Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
C |
A |
10: 76,293,899 (GRCm39) |
F252L |
possibly damaging |
Het |
4930447A16Rik |
T |
G |
15: 37,440,742 (GRCm39) |
|
probably benign |
Het |
Abca14 |
A |
T |
7: 119,815,408 (GRCm39) |
M219L |
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,498,159 (GRCm39) |
T918A |
probably damaging |
Het |
Acss3 |
C |
T |
10: 106,772,068 (GRCm39) |
S669N |
probably benign |
Het |
Adamts16 |
G |
A |
13: 70,927,637 (GRCm39) |
|
probably benign |
Het |
Adamtsl4 |
A |
G |
3: 95,588,412 (GRCm39) |
Y559H |
probably damaging |
Het |
Adgrg5 |
T |
A |
8: 95,661,108 (GRCm39) |
M106K |
probably damaging |
Het |
Akt1 |
T |
C |
12: 112,626,059 (GRCm39) |
N71S |
probably damaging |
Het |
Amer2 |
A |
C |
14: 60,615,894 (GRCm39) |
K30Q |
probably damaging |
Het |
Anapc5 |
T |
C |
5: 122,938,587 (GRCm39) |
K383E |
probably damaging |
Het |
Ano1 |
A |
G |
7: 144,207,987 (GRCm39) |
L258P |
probably damaging |
Het |
Arb2a |
A |
G |
13: 78,147,756 (GRCm39) |
T321A |
possibly damaging |
Het |
Arhgef10l |
A |
G |
4: 140,271,695 (GRCm39) |
S560P |
probably damaging |
Het |
Arhgef40 |
T |
A |
14: 52,241,162 (GRCm39) |
L1395Q |
probably damaging |
Het |
Arid1a |
A |
T |
4: 133,409,145 (GRCm39) |
D1787E |
unknown |
Het |
Ces2h |
T |
C |
8: 105,745,030 (GRCm39) |
L388P |
probably damaging |
Het |
Cryz |
T |
C |
3: 154,327,320 (GRCm39) |
V116A |
probably damaging |
Het |
Csrp1 |
G |
A |
1: 135,678,366 (GRCm39) |
A159T |
probably damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,434,517 (GRCm39) |
F447S |
probably damaging |
Het |
Cyp4a12a |
A |
T |
4: 115,184,702 (GRCm39) |
I328F |
probably damaging |
Het |
Cyth4 |
T |
G |
15: 78,492,371 (GRCm39) |
H133Q |
probably damaging |
Het |
Ddah2 |
A |
G |
17: 35,279,402 (GRCm39) |
I88V |
possibly damaging |
Het |
Dmbt1 |
T |
G |
7: 130,712,718 (GRCm39) |
I1563S |
possibly damaging |
Het |
Dnajc22 |
T |
C |
15: 98,999,114 (GRCm39) |
S100P |
probably benign |
Het |
Fancl |
T |
A |
11: 26,372,459 (GRCm39) |
D123E |
probably damaging |
Het |
Fbxo30 |
A |
G |
10: 11,166,772 (GRCm39) |
Q498R |
probably damaging |
Het |
Fgd4 |
T |
C |
16: 16,253,824 (GRCm39) |
H581R |
probably benign |
Het |
Gm2663 |
T |
C |
6: 40,974,900 (GRCm39) |
Q57R |
probably benign |
Het |
Gm7247 |
A |
T |
14: 51,602,804 (GRCm39) |
M47L |
possibly damaging |
Het |
Gsdmc2 |
T |
A |
15: 63,699,975 (GRCm39) |
|
probably null |
Het |
Hc |
A |
C |
2: 34,903,540 (GRCm39) |
F1038C |
probably damaging |
Het |
Heatr1 |
C |
A |
13: 12,429,359 (GRCm39) |
Q890K |
possibly damaging |
Het |
Hipk4 |
C |
A |
7: 27,228,429 (GRCm39) |
T293K |
probably damaging |
Het |
Hp1bp3 |
C |
A |
4: 137,948,943 (GRCm39) |
A2E |
probably damaging |
Het |
Il6 |
T |
C |
5: 30,219,945 (GRCm39) |
|
probably null |
Het |
Itga6 |
A |
G |
2: 71,648,828 (GRCm39) |
D104G |
probably benign |
Het |
Krt24 |
A |
G |
11: 99,173,277 (GRCm39) |
S293P |
probably damaging |
Het |
Krt4 |
C |
T |
15: 101,829,086 (GRCm39) |
R309Q |
probably damaging |
Het |
Krt40 |
A |
T |
11: 99,430,913 (GRCm39) |
W199R |
probably damaging |
Het |
Lamc1 |
T |
C |
1: 153,118,378 (GRCm39) |
E931G |
probably benign |
Het |
Lamp3 |
A |
T |
16: 19,519,961 (GRCm39) |
M74K |
probably benign |
Het |
Lgalsl2 |
A |
G |
7: 5,362,573 (GRCm39) |
D68G |
probably benign |
Het |
Magel2 |
G |
A |
7: 62,028,844 (GRCm39) |
V583I |
unknown |
Het |
Marchf7 |
T |
A |
2: 60,059,384 (GRCm39) |
Y37* |
probably null |
Het |
Mrpl36 |
A |
G |
13: 73,479,687 (GRCm39) |
K66E |
probably damaging |
Het |
Mrps35 |
G |
T |
6: 146,962,982 (GRCm39) |
E229* |
probably null |
Het |
Mtmr6 |
T |
C |
14: 60,536,441 (GRCm39) |
M557T |
probably benign |
Het |
Myocd |
A |
T |
11: 65,077,854 (GRCm39) |
I647N |
probably damaging |
Het |
Myom2 |
A |
C |
8: 15,181,151 (GRCm39) |
L1350F |
probably damaging |
Het |
Nhsl3 |
A |
G |
4: 129,116,148 (GRCm39) |
S884P |
probably damaging |
Het |
Nosip |
T |
A |
7: 44,726,033 (GRCm39) |
S197T |
probably benign |
Het |
Npat |
A |
G |
9: 53,473,791 (GRCm39) |
K528E |
probably benign |
Het |
Nyap2 |
A |
G |
1: 81,169,587 (GRCm39) |
T115A |
probably benign |
Het |
Obi1 |
T |
A |
14: 104,759,978 (GRCm39) |
K24M |
probably damaging |
Het |
Or10al6 |
A |
G |
17: 38,083,467 (GRCm39) |
R317G |
probably benign |
Het |
Or4a72 |
A |
G |
2: 89,405,737 (GRCm39) |
V111A |
probably damaging |
Het |
Or4c109 |
G |
T |
2: 88,818,489 (GRCm39) |
P19Q |
probably benign |
Het |
Or51b6 |
T |
A |
7: 103,556,249 (GRCm39) |
V201D |
possibly damaging |
Het |
Or5m3 |
A |
T |
2: 85,838,567 (GRCm39) |
Y149F |
probably damaging |
Het |
Or8g55 |
A |
G |
9: 39,785,354 (GRCm39) |
Q261R |
probably benign |
Het |
Orc1 |
T |
C |
4: 108,447,897 (GRCm39) |
V48A |
possibly damaging |
Het |
Pde6d |
T |
C |
1: 86,474,438 (GRCm39) |
E69G |
probably damaging |
Het |
Pdgfrb |
A |
T |
18: 61,216,406 (GRCm39) |
D1088V |
possibly damaging |
Het |
Peg12 |
A |
G |
7: 62,113,386 (GRCm39) |
V237A |
probably benign |
Het |
Phf8-ps |
T |
C |
17: 33,285,941 (GRCm39) |
N287S |
probably benign |
Het |
Piezo1 |
A |
G |
8: 123,209,451 (GRCm39) |
F2371L |
probably benign |
Het |
Podn |
T |
A |
4: 107,880,570 (GRCm39) |
S27C |
probably damaging |
Het |
Pom121l2 |
A |
G |
13: 22,166,904 (GRCm39) |
M392V |
possibly damaging |
Het |
Ppm1b |
A |
G |
17: 85,301,630 (GRCm39) |
K170R |
probably damaging |
Het |
Rab18 |
A |
T |
18: 6,770,113 (GRCm39) |
|
probably null |
Het |
Raet1d |
G |
A |
10: 22,246,911 (GRCm39) |
A80T |
probably damaging |
Het |
Rfx7 |
T |
A |
9: 72,524,967 (GRCm39) |
V719E |
probably benign |
Het |
Ror1 |
C |
T |
4: 100,265,038 (GRCm39) |
Q171* |
probably null |
Het |
Rufy4 |
G |
A |
1: 74,180,106 (GRCm39) |
V454M |
possibly damaging |
Het |
Ryr2 |
C |
T |
13: 11,866,074 (GRCm39) |
G292D |
possibly damaging |
Het |
Ryr3 |
G |
T |
2: 112,611,410 (GRCm39) |
N2257K |
probably benign |
Het |
Saal1 |
A |
G |
7: 46,348,913 (GRCm39) |
F306S |
possibly damaging |
Het |
Sap18 |
A |
G |
14: 58,036,021 (GRCm39) |
N69S |
probably damaging |
Het |
Sar1b |
A |
T |
11: 51,670,514 (GRCm39) |
|
probably null |
Het |
Serpina3n |
G |
T |
12: 104,375,473 (GRCm39) |
V182L |
probably damaging |
Het |
Setd3 |
A |
T |
12: 108,084,513 (GRCm39) |
H279Q |
probably damaging |
Het |
Slc18a2 |
C |
A |
19: 59,264,937 (GRCm39) |
A307E |
possibly damaging |
Het |
Slc4a10 |
A |
T |
2: 62,064,725 (GRCm39) |
D193V |
probably damaging |
Het |
Spire2 |
T |
C |
8: 124,059,657 (GRCm39) |
C52R |
probably damaging |
Het |
Syne2 |
A |
T |
12: 76,121,353 (GRCm39) |
I5940F |
probably damaging |
Het |
Sytl1 |
C |
T |
4: 132,983,471 (GRCm39) |
S355N |
probably damaging |
Het |
Tarbp1 |
C |
T |
8: 127,154,853 (GRCm39) |
V1424I |
probably damaging |
Het |
Tatdn3 |
A |
T |
1: 190,781,477 (GRCm39) |
|
probably null |
Het |
Tbpl1 |
T |
A |
10: 22,583,576 (GRCm39) |
E131D |
probably damaging |
Het |
Telo2 |
A |
T |
17: 25,324,382 (GRCm39) |
M501K |
probably damaging |
Het |
Terb1 |
A |
G |
8: 105,179,331 (GRCm39) |
V619A |
probably benign |
Het |
Tmem132e |
A |
G |
11: 82,335,989 (GRCm39) |
T1024A |
probably benign |
Het |
Tmem30a |
T |
C |
9: 79,681,500 (GRCm39) |
D223G |
probably damaging |
Het |
Tmprss11d |
A |
G |
5: 86,487,413 (GRCm39) |
V19A |
probably damaging |
Het |
Tnks |
A |
T |
8: 35,318,260 (GRCm39) |
S872T |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,890,724 (GRCm39) |
S356G |
probably benign |
Het |
Tob2 |
T |
C |
15: 81,735,400 (GRCm39) |
K190E |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,049,433 (GRCm39) |
V1240A |
possibly damaging |
Het |
Trim13 |
T |
A |
14: 61,842,335 (GRCm39) |
C117* |
probably null |
Het |
Trpv4 |
G |
A |
5: 114,772,666 (GRCm39) |
R308C |
probably damaging |
Het |
Ttn |
C |
G |
2: 76,585,676 (GRCm39) |
D21987H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,656,418 (GRCm39) |
|
probably null |
Het |
Upp1 |
A |
T |
11: 9,083,240 (GRCm39) |
M111L |
possibly damaging |
Het |
Vmn1r206 |
A |
T |
13: 22,804,358 (GRCm39) |
V283E |
probably damaging |
Het |
Vmn2r79 |
G |
T |
7: 86,651,634 (GRCm39) |
L344F |
probably benign |
Het |
Vmn2r93 |
T |
G |
17: 18,546,324 (GRCm39) |
I732S |
probably damaging |
Het |
Vmn2r96 |
G |
T |
17: 18,804,263 (GRCm39) |
M504I |
probably benign |
Het |
Vps39 |
T |
C |
2: 120,173,708 (GRCm39) |
Y147C |
probably damaging |
Het |
Zbtb20 |
T |
A |
16: 43,398,015 (GRCm39) |
C35S |
possibly damaging |
Het |
Zfp871 |
A |
T |
17: 32,993,751 (GRCm39) |
C475S |
probably damaging |
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 |
|
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 |
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 |
|