Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
G |
A |
15: 76,478,383 (GRCm39) |
D277N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,670,288 (GRCm39) |
S2353T |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,743,371 (GRCm39) |
N43K |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,185,937 (GRCm39) |
I12T |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,741,363 (GRCm39) |
L903P |
probably damaging |
Het |
Ankhd1 |
T |
G |
18: 36,780,878 (GRCm39) |
S1977A |
probably benign |
Het |
Ap1m2 |
T |
C |
9: 21,216,983 (GRCm39) |
M118V |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,548,639 (GRCm39) |
K846R |
possibly damaging |
Het |
Aqr |
C |
A |
2: 113,971,396 (GRCm39) |
E480* |
probably null |
Het |
Arl6 |
G |
T |
16: 59,434,199 (GRCm39) |
Q182K |
probably benign |
Het |
Arpc2 |
A |
G |
1: 74,294,034 (GRCm39) |
K106E |
probably benign |
Het |
Atp8a1 |
A |
C |
5: 67,889,524 (GRCm39) |
F599V |
|
Het |
B3galt5 |
A |
T |
16: 96,117,203 (GRCm39) |
I279F |
probably damaging |
Het |
Calcoco2 |
G |
T |
11: 95,991,104 (GRCm39) |
A211D |
unknown |
Het |
Ccdc33 |
T |
C |
9: 57,993,855 (GRCm39) |
E342G |
possibly damaging |
Het |
Ccdc88a |
C |
A |
11: 29,405,484 (GRCm39) |
Q386K |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,862,065 (GRCm39) |
K82E |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,503,575 (GRCm39) |
Y792N |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,658,254 (GRCm39) |
I653V |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,812,649 (GRCm39) |
R2826W |
unknown |
Het |
D6Ertd527e |
A |
G |
6: 87,088,908 (GRCm39) |
N357S |
unknown |
Het |
Dmgdh |
T |
A |
13: 93,857,123 (GRCm39) |
N742K |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,748,594 (GRCm39) |
N840S |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,475,821 (GRCm39) |
N565D |
probably benign |
Het |
Doc2g |
A |
G |
19: 4,054,390 (GRCm39) |
Y155C |
probably damaging |
Het |
Dot1l |
G |
A |
10: 80,624,361 (GRCm39) |
G943D |
probably damaging |
Het |
Dst |
T |
C |
1: 34,220,736 (GRCm39) |
V2180A |
probably benign |
Het |
Eftud2 |
A |
C |
11: 102,759,422 (GRCm39) |
Y160* |
probably null |
Het |
Ehd1 |
A |
T |
19: 6,331,262 (GRCm39) |
Q140L |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,443,172 (GRCm39) |
V252A |
probably benign |
Het |
F11 |
A |
T |
8: 45,694,566 (GRCm39) |
C598* |
probably null |
Het |
Fancm |
T |
A |
12: 65,137,758 (GRCm39) |
N316K |
probably benign |
Het |
Flnc |
T |
C |
6: 29,457,214 (GRCm39) |
V2372A |
probably damaging |
Het |
Fry |
A |
G |
5: 150,282,488 (GRCm39) |
R338G |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,591 (GRCm39) |
T136A |
probably benign |
Het |
Golga7b |
T |
C |
19: 42,255,462 (GRCm39) |
V113A |
possibly damaging |
Het |
Gpn3 |
G |
T |
5: 122,520,306 (GRCm39) |
V102L |
|
Het |
Herc2 |
A |
G |
7: 55,820,338 (GRCm39) |
N2859S |
possibly damaging |
Het |
Hpd |
A |
T |
5: 123,318,948 (GRCm39) |
|
probably null |
Het |
Hspg2 |
C |
T |
4: 137,266,887 (GRCm39) |
T1964I |
probably benign |
Het |
Hydin |
A |
T |
8: 111,220,965 (GRCm39) |
T1454S |
probably benign |
Het |
Irgm2 |
A |
T |
11: 58,110,872 (GRCm39) |
T188S |
possibly damaging |
Het |
Jak3 |
A |
G |
8: 72,131,366 (GRCm39) |
D77G |
probably damaging |
Het |
Kcnj4 |
G |
T |
15: 79,369,220 (GRCm39) |
F253L |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 25,106,895 (GRCm39) |
D1358E |
probably benign |
Het |
Klf1 |
C |
A |
8: 85,630,061 (GRCm39) |
C295* |
probably null |
Het |
Kmt2a |
C |
T |
9: 44,760,102 (GRCm39) |
W582* |
probably null |
Het |
Lrig2 |
A |
G |
3: 104,371,556 (GRCm39) |
C716R |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,765,004 (GRCm39) |
D2941N |
|
Het |
Lrpprc |
A |
T |
17: 85,020,262 (GRCm39) |
V1141E |
probably damaging |
Het |
Mrgprx1 |
C |
T |
7: 47,671,273 (GRCm39) |
G158D |
probably benign |
Het |
Muc5b |
C |
A |
7: 141,409,279 (GRCm39) |
A1121D |
unknown |
Het |
Nf1 |
G |
T |
11: 79,334,733 (GRCm39) |
V852L |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,118,286 (GRCm39) |
E670G |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,784,601 (GRCm39) |
T101A |
probably benign |
Het |
Or10a49 |
T |
C |
7: 108,467,563 (GRCm39) |
Y266C |
probably damaging |
Het |
Or2t35 |
T |
A |
14: 14,407,963 (GRCm38) |
I245K |
probably benign |
Het |
Or5b123 |
G |
A |
19: 13,597,365 (GRCm39) |
V237I |
probably benign |
Het |
P2rx2 |
T |
C |
5: 110,488,172 (GRCm39) |
T461A |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,799,194 (GRCm39) |
T419I |
probably damaging |
Het |
Patz1 |
T |
C |
11: 3,244,562 (GRCm39) |
V481A |
unknown |
Het |
Pdlim5 |
A |
G |
3: 142,018,058 (GRCm39) |
L179P |
probably benign |
Het |
Polq |
T |
C |
16: 36,848,176 (GRCm39) |
V261A |
probably damaging |
Het |
Ppm1a |
G |
A |
12: 72,837,451 (GRCm39) |
V333M |
possibly damaging |
Het |
R3hcc1l |
T |
C |
19: 42,552,671 (GRCm39) |
L556P |
probably benign |
Het |
Rabggta |
G |
A |
14: 55,956,375 (GRCm39) |
Q365* |
probably null |
Het |
Ranbp9 |
T |
C |
13: 43,578,519 (GRCm39) |
T185A |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,913 (GRCm39) |
N189H |
probably damaging |
Het |
Rnf17 |
A |
G |
14: 56,722,636 (GRCm39) |
T1066A |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,332,794 (GRCm39) |
A2669T |
|
Het |
Ros1 |
T |
A |
10: 51,996,931 (GRCm39) |
H1268L |
probably benign |
Het |
Rps6ka4 |
G |
T |
19: 6,809,354 (GRCm39) |
S433R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,759,092 (GRCm39) |
L3362P |
probably damaging |
Het |
Setd1b |
A |
T |
5: 123,298,046 (GRCm39) |
T1361S |
unknown |
Het |
Setd2 |
T |
C |
9: 110,377,570 (GRCm39) |
S462P |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,890,935 (GRCm39) |
Q132L |
probably benign |
Het |
Slx1b |
C |
A |
7: 126,291,698 (GRCm39) |
R122L |
probably damaging |
Het |
Sorbs2 |
A |
T |
8: 46,276,788 (GRCm39) |
T1167S |
probably benign |
Het |
Spdya |
A |
C |
17: 71,869,513 (GRCm39) |
T103P |
probably damaging |
Het |
Stfa2 |
A |
G |
16: 36,228,638 (GRCm39) |
S20P |
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,891,026 (GRCm39) |
T400A |
probably benign |
Het |
Tardbp |
A |
T |
4: 148,709,751 (GRCm39) |
D23E |
probably damaging |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tgm1 |
C |
T |
14: 55,948,441 (GRCm39) |
D237N |
probably benign |
Het |
Tgs1 |
T |
A |
4: 3,585,964 (GRCm39) |
N280K |
probably benign |
Het |
Tmem198 |
A |
T |
1: 75,459,272 (GRCm39) |
I76F |
possibly damaging |
Het |
Trpv2 |
A |
T |
11: 62,475,385 (GRCm39) |
Y266F |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,569,845 (GRCm39) |
G27016E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,781,824 (GRCm39) |
E1074G |
unknown |
Het |
Unc5b |
A |
T |
10: 60,613,322 (GRCm39) |
W305R |
probably damaging |
Het |
Usp38 |
A |
G |
8: 81,741,164 (GRCm39) |
|
probably benign |
Het |
Vmn1r79 |
A |
G |
7: 11,910,582 (GRCm39) |
T155A |
probably benign |
Het |
Vwce |
G |
A |
19: 10,615,481 (GRCm39) |
V121I |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,865,961 (GRCm39) |
D530E |
probably benign |
Het |
Wnt4 |
A |
G |
4: 137,023,929 (GRCm39) |
T299A |
probably benign |
Het |
Yeats2 |
T |
A |
16: 20,047,491 (GRCm39) |
Y1284* |
probably null |
Het |
Zfp113 |
A |
T |
5: 138,148,888 (GRCm39) |
Y85* |
probably null |
Het |
Zfp184 |
A |
G |
13: 22,144,096 (GRCm39) |
T601A |
probably benign |
Het |
Zfp655 |
A |
G |
5: 145,180,442 (GRCm39) |
E100G |
probably damaging |
Het |
|
Other mutations in Pik3ap1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Pik3ap1
|
APN |
19 |
41,364,329 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01697:Pik3ap1
|
APN |
19 |
41,313,018 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01743:Pik3ap1
|
APN |
19 |
41,281,267 (GRCm39) |
splice site |
probably benign |
|
IGL02006:Pik3ap1
|
APN |
19 |
41,291,032 (GRCm39) |
missense |
probably benign |
|
IGL02507:Pik3ap1
|
APN |
19 |
41,270,451 (GRCm39) |
splice site |
probably benign |
|
IGL02601:Pik3ap1
|
APN |
19 |
41,290,881 (GRCm39) |
missense |
probably benign |
0.08 |
Canvasback
|
UTSW |
19 |
41,310,069 (GRCm39) |
missense |
possibly damaging |
0.80 |
Eiderdown
|
UTSW |
19 |
41,312,924 (GRCm39) |
splice site |
silent |
|
Pintail
|
UTSW |
19 |
41,364,585 (GRCm39) |
missense |
probably benign |
0.00 |
Scaup
|
UTSW |
19 |
41,320,760 (GRCm39) |
missense |
probably damaging |
1.00 |
Scoter
|
UTSW |
19 |
41,310,024 (GRCm39) |
missense |
probably damaging |
1.00 |
sooni
|
UTSW |
19 |
41,316,348 (GRCm39) |
missense |
probably damaging |
1.00 |
sothe
|
UTSW |
19 |
41,356,683 (GRCm38) |
intron |
probably benign |
|
FR4449:Pik3ap1
|
UTSW |
19 |
41,270,385 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Pik3ap1
|
UTSW |
19 |
41,270,384 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Pik3ap1
|
UTSW |
19 |
41,270,384 (GRCm39) |
small insertion |
probably benign |
|
R0504:Pik3ap1
|
UTSW |
19 |
41,275,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Pik3ap1
|
UTSW |
19 |
41,313,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R0736:Pik3ap1
|
UTSW |
19 |
41,320,758 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0926:Pik3ap1
|
UTSW |
19 |
41,290,964 (GRCm39) |
missense |
probably benign |
0.00 |
R1521:Pik3ap1
|
UTSW |
19 |
41,309,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Pik3ap1
|
UTSW |
19 |
41,296,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Pik3ap1
|
UTSW |
19 |
41,320,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R1924:Pik3ap1
|
UTSW |
19 |
41,291,053 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1945:Pik3ap1
|
UTSW |
19 |
41,262,776 (GRCm39) |
missense |
probably benign |
|
R2327:Pik3ap1
|
UTSW |
19 |
41,284,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R2891:Pik3ap1
|
UTSW |
19 |
41,364,500 (GRCm39) |
missense |
probably benign |
0.00 |
R2892:Pik3ap1
|
UTSW |
19 |
41,364,500 (GRCm39) |
missense |
probably benign |
0.00 |
R2893:Pik3ap1
|
UTSW |
19 |
41,364,500 (GRCm39) |
missense |
probably benign |
0.00 |
R2894:Pik3ap1
|
UTSW |
19 |
41,364,500 (GRCm39) |
missense |
probably benign |
0.00 |
R2918:Pik3ap1
|
UTSW |
19 |
41,290,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4424:Pik3ap1
|
UTSW |
19 |
41,364,320 (GRCm39) |
missense |
probably benign |
0.00 |
R4654:Pik3ap1
|
UTSW |
19 |
41,316,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Pik3ap1
|
UTSW |
19 |
41,290,936 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4855:Pik3ap1
|
UTSW |
19 |
41,316,284 (GRCm39) |
missense |
probably benign |
0.13 |
R4885:Pik3ap1
|
UTSW |
19 |
41,364,365 (GRCm39) |
missense |
probably benign |
0.28 |
R5119:Pik3ap1
|
UTSW |
19 |
41,270,415 (GRCm39) |
missense |
probably benign |
0.18 |
R5261:Pik3ap1
|
UTSW |
19 |
41,364,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R5274:Pik3ap1
|
UTSW |
19 |
41,270,391 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5655:Pik3ap1
|
UTSW |
19 |
41,286,680 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5862:Pik3ap1
|
UTSW |
19 |
41,320,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R5924:Pik3ap1
|
UTSW |
19 |
41,284,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6015:Pik3ap1
|
UTSW |
19 |
41,316,640 (GRCm39) |
missense |
probably benign |
0.22 |
R6018:Pik3ap1
|
UTSW |
19 |
41,373,455 (GRCm39) |
start gained |
probably benign |
|
R6515:Pik3ap1
|
UTSW |
19 |
41,364,585 (GRCm39) |
missense |
probably benign |
0.00 |
R6792:Pik3ap1
|
UTSW |
19 |
41,310,065 (GRCm39) |
missense |
probably benign |
0.14 |
R7135:Pik3ap1
|
UTSW |
19 |
41,320,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Pik3ap1
|
UTSW |
19 |
41,309,965 (GRCm39) |
missense |
probably benign |
0.03 |
R7175:Pik3ap1
|
UTSW |
19 |
41,275,929 (GRCm39) |
missense |
probably damaging |
0.98 |
R7313:Pik3ap1
|
UTSW |
19 |
41,284,815 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7664:Pik3ap1
|
UTSW |
19 |
41,310,069 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7786:Pik3ap1
|
UTSW |
19 |
41,310,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8375:Pik3ap1
|
UTSW |
19 |
41,316,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R8707:Pik3ap1
|
UTSW |
19 |
41,313,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R8770:Pik3ap1
|
UTSW |
19 |
41,316,599 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9015:Pik3ap1
|
UTSW |
19 |
41,270,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Pik3ap1
|
UTSW |
19 |
41,312,924 (GRCm39) |
splice site |
silent |
|
R9369:Pik3ap1
|
UTSW |
19 |
41,317,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|