Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,846,002 (GRCm39) |
C811R |
possibly damaging |
Het |
Akap8l |
G |
A |
17: 32,557,416 (GRCm39) |
T65I |
possibly damaging |
Het |
Amdhd2 |
A |
G |
17: 24,376,829 (GRCm39) |
|
probably benign |
Het |
Arid4a |
T |
A |
12: 71,069,034 (GRCm39) |
|
probably null |
Het |
Armc2 |
C |
T |
10: 41,842,696 (GRCm39) |
|
probably null |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,258 (GRCm39) |
Y87C |
probably benign |
Het |
C030034I22Rik |
T |
A |
17: 69,725,106 (GRCm39) |
|
noncoding transcript |
Het |
Ccnb1-ps |
C |
A |
7: 41,755,499 (GRCm39) |
|
noncoding transcript |
Het |
Clasrp |
C |
A |
7: 19,319,165 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
T |
C |
4: 128,451,511 (GRCm39) |
F113S |
unknown |
Het |
Cyp4a14 |
C |
A |
4: 115,344,498 (GRCm39) |
G456W |
probably damaging |
Het |
Cyp4a30b |
A |
G |
4: 115,315,559 (GRCm39) |
H260R |
possibly damaging |
Het |
Dennd2b |
A |
T |
7: 109,156,637 (GRCm39) |
Y38N |
probably benign |
Het |
Dhx57 |
A |
T |
17: 80,558,805 (GRCm39) |
D1051E |
probably benign |
Het |
Eif4enif1 |
C |
T |
11: 3,192,586 (GRCm39) |
P805S |
probably damaging |
Het |
Eml5 |
C |
T |
12: 98,831,660 (GRCm39) |
D433N |
probably damaging |
Het |
Fan1 |
A |
G |
7: 64,012,938 (GRCm39) |
I668T |
probably benign |
Het |
Frmpd4 |
A |
T |
X: 166,260,243 (GRCm39) |
D1166E |
probably benign |
Homo |
Ftdc1 |
A |
T |
16: 58,434,342 (GRCm39) |
I125K |
probably benign |
Het |
Gm21759 |
T |
A |
5: 8,230,863 (GRCm39) |
|
probably benign |
Het |
Gm5454 |
C |
A |
13: 103,494,031 (GRCm39) |
|
noncoding transcript |
Het |
Gm9874 |
A |
T |
17: 30,704,763 (GRCm39) |
|
probably benign |
Het |
Gria2 |
G |
A |
3: 80,609,799 (GRCm39) |
T670I |
probably damaging |
Het |
Grid2ip |
C |
A |
5: 143,343,684 (GRCm39) |
Q127K |
probably benign |
Het |
Habp2 |
T |
A |
19: 56,276,423 (GRCm39) |
|
probably benign |
Het |
Hdhd2 |
T |
C |
18: 77,042,702 (GRCm39) |
F44L |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,614,467 (GRCm39) |
V1313D |
possibly damaging |
Het |
Ift172 |
C |
T |
5: 31,415,205 (GRCm39) |
V1335I |
probably benign |
Het |
Ighv2-2 |
G |
A |
12: 113,552,118 (GRCm39) |
T40I |
possibly damaging |
Het |
Kcnk10 |
T |
A |
12: 98,401,072 (GRCm39) |
R520S |
probably benign |
Het |
Kif1c |
A |
G |
11: 70,614,907 (GRCm39) |
E567G |
probably damaging |
Het |
Klf8 |
A |
T |
X: 152,165,678 (GRCm39) |
E82D |
probably damaging |
Homo |
Kpna7 |
T |
C |
5: 144,930,745 (GRCm39) |
T367A |
probably benign |
Het |
Lpo |
A |
G |
11: 87,707,350 (GRCm39) |
I221T |
possibly damaging |
Het |
Lrrn3 |
T |
C |
12: 41,502,722 (GRCm39) |
I532V |
probably benign |
Het |
Mapk7 |
C |
A |
11: 61,381,038 (GRCm39) |
|
probably benign |
Het |
Matr3 |
T |
A |
18: 35,705,349 (GRCm39) |
S91R |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,309,878 (GRCm39) |
P191L |
probably benign |
Het |
Mlxip |
A |
G |
5: 123,590,730 (GRCm39) |
M878V |
probably benign |
Het |
Mpp7 |
G |
A |
18: 7,461,678 (GRCm39) |
P65L |
possibly damaging |
Het |
Msh2 |
C |
A |
17: 87,993,012 (GRCm39) |
Q314K |
possibly damaging |
Het |
Mtm1 |
T |
C |
X: 70,339,968 (GRCm39) |
|
probably benign |
Homo |
Mtor |
T |
A |
4: 148,624,487 (GRCm39) |
M2089K |
probably benign |
Het |
Myo9b |
G |
A |
8: 71,786,981 (GRCm39) |
R721Q |
probably benign |
Het |
Nav1 |
A |
G |
1: 135,388,495 (GRCm39) |
|
silent |
Het |
Nell1 |
A |
T |
7: 49,899,405 (GRCm39) |
|
probably benign |
Het |
Nlrp4b |
C |
T |
7: 10,444,170 (GRCm39) |
Q40* |
probably null |
Het |
Nomo1 |
C |
A |
7: 45,696,361 (GRCm39) |
T293N |
probably damaging |
Het |
Notum |
A |
G |
11: 120,551,022 (GRCm39) |
V48A |
probably benign |
Het |
Npas3 |
C |
T |
12: 54,114,796 (GRCm39) |
R542* |
probably null |
Het |
Or10z1 |
T |
C |
1: 174,078,092 (GRCm39) |
S134G |
probably benign |
Het |
Or13a17 |
A |
G |
7: 140,271,198 (GRCm39) |
I127V |
possibly damaging |
Het |
Or13j1 |
C |
A |
4: 43,706,458 (GRCm39) |
V37L |
probably benign |
Het |
Or5t16 |
A |
T |
2: 86,819,192 (GRCm39) |
C109* |
probably null |
Het |
Ostc |
T |
C |
3: 130,497,157 (GRCm39) |
N80S |
probably damaging |
Het |
Palmd |
T |
C |
3: 116,717,400 (GRCm39) |
R366G |
possibly damaging |
Het |
Parp1 |
A |
G |
1: 180,401,230 (GRCm39) |
D45G |
probably damaging |
Het |
Pcdhga9 |
T |
A |
18: 37,870,524 (GRCm39) |
Y118N |
possibly damaging |
Het |
Pcnx3 |
A |
T |
19: 5,733,774 (GRCm39) |
|
probably benign |
Het |
Pes1 |
C |
A |
11: 3,926,834 (GRCm39) |
T372K |
probably benign |
Het |
Pkp4 |
C |
A |
2: 59,138,500 (GRCm39) |
T250K |
probably benign |
Het |
Plekhg5 |
T |
A |
4: 152,191,960 (GRCm39) |
C433S |
probably benign |
Het |
Plin2 |
A |
G |
4: 86,586,915 (GRCm39) |
M1T |
probably null |
Het |
Prdx4 |
A |
G |
X: 154,123,460 (GRCm39) |
V15A |
probably benign |
Homo |
Psmb8 |
T |
C |
17: 34,419,144 (GRCm39) |
I146T |
probably damaging |
Het |
Psmd13 |
A |
T |
7: 140,466,968 (GRCm39) |
T116S |
probably damaging |
Het |
Rel |
T |
C |
11: 23,711,129 (GRCm39) |
I13V |
probably benign |
Het |
Reln |
C |
T |
5: 22,254,789 (GRCm39) |
V527I |
possibly damaging |
Het |
Rnf6 |
T |
C |
5: 146,147,215 (GRCm39) |
Y601C |
probably benign |
Het |
Rps6kc1 |
T |
C |
1: 190,631,766 (GRCm39) |
I48M |
probably damaging |
Het |
Shoc1 |
A |
C |
4: 59,093,850 (GRCm39) |
L226R |
probably damaging |
Het |
Slc39a8 |
T |
A |
3: 135,592,554 (GRCm39) |
|
probably null |
Het |
Son |
A |
G |
16: 91,461,205 (GRCm39) |
|
probably null |
Het |
Sppl2c |
C |
T |
11: 104,078,141 (GRCm39) |
P314S |
probably benign |
Het |
Tnni3k |
C |
T |
3: 154,644,387 (GRCm39) |
|
probably null |
Het |
Vmn2r68 |
A |
C |
7: 84,882,834 (GRCm39) |
M306R |
probably benign |
Het |
Vmn2r70 |
T |
A |
7: 85,208,227 (GRCm39) |
Y750F |
probably damaging |
Het |
Vwa7 |
G |
A |
17: 35,240,218 (GRCm39) |
M395I |
probably damaging |
Het |
Zfp53 |
A |
T |
17: 21,728,340 (GRCm39) |
E124D |
probably benign |
Het |
Zzz3 |
T |
A |
3: 152,152,481 (GRCm39) |
|
silent |
Het |
|
Other mutations in Cfap54 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Cfap54
|
APN |
10 |
92,917,385 (GRCm39) |
missense |
unknown |
|
IGL02034:Cfap54
|
APN |
10 |
92,897,347 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02082:Cfap54
|
APN |
10 |
92,917,320 (GRCm39) |
missense |
unknown |
|
IGL02434:Cfap54
|
APN |
10 |
92,902,616 (GRCm39) |
missense |
probably benign |
0.20 |
R0011:Cfap54
|
UTSW |
10 |
92,901,087 (GRCm39) |
missense |
probably damaging |
0.97 |
R0011:Cfap54
|
UTSW |
10 |
92,901,087 (GRCm39) |
missense |
probably damaging |
0.97 |
R0032:Cfap54
|
UTSW |
10 |
92,768,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0032:Cfap54
|
UTSW |
10 |
92,768,559 (GRCm39) |
missense |
probably benign |
0.04 |
R0040:Cfap54
|
UTSW |
10 |
92,812,901 (GRCm39) |
missense |
probably benign |
0.33 |
R0044:Cfap54
|
UTSW |
10 |
92,871,295 (GRCm39) |
missense |
probably null |
0.46 |
R0086:Cfap54
|
UTSW |
10 |
92,864,456 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0104:Cfap54
|
UTSW |
10 |
92,864,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Cfap54
|
UTSW |
10 |
92,870,524 (GRCm39) |
unclassified |
probably benign |
|
R0234:Cfap54
|
UTSW |
10 |
92,735,022 (GRCm39) |
nonsense |
probably null |
|
R0308:Cfap54
|
UTSW |
10 |
92,721,226 (GRCm39) |
missense |
unknown |
|
R0332:Cfap54
|
UTSW |
10 |
92,871,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:Cfap54
|
UTSW |
10 |
92,612,075 (GRCm39) |
missense |
probably benign |
0.00 |
R0433:Cfap54
|
UTSW |
10 |
92,814,942 (GRCm39) |
splice site |
probably benign |
|
R0436:Cfap54
|
UTSW |
10 |
92,874,837 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0463:Cfap54
|
UTSW |
10 |
92,710,805 (GRCm39) |
critical splice donor site |
probably null |
|
R0523:Cfap54
|
UTSW |
10 |
92,744,745 (GRCm39) |
utr 3 prime |
probably benign |
|
R0551:Cfap54
|
UTSW |
10 |
92,860,984 (GRCm39) |
missense |
probably benign |
0.35 |
R0595:Cfap54
|
UTSW |
10 |
92,720,598 (GRCm39) |
missense |
unknown |
|
R0617:Cfap54
|
UTSW |
10 |
92,665,512 (GRCm39) |
splice site |
probably benign |
|
R0632:Cfap54
|
UTSW |
10 |
92,720,958 (GRCm39) |
missense |
unknown |
|
R0730:Cfap54
|
UTSW |
10 |
92,870,599 (GRCm39) |
missense |
probably benign |
0.05 |
R0786:Cfap54
|
UTSW |
10 |
92,803,397 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0883:Cfap54
|
UTSW |
10 |
92,706,531 (GRCm39) |
missense |
unknown |
|
R1004:Cfap54
|
UTSW |
10 |
92,902,558 (GRCm39) |
splice site |
probably benign |
|
R1033:Cfap54
|
UTSW |
10 |
92,675,311 (GRCm39) |
missense |
probably benign |
0.07 |
R1168:Cfap54
|
UTSW |
10 |
92,773,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Cfap54
|
UTSW |
10 |
92,711,856 (GRCm39) |
missense |
unknown |
|
R1429:Cfap54
|
UTSW |
10 |
92,656,900 (GRCm39) |
missense |
probably benign |
0.01 |
R1443:Cfap54
|
UTSW |
10 |
92,768,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cfap54
|
UTSW |
10 |
92,805,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1467:Cfap54
|
UTSW |
10 |
92,805,625 (GRCm39) |
missense |
probably benign |
0.01 |
R1557:Cfap54
|
UTSW |
10 |
92,820,089 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1687:Cfap54
|
UTSW |
10 |
92,768,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R1690:Cfap54
|
UTSW |
10 |
92,871,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1711:Cfap54
|
UTSW |
10 |
92,846,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Cfap54
|
UTSW |
10 |
92,883,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1769:Cfap54
|
UTSW |
10 |
92,740,125 (GRCm39) |
critical splice donor site |
probably null |
|
R1835:Cfap54
|
UTSW |
10 |
92,798,237 (GRCm39) |
missense |
probably benign |
0.35 |
R1889:Cfap54
|
UTSW |
10 |
92,870,572 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1915:Cfap54
|
UTSW |
10 |
92,720,564 (GRCm39) |
missense |
unknown |
|
R1958:Cfap54
|
UTSW |
10 |
92,833,204 (GRCm39) |
missense |
probably benign |
0.18 |
R2005:Cfap54
|
UTSW |
10 |
92,720,630 (GRCm39) |
missense |
unknown |
|
R2018:Cfap54
|
UTSW |
10 |
92,852,466 (GRCm39) |
missense |
probably benign |
0.00 |
R2045:Cfap54
|
UTSW |
10 |
92,874,671 (GRCm39) |
splice site |
probably null |
|
R2059:Cfap54
|
UTSW |
10 |
92,778,841 (GRCm39) |
unclassified |
probably benign |
|
R2100:Cfap54
|
UTSW |
10 |
92,837,799 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2110:Cfap54
|
UTSW |
10 |
92,722,229 (GRCm39) |
missense |
unknown |
|
R2392:Cfap54
|
UTSW |
10 |
92,860,873 (GRCm39) |
critical splice donor site |
probably null |
|
R2508:Cfap54
|
UTSW |
10 |
92,833,236 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2852:Cfap54
|
UTSW |
10 |
92,776,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Cfap54
|
UTSW |
10 |
92,881,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R2871:Cfap54
|
UTSW |
10 |
92,757,281 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3107:Cfap54
|
UTSW |
10 |
92,830,545 (GRCm39) |
missense |
probably benign |
0.04 |
R3108:Cfap54
|
UTSW |
10 |
92,830,545 (GRCm39) |
missense |
probably benign |
0.04 |
R3157:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3158:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3159:Cfap54
|
UTSW |
10 |
92,834,918 (GRCm39) |
missense |
probably benign |
0.03 |
R3161:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Cfap54
|
UTSW |
10 |
92,881,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R3508:Cfap54
|
UTSW |
10 |
92,721,286 (GRCm39) |
missense |
unknown |
|
R3730:Cfap54
|
UTSW |
10 |
92,847,335 (GRCm39) |
nonsense |
probably null |
|
R3770:Cfap54
|
UTSW |
10 |
92,714,398 (GRCm39) |
missense |
unknown |
|
R3776:Cfap54
|
UTSW |
10 |
92,880,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R3778:Cfap54
|
UTSW |
10 |
92,740,206 (GRCm39) |
utr 3 prime |
probably benign |
|
R3795:Cfap54
|
UTSW |
10 |
92,778,735 (GRCm39) |
unclassified |
probably benign |
|
R3834:Cfap54
|
UTSW |
10 |
92,636,985 (GRCm39) |
splice site |
probably benign |
|
R3891:Cfap54
|
UTSW |
10 |
92,874,708 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3932:Cfap54
|
UTSW |
10 |
92,665,619 (GRCm39) |
missense |
probably benign |
0.03 |
R3973:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3974:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3976:Cfap54
|
UTSW |
10 |
92,675,333 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3978:Cfap54
|
UTSW |
10 |
92,798,274 (GRCm39) |
missense |
probably benign |
0.01 |
R4190:Cfap54
|
UTSW |
10 |
92,720,885 (GRCm39) |
missense |
unknown |
|
R4389:Cfap54
|
UTSW |
10 |
92,803,362 (GRCm39) |
missense |
probably benign |
0.37 |
R4542:Cfap54
|
UTSW |
10 |
92,860,991 (GRCm39) |
missense |
probably benign |
0.12 |
R4564:Cfap54
|
UTSW |
10 |
92,675,402 (GRCm39) |
unclassified |
probably benign |
|
R4576:Cfap54
|
UTSW |
10 |
92,879,090 (GRCm39) |
critical splice donor site |
probably null |
|
R4620:Cfap54
|
UTSW |
10 |
92,805,619 (GRCm39) |
missense |
probably benign |
0.01 |
R4714:Cfap54
|
UTSW |
10 |
92,651,780 (GRCm39) |
missense |
probably benign |
0.01 |
R4762:Cfap54
|
UTSW |
10 |
92,897,315 (GRCm39) |
splice site |
probably null |
|
R4776:Cfap54
|
UTSW |
10 |
92,808,556 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4819:Cfap54
|
UTSW |
10 |
92,672,339 (GRCm39) |
nonsense |
probably null |
|
R4827:Cfap54
|
UTSW |
10 |
92,737,937 (GRCm39) |
utr 3 prime |
probably benign |
|
R4832:Cfap54
|
UTSW |
10 |
92,803,390 (GRCm39) |
missense |
probably benign |
0.01 |
R4965:Cfap54
|
UTSW |
10 |
92,902,661 (GRCm39) |
missense |
probably benign |
0.23 |
R5001:Cfap54
|
UTSW |
10 |
92,800,396 (GRCm39) |
missense |
probably benign |
0.01 |
R5060:Cfap54
|
UTSW |
10 |
92,875,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5067:Cfap54
|
UTSW |
10 |
92,902,628 (GRCm39) |
missense |
probably benign |
0.17 |
R5069:Cfap54
|
UTSW |
10 |
92,773,636 (GRCm39) |
missense |
probably benign |
|
R5094:Cfap54
|
UTSW |
10 |
92,734,861 (GRCm39) |
utr 3 prime |
probably benign |
|
R5109:Cfap54
|
UTSW |
10 |
92,773,753 (GRCm39) |
missense |
probably benign |
0.03 |
R5127:Cfap54
|
UTSW |
10 |
92,722,249 (GRCm39) |
splice site |
probably null |
|
R5143:Cfap54
|
UTSW |
10 |
92,865,020 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5147:Cfap54
|
UTSW |
10 |
92,773,700 (GRCm39) |
missense |
probably benign |
0.00 |
R5158:Cfap54
|
UTSW |
10 |
92,901,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Cfap54
|
UTSW |
10 |
92,880,885 (GRCm39) |
splice site |
probably null |
|
R5256:Cfap54
|
UTSW |
10 |
92,770,953 (GRCm39) |
nonsense |
probably null |
|
R5266:Cfap54
|
UTSW |
10 |
92,651,764 (GRCm39) |
missense |
probably benign |
0.16 |
R5304:Cfap54
|
UTSW |
10 |
92,656,968 (GRCm39) |
missense |
probably damaging |
0.97 |
R5369:Cfap54
|
UTSW |
10 |
92,897,119 (GRCm39) |
intron |
probably benign |
|
R5406:Cfap54
|
UTSW |
10 |
92,837,720 (GRCm39) |
missense |
probably benign |
0.33 |
R5471:Cfap54
|
UTSW |
10 |
92,864,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Cfap54
|
UTSW |
10 |
92,864,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5540:Cfap54
|
UTSW |
10 |
92,808,470 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5586:Cfap54
|
UTSW |
10 |
92,808,473 (GRCm39) |
nonsense |
probably null |
|
R5614:Cfap54
|
UTSW |
10 |
92,880,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5634:Cfap54
|
UTSW |
10 |
92,740,125 (GRCm39) |
critical splice donor site |
probably benign |
|
R5680:Cfap54
|
UTSW |
10 |
92,814,879 (GRCm39) |
nonsense |
probably null |
|
R5797:Cfap54
|
UTSW |
10 |
92,803,438 (GRCm39) |
missense |
probably benign |
0.11 |
R5859:Cfap54
|
UTSW |
10 |
92,852,386 (GRCm39) |
nonsense |
probably null |
|
R5878:Cfap54
|
UTSW |
10 |
92,800,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5910:Cfap54
|
UTSW |
10 |
92,901,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R5936:Cfap54
|
UTSW |
10 |
92,798,274 (GRCm39) |
missense |
probably benign |
0.01 |
R5994:Cfap54
|
UTSW |
10 |
92,874,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R6080:Cfap54
|
UTSW |
10 |
92,881,197 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6268:Cfap54
|
UTSW |
10 |
92,874,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R6296:Cfap54
|
UTSW |
10 |
92,902,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Cfap54
|
UTSW |
10 |
92,803,354 (GRCm39) |
missense |
probably benign |
0.04 |
R6545:Cfap54
|
UTSW |
10 |
92,672,319 (GRCm39) |
missense |
probably benign |
0.31 |
R6570:Cfap54
|
UTSW |
10 |
92,651,820 (GRCm39) |
missense |
unknown |
|
R6597:Cfap54
|
UTSW |
10 |
92,834,902 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6702:Cfap54
|
UTSW |
10 |
92,704,596 (GRCm39) |
missense |
unknown |
|
R6703:Cfap54
|
UTSW |
10 |
92,704,596 (GRCm39) |
missense |
unknown |
|
R6720:Cfap54
|
UTSW |
10 |
92,656,981 (GRCm39) |
missense |
probably benign |
0.07 |
R6841:Cfap54
|
UTSW |
10 |
92,710,877 (GRCm39) |
missense |
unknown |
|
R6910:Cfap54
|
UTSW |
10 |
92,672,374 (GRCm39) |
missense |
probably benign |
0.29 |
R6953:Cfap54
|
UTSW |
10 |
92,830,540 (GRCm39) |
missense |
probably benign |
0.19 |
R7009:Cfap54
|
UTSW |
10 |
92,710,881 (GRCm39) |
missense |
unknown |
|
R7129:Cfap54
|
UTSW |
10 |
92,852,433 (GRCm39) |
missense |
probably benign |
0.06 |
R7131:Cfap54
|
UTSW |
10 |
92,656,966 (GRCm39) |
missense |
probably benign |
0.03 |
R7171:Cfap54
|
UTSW |
10 |
92,612,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R7189:Cfap54
|
UTSW |
10 |
92,773,590 (GRCm39) |
missense |
unknown |
|
R7225:Cfap54
|
UTSW |
10 |
92,740,236 (GRCm39) |
missense |
unknown |
|
R7270:Cfap54
|
UTSW |
10 |
92,675,320 (GRCm39) |
missense |
probably benign |
0.03 |
R7323:Cfap54
|
UTSW |
10 |
92,637,000 (GRCm39) |
missense |
probably benign |
0.00 |
R7380:Cfap54
|
UTSW |
10 |
92,883,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7395:Cfap54
|
UTSW |
10 |
92,720,565 (GRCm39) |
missense |
unknown |
|
R7411:Cfap54
|
UTSW |
10 |
92,704,617 (GRCm39) |
missense |
unknown |
|
R7503:Cfap54
|
UTSW |
10 |
92,723,298 (GRCm39) |
splice site |
probably null |
|
R7622:Cfap54
|
UTSW |
10 |
92,792,806 (GRCm39) |
missense |
unknown |
|
R7679:Cfap54
|
UTSW |
10 |
92,803,374 (GRCm39) |
missense |
probably benign |
0.01 |
R7776:Cfap54
|
UTSW |
10 |
92,704,603 (GRCm39) |
missense |
unknown |
|
R7844:Cfap54
|
UTSW |
10 |
92,737,920 (GRCm39) |
missense |
unknown |
|
R7980:Cfap54
|
UTSW |
10 |
92,817,922 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7988:Cfap54
|
UTSW |
10 |
92,737,941 (GRCm39) |
missense |
unknown |
|
R8101:Cfap54
|
UTSW |
10 |
92,720,658 (GRCm39) |
missense |
unknown |
|
R8119:Cfap54
|
UTSW |
10 |
92,704,672 (GRCm39) |
missense |
unknown |
|
R8134:Cfap54
|
UTSW |
10 |
92,714,378 (GRCm39) |
missense |
unknown |
|
R8168:Cfap54
|
UTSW |
10 |
92,744,739 (GRCm39) |
missense |
unknown |
|
R8179:Cfap54
|
UTSW |
10 |
92,833,178 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8392:Cfap54
|
UTSW |
10 |
92,798,279 (GRCm39) |
missense |
unknown |
|
R8436:Cfap54
|
UTSW |
10 |
92,800,398 (GRCm39) |
missense |
unknown |
|
R8505:Cfap54
|
UTSW |
10 |
92,814,855 (GRCm39) |
missense |
probably benign |
0.03 |
R8671:Cfap54
|
UTSW |
10 |
92,790,934 (GRCm39) |
missense |
unknown |
|
R8716:Cfap54
|
UTSW |
10 |
92,800,494 (GRCm39) |
missense |
probably benign |
0.00 |
R8816:Cfap54
|
UTSW |
10 |
92,714,454 (GRCm39) |
missense |
unknown |
|
R8822:Cfap54
|
UTSW |
10 |
92,875,003 (GRCm39) |
missense |
probably benign |
0.09 |
R8827:Cfap54
|
UTSW |
10 |
92,774,110 (GRCm39) |
missense |
unknown |
|
R8920:Cfap54
|
UTSW |
10 |
92,776,199 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8924:Cfap54
|
UTSW |
10 |
92,837,685 (GRCm39) |
missense |
probably damaging |
0.99 |
R8954:Cfap54
|
UTSW |
10 |
92,879,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Cfap54
|
UTSW |
10 |
92,864,562 (GRCm39) |
nonsense |
probably null |
|
R9010:Cfap54
|
UTSW |
10 |
92,734,921 (GRCm39) |
missense |
unknown |
|
R9017:Cfap54
|
UTSW |
10 |
92,651,883 (GRCm39) |
missense |
probably benign |
0.07 |
R9093:Cfap54
|
UTSW |
10 |
92,651,770 (GRCm39) |
missense |
probably benign |
0.03 |
R9095:Cfap54
|
UTSW |
10 |
92,846,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9142:Cfap54
|
UTSW |
10 |
92,820,097 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9178:Cfap54
|
UTSW |
10 |
92,830,579 (GRCm39) |
missense |
probably benign |
0.10 |
R9196:Cfap54
|
UTSW |
10 |
92,873,753 (GRCm39) |
missense |
probably benign |
0.22 |
R9203:Cfap54
|
UTSW |
10 |
92,880,990 (GRCm39) |
missense |
probably benign |
0.30 |
R9258:Cfap54
|
UTSW |
10 |
92,770,960 (GRCm39) |
missense |
unknown |
|
R9275:Cfap54
|
UTSW |
10 |
92,875,048 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9287:Cfap54
|
UTSW |
10 |
92,805,565 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9289:Cfap54
|
UTSW |
10 |
92,656,936 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9310:Cfap54
|
UTSW |
10 |
92,798,177 (GRCm39) |
missense |
unknown |
|
R9397:Cfap54
|
UTSW |
10 |
92,833,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R9462:Cfap54
|
UTSW |
10 |
92,737,920 (GRCm39) |
missense |
unknown |
|
R9697:Cfap54
|
UTSW |
10 |
92,792,851 (GRCm39) |
missense |
unknown |
|
R9746:Cfap54
|
UTSW |
10 |
92,637,081 (GRCm39) |
missense |
probably benign |
0.03 |
R9755:Cfap54
|
UTSW |
10 |
92,757,230 (GRCm39) |
missense |
unknown |
|
X0022:Cfap54
|
UTSW |
10 |
92,768,476 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Cfap54
|
UTSW |
10 |
92,714,465 (GRCm39) |
missense |
unknown |
|
X0027:Cfap54
|
UTSW |
10 |
92,837,750 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0027:Cfap54
|
UTSW |
10 |
92,714,400 (GRCm39) |
missense |
unknown |
|
Z1177:Cfap54
|
UTSW |
10 |
92,814,888 (GRCm39) |
missense |
probably damaging |
1.00 |
|