Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730061H03Rik |
C |
T |
14: 55,797,574 (GRCm39) |
|
probably benign |
Het |
Acsf2 |
A |
C |
11: 94,460,155 (GRCm39) |
M399R |
possibly damaging |
Het |
Adra2c |
C |
A |
5: 35,438,268 (GRCm39) |
R347S |
probably benign |
Het |
Akap9 |
A |
G |
5: 4,011,466 (GRCm39) |
K723R |
possibly damaging |
Het |
Anxa9 |
A |
C |
3: 95,215,324 (GRCm39) |
|
probably benign |
Het |
Aqr |
T |
C |
2: 113,943,832 (GRCm39) |
H1102R |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,808,726 (GRCm39) |
F655Y |
probably damaging |
Het |
Arrdc2 |
A |
G |
8: 71,290,162 (GRCm39) |
V173A |
probably benign |
Het |
Aspm |
T |
C |
1: 139,405,748 (GRCm39) |
V1545A |
probably benign |
Het |
Bbs5 |
C |
T |
2: 69,477,578 (GRCm39) |
|
probably benign |
Het |
Bnip2 |
A |
G |
9: 69,910,716 (GRCm39) |
T255A |
possibly damaging |
Het |
Cacna1b |
T |
C |
2: 24,538,535 (GRCm39) |
T1531A |
probably damaging |
Het |
Cast |
T |
C |
13: 74,955,942 (GRCm39) |
K9R |
probably benign |
Het |
Cfap57 |
G |
T |
4: 118,450,251 (GRCm39) |
L624M |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,552,323 (GRCm39) |
M339L |
probably benign |
Het |
Dcst1 |
T |
A |
3: 89,265,110 (GRCm39) |
T247S |
probably benign |
Het |
Dnajc18 |
T |
A |
18: 35,816,372 (GRCm39) |
I189F |
possibly damaging |
Het |
Eef2kmt |
T |
C |
16: 5,066,876 (GRCm39) |
T126A |
probably benign |
Het |
Epha2 |
A |
G |
4: 141,049,016 (GRCm39) |
E624G |
probably damaging |
Het |
Erbb3 |
G |
A |
10: 128,408,317 (GRCm39) |
H866Y |
probably benign |
Het |
F13a1 |
C |
T |
13: 37,100,837 (GRCm39) |
|
probably null |
Het |
Fgd3 |
T |
A |
13: 49,432,078 (GRCm39) |
N392I |
probably damaging |
Het |
Fgf7 |
A |
T |
2: 125,930,160 (GRCm39) |
M98L |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,415,922 (GRCm39) |
S553T |
probably benign |
Het |
Glipr1 |
C |
A |
10: 111,829,411 (GRCm39) |
E117* |
probably null |
Het |
Gm11060 |
A |
T |
2: 104,924,128 (GRCm39) |
|
probably benign |
Het |
Gm4787 |
A |
G |
12: 81,424,403 (GRCm39) |
I585T |
probably damaging |
Het |
Gm6055 |
A |
T |
14: 48,316,915 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gpt2 |
T |
A |
8: 86,246,068 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,386,685 (GRCm39) |
Y345* |
probably null |
Het |
Hmcn1 |
T |
A |
1: 150,695,200 (GRCm39) |
T235S |
probably benign |
Het |
Igkv5-48 |
A |
G |
6: 69,703,738 (GRCm39) |
Y56H |
possibly damaging |
Het |
Il17re |
C |
T |
6: 113,446,530 (GRCm39) |
T427I |
probably benign |
Het |
Itpr3 |
A |
T |
17: 27,302,582 (GRCm39) |
D80V |
probably damaging |
Het |
Kif21a |
G |
T |
15: 90,833,213 (GRCm39) |
H1317N |
probably benign |
Het |
Kif28 |
T |
C |
1: 179,526,209 (GRCm39) |
K144E |
probably damaging |
Het |
Kif4-ps |
A |
C |
12: 101,113,330 (GRCm39) |
|
noncoding transcript |
Het |
Klk1b11 |
C |
T |
7: 43,427,160 (GRCm39) |
T148I |
probably damaging |
Het |
Klkb1 |
T |
A |
8: 45,739,995 (GRCm39) |
H99L |
probably damaging |
Het |
Kpna6 |
A |
C |
4: 129,550,198 (GRCm39) |
|
probably null |
Het |
Lama3 |
G |
T |
18: 12,685,883 (GRCm39) |
K1132N |
probably damaging |
Het |
Lcp1 |
T |
A |
14: 75,445,911 (GRCm39) |
L264* |
probably null |
Het |
Map2 |
T |
C |
1: 66,452,664 (GRCm39) |
V360A |
probably benign |
Het |
Med13 |
A |
T |
11: 86,189,673 (GRCm39) |
S1079T |
probably damaging |
Het |
Mettl13 |
A |
G |
1: 162,364,789 (GRCm39) |
M162T |
probably damaging |
Het |
Mppe1 |
T |
G |
18: 67,361,133 (GRCm39) |
E208A |
probably benign |
Het |
Msantd2 |
A |
C |
9: 37,400,675 (GRCm39) |
K19T |
possibly damaging |
Het |
Mylk3 |
A |
G |
8: 86,091,412 (GRCm39) |
V131A |
probably damaging |
Het |
Myocd |
A |
T |
11: 65,074,299 (GRCm39) |
S609T |
possibly damaging |
Het |
Ncbp3 |
G |
A |
11: 72,944,355 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,136,871 (GRCm39) |
L3203F |
probably damaging |
Het |
Notch2 |
C |
A |
3: 98,046,949 (GRCm39) |
T1756K |
probably benign |
Het |
Nphp4 |
A |
T |
4: 152,622,250 (GRCm39) |
R544W |
probably damaging |
Het |
Or3a1c |
A |
T |
11: 74,046,745 (GRCm39) |
Y255F |
probably benign |
Het |
Or4p18 |
T |
G |
2: 88,232,756 (GRCm39) |
H174P |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,222,578 (GRCm39) |
D273V |
probably damaging |
Het |
Parp4 |
T |
A |
14: 56,827,355 (GRCm39) |
V163E |
possibly damaging |
Het |
Pcdhgb1 |
C |
A |
18: 37,815,425 (GRCm39) |
Q639K |
probably benign |
Het |
Pcnx2 |
A |
G |
8: 126,577,869 (GRCm39) |
V936A |
probably benign |
Het |
Pcsk7 |
T |
A |
9: 45,830,160 (GRCm39) |
M418K |
probably damaging |
Het |
Pglyrp4 |
T |
C |
3: 90,640,314 (GRCm39) |
I188T |
probably benign |
Het |
Pgs1 |
A |
G |
11: 117,896,345 (GRCm39) |
R339G |
probably benign |
Het |
Pik3r3 |
A |
G |
4: 116,143,388 (GRCm39) |
I294V |
probably benign |
Het |
Pik3r6 |
A |
G |
11: 68,430,771 (GRCm39) |
D520G |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,704,610 (GRCm39) |
V442A |
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,931,917 (GRCm39) |
|
probably benign |
Het |
Ppp3ca |
C |
A |
3: 136,640,810 (GRCm39) |
Q454K |
possibly damaging |
Het |
Ppp5c |
A |
T |
7: 16,743,861 (GRCm39) |
M191K |
probably damaging |
Het |
Prl4a1 |
A |
T |
13: 28,207,308 (GRCm39) |
Y194F |
possibly damaging |
Het |
Ptpn21 |
G |
T |
12: 98,646,362 (GRCm39) |
T1032K |
probably damaging |
Het |
Ptprh |
A |
T |
7: 4,554,006 (GRCm39) |
|
probably null |
Het |
Ptprm |
T |
A |
17: 66,985,062 (GRCm39) |
R1447S |
probably benign |
Het |
Pxk |
T |
A |
14: 8,140,734 (GRCm38) |
D236E |
probably damaging |
Het |
Qars1 |
T |
C |
9: 108,386,130 (GRCm39) |
F107S |
probably damaging |
Het |
Rbbp6 |
A |
G |
7: 122,599,031 (GRCm39) |
|
probably benign |
Het |
Rptor |
A |
T |
11: 119,712,466 (GRCm39) |
|
probably benign |
Het |
Rtn4 |
T |
A |
11: 29,690,994 (GRCm39) |
M1095K |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,445 (GRCm39) |
H273L |
probably benign |
Het |
Sgce |
G |
A |
6: 4,689,630 (GRCm39) |
T401M |
probably benign |
Het |
Slc12a6 |
C |
T |
2: 112,188,870 (GRCm39) |
R1083W |
probably damaging |
Het |
Slc45a4 |
A |
T |
15: 73,456,299 (GRCm39) |
M635K |
probably damaging |
Het |
Slc6a1 |
T |
A |
6: 114,284,662 (GRCm39) |
V240D |
probably damaging |
Het |
Snx9 |
G |
A |
17: 5,952,794 (GRCm39) |
|
probably null |
Het |
Spred3 |
A |
G |
7: 28,867,249 (GRCm39) |
V49A |
probably damaging |
Het |
Tars1 |
A |
G |
15: 11,390,477 (GRCm39) |
F334S |
probably damaging |
Het |
Tdpoz1 |
A |
G |
3: 93,578,454 (GRCm39) |
V110A |
probably benign |
Het |
Tfrc |
T |
G |
16: 32,437,097 (GRCm39) |
V252G |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,528,128 (GRCm39) |
|
probably benign |
Het |
Txlnb |
T |
C |
10: 17,714,717 (GRCm39) |
V383A |
probably damaging |
Het |
Utp20 |
C |
A |
10: 88,652,811 (GRCm39) |
V368L |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,239,372 (GRCm39) |
V397E |
probably damaging |
Het |
Zdhhc12 |
G |
A |
2: 29,981,538 (GRCm39) |
R175W |
probably damaging |
Het |
Zfyve9 |
A |
G |
4: 108,538,097 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cfap46 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00480:Cfap46
|
APN |
7 |
139,240,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00493:Cfap46
|
APN |
7 |
139,194,359 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00505:Cfap46
|
APN |
7 |
139,240,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00508:Cfap46
|
APN |
7 |
139,240,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00514:Cfap46
|
APN |
7 |
139,240,605 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01394:Cfap46
|
APN |
7 |
139,246,895 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01621:Cfap46
|
APN |
7 |
139,186,523 (GRCm39) |
missense |
unknown |
|
IGL02171:Cfap46
|
APN |
7 |
139,246,972 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02343:Cfap46
|
APN |
7 |
139,262,425 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02679:Cfap46
|
APN |
7 |
139,194,386 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02687:Cfap46
|
APN |
7 |
139,187,117 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03180:Cfap46
|
APN |
7 |
139,183,168 (GRCm39) |
missense |
unknown |
|
IGL03329:Cfap46
|
APN |
7 |
139,181,081 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4449:Cfap46
|
UTSW |
7 |
139,218,711 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4737:Cfap46
|
UTSW |
7 |
139,218,846 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cfap46
|
UTSW |
7 |
139,218,846 (GRCm39) |
utr 3 prime |
probably benign |
|
PIT4651001:Cfap46
|
UTSW |
7 |
139,225,467 (GRCm39) |
missense |
|
|
R0051:Cfap46
|
UTSW |
7 |
139,255,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0051:Cfap46
|
UTSW |
7 |
139,255,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R0318:Cfap46
|
UTSW |
7 |
139,234,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R0358:Cfap46
|
UTSW |
7 |
139,231,449 (GRCm39) |
splice site |
probably benign |
|
R0650:Cfap46
|
UTSW |
7 |
139,185,571 (GRCm39) |
missense |
unknown |
|
R0675:Cfap46
|
UTSW |
7 |
139,255,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R0750:Cfap46
|
UTSW |
7 |
139,234,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R0931:Cfap46
|
UTSW |
7 |
139,235,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Cfap46
|
UTSW |
7 |
139,222,513 (GRCm39) |
missense |
probably benign |
0.42 |
R1251:Cfap46
|
UTSW |
7 |
139,181,181 (GRCm39) |
missense |
probably benign |
0.40 |
R1257:Cfap46
|
UTSW |
7 |
139,234,545 (GRCm39) |
nonsense |
probably null |
|
R1538:Cfap46
|
UTSW |
7 |
139,262,924 (GRCm39) |
missense |
probably null |
1.00 |
R1618:Cfap46
|
UTSW |
7 |
139,232,726 (GRCm39) |
missense |
probably benign |
0.04 |
R1655:Cfap46
|
UTSW |
7 |
139,222,436 (GRCm39) |
nonsense |
probably null |
|
R1824:Cfap46
|
UTSW |
7 |
139,219,518 (GRCm39) |
missense |
probably benign |
0.12 |
R1830:Cfap46
|
UTSW |
7 |
139,220,323 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1857:Cfap46
|
UTSW |
7 |
139,233,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1870:Cfap46
|
UTSW |
7 |
139,263,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Cfap46
|
UTSW |
7 |
139,259,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Cfap46
|
UTSW |
7 |
139,246,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Cfap46
|
UTSW |
7 |
139,263,677 (GRCm39) |
missense |
probably benign |
0.03 |
R2354:Cfap46
|
UTSW |
7 |
139,240,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R2367:Cfap46
|
UTSW |
7 |
139,233,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R3237:Cfap46
|
UTSW |
7 |
139,197,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R3617:Cfap46
|
UTSW |
7 |
139,219,515 (GRCm39) |
missense |
probably benign |
0.06 |
R3949:Cfap46
|
UTSW |
7 |
139,258,467 (GRCm39) |
missense |
probably benign |
0.12 |
R4239:Cfap46
|
UTSW |
7 |
139,246,203 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4240:Cfap46
|
UTSW |
7 |
139,246,203 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4297:Cfap46
|
UTSW |
7 |
139,232,589 (GRCm39) |
missense |
probably benign |
0.27 |
R4365:Cfap46
|
UTSW |
7 |
139,230,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R4516:Cfap46
|
UTSW |
7 |
139,239,998 (GRCm39) |
intron |
probably benign |
|
R4595:Cfap46
|
UTSW |
7 |
139,232,320 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4627:Cfap46
|
UTSW |
7 |
139,260,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Cfap46
|
UTSW |
7 |
139,237,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R4628:Cfap46
|
UTSW |
7 |
139,260,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Cfap46
|
UTSW |
7 |
139,260,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Cfap46
|
UTSW |
7 |
139,207,372 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4750:Cfap46
|
UTSW |
7 |
139,259,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4771:Cfap46
|
UTSW |
7 |
139,210,524 (GRCm39) |
missense |
probably null |
|
R4779:Cfap46
|
UTSW |
7 |
139,239,731 (GRCm39) |
intron |
probably benign |
|
R4812:Cfap46
|
UTSW |
7 |
139,215,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Cfap46
|
UTSW |
7 |
139,207,291 (GRCm39) |
missense |
probably benign |
0.12 |
R5033:Cfap46
|
UTSW |
7 |
139,183,776 (GRCm39) |
missense |
probably benign |
0.00 |
R5055:Cfap46
|
UTSW |
7 |
139,241,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R5254:Cfap46
|
UTSW |
7 |
139,258,430 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5288:Cfap46
|
UTSW |
7 |
139,193,423 (GRCm39) |
critical splice donor site |
probably null |
|
R5366:Cfap46
|
UTSW |
7 |
139,230,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Cfap46
|
UTSW |
7 |
139,207,389 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5371:Cfap46
|
UTSW |
7 |
139,212,097 (GRCm39) |
splice site |
probably null |
|
R5642:Cfap46
|
UTSW |
7 |
139,258,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R5690:Cfap46
|
UTSW |
7 |
139,218,269 (GRCm39) |
missense |
probably benign |
0.01 |
R5691:Cfap46
|
UTSW |
7 |
139,186,616 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5696:Cfap46
|
UTSW |
7 |
139,191,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R5844:Cfap46
|
UTSW |
7 |
139,230,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:Cfap46
|
UTSW |
7 |
139,231,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R6217:Cfap46
|
UTSW |
7 |
139,218,816 (GRCm39) |
utr 3 prime |
probably benign |
|
R6228:Cfap46
|
UTSW |
7 |
139,236,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Cfap46
|
UTSW |
7 |
139,218,816 (GRCm39) |
utr 3 prime |
probably benign |
|
R6253:Cfap46
|
UTSW |
7 |
139,218,816 (GRCm39) |
utr 3 prime |
probably benign |
|
R6285:Cfap46
|
UTSW |
7 |
139,241,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R6334:Cfap46
|
UTSW |
7 |
139,260,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Cfap46
|
UTSW |
7 |
139,194,321 (GRCm39) |
critical splice donor site |
probably null |
|
R6736:Cfap46
|
UTSW |
7 |
139,199,887 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6760:Cfap46
|
UTSW |
7 |
139,232,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R6773:Cfap46
|
UTSW |
7 |
139,222,477 (GRCm39) |
utr 3 prime |
probably benign |
|
R6835:Cfap46
|
UTSW |
7 |
139,232,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R6903:Cfap46
|
UTSW |
7 |
139,234,477 (GRCm39) |
critical splice donor site |
probably null |
|
R6912:Cfap46
|
UTSW |
7 |
139,219,616 (GRCm39) |
missense |
probably benign |
0.09 |
R7163:Cfap46
|
UTSW |
7 |
139,197,994 (GRCm39) |
critical splice donor site |
probably null |
|
R7232:Cfap46
|
UTSW |
7 |
139,197,493 (GRCm39) |
missense |
unknown |
|
R7327:Cfap46
|
UTSW |
7 |
139,215,062 (GRCm39) |
splice site |
probably null |
|
R7336:Cfap46
|
UTSW |
7 |
139,200,020 (GRCm39) |
missense |
unknown |
|
R7337:Cfap46
|
UTSW |
7 |
139,210,492 (GRCm39) |
critical splice donor site |
probably null |
|
R7437:Cfap46
|
UTSW |
7 |
139,230,753 (GRCm39) |
nonsense |
probably null |
|
R7450:Cfap46
|
UTSW |
7 |
139,197,353 (GRCm39) |
missense |
unknown |
|
R7495:Cfap46
|
UTSW |
7 |
139,183,112 (GRCm39) |
critical splice donor site |
probably null |
|
R7618:Cfap46
|
UTSW |
7 |
139,183,155 (GRCm39) |
missense |
|
|
R7623:Cfap46
|
UTSW |
7 |
139,198,266 (GRCm39) |
missense |
unknown |
|
R7765:Cfap46
|
UTSW |
7 |
139,231,480 (GRCm39) |
missense |
|
|
R7971:Cfap46
|
UTSW |
7 |
139,215,043 (GRCm39) |
missense |
unknown |
|
R8211:Cfap46
|
UTSW |
7 |
139,213,220 (GRCm39) |
missense |
unknown |
|
R8306:Cfap46
|
UTSW |
7 |
139,236,496 (GRCm39) |
missense |
|
|
R8354:Cfap46
|
UTSW |
7 |
139,233,414 (GRCm39) |
missense |
probably benign |
0.03 |
R8365:Cfap46
|
UTSW |
7 |
139,263,000 (GRCm39) |
nonsense |
probably null |
|
R8447:Cfap46
|
UTSW |
7 |
139,260,902 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8715:Cfap46
|
UTSW |
7 |
139,185,560 (GRCm39) |
missense |
|
|
R8805:Cfap46
|
UTSW |
7 |
139,211,979 (GRCm39) |
missense |
unknown |
|
R8830:Cfap46
|
UTSW |
7 |
139,195,565 (GRCm39) |
missense |
unknown |
|
R8912:Cfap46
|
UTSW |
7 |
139,260,097 (GRCm39) |
intron |
probably benign |
|
R8920:Cfap46
|
UTSW |
7 |
139,232,442 (GRCm39) |
missense |
|
|
R8977:Cfap46
|
UTSW |
7 |
139,259,849 (GRCm39) |
missense |
probably benign |
0.01 |
R9048:Cfap46
|
UTSW |
7 |
139,207,259 (GRCm39) |
missense |
unknown |
|
R9224:Cfap46
|
UTSW |
7 |
139,258,416 (GRCm39) |
nonsense |
probably null |
|
R9243:Cfap46
|
UTSW |
7 |
139,195,265 (GRCm39) |
intron |
probably benign |
|
R9252:Cfap46
|
UTSW |
7 |
139,198,165 (GRCm39) |
missense |
unknown |
|
R9276:Cfap46
|
UTSW |
7 |
139,201,207 (GRCm39) |
missense |
unknown |
|
R9301:Cfap46
|
UTSW |
7 |
139,222,461 (GRCm39) |
missense |
|
|
R9391:Cfap46
|
UTSW |
7 |
139,198,027 (GRCm39) |
missense |
unknown |
|
R9402:Cfap46
|
UTSW |
7 |
139,215,865 (GRCm39) |
missense |
unknown |
|
R9443:Cfap46
|
UTSW |
7 |
139,195,023 (GRCm39) |
missense |
|
|
R9564:Cfap46
|
UTSW |
7 |
139,231,471 (GRCm39) |
missense |
|
|
R9625:Cfap46
|
UTSW |
7 |
139,230,805 (GRCm39) |
missense |
|
|
R9626:Cfap46
|
UTSW |
7 |
139,230,805 (GRCm39) |
missense |
|
|
R9638:Cfap46
|
UTSW |
7 |
139,209,763 (GRCm39) |
missense |
unknown |
|
R9656:Cfap46
|
UTSW |
7 |
139,235,816 (GRCm39) |
missense |
|
|
R9658:Cfap46
|
UTSW |
7 |
139,246,229 (GRCm39) |
missense |
|
|
R9747:Cfap46
|
UTSW |
7 |
139,191,907 (GRCm39) |
missense |
unknown |
|
RF023:Cfap46
|
UTSW |
7 |
139,218,834 (GRCm39) |
|
|
|
W0251:Cfap46
|
UTSW |
7 |
139,183,862 (GRCm39) |
missense |
probably benign |
0.11 |
X0018:Cfap46
|
UTSW |
7 |
139,260,828 (GRCm39) |
missense |
probably benign |
0.03 |
X0064:Cfap46
|
UTSW |
7 |
139,183,363 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Cfap46
|
UTSW |
7 |
139,214,980 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Cfap46
|
UTSW |
7 |
139,219,464 (GRCm39) |
missense |
|
|
Z1177:Cfap46
|
UTSW |
7 |
139,210,542 (GRCm39) |
missense |
unknown |
|
Z1177:Cfap46
|
UTSW |
7 |
139,181,183 (GRCm39) |
missense |
unknown |
|
|