Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
T |
A |
16: 8,423,472 (GRCm39) |
L224Q |
probably damaging |
Het |
Abcc5 |
A |
G |
16: 20,211,529 (GRCm39) |
M478T |
probably benign |
Het |
Acot10 |
T |
C |
15: 20,665,871 (GRCm39) |
D290G |
possibly damaging |
Het |
Actr3b |
A |
G |
5: 26,036,688 (GRCm39) |
Q167R |
probably benign |
Het |
Actr8 |
C |
T |
14: 29,713,674 (GRCm39) |
R565* |
probably null |
Het |
Adcy7 |
C |
T |
8: 89,052,358 (GRCm39) |
|
probably null |
Het |
Adgrb3 |
C |
T |
1: 25,459,728 (GRCm39) |
V576I |
probably benign |
Het |
Adgrv1 |
T |
A |
13: 81,607,882 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
T |
13: 81,672,898 (GRCm39) |
|
probably null |
Het |
Ak2 |
A |
G |
4: 128,892,976 (GRCm39) |
D45G |
probably damaging |
Het |
Ak9 |
C |
G |
10: 41,298,403 (GRCm39) |
Q1489E |
unknown |
Het |
Ak9 |
A |
T |
10: 41,298,404 (GRCm39) |
Q1489L |
unknown |
Het |
Akap12 |
C |
A |
10: 4,306,268 (GRCm39) |
S1026Y |
possibly damaging |
Het |
Ankhd1 |
T |
G |
18: 36,744,862 (GRCm39) |
S601A |
possibly damaging |
Het |
Apba2 |
A |
T |
7: 64,389,628 (GRCm39) |
E508V |
probably damaging |
Het |
Arhgap18 |
A |
G |
10: 26,722,031 (GRCm39) |
M1V |
probably null |
Het |
Arhgef10l |
G |
A |
4: 140,270,073 (GRCm39) |
T865M |
possibly damaging |
Het |
Bdh1 |
T |
A |
16: 31,268,715 (GRCm39) |
V150D |
probably damaging |
Het |
Becn1 |
A |
G |
11: 101,186,200 (GRCm39) |
C135R |
probably damaging |
Het |
C2cd4d |
A |
G |
3: 94,271,226 (GRCm39) |
D164G |
probably benign |
Het |
Cacna1e |
C |
A |
1: 154,362,316 (GRCm39) |
V424F |
possibly damaging |
Het |
Capn7 |
C |
A |
14: 31,085,560 (GRCm39) |
T511K |
probably benign |
Het |
Cdc5l |
G |
A |
17: 45,718,943 (GRCm39) |
P558S |
probably benign |
Het |
Cep170 |
T |
A |
1: 176,609,975 (GRCm39) |
H112L |
probably damaging |
Het |
Cfap61 |
C |
T |
2: 145,789,053 (GRCm39) |
T19M |
probably benign |
Het |
Clca3a1 |
A |
G |
3: 144,463,821 (GRCm39) |
V152A |
probably benign |
Het |
Cnot10 |
G |
T |
9: 114,461,791 (GRCm39) |
T24K |
probably damaging |
Het |
Cntnap5b |
T |
A |
1: 100,306,800 (GRCm39) |
I839N |
possibly damaging |
Het |
Cyp4f13 |
A |
T |
17: 33,148,847 (GRCm39) |
D299E |
probably damaging |
Het |
Dclk1 |
A |
G |
3: 55,395,232 (GRCm39) |
E128G |
probably damaging |
Het |
Dennd1b |
T |
C |
1: 139,061,413 (GRCm39) |
I365T |
probably damaging |
Het |
Dgcr8 |
T |
C |
16: 18,102,274 (GRCm39) |
T3A |
probably damaging |
Het |
Dld |
A |
C |
12: 31,394,847 (GRCm39) |
I58S |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Faf1 |
C |
T |
4: 109,719,012 (GRCm39) |
L373F |
probably damaging |
Het |
Fam171b |
C |
T |
2: 83,707,042 (GRCm39) |
T304I |
probably benign |
Het |
Fcgrt |
A |
T |
7: 44,751,622 (GRCm39) |
|
probably null |
Het |
Gimap9 |
T |
C |
6: 48,655,285 (GRCm39) |
W291R |
probably damaging |
Het |
Gm4847 |
G |
A |
1: 166,457,892 (GRCm39) |
A487V |
probably damaging |
Het |
Gria4 |
T |
A |
9: 4,420,199 (GRCm39) |
I888F |
probably benign |
Het |
Hapln2 |
T |
A |
3: 87,930,600 (GRCm39) |
I224F |
probably damaging |
Het |
Herc1 |
T |
G |
9: 66,283,663 (GRCm39) |
L332R |
possibly damaging |
Het |
Hmgxb4 |
T |
C |
8: 75,749,927 (GRCm39) |
V481A |
probably benign |
Het |
Htr1d |
T |
C |
4: 136,170,109 (GRCm39) |
S113P |
probably damaging |
Het |
Ift81 |
T |
C |
5: 122,689,163 (GRCm39) |
Q651R |
probably benign |
Het |
Il17ra |
T |
C |
6: 120,452,234 (GRCm39) |
S199P |
probably damaging |
Het |
Itih2 |
T |
C |
2: 10,103,318 (GRCm39) |
N723S |
probably benign |
Het |
Jak1 |
A |
T |
4: 101,032,325 (GRCm39) |
V427E |
probably damaging |
Het |
Krt23 |
C |
T |
11: 99,376,584 (GRCm39) |
D191N |
probably damaging |
Het |
Lingo1 |
T |
A |
9: 56,526,934 (GRCm39) |
I552F |
possibly damaging |
Het |
Llgl2 |
G |
A |
11: 115,737,812 (GRCm39) |
R199Q |
probably benign |
Het |
Lrrc37a |
G |
T |
11: 103,392,042 (GRCm39) |
Q1128K |
possibly damaging |
Het |
Lrrc74a |
T |
C |
12: 86,783,263 (GRCm39) |
V36A |
probably benign |
Het |
M1ap |
T |
A |
6: 82,980,877 (GRCm39) |
D254E |
possibly damaging |
Het |
Mal2 |
C |
T |
15: 54,434,794 (GRCm39) |
|
probably benign |
Het |
Mbnl2 |
A |
G |
14: 120,622,833 (GRCm39) |
T124A |
probably benign |
Het |
Nfatc1 |
A |
G |
18: 80,755,885 (GRCm39) |
S33P |
probably benign |
Het |
Nfkbid |
A |
G |
7: 30,125,162 (GRCm39) |
N253S |
probably damaging |
Het |
Ngfr |
T |
A |
11: 95,465,267 (GRCm39) |
I194F |
probably benign |
Het |
Nhsl1 |
A |
G |
10: 18,345,789 (GRCm39) |
|
probably benign |
Het |
Nol9 |
T |
A |
4: 152,125,691 (GRCm39) |
I214N |
possibly damaging |
Het |
Or1o3 |
A |
G |
17: 37,573,635 (GRCm39) |
S307P |
probably benign |
Het |
Or5p56 |
T |
C |
7: 107,590,307 (GRCm39) |
L245P |
probably damaging |
Het |
Or8k3 |
T |
A |
2: 86,058,578 (GRCm39) |
T246S |
possibly damaging |
Het |
Pax3 |
C |
T |
1: 78,169,186 (GRCm39) |
S160N |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,122,267 (GRCm39) |
|
probably null |
Het |
Pde5a |
A |
C |
3: 122,522,956 (GRCm39) |
E21A |
probably benign |
Het |
Plcxd1 |
A |
G |
5: 110,250,469 (GRCm39) |
E270G |
probably damaging |
Het |
Plxna1 |
T |
A |
6: 89,333,586 (GRCm39) |
K348* |
probably null |
Het |
Pramel34 |
A |
T |
5: 93,785,937 (GRCm39) |
N114K |
probably benign |
Het |
Prb1b |
T |
A |
6: 132,289,692 (GRCm39) |
H44L |
unknown |
Het |
Psg21 |
G |
T |
7: 18,388,926 (GRCm39) |
D55E |
possibly damaging |
Het |
Rasa1 |
C |
A |
13: 85,381,814 (GRCm39) |
A493S |
probably benign |
Het |
Raver2 |
A |
G |
4: 100,990,814 (GRCm39) |
I396V |
probably benign |
Het |
Rpa2 |
A |
G |
4: 132,502,331 (GRCm39) |
K138E |
probably benign |
Het |
Rsad1 |
T |
C |
11: 94,439,062 (GRCm39) |
N133D |
probably damaging |
Het |
Rusc1 |
T |
C |
3: 88,999,188 (GRCm39) |
D198G |
probably benign |
Het |
Samsn1 |
A |
T |
16: 75,667,803 (GRCm39) |
Y258N |
probably damaging |
Het |
Scap |
A |
G |
9: 110,203,135 (GRCm39) |
N270D |
probably benign |
Het |
Shisal2a |
A |
T |
4: 108,225,052 (GRCm39) |
I170N |
probably damaging |
Het |
Smpd4 |
T |
C |
16: 17,449,877 (GRCm39) |
Y200H |
probably damaging |
Het |
Steap2 |
A |
G |
5: 5,725,881 (GRCm39) |
V381A |
probably damaging |
Het |
Syk |
C |
T |
13: 52,765,089 (GRCm39) |
T72I |
probably damaging |
Het |
Tbc1d14 |
T |
C |
5: 36,729,228 (GRCm39) |
D66G |
possibly damaging |
Het |
Tcp11 |
A |
G |
17: 28,290,691 (GRCm39) |
Y223H |
probably benign |
Het |
Timm9 |
A |
G |
12: 71,173,124 (GRCm39) |
S8P |
probably benign |
Het |
Tmpo |
T |
C |
10: 91,000,069 (GRCm39) |
|
probably null |
Het |
Vezf1 |
T |
C |
11: 87,967,012 (GRCm39) |
M81T |
probably benign |
Het |
Vipr1 |
T |
A |
9: 121,493,719 (GRCm39) |
W257R |
probably damaging |
Het |
Vmn1r237 |
G |
A |
17: 21,534,556 (GRCm39) |
G93D |
probably damaging |
Het |
Vmn2r6 |
A |
G |
3: 64,445,424 (GRCm39) |
V678A |
probably benign |
Het |
Vmn2r85 |
T |
C |
10: 130,261,330 (GRCm39) |
T336A |
possibly damaging |
Het |
Xpnpep3 |
C |
A |
15: 81,322,300 (GRCm39) |
D296E |
probably benign |
Het |
Zfp35 |
C |
A |
18: 24,137,118 (GRCm39) |
H487Q |
probably benign |
Het |
Zfp606 |
A |
T |
7: 12,227,928 (GRCm39) |
Y625F |
probably damaging |
Het |
Zfp677 |
A |
G |
17: 21,617,530 (GRCm39) |
T196A |
possibly damaging |
Het |
Zmym1 |
T |
C |
4: 126,941,677 (GRCm39) |
I904V |
probably damaging |
Het |
|
Other mutations in Dlg5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Dlg5
|
APN |
14 |
24,241,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00164:Dlg5
|
APN |
14 |
24,208,532 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL00767:Dlg5
|
APN |
14 |
24,215,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01284:Dlg5
|
APN |
14 |
24,196,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Dlg5
|
APN |
14 |
24,252,419 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01532:Dlg5
|
APN |
14 |
24,208,660 (GRCm39) |
missense |
probably benign |
|
IGL01621:Dlg5
|
APN |
14 |
24,198,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Dlg5
|
APN |
14 |
24,188,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01733:Dlg5
|
APN |
14 |
24,220,517 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02048:Dlg5
|
APN |
14 |
24,222,271 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02103:Dlg5
|
APN |
14 |
24,194,414 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Dlg5
|
APN |
14 |
24,208,419 (GRCm39) |
missense |
probably benign |
|
IGL02146:Dlg5
|
APN |
14 |
24,252,429 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02392:Dlg5
|
APN |
14 |
24,200,277 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02427:Dlg5
|
APN |
14 |
24,216,275 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Dlg5
|
APN |
14 |
24,241,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Dlg5
|
APN |
14 |
24,196,319 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02933:Dlg5
|
APN |
14 |
24,208,567 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02965:Dlg5
|
APN |
14 |
24,222,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02988:Dlg5
|
APN |
14 |
24,216,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Dlg5
|
APN |
14 |
24,220,522 (GRCm39) |
missense |
probably benign |
0.03 |
legerdemain
|
UTSW |
14 |
24,214,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Dlg5
|
UTSW |
14 |
24,197,274 (GRCm39) |
missense |
probably benign |
|
R0131:Dlg5
|
UTSW |
14 |
24,188,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Dlg5
|
UTSW |
14 |
24,196,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Dlg5
|
UTSW |
14 |
24,226,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Dlg5
|
UTSW |
14 |
24,185,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Dlg5
|
UTSW |
14 |
24,185,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0981:Dlg5
|
UTSW |
14 |
24,204,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Dlg5
|
UTSW |
14 |
24,226,676 (GRCm39) |
missense |
probably benign |
0.06 |
R1402:Dlg5
|
UTSW |
14 |
24,226,676 (GRCm39) |
missense |
probably benign |
0.06 |
R1438:Dlg5
|
UTSW |
14 |
24,204,673 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1449:Dlg5
|
UTSW |
14 |
24,185,711 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1465:Dlg5
|
UTSW |
14 |
24,204,764 (GRCm39) |
splice site |
probably null |
|
R1465:Dlg5
|
UTSW |
14 |
24,204,764 (GRCm39) |
splice site |
probably null |
|
R1543:Dlg5
|
UTSW |
14 |
24,194,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Dlg5
|
UTSW |
14 |
24,199,512 (GRCm39) |
missense |
probably benign |
0.28 |
R1899:Dlg5
|
UTSW |
14 |
24,198,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Dlg5
|
UTSW |
14 |
24,226,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1921:Dlg5
|
UTSW |
14 |
24,226,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Dlg5
|
UTSW |
14 |
24,206,537 (GRCm39) |
splice site |
probably benign |
|
R1968:Dlg5
|
UTSW |
14 |
24,214,187 (GRCm39) |
nonsense |
probably null |
|
R2049:Dlg5
|
UTSW |
14 |
24,204,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Dlg5
|
UTSW |
14 |
24,186,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Dlg5
|
UTSW |
14 |
24,227,826 (GRCm39) |
nonsense |
probably null |
|
R2139:Dlg5
|
UTSW |
14 |
24,220,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Dlg5
|
UTSW |
14 |
24,187,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R2283:Dlg5
|
UTSW |
14 |
24,208,731 (GRCm39) |
missense |
probably benign |
0.00 |
R2293:Dlg5
|
UTSW |
14 |
24,208,180 (GRCm39) |
missense |
probably benign |
|
R2356:Dlg5
|
UTSW |
14 |
24,220,496 (GRCm39) |
critical splice donor site |
probably null |
|
R2362:Dlg5
|
UTSW |
14 |
24,208,755 (GRCm39) |
missense |
probably benign |
0.04 |
R2513:Dlg5
|
UTSW |
14 |
24,214,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R3084:Dlg5
|
UTSW |
14 |
24,216,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R3086:Dlg5
|
UTSW |
14 |
24,216,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R3750:Dlg5
|
UTSW |
14 |
24,215,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R3780:Dlg5
|
UTSW |
14 |
24,240,378 (GRCm39) |
unclassified |
probably benign |
|
R3782:Dlg5
|
UTSW |
14 |
24,240,378 (GRCm39) |
unclassified |
probably benign |
|
R3828:Dlg5
|
UTSW |
14 |
24,196,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R4079:Dlg5
|
UTSW |
14 |
24,198,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4393:Dlg5
|
UTSW |
14 |
24,228,057 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4615:Dlg5
|
UTSW |
14 |
24,208,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Dlg5
|
UTSW |
14 |
24,187,249 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4712:Dlg5
|
UTSW |
14 |
24,228,051 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4796:Dlg5
|
UTSW |
14 |
24,194,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dlg5
|
UTSW |
14 |
24,204,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Dlg5
|
UTSW |
14 |
24,204,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Dlg5
|
UTSW |
14 |
24,204,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R5022:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5023:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Dlg5
|
UTSW |
14 |
24,186,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5234:Dlg5
|
UTSW |
14 |
24,242,930 (GRCm39) |
missense |
probably damaging |
0.98 |
R5561:Dlg5
|
UTSW |
14 |
24,227,860 (GRCm39) |
missense |
probably benign |
0.03 |
R5567:Dlg5
|
UTSW |
14 |
24,242,981 (GRCm39) |
nonsense |
probably null |
|
R5570:Dlg5
|
UTSW |
14 |
24,242,981 (GRCm39) |
nonsense |
probably null |
|
R5640:Dlg5
|
UTSW |
14 |
24,220,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Dlg5
|
UTSW |
14 |
24,208,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R5711:Dlg5
|
UTSW |
14 |
24,200,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Dlg5
|
UTSW |
14 |
24,196,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R5900:Dlg5
|
UTSW |
14 |
24,199,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5964:Dlg5
|
UTSW |
14 |
24,214,157 (GRCm39) |
missense |
probably benign |
|
R6240:Dlg5
|
UTSW |
14 |
24,199,596 (GRCm39) |
splice site |
probably null |
|
R6276:Dlg5
|
UTSW |
14 |
24,214,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Dlg5
|
UTSW |
14 |
24,208,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Dlg5
|
UTSW |
14 |
24,188,774 (GRCm39) |
missense |
probably benign |
0.45 |
R6527:Dlg5
|
UTSW |
14 |
24,240,516 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6593:Dlg5
|
UTSW |
14 |
24,200,720 (GRCm39) |
missense |
probably benign |
0.01 |
R6687:Dlg5
|
UTSW |
14 |
24,240,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6965:Dlg5
|
UTSW |
14 |
24,199,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Dlg5
|
UTSW |
14 |
24,196,263 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7075:Dlg5
|
UTSW |
14 |
24,227,865 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7149:Dlg5
|
UTSW |
14 |
24,240,492 (GRCm39) |
missense |
probably benign |
0.00 |
R7182:Dlg5
|
UTSW |
14 |
24,294,924 (GRCm39) |
missense |
|
|
R7203:Dlg5
|
UTSW |
14 |
24,188,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Dlg5
|
UTSW |
14 |
24,186,706 (GRCm39) |
nonsense |
probably null |
|
R7359:Dlg5
|
UTSW |
14 |
24,214,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Dlg5
|
UTSW |
14 |
24,227,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R7485:Dlg5
|
UTSW |
14 |
24,198,390 (GRCm39) |
missense |
probably benign |
|
R7629:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Dlg5
|
UTSW |
14 |
24,207,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R7804:Dlg5
|
UTSW |
14 |
24,215,388 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7861:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7864:Dlg5
|
UTSW |
14 |
24,295,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R7874:Dlg5
|
UTSW |
14 |
24,185,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Dlg5
|
UTSW |
14 |
24,187,192 (GRCm39) |
splice site |
probably null |
|
R7981:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8147:Dlg5
|
UTSW |
14 |
24,208,395 (GRCm39) |
missense |
probably benign |
0.07 |
R8204:Dlg5
|
UTSW |
14 |
24,210,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Dlg5
|
UTSW |
14 |
24,210,336 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8287:Dlg5
|
UTSW |
14 |
24,214,453 (GRCm39) |
missense |
probably benign |
0.40 |
R8296:Dlg5
|
UTSW |
14 |
24,198,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8317:Dlg5
|
UTSW |
14 |
24,241,298 (GRCm39) |
missense |
probably damaging |
0.98 |
R8327:Dlg5
|
UTSW |
14 |
24,196,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R8352:Dlg5
|
UTSW |
14 |
24,241,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8409:Dlg5
|
UTSW |
14 |
24,226,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Dlg5
|
UTSW |
14 |
24,241,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Dlg5
|
UTSW |
14 |
24,208,213 (GRCm39) |
missense |
probably benign |
|
R8540:Dlg5
|
UTSW |
14 |
24,208,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R8701:Dlg5
|
UTSW |
14 |
24,226,768 (GRCm39) |
missense |
probably benign |
0.04 |
R8925:Dlg5
|
UTSW |
14 |
24,206,547 (GRCm39) |
missense |
|
|
R8927:Dlg5
|
UTSW |
14 |
24,206,547 (GRCm39) |
missense |
|
|
R9025:Dlg5
|
UTSW |
14 |
24,199,546 (GRCm39) |
missense |
probably benign |
0.00 |
R9102:Dlg5
|
UTSW |
14 |
24,199,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R9138:Dlg5
|
UTSW |
14 |
24,295,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R9165:Dlg5
|
UTSW |
14 |
24,196,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9250:Dlg5
|
UTSW |
14 |
24,240,543 (GRCm39) |
missense |
probably benign |
0.07 |
R9267:Dlg5
|
UTSW |
14 |
24,204,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:Dlg5
|
UTSW |
14 |
24,242,881 (GRCm39) |
missense |
probably damaging |
0.99 |
R9291:Dlg5
|
UTSW |
14 |
24,241,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R9387:Dlg5
|
UTSW |
14 |
24,197,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R9729:Dlg5
|
UTSW |
14 |
24,204,681 (GRCm39) |
missense |
probably benign |
0.00 |
RF005:Dlg5
|
UTSW |
14 |
24,208,561 (GRCm39) |
nonsense |
probably null |
|
YA93:Dlg5
|
UTSW |
14 |
24,205,201 (GRCm39) |
unclassified |
probably benign |
|
Z1088:Dlg5
|
UTSW |
14 |
24,208,162 (GRCm39) |
missense |
probably damaging |
1.00 |
|