Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
T |
C |
8: 84,729,637 (GRCm39) |
|
probably benign |
Het |
A530064D06Rik |
G |
A |
17: 48,473,824 (GRCm39) |
T31I |
probably benign |
Het |
Abca17 |
A |
G |
17: 24,500,223 (GRCm39) |
F1323L |
probably benign |
Het |
Abcf3 |
T |
A |
16: 20,369,237 (GRCm39) |
N206K |
probably damaging |
Het |
Adam10 |
A |
G |
9: 70,673,223 (GRCm39) |
|
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,172,390 (GRCm39) |
Q451L |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,708,752 (GRCm39) |
I413N |
probably benign |
Het |
Asb18 |
G |
T |
1: 89,920,893 (GRCm39) |
A128E |
probably damaging |
Het |
Atf7ip2 |
T |
C |
16: 10,059,743 (GRCm39) |
S428P |
possibly damaging |
Het |
Atp8b5 |
G |
T |
4: 43,291,672 (GRCm39) |
C15F |
possibly damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,146 (GRCm39) |
E2235G |
probably damaging |
Het |
Blnk |
G |
T |
19: 40,926,111 (GRCm39) |
S330* |
probably null |
Het |
Bpnt1 |
T |
G |
1: 185,088,808 (GRCm39) |
N319K |
probably benign |
Het |
Brip1 |
G |
A |
11: 86,043,493 (GRCm39) |
T357I |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,725,104 (GRCm39) |
D288E |
probably benign |
Het |
Calcoco2 |
A |
G |
11: 95,998,354 (GRCm39) |
V23A |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,780,766 (GRCm39) |
E1217K |
probably damaging |
Het |
Ccdc154 |
G |
T |
17: 25,386,259 (GRCm39) |
|
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,120,935 (GRCm39) |
|
probably benign |
Het |
Clec4a3 |
A |
G |
6: 122,930,993 (GRCm39) |
|
probably null |
Het |
Cpne2 |
T |
A |
8: 95,274,970 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,573,710 (GRCm39) |
|
probably null |
Het |
Cyp26c1 |
A |
G |
19: 37,675,009 (GRCm39) |
H110R |
probably damaging |
Het |
Cyp2j13 |
A |
G |
4: 95,959,932 (GRCm39) |
Y75H |
probably damaging |
Het |
Defb43 |
T |
A |
14: 63,249,287 (GRCm39) |
V10D |
probably damaging |
Het |
Dhx36 |
G |
A |
3: 62,401,162 (GRCm39) |
S368L |
possibly damaging |
Het |
Dock6 |
G |
A |
9: 21,715,923 (GRCm39) |
|
probably benign |
Het |
Elp2 |
T |
C |
18: 24,745,499 (GRCm39) |
|
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,750,249 (GRCm39) |
L453P |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,755,065 (GRCm39) |
D903E |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,500,335 (GRCm39) |
|
probably benign |
Het |
Ep400 |
G |
A |
5: 110,836,062 (GRCm39) |
T1899M |
unknown |
Het |
Fancg |
A |
G |
4: 43,002,998 (GRCm39) |
S620P |
probably benign |
Het |
Fbxo42 |
G |
A |
4: 140,922,550 (GRCm39) |
V239M |
probably damaging |
Het |
Fermt2 |
T |
C |
14: 45,706,776 (GRCm39) |
D340G |
probably benign |
Het |
Filip1 |
A |
T |
9: 79,726,672 (GRCm39) |
V649E |
probably damaging |
Het |
Fut8 |
G |
A |
12: 77,521,791 (GRCm39) |
E477K |
probably damaging |
Het |
Gbp3 |
G |
A |
3: 142,271,151 (GRCm39) |
G185D |
probably benign |
Het |
Gclc |
G |
T |
9: 77,694,080 (GRCm39) |
D345Y |
probably damaging |
Het |
Gfus |
A |
G |
15: 75,800,807 (GRCm39) |
V27A |
possibly damaging |
Het |
Gkn2 |
A |
G |
6: 87,352,800 (GRCm39) |
D43G |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,279,166 (GRCm39) |
|
probably benign |
Het |
Greb1l |
C |
T |
18: 10,474,303 (GRCm39) |
T206I |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,905,611 (GRCm39) |
N452S |
probably benign |
Het |
Hcn2 |
G |
C |
10: 79,570,066 (GRCm39) |
|
probably null |
Het |
Hpn |
T |
C |
7: 30,808,585 (GRCm39) |
K76E |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,280,591 (GRCm39) |
D3268G |
probably damaging |
Het |
Immt |
A |
T |
6: 71,848,541 (GRCm39) |
Q467L |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,936,778 (GRCm39) |
S1636G |
probably benign |
Het |
Kcnh8 |
T |
A |
17: 53,285,141 (GRCm39) |
L1037* |
probably null |
Het |
Klhl33 |
T |
C |
14: 51,129,851 (GRCm39) |
T548A |
probably damaging |
Het |
Klri2 |
T |
C |
6: 129,717,171 (GRCm39) |
I71V |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,609,363 (GRCm39) |
C254S |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,610,647 (GRCm39) |
I1170T |
possibly damaging |
Het |
Med12l |
A |
G |
3: 59,172,350 (GRCm39) |
Q1702R |
probably damaging |
Het |
Mga |
A |
T |
2: 119,750,391 (GRCm39) |
|
probably null |
Het |
Mis18a |
A |
T |
16: 90,517,561 (GRCm39) |
I172K |
possibly damaging |
Het |
Mrgpre |
T |
C |
7: 143,335,254 (GRCm39) |
D83G |
probably benign |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Mrpl39 |
T |
C |
16: 84,531,282 (GRCm39) |
|
probably benign |
Het |
Mrrf |
C |
T |
2: 36,043,710 (GRCm39) |
A149V |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,432,024 (GRCm39) |
M2338K |
possibly damaging |
Het |
N4bp2 |
T |
C |
5: 65,964,780 (GRCm39) |
I943T |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,998,773 (GRCm39) |
N1254K |
probably benign |
Het |
Ncoa1 |
A |
T |
12: 4,299,758 (GRCm39) |
|
probably null |
Het |
Ncor2 |
C |
T |
5: 125,126,451 (GRCm39) |
A136T |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,421,025 (GRCm39) |
|
probably benign |
Het |
Or13a25 |
A |
G |
7: 140,247,590 (GRCm39) |
D123G |
probably damaging |
Het |
Or5p59 |
C |
A |
7: 107,703,363 (GRCm39) |
Y282* |
probably null |
Het |
Or8b39 |
T |
A |
9: 37,996,423 (GRCm39) |
M97K |
possibly damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,681 (GRCm39) |
I247N |
possibly damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,440,795 (GRCm39) |
M35T |
probably benign |
Het |
Per3 |
T |
C |
4: 151,113,288 (GRCm39) |
I347V |
probably benign |
Het |
Pex13 |
G |
A |
11: 23,615,831 (GRCm39) |
P5L |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,602,322 (GRCm39) |
W38R |
probably damaging |
Het |
Plekhf1 |
A |
T |
7: 37,920,826 (GRCm39) |
D247E |
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,042,184 (GRCm39) |
S1607P |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,635,194 (GRCm39) |
H1344L |
possibly damaging |
Het |
Potefam1 |
A |
C |
2: 111,034,482 (GRCm39) |
V350G |
possibly damaging |
Het |
Ptk7 |
T |
G |
17: 46,901,238 (GRCm39) |
N196H |
possibly damaging |
Het |
Rab27a |
G |
T |
9: 72,982,715 (GRCm39) |
D7Y |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,630,505 (GRCm39) |
C82* |
probably null |
Het |
Rccd1 |
A |
T |
7: 79,969,965 (GRCm39) |
|
probably benign |
Het |
Riiad1 |
T |
C |
3: 94,379,546 (GRCm39) |
I56V |
possibly damaging |
Het |
Rnase4 |
A |
G |
14: 51,342,507 (GRCm39) |
E77G |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,441 (GRCm39) |
I157N |
possibly damaging |
Het |
Rnf207 |
T |
C |
4: 152,391,925 (GRCm39) |
R623G |
probably benign |
Het |
Rpusd1 |
T |
G |
17: 25,947,498 (GRCm39) |
F62V |
possibly damaging |
Het |
Rxfp1 |
T |
C |
3: 79,570,600 (GRCm39) |
|
probably null |
Het |
Scfd1 |
A |
T |
12: 51,459,411 (GRCm39) |
Q324L |
probably benign |
Het |
Skint3 |
G |
T |
4: 112,112,974 (GRCm39) |
E195* |
probably null |
Het |
Slc7a10 |
A |
T |
7: 34,896,758 (GRCm39) |
T165S |
probably benign |
Het |
Smagp |
A |
G |
15: 100,519,733 (GRCm39) |
I97T |
probably damaging |
Het |
Sostdc1 |
A |
G |
12: 36,367,340 (GRCm39) |
H172R |
probably damaging |
Het |
Spast |
A |
G |
17: 74,646,446 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
T |
6: 48,467,325 (GRCm39) |
|
probably benign |
Het |
Ston2 |
C |
T |
12: 91,707,240 (GRCm39) |
|
probably null |
Het |
Tas2r103 |
T |
G |
6: 133,013,313 (GRCm39) |
E251A |
probably benign |
Het |
Tbc1d2b |
A |
T |
9: 90,104,558 (GRCm39) |
|
probably benign |
Het |
Telo2 |
G |
A |
17: 25,332,139 (GRCm39) |
P143L |
probably benign |
Het |
Tgfbi |
A |
T |
13: 56,786,539 (GRCm39) |
Y674F |
probably null |
Het |
Tha1 |
T |
A |
11: 117,763,983 (GRCm39) |
|
probably benign |
Het |
Timp4 |
T |
A |
6: 115,226,814 (GRCm39) |
S110C |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,935 (GRCm39) |
K324R |
probably benign |
Het |
Tnip3 |
A |
G |
6: 65,574,347 (GRCm39) |
E137G |
probably damaging |
Het |
Top6bl |
A |
G |
19: 4,676,216 (GRCm39) |
S639P |
probably damaging |
Het |
Trak1 |
T |
C |
9: 121,278,021 (GRCm39) |
|
probably null |
Het |
Trim47 |
A |
G |
11: 115,999,178 (GRCm39) |
S233P |
probably benign |
Het |
Tspoap1 |
A |
T |
11: 87,653,635 (GRCm39) |
E155V |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,194,209 (GRCm39) |
L1343Q |
probably damaging |
Het |
Utp14b |
T |
C |
1: 78,642,452 (GRCm39) |
S117P |
probably benign |
Het |
Vmn1r124 |
A |
T |
7: 20,994,436 (GRCm39) |
V36D |
probably damaging |
Het |
Wdr27 |
T |
C |
17: 15,148,658 (GRCm39) |
T112A |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,367 (GRCm39) |
T1630A |
probably benign |
Het |
Zfp352 |
A |
G |
4: 90,112,156 (GRCm39) |
T99A |
probably benign |
Het |
|
Other mutations in Myo18b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Myo18b
|
APN |
5 |
113,021,997 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00847:Myo18b
|
APN |
5 |
112,978,255 (GRCm39) |
splice site |
probably benign |
|
IGL00848:Myo18b
|
APN |
5 |
113,019,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00969:Myo18b
|
APN |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
IGL01018:Myo18b
|
APN |
5 |
112,957,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01448:Myo18b
|
APN |
5 |
112,959,570 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01490:Myo18b
|
APN |
5 |
112,957,566 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01556:Myo18b
|
APN |
5 |
112,905,315 (GRCm39) |
splice site |
probably benign |
|
IGL01637:Myo18b
|
APN |
5 |
112,988,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01819:Myo18b
|
APN |
5 |
113,025,916 (GRCm39) |
missense |
unknown |
|
IGL02007:Myo18b
|
APN |
5 |
113,022,838 (GRCm39) |
unclassified |
probably benign |
|
IGL02146:Myo18b
|
APN |
5 |
112,991,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02229:Myo18b
|
APN |
5 |
113,025,976 (GRCm39) |
missense |
unknown |
|
IGL02319:Myo18b
|
APN |
5 |
112,939,005 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02398:Myo18b
|
APN |
5 |
112,978,178 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02420:Myo18b
|
APN |
5 |
112,975,852 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02626:Myo18b
|
APN |
5 |
113,025,951 (GRCm39) |
missense |
unknown |
|
IGL02815:Myo18b
|
APN |
5 |
112,957,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Myo18b
|
APN |
5 |
112,923,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Myo18b
|
APN |
5 |
112,863,377 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02995:Myo18b
|
APN |
5 |
112,923,279 (GRCm39) |
splice site |
probably benign |
|
IGL03019:Myo18b
|
APN |
5 |
112,840,263 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03039:Myo18b
|
APN |
5 |
112,988,637 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Myo18b
|
APN |
5 |
113,021,856 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03123:Myo18b
|
APN |
5 |
113,022,804 (GRCm39) |
unclassified |
probably benign |
|
IGL03288:Myo18b
|
APN |
5 |
112,937,863 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03391:Myo18b
|
APN |
5 |
113,022,345 (GRCm39) |
unclassified |
probably benign |
|
klippel
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4651001:Myo18b
|
UTSW |
5 |
112,982,301 (GRCm39) |
missense |
probably benign |
0.01 |
R0271:Myo18b
|
UTSW |
5 |
112,957,551 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0277:Myo18b
|
UTSW |
5 |
112,841,213 (GRCm39) |
splice site |
probably benign |
|
R0352:Myo18b
|
UTSW |
5 |
113,022,389 (GRCm39) |
unclassified |
probably benign |
|
R0504:Myo18b
|
UTSW |
5 |
113,021,442 (GRCm39) |
unclassified |
probably benign |
|
R0539:Myo18b
|
UTSW |
5 |
112,871,734 (GRCm39) |
missense |
probably damaging |
0.99 |
R0599:Myo18b
|
UTSW |
5 |
113,013,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Myo18b
|
UTSW |
5 |
112,946,700 (GRCm39) |
missense |
probably benign |
0.38 |
R0659:Myo18b
|
UTSW |
5 |
112,908,193 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0847:Myo18b
|
UTSW |
5 |
113,022,354 (GRCm39) |
unclassified |
probably benign |
|
R1082:Myo18b
|
UTSW |
5 |
112,908,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R1116:Myo18b
|
UTSW |
5 |
112,951,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Myo18b
|
UTSW |
5 |
112,978,185 (GRCm39) |
missense |
probably benign |
0.12 |
R1280:Myo18b
|
UTSW |
5 |
112,871,671 (GRCm39) |
critical splice donor site |
probably null |
|
R1444:Myo18b
|
UTSW |
5 |
112,923,117 (GRCm39) |
critical splice donor site |
probably null |
|
R1446:Myo18b
|
UTSW |
5 |
112,905,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Myo18b
|
UTSW |
5 |
112,840,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Myo18b
|
UTSW |
5 |
113,023,132 (GRCm39) |
nonsense |
probably null |
|
R1601:Myo18b
|
UTSW |
5 |
113,019,364 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1903:Myo18b
|
UTSW |
5 |
112,840,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1935:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R1936:Myo18b
|
UTSW |
5 |
112,908,222 (GRCm39) |
missense |
probably benign |
0.04 |
R2008:Myo18b
|
UTSW |
5 |
113,021,423 (GRCm39) |
missense |
probably benign |
|
R2127:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Myo18b
|
UTSW |
5 |
112,978,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Myo18b
|
UTSW |
5 |
113,021,892 (GRCm39) |
missense |
probably benign |
0.01 |
R2170:Myo18b
|
UTSW |
5 |
112,871,724 (GRCm39) |
missense |
probably benign |
0.23 |
R2258:Myo18b
|
UTSW |
5 |
113,022,529 (GRCm39) |
unclassified |
probably benign |
|
R2265:Myo18b
|
UTSW |
5 |
112,930,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Myo18b
|
UTSW |
5 |
113,006,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Myo18b
|
UTSW |
5 |
112,840,993 (GRCm39) |
missense |
probably benign |
0.01 |
R3160:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3162:Myo18b
|
UTSW |
5 |
112,840,594 (GRCm39) |
missense |
probably damaging |
0.99 |
R3777:Myo18b
|
UTSW |
5 |
112,905,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R4240:Myo18b
|
UTSW |
5 |
112,951,053 (GRCm39) |
critical splice donor site |
probably null |
|
R4243:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4245:Myo18b
|
UTSW |
5 |
112,840,261 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4533:Myo18b
|
UTSW |
5 |
112,840,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Myo18b
|
UTSW |
5 |
112,994,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Myo18b
|
UTSW |
5 |
113,023,041 (GRCm39) |
unclassified |
probably benign |
|
R4755:Myo18b
|
UTSW |
5 |
113,022,340 (GRCm39) |
nonsense |
probably null |
|
R4771:Myo18b
|
UTSW |
5 |
112,840,093 (GRCm39) |
nonsense |
probably null |
|
R4812:Myo18b
|
UTSW |
5 |
112,957,584 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4840:Myo18b
|
UTSW |
5 |
113,021,895 (GRCm39) |
missense |
probably benign |
0.02 |
R4888:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R4995:Myo18b
|
UTSW |
5 |
112,908,258 (GRCm39) |
missense |
probably damaging |
0.99 |
R5001:Myo18b
|
UTSW |
5 |
112,909,206 (GRCm39) |
missense |
probably damaging |
0.99 |
R5015:Myo18b
|
UTSW |
5 |
112,937,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Myo18b
|
UTSW |
5 |
113,023,083 (GRCm39) |
unclassified |
probably benign |
|
R5070:Myo18b
|
UTSW |
5 |
112,909,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5105:Myo18b
|
UTSW |
5 |
112,988,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Myo18b
|
UTSW |
5 |
113,022,346 (GRCm39) |
unclassified |
probably benign |
|
R5130:Myo18b
|
UTSW |
5 |
113,021,769 (GRCm39) |
missense |
probably benign |
0.06 |
R5186:Myo18b
|
UTSW |
5 |
113,019,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Myo18b
|
UTSW |
5 |
112,905,439 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5535:Myo18b
|
UTSW |
5 |
112,937,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Myo18b
|
UTSW |
5 |
113,016,161 (GRCm39) |
missense |
probably damaging |
0.96 |
R5810:Myo18b
|
UTSW |
5 |
112,982,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Myo18b
|
UTSW |
5 |
112,950,196 (GRCm39) |
splice site |
probably null |
|
R6065:Myo18b
|
UTSW |
5 |
112,840,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6104:Myo18b
|
UTSW |
5 |
113,022,157 (GRCm39) |
unclassified |
probably benign |
|
R6113:Myo18b
|
UTSW |
5 |
113,014,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo18b
|
UTSW |
5 |
113,022,038 (GRCm39) |
missense |
probably benign |
0.01 |
R6167:Myo18b
|
UTSW |
5 |
113,020,373 (GRCm39) |
splice site |
probably null |
|
R6220:Myo18b
|
UTSW |
5 |
112,905,373 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6276:Myo18b
|
UTSW |
5 |
112,959,508 (GRCm39) |
missense |
probably benign |
0.31 |
R6290:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6291:Myo18b
|
UTSW |
5 |
113,013,601 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6795:Myo18b
|
UTSW |
5 |
112,994,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R6798:Myo18b
|
UTSW |
5 |
112,909,252 (GRCm39) |
missense |
probably damaging |
0.98 |
R6817:Myo18b
|
UTSW |
5 |
112,978,104 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Myo18b
|
UTSW |
5 |
112,950,258 (GRCm39) |
missense |
probably benign |
0.12 |
R7034:Myo18b
|
UTSW |
5 |
112,871,770 (GRCm39) |
nonsense |
probably null |
|
R7097:Myo18b
|
UTSW |
5 |
113,022,271 (GRCm39) |
missense |
unknown |
|
R7145:Myo18b
|
UTSW |
5 |
112,965,545 (GRCm39) |
nonsense |
probably null |
|
R7201:Myo18b
|
UTSW |
5 |
112,863,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Myo18b
|
UTSW |
5 |
112,923,154 (GRCm39) |
missense |
probably benign |
0.01 |
R7265:Myo18b
|
UTSW |
5 |
112,959,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Myo18b
|
UTSW |
5 |
113,021,971 (GRCm39) |
missense |
probably benign |
0.25 |
R7466:Myo18b
|
UTSW |
5 |
112,871,758 (GRCm39) |
missense |
probably benign |
0.02 |
R7487:Myo18b
|
UTSW |
5 |
112,982,299 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7571:Myo18b
|
UTSW |
5 |
112,978,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Myo18b
|
UTSW |
5 |
113,025,969 (GRCm39) |
missense |
unknown |
|
R7612:Myo18b
|
UTSW |
5 |
113,013,168 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7617:Myo18b
|
UTSW |
5 |
112,905,319 (GRCm39) |
critical splice donor site |
probably null |
|
R7696:Myo18b
|
UTSW |
5 |
112,840,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myo18b
|
UTSW |
5 |
113,022,891 (GRCm39) |
missense |
unknown |
|
R8047:Myo18b
|
UTSW |
5 |
112,871,681 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8070:Myo18b
|
UTSW |
5 |
112,938,986 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Myo18b
|
UTSW |
5 |
113,027,376 (GRCm39) |
start gained |
probably benign |
|
R8247:Myo18b
|
UTSW |
5 |
112,840,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8276:Myo18b
|
UTSW |
5 |
112,943,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8313:Myo18b
|
UTSW |
5 |
113,023,045 (GRCm39) |
missense |
unknown |
|
R8375:Myo18b
|
UTSW |
5 |
112,908,259 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8432:Myo18b
|
UTSW |
5 |
112,912,378 (GRCm39) |
missense |
probably benign |
0.00 |
R8475:Myo18b
|
UTSW |
5 |
113,021,422 (GRCm39) |
nonsense |
probably null |
|
R8482:Myo18b
|
UTSW |
5 |
113,019,489 (GRCm39) |
nonsense |
probably null |
|
R8671:Myo18b
|
UTSW |
5 |
113,022,609 (GRCm39) |
missense |
unknown |
|
R8681:Myo18b
|
UTSW |
5 |
113,021,429 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8918:Myo18b
|
UTSW |
5 |
113,022,873 (GRCm39) |
unclassified |
probably benign |
|
R8941:Myo18b
|
UTSW |
5 |
113,022,795 (GRCm39) |
unclassified |
probably benign |
|
R8962:Myo18b
|
UTSW |
5 |
113,006,346 (GRCm39) |
missense |
probably benign |
0.24 |
R8972:Myo18b
|
UTSW |
5 |
112,841,164 (GRCm39) |
missense |
probably benign |
0.00 |
R9116:Myo18b
|
UTSW |
5 |
112,975,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R9209:Myo18b
|
UTSW |
5 |
113,022,927 (GRCm39) |
missense |
unknown |
|
R9358:Myo18b
|
UTSW |
5 |
112,943,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9469:Myo18b
|
UTSW |
5 |
112,994,247 (GRCm39) |
missense |
probably benign |
0.15 |
R9607:Myo18b
|
UTSW |
5 |
113,022,544 (GRCm39) |
missense |
unknown |
|
R9659:Myo18b
|
UTSW |
5 |
113,022,382 (GRCm39) |
missense |
unknown |
|
Z1088:Myo18b
|
UTSW |
5 |
112,905,350 (GRCm39) |
missense |
probably benign |
0.25 |
Z1088:Myo18b
|
UTSW |
5 |
112,840,809 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1176:Myo18b
|
UTSW |
5 |
112,979,056 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo18b
|
UTSW |
5 |
112,957,604 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1176:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
113,021,407 (GRCm39) |
nonsense |
probably null |
|
Z1177:Myo18b
|
UTSW |
5 |
112,910,587 (GRCm39) |
missense |
not run |
|
Z1177:Myo18b
|
UTSW |
5 |
112,840,765 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo18b
|
UTSW |
5 |
113,023,018 (GRCm39) |
nonsense |
probably null |
|
|