Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambn |
T |
C |
5: 88,615,387 (GRCm39) |
L272P |
possibly damaging |
Het |
Ash2l |
C |
A |
8: 26,317,348 (GRCm39) |
G335V |
probably damaging |
Het |
Atp13a1 |
T |
A |
8: 70,251,966 (GRCm39) |
|
probably null |
Het |
Atp13a2 |
G |
A |
4: 140,734,295 (GRCm39) |
R1139Q |
possibly damaging |
Het |
Atxn2 |
T |
A |
5: 121,934,460 (GRCm39) |
N886K |
possibly damaging |
Het |
Celsr3 |
G |
T |
9: 108,720,150 (GRCm39) |
C2512F |
probably damaging |
Het |
Cfap221 |
A |
G |
1: 119,875,843 (GRCm39) |
V449A |
probably benign |
Het |
Cfhr2 |
A |
T |
1: 139,758,839 (GRCm39) |
C70* |
probably null |
Het |
Chfr |
C |
A |
5: 110,306,671 (GRCm39) |
P472Q |
probably benign |
Het |
Crybg2 |
G |
A |
4: 133,788,193 (GRCm39) |
R22Q |
probably damaging |
Het |
Eef2k |
T |
C |
7: 120,483,995 (GRCm39) |
F244L |
probably damaging |
Het |
Efcab11 |
A |
T |
12: 99,849,614 (GRCm39) |
M23K |
|
Het |
Eif4a3l2 |
A |
G |
6: 116,528,329 (GRCm39) |
I69V |
probably benign |
Het |
Ercc8 |
T |
A |
13: 108,305,967 (GRCm39) |
M114K |
possibly damaging |
Het |
Fam217a |
T |
C |
13: 35,094,298 (GRCm39) |
Y487C |
probably benign |
Het |
Farsb |
T |
C |
1: 78,447,821 (GRCm39) |
N205S |
probably benign |
Het |
Glra1 |
A |
G |
11: 55,405,904 (GRCm39) |
F370S |
probably benign |
Het |
Gm12258 |
T |
A |
11: 58,749,299 (GRCm39) |
M158K |
|
Het |
Gm14305 |
T |
A |
2: 176,412,736 (GRCm39) |
H209Q |
probably damaging |
Het |
Gm4924 |
A |
T |
10: 82,214,035 (GRCm39) |
Q611L |
unknown |
Het |
H4c11 |
A |
G |
13: 21,919,321 (GRCm39) |
H19R |
unknown |
Het |
Haus6 |
T |
C |
4: 86,501,924 (GRCm39) |
E649G |
possibly damaging |
Het |
Hlcs |
C |
T |
16: 94,063,585 (GRCm39) |
D345N |
possibly damaging |
Het |
Htt |
C |
A |
5: 35,010,238 (GRCm39) |
Q1564K |
probably benign |
Het |
Itpr1 |
G |
A |
6: 108,355,151 (GRCm39) |
V481I |
probably benign |
Het |
Jak3 |
T |
C |
8: 72,134,960 (GRCm39) |
I531T |
probably damaging |
Het |
Kng1 |
T |
A |
16: 22,898,428 (GRCm39) |
H609Q |
probably benign |
Het |
Npnt |
A |
G |
3: 132,653,889 (GRCm39) |
S31P |
probably damaging |
Het |
Or1r1 |
A |
T |
11: 73,875,121 (GRCm39) |
F104L |
possibly damaging |
Het |
Or4c100 |
A |
T |
2: 88,355,990 (GRCm39) |
Q21L |
possibly damaging |
Het |
Or8h8 |
T |
A |
2: 86,753,092 (GRCm39) |
K261N |
probably damaging |
Het |
Paxx |
A |
T |
2: 25,350,238 (GRCm39) |
L123Q |
probably damaging |
Het |
Prdm13 |
C |
T |
4: 21,683,528 (GRCm39) |
R144Q |
unknown |
Het |
Rab2b |
C |
A |
14: 52,516,802 (GRCm39) |
|
probably benign |
Het |
Rnf207 |
A |
G |
4: 152,396,237 (GRCm39) |
I509T |
probably damaging |
Het |
Ropn1l |
T |
C |
15: 31,453,655 (GRCm39) |
Q12R |
|
Het |
Ryr3 |
T |
G |
2: 112,705,373 (GRCm39) |
Y847S |
probably damaging |
Het |
Slc1a6 |
A |
T |
10: 78,648,646 (GRCm39) |
T456S |
possibly damaging |
Het |
Slc26a2 |
A |
T |
18: 61,331,901 (GRCm39) |
M510K |
possibly damaging |
Het |
Slc5a9 |
T |
C |
4: 111,741,036 (GRCm39) |
T537A |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,031,939 (GRCm39) |
Y132H |
unknown |
Het |
Sltm |
T |
C |
9: 70,492,132 (GRCm39) |
L725S |
probably damaging |
Het |
Spz1 |
A |
G |
13: 92,712,435 (GRCm39) |
C14R |
probably benign |
Het |
Srrm4 |
T |
A |
5: 116,609,301 (GRCm39) |
Q172L |
unknown |
Het |
Synj2bp |
T |
C |
12: 81,551,289 (GRCm39) |
D92G |
probably benign |
Het |
Tmem169 |
A |
C |
1: 72,340,229 (GRCm39) |
T220P |
probably benign |
Het |
Ttn |
T |
A |
2: 76,718,372 (GRCm39) |
I7270F |
unknown |
Het |
Txndc16 |
T |
G |
14: 45,420,611 (GRCm39) |
N137H |
probably benign |
Het |
Ubr5 |
A |
G |
15: 37,976,389 (GRCm39) |
Y2499H |
|
Het |
Ugt2b38 |
T |
C |
5: 87,558,305 (GRCm39) |
D452G |
probably damaging |
Het |
Zfp12 |
T |
A |
5: 143,231,257 (GRCm39) |
I560N |
possibly damaging |
Het |
Zfp60 |
A |
G |
7: 27,448,937 (GRCm39) |
K535R |
possibly damaging |
Het |
Zfp960 |
T |
A |
17: 17,308,761 (GRCm39) |
C492S |
probably damaging |
Het |
|
Other mutations in Mdn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Mdn1
|
APN |
4 |
32,723,651 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00426:Mdn1
|
APN |
4 |
32,719,214 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00570:Mdn1
|
APN |
4 |
32,735,719 (GRCm39) |
missense |
probably benign |
|
IGL00573:Mdn1
|
APN |
4 |
32,666,619 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00983:Mdn1
|
APN |
4 |
32,735,525 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Mdn1
|
APN |
4 |
32,730,864 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01359:Mdn1
|
APN |
4 |
32,743,686 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01457:Mdn1
|
APN |
4 |
32,715,922 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01530:Mdn1
|
APN |
4 |
32,711,938 (GRCm39) |
splice site |
probably benign |
|
IGL01684:Mdn1
|
APN |
4 |
32,726,857 (GRCm39) |
missense |
probably benign |
|
IGL01753:Mdn1
|
APN |
4 |
32,708,483 (GRCm39) |
missense |
probably benign |
|
IGL01901:Mdn1
|
APN |
4 |
32,669,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01952:Mdn1
|
APN |
4 |
32,723,657 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01960:Mdn1
|
APN |
4 |
32,758,393 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02019:Mdn1
|
APN |
4 |
32,749,948 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02100:Mdn1
|
APN |
4 |
32,715,708 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02117:Mdn1
|
APN |
4 |
32,709,364 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02154:Mdn1
|
APN |
4 |
32,740,395 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02216:Mdn1
|
APN |
4 |
32,739,092 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02371:Mdn1
|
APN |
4 |
32,676,860 (GRCm39) |
splice site |
probably benign |
|
IGL02396:Mdn1
|
APN |
4 |
32,700,120 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02454:Mdn1
|
APN |
4 |
32,694,674 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02502:Mdn1
|
APN |
4 |
32,670,579 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02883:Mdn1
|
APN |
4 |
32,763,199 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02946:Mdn1
|
APN |
4 |
32,734,366 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02950:Mdn1
|
APN |
4 |
32,713,360 (GRCm39) |
splice site |
probably benign |
|
IGL03076:Mdn1
|
APN |
4 |
32,735,564 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03129:Mdn1
|
APN |
4 |
32,729,994 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03234:Mdn1
|
APN |
4 |
32,732,842 (GRCm39) |
missense |
probably benign |
0.06 |
3-1:Mdn1
|
UTSW |
4 |
32,725,967 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03046:Mdn1
|
UTSW |
4 |
32,694,495 (GRCm39) |
missense |
possibly damaging |
0.73 |
P0035:Mdn1
|
UTSW |
4 |
32,749,934 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4508001:Mdn1
|
UTSW |
4 |
32,719,223 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4618001:Mdn1
|
UTSW |
4 |
32,746,527 (GRCm39) |
missense |
probably benign |
0.20 |
R0008:Mdn1
|
UTSW |
4 |
32,718,317 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0110:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0125:Mdn1
|
UTSW |
4 |
32,729,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R0257:Mdn1
|
UTSW |
4 |
32,693,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R0266:Mdn1
|
UTSW |
4 |
32,741,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R0349:Mdn1
|
UTSW |
4 |
32,750,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R0362:Mdn1
|
UTSW |
4 |
32,746,439 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0421:Mdn1
|
UTSW |
4 |
32,684,707 (GRCm39) |
missense |
probably benign |
0.39 |
R0450:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0465:Mdn1
|
UTSW |
4 |
32,699,204 (GRCm39) |
splice site |
probably benign |
|
R0469:Mdn1
|
UTSW |
4 |
32,738,619 (GRCm39) |
missense |
probably benign |
0.20 |
R0477:Mdn1
|
UTSW |
4 |
32,750,928 (GRCm39) |
missense |
probably benign |
0.02 |
R0481:Mdn1
|
UTSW |
4 |
32,767,182 (GRCm39) |
splice site |
probably benign |
|
R0504:Mdn1
|
UTSW |
4 |
32,698,916 (GRCm39) |
splice site |
probably benign |
|
R0522:Mdn1
|
UTSW |
4 |
32,672,837 (GRCm39) |
missense |
probably benign |
0.09 |
R0550:Mdn1
|
UTSW |
4 |
32,730,479 (GRCm39) |
missense |
probably benign |
0.13 |
R0607:Mdn1
|
UTSW |
4 |
32,732,829 (GRCm39) |
missense |
probably benign |
0.36 |
R0607:Mdn1
|
UTSW |
4 |
32,712,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R0664:Mdn1
|
UTSW |
4 |
32,768,011 (GRCm39) |
nonsense |
probably null |
|
R0701:Mdn1
|
UTSW |
4 |
32,699,263 (GRCm39) |
missense |
probably benign |
0.00 |
R0801:Mdn1
|
UTSW |
4 |
32,668,895 (GRCm39) |
missense |
probably benign |
0.04 |
R0841:Mdn1
|
UTSW |
4 |
32,752,032 (GRCm39) |
missense |
probably benign |
0.23 |
R0849:Mdn1
|
UTSW |
4 |
32,741,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R0893:Mdn1
|
UTSW |
4 |
32,701,713 (GRCm39) |
missense |
probably benign |
0.01 |
R1114:Mdn1
|
UTSW |
4 |
32,746,568 (GRCm39) |
critical splice donor site |
probably null |
|
R1137:Mdn1
|
UTSW |
4 |
32,694,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1185:Mdn1
|
UTSW |
4 |
32,735,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1257:Mdn1
|
UTSW |
4 |
32,667,089 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1356:Mdn1
|
UTSW |
4 |
32,700,334 (GRCm39) |
splice site |
probably benign |
|
R1466:Mdn1
|
UTSW |
4 |
32,730,788 (GRCm39) |
missense |
probably benign |
0.28 |
R1466:Mdn1
|
UTSW |
4 |
32,730,788 (GRCm39) |
missense |
probably benign |
0.28 |
R1518:Mdn1
|
UTSW |
4 |
32,739,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Mdn1
|
UTSW |
4 |
32,723,501 (GRCm39) |
missense |
probably null |
0.10 |
R1574:Mdn1
|
UTSW |
4 |
32,722,315 (GRCm39) |
missense |
probably benign |
|
R1574:Mdn1
|
UTSW |
4 |
32,722,315 (GRCm39) |
missense |
probably benign |
|
R1591:Mdn1
|
UTSW |
4 |
32,700,092 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1678:Mdn1
|
UTSW |
4 |
32,663,050 (GRCm39) |
missense |
probably damaging |
0.99 |
R1696:Mdn1
|
UTSW |
4 |
32,700,417 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1707:Mdn1
|
UTSW |
4 |
32,693,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Mdn1
|
UTSW |
4 |
32,773,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Mdn1
|
UTSW |
4 |
32,700,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Mdn1
|
UTSW |
4 |
32,720,761 (GRCm39) |
missense |
probably damaging |
0.97 |
R1858:Mdn1
|
UTSW |
4 |
32,730,881 (GRCm39) |
missense |
probably benign |
0.17 |
R1870:Mdn1
|
UTSW |
4 |
32,763,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1887:Mdn1
|
UTSW |
4 |
32,742,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Mdn1
|
UTSW |
4 |
32,760,839 (GRCm39) |
small deletion |
probably benign |
|
R2075:Mdn1
|
UTSW |
4 |
32,716,058 (GRCm39) |
missense |
probably benign |
0.03 |
R2103:Mdn1
|
UTSW |
4 |
32,738,712 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2104:Mdn1
|
UTSW |
4 |
32,743,843 (GRCm39) |
splice site |
probably null |
|
R2110:Mdn1
|
UTSW |
4 |
32,700,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Mdn1
|
UTSW |
4 |
32,700,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Mdn1
|
UTSW |
4 |
32,716,271 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2221:Mdn1
|
UTSW |
4 |
32,763,306 (GRCm39) |
missense |
probably benign |
0.37 |
R2240:Mdn1
|
UTSW |
4 |
32,765,701 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2351:Mdn1
|
UTSW |
4 |
32,750,010 (GRCm39) |
missense |
probably benign |
0.21 |
R2421:Mdn1
|
UTSW |
4 |
32,723,621 (GRCm39) |
missense |
probably damaging |
0.96 |
R3036:Mdn1
|
UTSW |
4 |
32,750,013 (GRCm39) |
missense |
probably damaging |
0.99 |
R3434:Mdn1
|
UTSW |
4 |
32,733,726 (GRCm39) |
critical splice donor site |
probably null |
|
R3435:Mdn1
|
UTSW |
4 |
32,733,726 (GRCm39) |
critical splice donor site |
probably null |
|
R3783:Mdn1
|
UTSW |
4 |
32,720,818 (GRCm39) |
missense |
probably benign |
0.01 |
R3811:Mdn1
|
UTSW |
4 |
32,693,506 (GRCm39) |
nonsense |
probably null |
|
R3973:Mdn1
|
UTSW |
4 |
32,722,363 (GRCm39) |
missense |
probably benign |
0.00 |
R4154:Mdn1
|
UTSW |
4 |
32,707,475 (GRCm39) |
missense |
probably damaging |
0.96 |
R4372:Mdn1
|
UTSW |
4 |
32,743,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4393:Mdn1
|
UTSW |
4 |
32,754,482 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4438:Mdn1
|
UTSW |
4 |
32,704,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Mdn1
|
UTSW |
4 |
32,668,860 (GRCm39) |
missense |
probably benign |
0.00 |
R4509:Mdn1
|
UTSW |
4 |
32,715,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4538:Mdn1
|
UTSW |
4 |
32,722,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Mdn1
|
UTSW |
4 |
32,754,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R4570:Mdn1
|
UTSW |
4 |
32,741,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Mdn1
|
UTSW |
4 |
32,707,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Mdn1
|
UTSW |
4 |
32,730,749 (GRCm39) |
splice site |
probably null |
|
R4667:Mdn1
|
UTSW |
4 |
32,679,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Mdn1
|
UTSW |
4 |
32,666,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Mdn1
|
UTSW |
4 |
32,683,583 (GRCm39) |
nonsense |
probably null |
|
R4807:Mdn1
|
UTSW |
4 |
32,685,651 (GRCm39) |
splice site |
probably null |
|
R4923:Mdn1
|
UTSW |
4 |
32,671,608 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4951:Mdn1
|
UTSW |
4 |
32,707,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R4963:Mdn1
|
UTSW |
4 |
32,756,512 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:Mdn1
|
UTSW |
4 |
32,739,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Mdn1
|
UTSW |
4 |
32,734,418 (GRCm39) |
missense |
probably benign |
0.01 |
R5122:Mdn1
|
UTSW |
4 |
32,670,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Mdn1
|
UTSW |
4 |
32,774,008 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5164:Mdn1
|
UTSW |
4 |
32,759,011 (GRCm39) |
splice site |
probably null |
|
R5215:Mdn1
|
UTSW |
4 |
32,741,418 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5217:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5219:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5365:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5366:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5368:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5445:Mdn1
|
UTSW |
4 |
32,723,690 (GRCm39) |
missense |
probably damaging |
0.98 |
R5462:Mdn1
|
UTSW |
4 |
32,720,897 (GRCm39) |
missense |
probably benign |
|
R5522:Mdn1
|
UTSW |
4 |
32,685,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Mdn1
|
UTSW |
4 |
32,767,961 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5578:Mdn1
|
UTSW |
4 |
32,728,167 (GRCm39) |
missense |
probably benign |
0.04 |
R5605:Mdn1
|
UTSW |
4 |
32,765,664 (GRCm39) |
missense |
probably benign |
|
R5621:Mdn1
|
UTSW |
4 |
32,716,371 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5636:Mdn1
|
UTSW |
4 |
32,695,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Mdn1
|
UTSW |
4 |
32,667,467 (GRCm39) |
splice site |
probably null |
|
R5780:Mdn1
|
UTSW |
4 |
32,722,950 (GRCm39) |
missense |
probably benign |
0.02 |
R5838:Mdn1
|
UTSW |
4 |
32,754,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R5857:Mdn1
|
UTSW |
4 |
32,670,646 (GRCm39) |
missense |
probably benign |
0.09 |
R5895:Mdn1
|
UTSW |
4 |
32,695,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R5943:Mdn1
|
UTSW |
4 |
32,678,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Mdn1
|
UTSW |
4 |
32,741,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Mdn1
|
UTSW |
4 |
32,715,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6075:Mdn1
|
UTSW |
4 |
32,689,581 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6151:Mdn1
|
UTSW |
4 |
32,684,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Mdn1
|
UTSW |
4 |
32,716,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6181:Mdn1
|
UTSW |
4 |
32,715,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Mdn1
|
UTSW |
4 |
32,696,269 (GRCm39) |
missense |
probably benign |
0.12 |
R6249:Mdn1
|
UTSW |
4 |
32,708,484 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6251:Mdn1
|
UTSW |
4 |
32,748,590 (GRCm39) |
missense |
probably benign |
0.13 |
R6253:Mdn1
|
UTSW |
4 |
32,749,593 (GRCm39) |
missense |
probably benign |
0.25 |
R6273:Mdn1
|
UTSW |
4 |
32,715,979 (GRCm39) |
missense |
probably benign |
0.01 |
R6297:Mdn1
|
UTSW |
4 |
32,730,054 (GRCm39) |
nonsense |
probably null |
|
R6384:Mdn1
|
UTSW |
4 |
32,670,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6463:Mdn1
|
UTSW |
4 |
32,773,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R6528:Mdn1
|
UTSW |
4 |
32,713,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Mdn1
|
UTSW |
4 |
32,774,041 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6762:Mdn1
|
UTSW |
4 |
32,676,786 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6794:Mdn1
|
UTSW |
4 |
32,741,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Mdn1
|
UTSW |
4 |
32,748,614 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6935:Mdn1
|
UTSW |
4 |
32,774,041 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6980:Mdn1
|
UTSW |
4 |
32,726,942 (GRCm39) |
critical splice donor site |
probably null |
|
R6995:Mdn1
|
UTSW |
4 |
32,733,374 (GRCm39) |
missense |
probably benign |
0.03 |
R7048:Mdn1
|
UTSW |
4 |
32,767,969 (GRCm39) |
missense |
probably benign |
0.00 |
R7082:Mdn1
|
UTSW |
4 |
32,762,341 (GRCm39) |
missense |
probably benign |
|
R7158:Mdn1
|
UTSW |
4 |
32,725,121 (GRCm39) |
missense |
probably benign |
0.09 |
R7168:Mdn1
|
UTSW |
4 |
32,719,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Mdn1
|
UTSW |
4 |
32,694,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Mdn1
|
UTSW |
4 |
32,701,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Mdn1
|
UTSW |
4 |
32,695,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Mdn1
|
UTSW |
4 |
32,725,944 (GRCm39) |
missense |
probably benign |
0.12 |
R7330:Mdn1
|
UTSW |
4 |
32,723,685 (GRCm39) |
missense |
probably benign |
0.16 |
R7363:Mdn1
|
UTSW |
4 |
32,691,729 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Mdn1
|
UTSW |
4 |
32,773,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R7452:Mdn1
|
UTSW |
4 |
32,739,030 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7523:Mdn1
|
UTSW |
4 |
32,667,270 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7594:Mdn1
|
UTSW |
4 |
32,696,359 (GRCm39) |
missense |
probably benign |
0.27 |
R7605:Mdn1
|
UTSW |
4 |
32,694,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7661:Mdn1
|
UTSW |
4 |
32,691,229 (GRCm39) |
missense |
probably benign |
0.08 |
R7689:Mdn1
|
UTSW |
4 |
32,739,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Mdn1
|
UTSW |
4 |
32,741,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Mdn1
|
UTSW |
4 |
32,741,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R7714:Mdn1
|
UTSW |
4 |
32,722,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7718:Mdn1
|
UTSW |
4 |
32,718,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Mdn1
|
UTSW |
4 |
32,734,421 (GRCm39) |
missense |
probably benign |
|
R7787:Mdn1
|
UTSW |
4 |
32,741,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R8111:Mdn1
|
UTSW |
4 |
32,674,003 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8222:Mdn1
|
UTSW |
4 |
32,707,477 (GRCm39) |
missense |
probably benign |
0.09 |
R8246:Mdn1
|
UTSW |
4 |
32,657,284 (GRCm39) |
missense |
probably benign |
0.06 |
R8267:Mdn1
|
UTSW |
4 |
32,742,485 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8286:Mdn1
|
UTSW |
4 |
32,731,960 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8305:Mdn1
|
UTSW |
4 |
32,725,107 (GRCm39) |
missense |
probably benign |
|
R8318:Mdn1
|
UTSW |
4 |
32,735,897 (GRCm39) |
critical splice donor site |
probably null |
|
R8379:Mdn1
|
UTSW |
4 |
32,756,453 (GRCm39) |
missense |
probably null |
1.00 |
R8384:Mdn1
|
UTSW |
4 |
32,765,680 (GRCm39) |
missense |
probably benign |
0.05 |
R8514:Mdn1
|
UTSW |
4 |
32,739,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Mdn1
|
UTSW |
4 |
32,743,830 (GRCm39) |
missense |
probably benign |
0.08 |
R8672:Mdn1
|
UTSW |
4 |
32,768,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Mdn1
|
UTSW |
4 |
32,725,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8769:Mdn1
|
UTSW |
4 |
32,751,390 (GRCm39) |
missense |
probably damaging |
0.97 |
R8896:Mdn1
|
UTSW |
4 |
32,678,328 (GRCm39) |
missense |
probably benign |
0.28 |
R8918:Mdn1
|
UTSW |
4 |
32,744,579 (GRCm39) |
nonsense |
probably null |
|
R8920:Mdn1
|
UTSW |
4 |
32,719,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Mdn1
|
UTSW |
4 |
32,672,837 (GRCm39) |
nonsense |
probably null |
|
R8997:Mdn1
|
UTSW |
4 |
32,773,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9120:Mdn1
|
UTSW |
4 |
32,701,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Mdn1
|
UTSW |
4 |
32,676,812 (GRCm39) |
missense |
probably benign |
0.24 |
R9131:Mdn1
|
UTSW |
4 |
32,762,275 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9200:Mdn1
|
UTSW |
4 |
32,760,791 (GRCm39) |
missense |
probably benign |
0.00 |
R9226:Mdn1
|
UTSW |
4 |
32,694,612 (GRCm39) |
missense |
probably benign |
0.25 |
R9235:Mdn1
|
UTSW |
4 |
32,739,122 (GRCm39) |
missense |
probably benign |
0.10 |
R9293:Mdn1
|
UTSW |
4 |
32,707,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9315:Mdn1
|
UTSW |
4 |
32,760,911 (GRCm39) |
missense |
probably benign |
0.00 |
R9338:Mdn1
|
UTSW |
4 |
32,666,536 (GRCm39) |
missense |
probably benign |
0.00 |
R9353:Mdn1
|
UTSW |
4 |
32,693,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R9393:Mdn1
|
UTSW |
4 |
32,713,825 (GRCm39) |
missense |
|
|
R9420:Mdn1
|
UTSW |
4 |
32,678,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R9475:Mdn1
|
UTSW |
4 |
32,739,849 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9583:Mdn1
|
UTSW |
4 |
32,741,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R9600:Mdn1
|
UTSW |
4 |
32,684,723 (GRCm39) |
nonsense |
probably null |
|
R9640:Mdn1
|
UTSW |
4 |
32,754,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Mdn1
|
UTSW |
4 |
32,745,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R9744:Mdn1
|
UTSW |
4 |
32,715,711 (GRCm39) |
missense |
possibly damaging |
0.91 |
X0066:Mdn1
|
UTSW |
4 |
32,739,030 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,696,244 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,668,944 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mdn1
|
UTSW |
4 |
32,667,102 (GRCm39) |
missense |
probably benign |
0.01 |
|