Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
C |
G |
8: 25,140,893 (GRCm39) |
G286A |
probably damaging |
Het |
Adcy1 |
G |
A |
11: 7,089,142 (GRCm39) |
A519T |
probably benign |
Het |
Anxa2 |
T |
A |
9: 69,371,762 (GRCm39) |
S2T |
possibly damaging |
Het |
Ap3m1 |
G |
A |
14: 21,089,217 (GRCm39) |
S261L |
possibly damaging |
Het |
Baz2b |
A |
T |
2: 59,743,067 (GRCm39) |
|
probably benign |
Het |
Brdt |
T |
A |
5: 107,507,090 (GRCm39) |
S497T |
probably benign |
Het |
Cdh11 |
A |
G |
8: 103,406,404 (GRCm39) |
F23S |
probably benign |
Het |
Cdh16 |
A |
C |
8: 105,344,434 (GRCm39) |
L540R |
probably damaging |
Het |
Ces5a |
A |
T |
8: 94,261,205 (GRCm39) |
L74Q |
probably damaging |
Het |
Cfap69 |
A |
G |
5: 5,654,306 (GRCm39) |
S543P |
probably damaging |
Het |
Cma1 |
T |
A |
14: 56,181,191 (GRCm39) |
R58S |
possibly damaging |
Het |
Csmd3 |
C |
T |
15: 47,701,975 (GRCm39) |
D1599N |
probably damaging |
Het |
Cyld |
A |
G |
8: 89,471,940 (GRCm39) |
K857R |
probably benign |
Het |
Cyp3a16 |
T |
C |
5: 145,388,667 (GRCm39) |
D270G |
probably damaging |
Het |
D1Pas1 |
T |
C |
1: 186,700,286 (GRCm39) |
S72P |
possibly damaging |
Het |
Ddx3y |
T |
C |
Y: 1,266,389 (GRCm39) |
E331G |
probably benign |
Het |
Degs1l |
T |
A |
1: 180,882,496 (GRCm39) |
I86K |
probably benign |
Het |
Dis3l2 |
T |
C |
1: 86,782,189 (GRCm39) |
|
probably benign |
Het |
Dop1a |
G |
T |
9: 86,403,418 (GRCm39) |
W1539C |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,566,323 (GRCm39) |
K917E |
probably benign |
Het |
Ecpas |
G |
A |
4: 58,844,165 (GRCm39) |
R534* |
probably null |
Het |
Efcab3 |
T |
C |
11: 104,990,851 (GRCm39) |
I5462T |
probably damaging |
Het |
Eif1ad15 |
A |
T |
12: 88,288,191 (GRCm39) |
S21T |
unknown |
Het |
Epo |
A |
G |
5: 137,483,447 (GRCm39) |
|
probably benign |
Het |
Figla |
T |
A |
6: 85,997,624 (GRCm39) |
|
probably benign |
Het |
Flvcr1 |
T |
C |
1: 190,753,353 (GRCm39) |
D273G |
probably benign |
Het |
Fryl |
T |
A |
5: 73,179,465 (GRCm39) |
R304* |
probably null |
Het |
Gcm1 |
T |
G |
9: 77,972,326 (GRCm39) |
D422E |
possibly damaging |
Het |
Get3 |
A |
T |
8: 85,746,403 (GRCm39) |
Y148* |
probably null |
Het |
Ggt6 |
A |
G |
11: 72,328,367 (GRCm39) |
D251G |
possibly damaging |
Het |
Git2 |
A |
G |
5: 114,904,511 (GRCm39) |
|
probably null |
Het |
Gm18856 |
A |
T |
13: 14,139,376 (GRCm39) |
|
probably benign |
Het |
Gm20939 |
T |
A |
17: 95,183,252 (GRCm39) |
|
probably benign |
Het |
Gpr176 |
A |
G |
2: 118,109,913 (GRCm39) |
Y449H |
probably benign |
Het |
H2-Eb1 |
A |
G |
17: 34,533,366 (GRCm39) |
E196G |
probably damaging |
Het |
H2-M10.6 |
A |
G |
17: 37,124,799 (GRCm39) |
T239A |
possibly damaging |
Het |
Haus5 |
T |
C |
7: 30,358,825 (GRCm39) |
N237S |
possibly damaging |
Het |
Hectd3 |
T |
C |
4: 116,857,882 (GRCm39) |
M605T |
probably damaging |
Het |
Hps3 |
T |
C |
3: 20,084,691 (GRCm39) |
I166V |
probably benign |
Het |
Ighv5-21 |
A |
T |
12: 114,286,434 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
C |
T |
11: 69,294,418 (GRCm39) |
G1218D |
unknown |
Het |
Klhl30 |
A |
G |
1: 91,285,636 (GRCm39) |
|
probably null |
Het |
Kmt2a |
A |
T |
9: 44,729,747 (GRCm39) |
S3523R |
probably benign |
Het |
Lnpep |
A |
T |
17: 17,788,661 (GRCm39) |
N481K |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 41,231,861 (GRCm39) |
H1203R |
probably benign |
Het |
Lrrc8a |
C |
T |
2: 30,146,661 (GRCm39) |
R492W |
probably damaging |
Het |
Magel2 |
T |
A |
7: 62,030,342 (GRCm39) |
V1082D |
unknown |
Het |
Memo1 |
A |
C |
17: 74,552,049 (GRCm39) |
H82Q |
probably null |
Het |
Myh13 |
A |
T |
11: 67,252,115 (GRCm39) |
T1408S |
probably benign |
Het |
Myh2 |
A |
T |
11: 67,085,451 (GRCm39) |
N1792Y |
possibly damaging |
Het |
Myo1e |
A |
T |
9: 70,275,969 (GRCm39) |
N728I |
possibly damaging |
Het |
Myo1e |
T |
C |
9: 70,285,997 (GRCm39) |
|
probably benign |
Het |
Myo5c |
T |
C |
9: 75,196,337 (GRCm39) |
|
probably benign |
Het |
Or11l3 |
T |
A |
11: 58,516,319 (GRCm39) |
L184F |
probably damaging |
Het |
Or1e19 |
A |
G |
11: 73,316,188 (GRCm39) |
V207A |
probably benign |
Het |
Or2d2b |
T |
C |
7: 106,705,643 (GRCm39) |
I142V |
probably benign |
Het |
Or4c11c |
T |
A |
2: 88,661,749 (GRCm39) |
M96K |
possibly damaging |
Het |
Or51g1 |
T |
A |
7: 102,633,478 (GRCm39) |
T298S |
probably damaging |
Het |
Or52e3 |
T |
C |
7: 102,868,967 (GRCm39) |
F14S |
probably damaging |
Het |
Parp2 |
C |
T |
14: 51,047,543 (GRCm39) |
A18V |
probably benign |
Het |
Peli1 |
T |
A |
11: 21,098,110 (GRCm39) |
C282S |
probably damaging |
Het |
Phf8-ps |
G |
T |
17: 33,286,598 (GRCm39) |
S68* |
probably null |
Het |
Piezo2 |
T |
C |
18: 63,252,006 (GRCm39) |
M404V |
possibly damaging |
Het |
Pkn1 |
T |
A |
8: 84,404,592 (GRCm39) |
Q496L |
possibly damaging |
Het |
Pla2r1 |
A |
T |
2: 60,262,317 (GRCm39) |
F1093L |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 101,022,680 (GRCm39) |
V323A |
probably damaging |
Het |
Pramel16 |
T |
A |
4: 143,676,453 (GRCm39) |
Y217F |
probably benign |
Het |
Prg2 |
C |
T |
2: 84,812,342 (GRCm39) |
|
probably benign |
Het |
Ptprb |
G |
A |
10: 116,182,958 (GRCm39) |
G1545S |
probably benign |
Het |
Rbm19 |
A |
G |
5: 120,258,307 (GRCm39) |
D174G |
possibly damaging |
Het |
Rhbdf2 |
T |
A |
11: 116,491,974 (GRCm39) |
T526S |
probably damaging |
Het |
Rpusd4 |
A |
G |
9: 35,179,310 (GRCm39) |
N42S |
probably benign |
Het |
Ryr3 |
T |
A |
2: 112,477,361 (GRCm39) |
Q4455L |
possibly damaging |
Het |
Sema4a |
G |
T |
3: 88,358,668 (GRCm39) |
H30Q |
probably damaging |
Het |
Skint1 |
G |
A |
4: 111,878,653 (GRCm39) |
|
probably null |
Het |
Slc1a3 |
A |
G |
15: 8,675,153 (GRCm39) |
V284A |
probably benign |
Het |
Slc30a9 |
A |
T |
5: 67,497,318 (GRCm39) |
K288* |
probably null |
Het |
Slc36a1 |
G |
T |
11: 55,119,164 (GRCm39) |
A380S |
probably benign |
Het |
Slc47a1 |
G |
A |
11: 61,268,833 (GRCm39) |
|
probably benign |
Het |
Snx19 |
A |
T |
9: 30,340,296 (GRCm39) |
E478V |
probably benign |
Het |
Spag6 |
T |
C |
2: 18,738,916 (GRCm39) |
|
probably benign |
Het |
Stag1 |
A |
T |
9: 100,668,740 (GRCm39) |
T223S |
probably damaging |
Het |
Terb1 |
A |
T |
8: 105,224,732 (GRCm39) |
|
probably benign |
Het |
Terf1 |
A |
G |
1: 15,876,170 (GRCm39) |
D90G |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 34,061,302 (GRCm39) |
D518G |
probably damaging |
Het |
Tmem174 |
T |
A |
13: 98,773,546 (GRCm39) |
M95L |
possibly damaging |
Het |
Tnnt3 |
GTCCAGGCATCTC |
GTC |
7: 142,066,364 (GRCm39) |
|
probably benign |
Het |
Usp28 |
A |
G |
9: 48,896,803 (GRCm39) |
D8G |
probably benign |
Het |
Vmn2r105 |
T |
C |
17: 20,444,840 (GRCm39) |
T551A |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,595,549 (GRCm39) |
I701V |
probably benign |
Het |
Vmn2r13 |
A |
C |
5: 109,339,943 (GRCm39) |
F11V |
probably benign |
Het |
Vmn2r85 |
G |
C |
10: 130,261,443 (GRCm39) |
S298* |
probably null |
Het |
Wdr6 |
C |
G |
9: 108,452,554 (GRCm39) |
W443S |
probably damaging |
Het |
Wipi1 |
A |
G |
11: 109,474,016 (GRCm39) |
V210A |
probably damaging |
Het |
Zfp317 |
A |
G |
9: 19,556,532 (GRCm39) |
T47A |
probably benign |
Het |
Zfp61 |
T |
C |
7: 23,991,714 (GRCm39) |
T146A |
probably benign |
Het |
Zfp964 |
A |
G |
8: 70,116,567 (GRCm39) |
E389G |
unknown |
Het |
Zfyve16 |
T |
C |
13: 92,640,985 (GRCm39) |
D1253G |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,929,669 (GRCm39) |
K212R |
possibly damaging |
Het |
Zswim7 |
G |
A |
11: 62,158,299 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cfap74 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01607:Cfap74
|
APN |
4 |
155,503,443 (GRCm39) |
missense |
possibly damaging |
0.95 |
paranoid
|
UTSW |
4 |
155,538,481 (GRCm39) |
utr 5 prime |
probably benign |
|
sensibile
|
UTSW |
4 |
155,525,743 (GRCm39) |
missense |
probably null |
0.03 |
touchy
|
UTSW |
4 |
155,547,529 (GRCm39) |
missense |
probably benign |
0.27 |
FR4304:Cfap74
|
UTSW |
4 |
155,500,217 (GRCm39) |
missense |
possibly damaging |
0.93 |
P0007:Cfap74
|
UTSW |
4 |
155,506,685 (GRCm39) |
missense |
possibly damaging |
0.83 |
PIT4434001:Cfap74
|
UTSW |
4 |
155,548,421 (GRCm39) |
missense |
unknown |
|
R0025:Cfap74
|
UTSW |
4 |
155,510,572 (GRCm39) |
missense |
probably benign |
0.22 |
R0034:Cfap74
|
UTSW |
4 |
155,545,344 (GRCm39) |
splice site |
probably benign |
|
R0193:Cfap74
|
UTSW |
4 |
155,510,572 (GRCm39) |
missense |
probably benign |
0.22 |
R0306:Cfap74
|
UTSW |
4 |
155,549,896 (GRCm39) |
unclassified |
probably benign |
|
R0427:Cfap74
|
UTSW |
4 |
155,525,734 (GRCm39) |
missense |
probably benign |
0.02 |
R0905:Cfap74
|
UTSW |
4 |
155,503,153 (GRCm39) |
critical splice donor site |
probably null |
|
R1116:Cfap74
|
UTSW |
4 |
155,518,453 (GRCm39) |
missense |
probably benign |
0.15 |
R1548:Cfap74
|
UTSW |
4 |
155,518,502 (GRCm39) |
missense |
probably benign |
0.45 |
R1950:Cfap74
|
UTSW |
4 |
155,511,887 (GRCm39) |
critical splice donor site |
probably null |
|
R2009:Cfap74
|
UTSW |
4 |
155,504,724 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2135:Cfap74
|
UTSW |
4 |
155,514,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Cfap74
|
UTSW |
4 |
155,514,397 (GRCm39) |
missense |
probably damaging |
0.97 |
R2154:Cfap74
|
UTSW |
4 |
155,513,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2413:Cfap74
|
UTSW |
4 |
155,503,081 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2418:Cfap74
|
UTSW |
4 |
155,540,166 (GRCm39) |
utr 5 prime |
probably benign |
|
R2930:Cfap74
|
UTSW |
4 |
155,522,627 (GRCm39) |
missense |
probably damaging |
0.97 |
R3965:Cfap74
|
UTSW |
4 |
155,531,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R4078:Cfap74
|
UTSW |
4 |
155,540,128 (GRCm39) |
missense |
probably damaging |
0.98 |
R4238:Cfap74
|
UTSW |
4 |
155,547,529 (GRCm39) |
missense |
probably benign |
0.27 |
R4239:Cfap74
|
UTSW |
4 |
155,547,529 (GRCm39) |
missense |
probably benign |
0.27 |
R4240:Cfap74
|
UTSW |
4 |
155,547,529 (GRCm39) |
missense |
probably benign |
0.27 |
R4491:Cfap74
|
UTSW |
4 |
155,513,628 (GRCm39) |
missense |
probably benign |
0.22 |
R4731:Cfap74
|
UTSW |
4 |
155,548,059 (GRCm39) |
intron |
probably benign |
|
R5333:Cfap74
|
UTSW |
4 |
155,521,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R5362:Cfap74
|
UTSW |
4 |
155,522,623 (GRCm39) |
missense |
probably damaging |
0.98 |
R5425:Cfap74
|
UTSW |
4 |
155,540,149 (GRCm39) |
utr 5 prime |
probably benign |
|
R5468:Cfap74
|
UTSW |
4 |
155,510,498 (GRCm39) |
missense |
probably benign |
0.27 |
R5839:Cfap74
|
UTSW |
4 |
155,507,207 (GRCm39) |
critical splice donor site |
probably null |
|
R6010:Cfap74
|
UTSW |
4 |
155,538,495 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6284:Cfap74
|
UTSW |
4 |
155,536,253 (GRCm39) |
missense |
probably damaging |
0.96 |
R6323:Cfap74
|
UTSW |
4 |
155,548,395 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6389:Cfap74
|
UTSW |
4 |
155,507,793 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6513:Cfap74
|
UTSW |
4 |
155,525,743 (GRCm39) |
missense |
probably null |
0.03 |
R6527:Cfap74
|
UTSW |
4 |
155,506,722 (GRCm39) |
splice site |
probably null |
|
R6785:Cfap74
|
UTSW |
4 |
155,538,481 (GRCm39) |
utr 5 prime |
probably benign |
|
R6980:Cfap74
|
UTSW |
4 |
155,550,809 (GRCm39) |
unclassified |
probably benign |
|
R7039:Cfap74
|
UTSW |
4 |
155,538,565 (GRCm39) |
critical splice donor site |
probably null |
|
R7077:Cfap74
|
UTSW |
4 |
155,540,134 (GRCm39) |
missense |
unknown |
|
R7116:Cfap74
|
UTSW |
4 |
155,539,518 (GRCm39) |
missense |
unknown |
|
R7202:Cfap74
|
UTSW |
4 |
155,510,654 (GRCm39) |
splice site |
probably null |
|
R7227:Cfap74
|
UTSW |
4 |
155,545,405 (GRCm39) |
nonsense |
probably null |
|
R7228:Cfap74
|
UTSW |
4 |
155,549,507 (GRCm39) |
missense |
unknown |
|
R7261:Cfap74
|
UTSW |
4 |
155,549,831 (GRCm39) |
missense |
unknown |
|
R7315:Cfap74
|
UTSW |
4 |
155,547,476 (GRCm39) |
missense |
unknown |
|
R7337:Cfap74
|
UTSW |
4 |
155,544,472 (GRCm39) |
missense |
unknown |
|
R7354:Cfap74
|
UTSW |
4 |
155,549,804 (GRCm39) |
missense |
unknown |
|
R7533:Cfap74
|
UTSW |
4 |
155,500,200 (GRCm39) |
missense |
|
|
R7673:Cfap74
|
UTSW |
4 |
155,547,513 (GRCm39) |
missense |
unknown |
|
R7798:Cfap74
|
UTSW |
4 |
155,507,079 (GRCm39) |
missense |
|
|
R7829:Cfap74
|
UTSW |
4 |
155,513,694 (GRCm39) |
missense |
|
|
R7897:Cfap74
|
UTSW |
4 |
155,514,351 (GRCm39) |
missense |
|
|
R8099:Cfap74
|
UTSW |
4 |
155,539,489 (GRCm39) |
missense |
unknown |
|
R8126:Cfap74
|
UTSW |
4 |
155,511,831 (GRCm39) |
missense |
|
|
R8769:Cfap74
|
UTSW |
4 |
155,503,105 (GRCm39) |
missense |
|
|
R8873:Cfap74
|
UTSW |
4 |
155,539,465 (GRCm39) |
missense |
unknown |
|
R8893:Cfap74
|
UTSW |
4 |
155,531,152 (GRCm39) |
missense |
unknown |
|
R8900:Cfap74
|
UTSW |
4 |
155,521,187 (GRCm39) |
missense |
|
|
R8954:Cfap74
|
UTSW |
4 |
155,521,187 (GRCm39) |
missense |
|
|
R8957:Cfap74
|
UTSW |
4 |
155,521,187 (GRCm39) |
missense |
|
|
R8982:Cfap74
|
UTSW |
4 |
155,521,187 (GRCm39) |
missense |
|
|
R9008:Cfap74
|
UTSW |
4 |
155,503,121 (GRCm39) |
missense |
|
|
R9406:Cfap74
|
UTSW |
4 |
155,510,626 (GRCm39) |
nonsense |
probably null |
|
R9606:Cfap74
|
UTSW |
4 |
155,509,133 (GRCm39) |
missense |
|
|
R9641:Cfap74
|
UTSW |
4 |
155,549,054 (GRCm39) |
missense |
unknown |
|
R9647:Cfap74
|
UTSW |
4 |
155,549,373 (GRCm39) |
missense |
unknown |
|
R9655:Cfap74
|
UTSW |
4 |
155,522,665 (GRCm39) |
missense |
|
|
R9761:Cfap74
|
UTSW |
4 |
155,550,844 (GRCm39) |
missense |
unknown |
|
R9797:Cfap74
|
UTSW |
4 |
155,514,402 (GRCm39) |
missense |
|
|
T0970:Cfap74
|
UTSW |
4 |
155,547,574 (GRCm39) |
splice site |
probably null |
|
X0066:Cfap74
|
UTSW |
4 |
155,548,421 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cfap74
|
UTSW |
4 |
155,510,575 (GRCm39) |
missense |
|
|
Z1177:Cfap74
|
UTSW |
4 |
155,539,370 (GRCm39) |
start gained |
probably benign |
|
|