
T |
G |
6: 42,118,218 (GRCm39) |
F117V |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,936,467 (GRCm39) |
Y1527C |
probably damaging |
Het |
Tenm4 |
A |
C |
7: 96,423,253 (GRCm39) |
K683Q |
probably damaging |
Het |
Tfeb |
T |
A |
17: 48,099,152 (GRCm39) |
|
probably null |
Het |
Tmco4 |
T |
C |
4: 138,725,350 (GRCm39) |
S121P |
probably damaging |
Het |
Tmprss11d |
C |
T |
5: 86,454,140 (GRCm39) |
V222M |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,893,378 (GRCm39) |
W440R |
probably damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,276,562 (GRCm39) |
T848A |
probably benign |
Het |
Tssk1 |
G |
A |
16: 17,712,926 (GRCm39) |
R237H |
probably benign |
Het |
Ttll4 |
A |
T |
1: 74,718,166 (GRCm39) |
T6S |
possibly damaging |
Het |
Ttn |
G |
T |
2: 76,552,141 (GRCm39) |
Y29419* |
probably null |
Het |
Ttn |
A |
G |
2: 76,599,947 (GRCm39) |
Y19076H |
probably damaging |
Het |
Ubr3 |
T |
A |
2: 69,789,947 (GRCm39) |
V867D |
probably damaging |
Het |
Usp29 |
A |
G |
7: 6,964,390 (GRCm39) |
T78A |
probably damaging |
Het |
Utrn |
T |
G |
10: 12,530,489 (GRCm39) |
Q2108P |
probably benign |
Het |
Vcan |
T |
C |
13: 89,853,908 (GRCm39) |
N351D |
probably damaging |
Het |
Vmn1r61 |
A |
T |
7: 5,614,124 (GRCm39) |
Y63* |
probably null |
Het |
Vmn1r61 |
A |
T |
7: 5,614,126 (GRCm39) |
Y63N |
probably benign |
Het |
Vmn1r85 |
A |
T |
7: 12,818,788 (GRCm39) |
W119R |
probably damaging |
Het |
Zbtb21 |
A |
C |
16: 97,751,655 (GRCm39) |
V190G |
possibly damaging |
Het |
Zfp157 |
C |
A |
5: 138,443,051 (GRCm39) |
T14N |
probably damaging |
Het |
Zfp942 |
A |
T |
17: 22,148,400 (GRCm39) |
H76Q |
probably damaging |
Het |
|
Other mutations in Als2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00772:Als2
|
APN |
1 |
59,209,055 (GRCm39) |
nonsense |
probably null |
|
IGL00924:Als2
|
APN |
1 |
59,255,021 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00949:Als2
|
APN |
1 |
59,254,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Als2
|
APN |
1 |
59,254,541 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01090:Als2
|
APN |
1 |
59,254,775 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01116:Als2
|
APN |
1 |
59,225,163 (GRCm39) |
splice site |
probably benign |
|
IGL02001:Als2
|
APN |
1 |
59,219,347 (GRCm39) |
splice site |
probably benign |
|
IGL02075:Als2
|
APN |
1 |
59,246,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02441:Als2
|
APN |
1 |
59,254,631 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02728:Als2
|
APN |
1 |
59,235,506 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02740:Als2
|
APN |
1 |
59,209,078 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02885:Als2
|
APN |
1 |
59,206,650 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02896:Als2
|
APN |
1 |
59,222,946 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02978:Als2
|
APN |
1 |
59,254,324 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03032:Als2
|
APN |
1 |
59,255,189 (GRCm39) |
splice site |
probably benign |
|
IGL03065:Als2
|
APN |
1 |
59,255,031 (GRCm39) |
missense |
probably benign |
|
IGL03212:Als2
|
APN |
1 |
59,242,085 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03226:Als2
|
APN |
1 |
59,225,679 (GRCm39) |
missense |
probably benign |
0.43 |
R0014:Als2
|
UTSW |
1 |
59,250,547 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0243:Als2
|
UTSW |
1 |
59,254,546 (GRCm39) |
missense |
probably benign |
|
R0326:Als2
|
UTSW |
1 |
59,219,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R0376:Als2
|
UTSW |
1 |
59,254,724 (GRCm39) |
missense |
probably benign |
0.00 |
R0605:Als2
|
UTSW |
1 |
59,207,573 (GRCm39) |
missense |
probably benign |
0.02 |
R1607:Als2
|
UTSW |
1 |
59,219,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R1631:Als2
|
UTSW |
1 |
59,257,226 (GRCm39) |
missense |
probably benign |
0.00 |
R1657:Als2
|
UTSW |
1 |
59,219,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Als2
|
UTSW |
1 |
59,214,150 (GRCm39) |
missense |
probably benign |
|
R1950:Als2
|
UTSW |
1 |
59,224,760 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1970:Als2
|
UTSW |
1 |
59,254,328 (GRCm39) |
missense |
probably benign |
0.34 |
R2151:Als2
|
UTSW |
1 |
59,246,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2292:Als2
|
UTSW |
1 |
59,226,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Als2
|
UTSW |
1 |
59,254,276 (GRCm39) |
missense |
probably benign |
0.00 |
R2849:Als2
|
UTSW |
1 |
59,245,697 (GRCm39) |
missense |
probably damaging |
0.97 |
R2869:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R2873:Als2
|
UTSW |
1 |
59,250,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R3054:Als2
|
UTSW |
1 |
59,254,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Als2
|
UTSW |
1 |
59,226,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Als2
|
UTSW |
1 |
59,209,167 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3276:Als2
|
UTSW |
1 |
59,209,167 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3801:Als2
|
UTSW |
1 |
59,206,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Als2
|
UTSW |
1 |
59,206,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Als2
|
UTSW |
1 |
59,209,609 (GRCm39) |
missense |
probably benign |
0.08 |
R3884:Als2
|
UTSW |
1 |
59,224,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R4012:Als2
|
UTSW |
1 |
59,226,575 (GRCm39) |
missense |
probably benign |
0.09 |
R4033:Als2
|
UTSW |
1 |
59,235,400 (GRCm39) |
missense |
probably benign |
|
R4201:Als2
|
UTSW |
1 |
59,219,313 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4321:Als2
|
UTSW |
1 |
59,206,613 (GRCm39) |
splice site |
probably benign |
|
R4707:Als2
|
UTSW |
1 |
59,254,472 (GRCm39) |
missense |
probably benign |
|
R4784:Als2
|
UTSW |
1 |
59,254,472 (GRCm39) |
missense |
probably benign |
|
R4991:Als2
|
UTSW |
1 |
59,246,927 (GRCm39) |
missense |
probably benign |
0.10 |
R5068:Als2
|
UTSW |
1 |
59,250,433 (GRCm39) |
missense |
probably benign |
0.13 |
R5110:Als2
|
UTSW |
1 |
59,224,600 (GRCm39) |
missense |
probably damaging |
0.98 |
R5141:Als2
|
UTSW |
1 |
59,209,611 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5394:Als2
|
UTSW |
1 |
59,214,105 (GRCm39) |
missense |
probably benign |
0.06 |
R5621:Als2
|
UTSW |
1 |
59,231,049 (GRCm39) |
missense |
probably benign |
0.33 |
R5685:Als2
|
UTSW |
1 |
59,218,250 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5987:Als2
|
UTSW |
1 |
59,245,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6012:Als2
|
UTSW |
1 |
59,224,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Als2
|
UTSW |
1 |
59,242,228 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6222:Als2
|
UTSW |
1 |
59,219,284 (GRCm39) |
missense |
probably benign |
0.04 |
R6367:Als2
|
UTSW |
1 |
59,238,299 (GRCm39) |
missense |
probably benign |
0.04 |
R6394:Als2
|
UTSW |
1 |
59,206,356 (GRCm39) |
missense |
probably damaging |
0.99 |
R6866:Als2
|
UTSW |
1 |
59,250,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6965:Als2
|
UTSW |
1 |
59,209,716 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7038:Als2
|
UTSW |
1 |
59,206,673 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7178:Als2
|
UTSW |
1 |
59,246,971 (GRCm39) |
missense |
probably damaging |
0.96 |
R7494:Als2
|
UTSW |
1 |
59,222,325 (GRCm39) |
splice site |
probably null |
|
R7541:Als2
|
UTSW |
1 |
59,206,775 (GRCm39) |
splice site |
probably null |
|
R7601:Als2
|
UTSW |
1 |
59,209,161 (GRCm39) |
missense |
probably benign |
0.17 |
R8380:Als2
|
UTSW |
1 |
59,250,467 (GRCm39) |
missense |
probably benign |
|
R8478:Als2
|
UTSW |
1 |
59,225,175 (GRCm39) |
missense |
probably damaging |
0.96 |
R8492:Als2
|
UTSW |
1 |
59,250,503 (GRCm39) |
missense |
probably damaging |
0.98 |
R9048:Als2
|
UTSW |
1 |
59,225,670 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9090:Als2
|
UTSW |
1 |
59,242,189 (GRCm39) |
missense |
probably benign |
0.01 |
R9128:Als2
|
UTSW |
1 |
59,219,709 (GRCm39) |
missense |
probably benign |
0.00 |
R9206:Als2
|
UTSW |
1 |
59,224,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Als2
|
UTSW |
1 |
59,242,189 (GRCm39) |
missense |
probably benign |
0.01 |
R9430:Als2
|
UTSW |
1 |
59,231,198 (GRCm39) |
missense |
probably benign |
0.00 |
R9455:Als2
|
UTSW |
1 |
59,219,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R9482:Als2
|
UTSW |
1 |
59,231,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Als2
|
UTSW |
1 |
59,206,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R9544:Als2
|
UTSW |
1 |
59,250,468 (GRCm39) |
missense |
probably benign |
0.00 |
R9796:Als2
|
UTSW |
1 |
59,209,601 (GRCm39) |
missense |
probably benign |
0.04 |
|