Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
A |
1: 12,045,177 (GRCm39) |
A443E |
unknown |
Het |
Acacb |
A |
T |
5: 114,334,770 (GRCm39) |
Y613F |
probably benign |
Het |
Adam23 |
A |
C |
1: 63,596,615 (GRCm39) |
I566L |
probably benign |
Het |
Adar |
G |
T |
3: 89,646,589 (GRCm39) |
R338L |
probably benign |
Het |
Akap14 |
C |
T |
X: 36,420,779 (GRCm39) |
A476T |
probably damaging |
Het |
Amotl1 |
T |
A |
9: 14,486,697 (GRCm39) |
Q399L |
probably benign |
Het |
Ankrd16 |
T |
G |
2: 11,783,407 (GRCm39) |
L3R |
probably benign |
Het |
Arfgap1 |
G |
C |
2: 180,615,881 (GRCm39) |
G187R |
probably damaging |
Het |
Arhgap19 |
A |
T |
19: 41,767,592 (GRCm39) |
V399D |
probably benign |
Het |
Arl4d |
A |
G |
11: 101,557,578 (GRCm39) |
T35A |
probably damaging |
Het |
Atr |
T |
A |
9: 95,747,150 (GRCm39) |
I144N |
probably damaging |
Het |
Bptf |
A |
G |
11: 106,964,127 (GRCm39) |
M1574T |
probably benign |
Het |
Cacna1h |
T |
A |
17: 25,599,781 (GRCm39) |
D1684V |
probably damaging |
Het |
Celsr1 |
C |
A |
15: 85,916,960 (GRCm39) |
V338F |
probably damaging |
Het |
Cep164 |
T |
C |
9: 45,734,938 (GRCm39) |
|
probably benign |
Het |
Clock |
C |
A |
5: 76,388,756 (GRCm39) |
G390C |
possibly damaging |
Het |
Col6a6 |
A |
G |
9: 105,658,301 (GRCm39) |
F637S |
probably damaging |
Het |
Crebrf |
T |
A |
17: 26,961,937 (GRCm39) |
Y345N |
probably benign |
Het |
Cstdc3 |
A |
T |
16: 36,128,449 (GRCm39) |
I15F |
probably damaging |
Het |
Cul1 |
A |
G |
6: 47,502,458 (GRCm39) |
|
probably null |
Het |
Cyb5r4 |
C |
T |
9: 86,923,332 (GRCm39) |
S185L |
probably benign |
Het |
Cyp3a57 |
T |
C |
5: 145,318,059 (GRCm39) |
Y347H |
probably damaging |
Het |
Dgkq |
G |
T |
5: 108,801,597 (GRCm39) |
T487K |
probably benign |
Het |
Dmkn |
T |
C |
7: 30,463,990 (GRCm39) |
V143A |
probably benign |
Het |
Dmp1 |
A |
T |
5: 104,355,496 (GRCm39) |
E32V |
possibly damaging |
Het |
Dsc3 |
T |
C |
18: 20,098,773 (GRCm39) |
D802G |
probably damaging |
Het |
Dse |
T |
C |
10: 34,029,225 (GRCm39) |
T622A |
probably benign |
Het |
Duxf4 |
A |
G |
10: 58,071,602 (GRCm39) |
V204A |
probably benign |
Het |
Dyrk1b |
A |
T |
7: 27,882,071 (GRCm39) |
|
probably null |
Het |
Ehd2 |
T |
C |
7: 15,686,113 (GRCm39) |
T320A |
probably benign |
Het |
Eif3a |
A |
C |
19: 60,770,635 (GRCm39) |
L71V |
probably damaging |
Het |
Eif4e1b |
A |
G |
13: 54,935,091 (GRCm39) |
|
probably null |
Het |
Fam131b |
A |
G |
6: 42,295,914 (GRCm39) |
F161L |
probably damaging |
Het |
Fam171b |
A |
T |
2: 83,683,725 (GRCm39) |
M81L |
probably benign |
Het |
Gal3st4 |
T |
C |
5: 138,269,050 (GRCm39) |
|
probably null |
Het |
Gdf11 |
A |
T |
10: 128,722,315 (GRCm39) |
V180E |
probably damaging |
Het |
Grin3a |
T |
A |
4: 49,792,437 (GRCm39) |
Y432F |
probably benign |
Het |
Hif1a |
C |
A |
12: 73,990,929 (GRCm39) |
H708N |
probably benign |
Het |
Hmcn2 |
G |
T |
2: 31,305,295 (GRCm39) |
|
probably null |
Het |
Hs3st6 |
T |
A |
17: 24,976,973 (GRCm39) |
M151K |
possibly damaging |
Het |
Hyal2 |
T |
A |
9: 107,449,537 (GRCm39) |
L431Q |
probably benign |
Het |
Hyal6 |
A |
T |
6: 24,740,857 (GRCm39) |
T337S |
probably benign |
Het |
Igsf5 |
A |
T |
16: 96,187,829 (GRCm39) |
|
probably null |
Het |
Kif13a |
G |
A |
13: 47,018,314 (GRCm39) |
|
probably benign |
Het |
Krtap19-3 |
G |
A |
16: 88,674,878 (GRCm39) |
|
probably benign |
Het |
Lgalsl |
T |
C |
11: 20,779,420 (GRCm39) |
D75G |
probably benign |
Het |
Lrrc56 |
A |
G |
7: 140,787,421 (GRCm39) |
M353V |
probably benign |
Het |
Ltbp2 |
T |
A |
12: 84,877,555 (GRCm39) |
K337* |
probably null |
Het |
Medag |
A |
G |
5: 149,353,259 (GRCm39) |
I151M |
probably damaging |
Het |
Meiob |
T |
C |
17: 25,042,544 (GRCm39) |
V124A |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,451,799 (GRCm39) |
H379R |
probably benign |
Het |
Mpg |
A |
G |
11: 32,181,957 (GRCm39) |
|
probably null |
Het |
Ncoa6 |
G |
T |
2: 155,263,559 (GRCm39) |
Q292K |
probably benign |
Het |
Ndufaf6 |
G |
T |
4: 11,053,474 (GRCm39) |
H277Q |
probably benign |
Het |
Nlrp4c |
A |
G |
7: 6,087,655 (GRCm39) |
I763V |
probably benign |
Het |
Nlrp5 |
A |
T |
7: 23,117,586 (GRCm39) |
I437F |
probably damaging |
Het |
Noc2l |
G |
A |
4: 156,329,727 (GRCm39) |
R435Q |
probably damaging |
Het |
Nova2 |
T |
C |
7: 18,692,326 (GRCm39) |
I485T |
probably damaging |
Het |
Nrxn2 |
G |
A |
19: 6,538,825 (GRCm39) |
V794I |
probably benign |
Het |
Nup210l |
A |
G |
3: 90,061,806 (GRCm39) |
T662A |
probably damaging |
Het |
Or2ad1 |
A |
T |
13: 21,326,564 (GRCm39) |
I221N |
probably damaging |
Het |
Or2b28 |
A |
G |
13: 21,531,346 (GRCm39) |
M83V |
possibly damaging |
Het |
Or2p2 |
A |
T |
13: 21,256,641 (GRCm39) |
F277I |
probably damaging |
Het |
Or51aa2 |
G |
A |
7: 103,187,859 (GRCm39) |
T194I |
probably damaging |
Het |
Or51e2 |
A |
C |
7: 102,391,571 (GRCm39) |
I213S |
probably damaging |
Het |
Or51l14 |
G |
A |
7: 103,101,332 (GRCm39) |
V263I |
probably benign |
Het |
Or9g8 |
T |
C |
2: 85,607,582 (GRCm39) |
L218P |
probably damaging |
Het |
Pelp1 |
G |
A |
11: 70,285,568 (GRCm39) |
P767S |
probably damaging |
Het |
Pfdn1 |
C |
A |
18: 36,584,153 (GRCm39) |
M60I |
probably benign |
Het |
Plaat1 |
G |
A |
16: 29,036,470 (GRCm39) |
G36D |
probably damaging |
Het |
Plcxd3 |
T |
A |
15: 4,546,093 (GRCm39) |
|
probably benign |
Het |
Plekhg1 |
C |
A |
10: 3,895,917 (GRCm39) |
D436E |
possibly damaging |
Het |
Ppfibp1 |
G |
A |
6: 146,892,090 (GRCm39) |
V117I |
probably benign |
Het |
Prss44 |
A |
G |
9: 110,643,177 (GRCm39) |
K24R |
probably benign |
Het |
Ptger1 |
G |
T |
8: 84,395,107 (GRCm39) |
G195W |
probably benign |
Het |
Ptgs1 |
A |
C |
2: 36,132,782 (GRCm39) |
D260A |
probably benign |
Het |
Ptprd |
T |
A |
4: 75,865,384 (GRCm39) |
T1198S |
probably damaging |
Het |
Qsox2 |
A |
G |
2: 26,104,074 (GRCm39) |
S319P |
probably damaging |
Het |
Rab35 |
A |
G |
5: 115,778,147 (GRCm39) |
I38V |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 71,861,408 (GRCm39) |
I33V |
possibly damaging |
Het |
Rbbp8nl |
C |
T |
2: 179,924,006 (GRCm39) |
|
probably benign |
Het |
Riok1 |
A |
T |
13: 38,242,694 (GRCm39) |
K473* |
probably null |
Het |
Rtca |
C |
T |
3: 116,287,764 (GRCm39) |
G288S |
probably benign |
Het |
Sag |
A |
T |
1: 87,742,570 (GRCm39) |
D114V |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sec61g |
A |
G |
11: 16,456,371 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
A |
T |
4: 124,623,288 (GRCm39) |
I440F |
probably damaging |
Het |
Sgta |
T |
C |
10: 80,884,695 (GRCm39) |
K205E |
possibly damaging |
Het |
Slc36a4 |
A |
G |
9: 15,632,006 (GRCm39) |
T61A |
probably damaging |
Het |
Slc5a4a |
T |
C |
10: 76,002,569 (GRCm39) |
S242P |
probably benign |
Het |
Srgap3 |
A |
T |
6: 112,748,479 (GRCm39) |
L391Q |
probably damaging |
Het |
Stard13 |
T |
C |
5: 151,018,903 (GRCm39) |
Y60C |
probably damaging |
Het |
Styxl2 |
T |
C |
1: 165,928,415 (GRCm39) |
Y399C |
possibly damaging |
Het |
Syt12 |
G |
T |
19: 4,497,825 (GRCm39) |
H386N |
probably damaging |
Het |
Thyn1 |
T |
A |
9: 26,915,070 (GRCm39) |
M74K |
probably benign |
Het |
Tmem130 |
C |
A |
5: 144,689,093 (GRCm39) |
|
probably null |
Het |
Trim71 |
A |
G |
9: 114,392,016 (GRCm39) |
V57A |
possibly damaging |
Het |
Twf1 |
T |
C |
15: 94,483,428 (GRCm39) |
|
probably benign |
Het |
Tyro3 |
T |
A |
2: 119,632,176 (GRCm39) |
I81N |
possibly damaging |
Het |
Unc13a |
A |
T |
8: 72,105,043 (GRCm39) |
C740S |
probably damaging |
Het |
Vmn1r15 |
A |
T |
6: 57,235,616 (GRCm39) |
K161N |
probably benign |
Het |
Vmn1r16 |
A |
T |
6: 57,299,884 (GRCm39) |
I246N |
probably damaging |
Het |
Vmn1r42 |
A |
G |
6: 89,821,597 (GRCm39) |
I324T |
probably benign |
Het |
Vmn2r35 |
T |
C |
7: 7,819,805 (GRCm39) |
Y155C |
possibly damaging |
Het |
Wif1 |
T |
A |
10: 120,919,788 (GRCm39) |
|
probably null |
Het |
Wscd2 |
G |
A |
5: 113,689,231 (GRCm39) |
R79Q |
possibly damaging |
Het |
Zan |
G |
T |
5: 137,404,139 (GRCm39) |
|
probably benign |
Het |
Zfp9 |
G |
T |
6: 118,442,021 (GRCm39) |
H214N |
probably benign |
Het |
Zfp985 |
A |
T |
4: 147,667,315 (GRCm39) |
Y61F |
probably benign |
Het |
Zscan30 |
A |
G |
18: 24,104,524 (GRCm39) |
|
noncoding transcript |
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 |
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 |
R7166:Mdn1
|
UTSW |
4 |
32,746,446 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|