Other mutations in this stock |
Total: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
C |
9: 57,165,635 (GRCm39) |
S246R |
possibly damaging |
Het |
Abca13 |
C |
T |
11: 9,416,411 (GRCm39) |
R4058C |
probably benign |
Het |
Acacb |
A |
T |
5: 114,303,795 (GRCm39) |
R73* |
probably null |
Het |
Adam22 |
C |
T |
5: 8,184,525 (GRCm39) |
C489Y |
probably damaging |
Het |
Agap3 |
A |
T |
5: 24,698,011 (GRCm39) |
K460I |
probably damaging |
Het |
Ak4 |
T |
C |
4: 101,320,833 (GRCm39) |
I214T |
possibly damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Arrb2 |
T |
A |
11: 70,328,808 (GRCm39) |
H221Q |
probably damaging |
Het |
Atl1 |
T |
G |
12: 70,006,049 (GRCm39) |
F452V |
probably damaging |
Het |
Atp8b5 |
A |
G |
4: 43,357,063 (GRCm39) |
T604A |
probably damaging |
Het |
Bglap3 |
T |
C |
3: 88,276,068 (GRCm39) |
I95V |
probably benign |
Het |
Ccdc88a |
G |
T |
11: 29,411,788 (GRCm39) |
M532I |
probably benign |
Het |
Ccnl1 |
A |
G |
3: 65,854,332 (GRCm39) |
S430P |
possibly damaging |
Het |
Cdhr18 |
C |
T |
14: 13,829,657 (GRCm38) |
S695N |
possibly damaging |
Het |
Cdk5rap2 |
A |
T |
4: 70,321,791 (GRCm39) |
|
probably null |
Het |
Cep126 |
A |
T |
9: 8,120,748 (GRCm39) |
Y92N |
possibly damaging |
Het |
Cfap44 |
A |
C |
16: 44,242,737 (GRCm39) |
T714P |
probably benign |
Het |
Cnga1 |
T |
G |
5: 72,774,068 (GRCm39) |
D90A |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,469,749 (GRCm39) |
I1369V |
possibly damaging |
Het |
Coq3 |
T |
C |
4: 21,910,466 (GRCm39) |
S314P |
probably damaging |
Het |
Crhr1 |
A |
G |
11: 104,060,675 (GRCm39) |
R151G |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,806,167 (GRCm39) |
I930V |
probably damaging |
Het |
Ctcf |
T |
A |
8: 106,402,620 (GRCm39) |
|
probably null |
Het |
Dct |
T |
C |
14: 118,271,690 (GRCm39) |
N380S |
probably benign |
Het |
Decr2 |
A |
T |
17: 26,306,387 (GRCm39) |
L83Q |
probably damaging |
Het |
Depdc5 |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
5: 33,067,751 (GRCm39) |
|
probably benign |
Het |
Dgkb |
T |
C |
12: 38,216,776 (GRCm39) |
|
probably null |
Het |
Dnah1 |
T |
C |
14: 31,041,716 (GRCm39) |
D85G |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,574,637 (GRCm39) |
D1709G |
probably damaging |
Het |
Dsc1 |
A |
T |
18: 20,229,045 (GRCm39) |
V415D |
probably damaging |
Het |
Duox2 |
T |
A |
2: 122,125,832 (GRCm39) |
I296F |
probably damaging |
Het |
Ece2 |
T |
A |
16: 20,463,922 (GRCm39) |
L890H |
probably damaging |
Het |
Ecsit |
A |
G |
9: 21,987,815 (GRCm39) |
S75P |
possibly damaging |
Het |
Enpp3 |
A |
G |
10: 24,654,687 (GRCm39) |
C664R |
probably damaging |
Het |
Evpl |
G |
T |
11: 116,117,854 (GRCm39) |
D778E |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,448,663 (GRCm39) |
|
probably null |
Het |
Fam217b |
A |
T |
2: 178,062,374 (GRCm39) |
I113F |
probably benign |
Het |
Galnt6 |
G |
A |
15: 100,613,999 (GRCm39) |
P101S |
possibly damaging |
Het |
Gm379 |
G |
A |
X: 107,707,870 (GRCm39) |
Q210* |
probably null |
Het |
Grk4 |
A |
T |
5: 34,833,531 (GRCm39) |
|
probably null |
Het |
Gtf3c4 |
A |
G |
2: 28,729,968 (GRCm39) |
V91A |
probably benign |
Het |
Hcfc2 |
G |
T |
10: 82,538,392 (GRCm39) |
G143V |
probably damaging |
Het |
Heatr4 |
A |
C |
12: 84,005,221 (GRCm39) |
H710Q |
probably damaging |
Het |
Htr3a |
A |
T |
9: 48,817,681 (GRCm39) |
D97E |
probably damaging |
Het |
Htr4 |
T |
G |
18: 62,561,193 (GRCm39) |
F151L |
probably benign |
Het |
Il22ra1 |
A |
T |
4: 135,478,219 (GRCm39) |
Q430L |
probably damaging |
Het |
Invs |
T |
A |
4: 48,402,824 (GRCm39) |
|
probably null |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Irs1 |
T |
C |
1: 82,267,182 (GRCm39) |
S345G |
probably damaging |
Het |
Kdm4a |
A |
G |
4: 118,017,596 (GRCm39) |
V490A |
probably benign |
Het |
Kif26a |
C |
T |
12: 112,141,974 (GRCm39) |
R743C |
probably damaging |
Het |
Kif28 |
A |
G |
1: 179,530,088 (GRCm39) |
V691A |
possibly damaging |
Het |
Klhl5 |
T |
A |
5: 65,324,330 (GRCm39) |
L696Q |
probably benign |
Het |
Krtap5-1 |
T |
C |
7: 141,850,084 (GRCm39) |
|
probably benign |
Het |
Lama2 |
A |
C |
10: 27,064,395 (GRCm39) |
D1195E |
probably damaging |
Het |
Lamb1 |
T |
G |
12: 31,379,209 (GRCm39) |
L1722R |
probably damaging |
Het |
Lrp11 |
T |
A |
10: 7,499,544 (GRCm39) |
L245Q |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,876,879 (GRCm39) |
E422G |
probably benign |
Het |
Man2b1 |
T |
A |
8: 85,813,451 (GRCm39) |
D214E |
probably damaging |
Het |
Mlxipl |
A |
T |
5: 135,162,422 (GRCm39) |
D628V |
possibly damaging |
Het |
Msantd5f6 |
T |
A |
4: 73,321,675 (GRCm39) |
Y120F |
probably damaging |
Het |
Myo18b |
G |
A |
5: 112,840,624 (GRCm39) |
R2390C |
probably damaging |
Het |
Mypn |
T |
A |
10: 62,959,176 (GRCm39) |
R1048S |
probably benign |
Het |
Napepld |
A |
G |
5: 21,870,270 (GRCm39) |
S383P |
probably damaging |
Het |
Napsa |
A |
G |
7: 44,231,160 (GRCm39) |
T130A |
probably damaging |
Het |
Nbr1 |
T |
C |
11: 101,465,978 (GRCm39) |
I716T |
probably damaging |
Het |
Nexn |
A |
T |
3: 151,953,818 (GRCm39) |
M212K |
probably damaging |
Het |
Nlrp9b |
T |
A |
7: 19,757,182 (GRCm39) |
S140T |
probably benign |
Het |
Nxpe2 |
T |
C |
9: 48,230,906 (GRCm39) |
T488A |
probably benign |
Het |
Or10g3 |
T |
G |
14: 52,610,174 (GRCm39) |
Q112P |
possibly damaging |
Het |
Or10v1 |
A |
T |
19: 11,873,913 (GRCm39) |
Y176F |
probably benign |
Het |
Or5ac25 |
A |
T |
16: 59,182,526 (GRCm39) |
D18E |
probably benign |
Het |
Or7g12 |
A |
T |
9: 18,900,192 (GRCm39) |
K303* |
probably null |
Het |
Or8k20 |
C |
T |
2: 86,106,190 (GRCm39) |
V214I |
probably benign |
Het |
Osbpl5 |
T |
C |
7: 143,256,918 (GRCm39) |
D404G |
possibly damaging |
Het |
Pan2 |
T |
G |
10: 128,144,237 (GRCm39) |
L162R |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,416,235 (GRCm39) |
V545F |
probably damaging |
Het |
Pcdh18 |
A |
G |
3: 49,709,896 (GRCm39) |
V473A |
probably benign |
Het |
Plb1 |
A |
T |
5: 32,448,582 (GRCm39) |
N350I |
probably damaging |
Het |
Polr1a |
A |
G |
6: 71,944,898 (GRCm39) |
K1318R |
probably benign |
Het |
Ppp1r18 |
C |
T |
17: 36,184,738 (GRCm39) |
P130S |
probably damaging |
Het |
Prss48 |
C |
T |
3: 85,905,614 (GRCm39) |
W86* |
probably null |
Het |
Rab3c |
A |
T |
13: 110,220,744 (GRCm39) |
I137N |
probably damaging |
Het |
Rab3gap2 |
G |
C |
1: 184,954,099 (GRCm39) |
R57P |
probably benign |
Het |
Rad54l2 |
A |
C |
9: 106,570,916 (GRCm39) |
|
probably null |
Het |
Ralgapb |
C |
A |
2: 158,337,483 (GRCm39) |
N1147K |
probably benign |
Het |
Rfx7 |
C |
T |
9: 72,524,093 (GRCm39) |
R428C |
probably damaging |
Het |
Robo1 |
A |
G |
16: 72,757,092 (GRCm39) |
Q351R |
probably null |
Het |
Samd4 |
T |
C |
14: 47,311,585 (GRCm39) |
F81S |
probably damaging |
Het |
Shprh |
T |
A |
10: 11,059,541 (GRCm39) |
Y1097* |
probably null |
Het |
Sik3 |
C |
G |
9: 46,132,387 (GRCm39) |
H1276Q |
probably benign |
Het |
Slc24a4 |
T |
A |
12: 102,097,876 (GRCm39) |
D79E |
probably benign |
Het |
Slc7a13 |
A |
T |
4: 19,839,254 (GRCm39) |
I286F |
probably benign |
Het |
Smarca1 |
G |
A |
X: 46,938,840 (GRCm39) |
Q723* |
probably null |
Het |
Spata31d1b |
T |
C |
13: 59,865,882 (GRCm39) |
L1010P |
probably damaging |
Het |
Sult2a1 |
T |
C |
7: 13,569,900 (GRCm39) |
S111G |
possibly damaging |
Het |
Tecpr2 |
C |
T |
12: 110,914,346 (GRCm39) |
T1219M |
probably damaging |
Het |
Tesk1 |
T |
C |
4: 43,446,998 (GRCm39) |
M462T |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,666,196 (GRCm39) |
S239R |
probably benign |
Het |
Tmem171 |
C |
A |
13: 98,822,924 (GRCm39) |
G292* |
probably null |
Het |
Tmtc2 |
G |
T |
10: 105,025,969 (GRCm39) |
T833N |
probably benign |
Het |
Tnc |
G |
T |
4: 63,918,299 (GRCm39) |
T1204K |
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 18,883,937 (GRCm39) |
K148E |
probably benign |
Het |
Tnrc18 |
G |
A |
5: 142,800,895 (GRCm39) |
S21F |
probably damaging |
Het |
Tns4 |
T |
C |
11: 98,966,401 (GRCm39) |
T425A |
probably damaging |
Het |
Tox |
T |
A |
4: 6,688,948 (GRCm39) |
Y472F |
probably damaging |
Het |
Trak2 |
A |
T |
1: 58,958,014 (GRCm39) |
|
probably null |
Het |
Trim33 |
T |
A |
3: 103,244,760 (GRCm39) |
Y716N |
probably damaging |
Het |
Trrap |
T |
G |
5: 144,752,863 (GRCm39) |
I1813R |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 78,978,361 (GRCm39) |
E137G |
probably benign |
Het |
Ube2j2 |
A |
G |
4: 156,033,483 (GRCm39) |
K19R |
probably benign |
Het |
Ubxn2b |
T |
C |
4: 6,208,889 (GRCm39) |
I206T |
possibly damaging |
Het |
Usp40 |
A |
G |
1: 87,909,778 (GRCm39) |
F559L |
probably benign |
Het |
Utp4 |
T |
A |
8: 107,638,982 (GRCm39) |
|
probably null |
Het |
Vac14 |
A |
G |
8: 111,409,166 (GRCm39) |
N524S |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,801,334 (GRCm39) |
S605P |
probably damaging |
Het |
Vwa5b2 |
G |
T |
16: 20,423,582 (GRCm39) |
S1165I |
possibly damaging |
Het |
Zdhhc19 |
C |
T |
16: 32,317,231 (GRCm39) |
R28* |
probably null |
Het |
Zfp106 |
T |
C |
2: 120,357,329 (GRCm39) |
I1189V |
probably benign |
Het |
Zfp189 |
C |
T |
4: 49,529,511 (GRCm39) |
Q205* |
probably null |
Het |
|
Other mutations in Dnajc13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Dnajc13
|
APN |
9 |
104,039,979 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00754:Dnajc13
|
APN |
9 |
104,051,697 (GRCm39) |
nonsense |
probably null |
|
IGL00914:Dnajc13
|
APN |
9 |
104,090,081 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01014:Dnajc13
|
APN |
9 |
104,080,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01077:Dnajc13
|
APN |
9 |
104,108,220 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01137:Dnajc13
|
APN |
9 |
104,037,689 (GRCm39) |
missense |
probably benign |
|
IGL01305:Dnajc13
|
APN |
9 |
104,107,836 (GRCm39) |
splice site |
probably null |
|
IGL01707:Dnajc13
|
APN |
9 |
104,106,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01868:Dnajc13
|
APN |
9 |
104,039,944 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01950:Dnajc13
|
APN |
9 |
104,067,631 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02102:Dnajc13
|
APN |
9 |
104,106,208 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02350:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02357:Dnajc13
|
APN |
9 |
104,039,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02470:Dnajc13
|
APN |
9 |
104,052,946 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02888:Dnajc13
|
APN |
9 |
104,057,261 (GRCm39) |
splice site |
probably benign |
|
IGL03079:Dnajc13
|
APN |
9 |
104,090,068 (GRCm39) |
nonsense |
probably null |
|
IGL03179:Dnajc13
|
APN |
9 |
104,044,634 (GRCm39) |
missense |
probably benign |
0.42 |
IGL03293:Dnajc13
|
APN |
9 |
104,051,625 (GRCm39) |
missense |
possibly damaging |
0.64 |
impressario
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
Kaiser
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
BB018:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4142001:Dnajc13
|
UTSW |
9 |
104,115,672 (GRCm39) |
missense |
probably damaging |
0.96 |
R0323:Dnajc13
|
UTSW |
9 |
104,034,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R0361:Dnajc13
|
UTSW |
9 |
104,044,258 (GRCm39) |
missense |
probably benign |
0.18 |
R0480:Dnajc13
|
UTSW |
9 |
104,077,708 (GRCm39) |
missense |
probably damaging |
0.98 |
R0558:Dnajc13
|
UTSW |
9 |
104,079,151 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0707:Dnajc13
|
UTSW |
9 |
104,049,781 (GRCm39) |
missense |
probably benign |
0.12 |
R0831:Dnajc13
|
UTSW |
9 |
104,049,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1234:Dnajc13
|
UTSW |
9 |
104,091,356 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1433:Dnajc13
|
UTSW |
9 |
104,057,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Dnajc13
|
UTSW |
9 |
104,056,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1464:Dnajc13
|
UTSW |
9 |
104,091,366 (GRCm39) |
missense |
probably benign |
0.10 |
R1489:Dnajc13
|
UTSW |
9 |
104,108,234 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1575:Dnajc13
|
UTSW |
9 |
104,034,037 (GRCm39) |
missense |
probably benign |
0.29 |
R1750:Dnajc13
|
UTSW |
9 |
104,098,676 (GRCm39) |
missense |
probably damaging |
0.98 |
R2066:Dnajc13
|
UTSW |
9 |
104,098,640 (GRCm39) |
missense |
probably benign |
0.01 |
R2206:Dnajc13
|
UTSW |
9 |
104,080,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3160:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3162:Dnajc13
|
UTSW |
9 |
104,097,097 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4158:Dnajc13
|
UTSW |
9 |
104,067,641 (GRCm39) |
missense |
probably damaging |
0.96 |
R4460:Dnajc13
|
UTSW |
9 |
104,058,262 (GRCm39) |
missense |
probably damaging |
0.96 |
R4537:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4538:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4631:Dnajc13
|
UTSW |
9 |
104,067,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Dnajc13
|
UTSW |
9 |
104,084,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Dnajc13
|
UTSW |
9 |
104,091,017 (GRCm39) |
missense |
probably benign |
|
R4731:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4732:Dnajc13
|
UTSW |
9 |
104,064,004 (GRCm39) |
intron |
probably benign |
|
R4758:Dnajc13
|
UTSW |
9 |
104,049,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4802:Dnajc13
|
UTSW |
9 |
104,052,926 (GRCm39) |
missense |
probably benign |
0.16 |
R4928:Dnajc13
|
UTSW |
9 |
104,110,837 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4944:Dnajc13
|
UTSW |
9 |
104,044,586 (GRCm39) |
unclassified |
probably benign |
|
R4979:Dnajc13
|
UTSW |
9 |
104,063,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Dnajc13
|
UTSW |
9 |
104,108,185 (GRCm39) |
missense |
probably benign |
0.39 |
R5190:Dnajc13
|
UTSW |
9 |
104,051,724 (GRCm39) |
missense |
probably benign |
0.00 |
R5256:Dnajc13
|
UTSW |
9 |
104,080,528 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5452:Dnajc13
|
UTSW |
9 |
104,069,313 (GRCm39) |
missense |
probably benign |
0.01 |
R5657:Dnajc13
|
UTSW |
9 |
104,105,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R5752:Dnajc13
|
UTSW |
9 |
104,069,973 (GRCm39) |
splice site |
probably null |
|
R5789:Dnajc13
|
UTSW |
9 |
104,091,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Dnajc13
|
UTSW |
9 |
104,053,865 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5846:Dnajc13
|
UTSW |
9 |
104,067,584 (GRCm39) |
missense |
probably damaging |
0.99 |
R5982:Dnajc13
|
UTSW |
9 |
104,061,814 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6189:Dnajc13
|
UTSW |
9 |
104,091,085 (GRCm39) |
missense |
probably benign |
0.12 |
R6355:Dnajc13
|
UTSW |
9 |
104,080,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R6483:Dnajc13
|
UTSW |
9 |
104,085,003 (GRCm39) |
missense |
probably damaging |
0.96 |
R6613:Dnajc13
|
UTSW |
9 |
104,091,076 (GRCm39) |
missense |
probably benign |
0.07 |
R6962:Dnajc13
|
UTSW |
9 |
104,058,208 (GRCm39) |
missense |
probably benign |
0.02 |
R7048:Dnajc13
|
UTSW |
9 |
104,080,613 (GRCm39) |
critical splice donor site |
probably null |
|
R7101:Dnajc13
|
UTSW |
9 |
104,042,221 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7304:Dnajc13
|
UTSW |
9 |
104,115,713 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Dnajc13
|
UTSW |
9 |
104,107,230 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7366:Dnajc13
|
UTSW |
9 |
104,061,905 (GRCm39) |
missense |
probably benign |
0.43 |
R7528:Dnajc13
|
UTSW |
9 |
104,056,164 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7635:Dnajc13
|
UTSW |
9 |
104,039,566 (GRCm39) |
missense |
probably benign |
|
R7673:Dnajc13
|
UTSW |
9 |
104,110,891 (GRCm39) |
missense |
probably benign |
0.09 |
R7856:Dnajc13
|
UTSW |
9 |
104,044,684 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7931:Dnajc13
|
UTSW |
9 |
104,095,763 (GRCm39) |
missense |
probably benign |
0.02 |
R7995:Dnajc13
|
UTSW |
9 |
104,051,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Dnajc13
|
UTSW |
9 |
104,067,590 (GRCm39) |
missense |
probably benign |
0.00 |
R8354:Dnajc13
|
UTSW |
9 |
104,094,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Dnajc13
|
UTSW |
9 |
104,057,338 (GRCm39) |
missense |
probably benign |
|
R8686:Dnajc13
|
UTSW |
9 |
104,048,004 (GRCm39) |
missense |
probably benign |
0.00 |
R8707:Dnajc13
|
UTSW |
9 |
104,069,847 (GRCm39) |
missense |
probably damaging |
0.96 |
R8847:Dnajc13
|
UTSW |
9 |
104,057,360 (GRCm39) |
nonsense |
probably null |
|
R8868:Dnajc13
|
UTSW |
9 |
104,042,987 (GRCm39) |
missense |
probably benign |
0.13 |
R8986:Dnajc13
|
UTSW |
9 |
104,057,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Dnajc13
|
UTSW |
9 |
104,085,039 (GRCm39) |
missense |
probably benign |
0.02 |
R9334:Dnajc13
|
UTSW |
9 |
104,051,659 (GRCm39) |
missense |
probably benign |
0.00 |
R9353:Dnajc13
|
UTSW |
9 |
104,067,571 (GRCm39) |
missense |
probably benign |
0.31 |
R9470:Dnajc13
|
UTSW |
9 |
104,107,919 (GRCm39) |
missense |
probably benign |
0.01 |
R9528:Dnajc13
|
UTSW |
9 |
104,114,904 (GRCm39) |
missense |
probably benign |
|
R9578:Dnajc13
|
UTSW |
9 |
104,115,726 (GRCm39) |
missense |
probably benign |
0.04 |
R9658:Dnajc13
|
UTSW |
9 |
104,115,728 (GRCm39) |
missense |
probably benign |
0.11 |
R9691:Dnajc13
|
UTSW |
9 |
104,042,211 (GRCm39) |
missense |
probably damaging |
1.00 |
X0017:Dnajc13
|
UTSW |
9 |
104,115,677 (GRCm39) |
missense |
possibly damaging |
0.90 |
X0028:Dnajc13
|
UTSW |
9 |
104,042,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|