Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aar2 |
T |
G |
2: 156,392,893 (GRCm39) |
V94G |
probably benign |
Het |
Acp5 |
A |
T |
9: 22,041,218 (GRCm39) |
S70T |
possibly damaging |
Het |
Adcy1 |
C |
G |
11: 7,089,162 (GRCm39) |
N525K |
possibly damaging |
Het |
Aknad1 |
A |
G |
3: 108,688,555 (GRCm39) |
M628V |
probably benign |
Het |
Alg8 |
A |
T |
7: 97,032,891 (GRCm39) |
|
probably null |
Het |
Cacna1d |
A |
G |
14: 29,845,453 (GRCm39) |
V572A |
probably benign |
Het |
Ccdc158 |
A |
C |
5: 92,809,977 (GRCm39) |
M177R |
probably benign |
Het |
Ccdc191 |
A |
T |
16: 43,767,859 (GRCm39) |
R678* |
probably null |
Het |
Cdkn2d |
C |
A |
9: 21,202,288 (GRCm39) |
|
probably benign |
Het |
Cdx2 |
G |
T |
5: 147,240,097 (GRCm39) |
T193K |
probably damaging |
Het |
Cfap44 |
T |
A |
16: 44,242,681 (GRCm39) |
M695K |
probably benign |
Het |
Cfap70 |
A |
C |
14: 20,498,673 (GRCm39) |
S5A |
probably benign |
Het |
Chd9 |
T |
C |
8: 91,659,456 (GRCm39) |
S139P |
probably damaging |
Het |
Chmp7 |
A |
G |
14: 69,958,446 (GRCm39) |
V241A |
probably damaging |
Het |
Cnga1 |
A |
G |
5: 72,762,374 (GRCm39) |
I380T |
probably damaging |
Het |
Cts6 |
T |
A |
13: 61,349,633 (GRCm39) |
E53D |
probably damaging |
Het |
Dclk3 |
A |
T |
9: 111,311,696 (GRCm39) |
N646I |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,738 (GRCm39) |
S4673G |
probably benign |
Het |
Dock4 |
G |
T |
12: 40,787,539 (GRCm39) |
S818I |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,041,461 (GRCm39) |
Q156* |
probably null |
Het |
Fam163b |
T |
C |
2: 27,002,646 (GRCm39) |
N117S |
probably damaging |
Het |
Fam89a |
A |
G |
8: 125,467,971 (GRCm39) |
Y114H |
probably damaging |
Het |
Flcn |
T |
C |
11: 59,691,902 (GRCm39) |
N249S |
probably benign |
Het |
Gm20422 |
T |
C |
8: 70,219,365 (GRCm39) |
Y53C |
probably damaging |
Het |
Gnai1 |
A |
G |
5: 18,478,548 (GRCm39) |
S206P |
probably damaging |
Het |
H1f6 |
G |
T |
13: 23,880,307 (GRCm39) |
K153N |
possibly damaging |
Het |
Hal |
T |
C |
10: 93,339,344 (GRCm39) |
S478P |
possibly damaging |
Het |
Haus3 |
G |
A |
5: 34,323,600 (GRCm39) |
P337S |
possibly damaging |
Het |
Hectd1 |
T |
A |
12: 51,816,101 (GRCm39) |
M1324L |
possibly damaging |
Het |
Hspa9 |
A |
T |
18: 35,079,699 (GRCm39) |
Y243* |
probably null |
Het |
Htr3a |
T |
C |
9: 48,817,686 (GRCm39) |
T96A |
probably benign |
Het |
Ift140 |
C |
A |
17: 25,264,497 (GRCm39) |
C557* |
probably null |
Het |
Jph3 |
A |
G |
8: 122,480,459 (GRCm39) |
Q379R |
possibly damaging |
Het |
Kcnb1 |
A |
G |
2: 166,946,889 (GRCm39) |
V653A |
probably benign |
Het |
Krt17 |
G |
A |
11: 100,151,704 (GRCm39) |
R30* |
probably null |
Het |
Lamb3 |
A |
T |
1: 193,003,361 (GRCm39) |
D100V |
probably damaging |
Het |
Map2 |
A |
G |
1: 66,455,265 (GRCm39) |
D1385G |
probably damaging |
Het |
Map3k21 |
A |
G |
8: 126,671,709 (GRCm39) |
D999G |
possibly damaging |
Het |
Marf1 |
T |
C |
16: 13,969,147 (GRCm39) |
I109V |
probably benign |
Het |
Mcam |
T |
G |
9: 44,051,502 (GRCm39) |
|
probably null |
Het |
Med18 |
T |
C |
4: 132,187,337 (GRCm39) |
H99R |
probably damaging |
Het |
Mettl25 |
C |
T |
10: 105,662,386 (GRCm39) |
V195I |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,192,518 (GRCm39) |
T1466A |
probably benign |
Het |
Myo1e |
A |
T |
9: 70,249,408 (GRCm39) |
I503F |
possibly damaging |
Het |
Myo3b |
T |
A |
2: 69,935,769 (GRCm39) |
C61S |
probably benign |
Het |
Myorg |
A |
T |
4: 41,498,912 (GRCm39) |
N239K |
probably benign |
Het |
Nf1 |
A |
T |
11: 79,309,400 (GRCm39) |
K438M |
possibly damaging |
Het |
Nlrp9c |
A |
G |
7: 26,077,437 (GRCm39) |
S727P |
possibly damaging |
Het |
Nmbr |
C |
T |
10: 14,646,139 (GRCm39) |
Q338* |
probably null |
Het |
Nt5e |
A |
G |
9: 88,249,385 (GRCm39) |
S440G |
possibly damaging |
Het |
Nubp2 |
T |
C |
17: 25,103,445 (GRCm39) |
E144G |
probably damaging |
Het |
Or12e7 |
T |
C |
2: 87,288,381 (GRCm39) |
F291L |
probably benign |
Het |
Or2ag1b |
A |
G |
7: 106,288,462 (GRCm39) |
Y159H |
probably benign |
Het |
Or52s1 |
G |
A |
7: 102,861,933 (GRCm39) |
V289M |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,642,557 (GRCm39) |
N1291I |
probably damaging |
Het |
Pa2g4 |
T |
C |
10: 128,399,511 (GRCm39) |
K51R |
probably benign |
Het |
Pcdhb12 |
A |
G |
18: 37,569,780 (GRCm39) |
I309V |
probably benign |
Het |
Pck1 |
T |
G |
2: 172,998,861 (GRCm39) |
I373S |
possibly damaging |
Het |
Pga5 |
A |
G |
19: 10,646,817 (GRCm39) |
Y305H |
probably damaging |
Het |
Plxnd1 |
G |
T |
6: 115,945,754 (GRCm39) |
D906E |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,256,927 (GRCm39) |
E98G |
possibly damaging |
Het |
Rab39 |
G |
A |
9: 53,617,330 (GRCm39) |
T29I |
probably damaging |
Het |
Raet1e |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Rars2 |
A |
C |
4: 34,656,030 (GRCm39) |
Q421P |
probably benign |
Het |
Rars2 |
T |
C |
4: 34,645,838 (GRCm39) |
Y252H |
probably damaging |
Het |
Rasa2 |
A |
T |
9: 96,450,460 (GRCm39) |
D479E |
probably damaging |
Het |
Rbl2 |
A |
T |
8: 91,833,135 (GRCm39) |
T689S |
probably damaging |
Het |
Rims4 |
C |
T |
2: 163,705,945 (GRCm39) |
V230M |
probably benign |
Het |
Skp2 |
A |
C |
15: 9,127,971 (GRCm39) |
|
probably null |
Het |
Slc35f4 |
A |
T |
14: 49,541,713 (GRCm39) |
I347N |
possibly damaging |
Het |
Slc4a2 |
A |
T |
5: 24,641,272 (GRCm39) |
|
probably null |
Het |
Slc52a3 |
T |
C |
2: 151,850,076 (GRCm39) |
*461Q |
probably null |
Het |
Slc6a1 |
G |
A |
6: 114,279,761 (GRCm39) |
V142I |
probably benign |
Het |
Susd5 |
A |
G |
9: 113,925,977 (GRCm39) |
*620W |
probably null |
Het |
Timm21 |
T |
C |
18: 84,965,791 (GRCm39) |
N239S |
probably damaging |
Het |
Tmem63c |
T |
C |
12: 87,122,413 (GRCm39) |
W404R |
probably damaging |
Het |
Tnrc6b |
A |
G |
15: 80,772,065 (GRCm39) |
D1118G |
probably damaging |
Het |
Traf2 |
G |
C |
2: 25,427,138 (GRCm39) |
A71G |
possibly damaging |
Het |
Trim54 |
A |
G |
5: 31,291,463 (GRCm39) |
M195V |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,850,987 (GRCm39) |
E741K |
probably damaging |
Het |
Trp73 |
AGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTG |
4: 154,146,981 (GRCm39) |
|
probably benign |
Het |
Trpm5 |
G |
T |
7: 142,636,695 (GRCm39) |
T414N |
probably damaging |
Het |
Vps51 |
G |
T |
19: 6,121,467 (GRCm39) |
S185* |
probably null |
Het |
Zfp329 |
G |
T |
7: 12,544,756 (GRCm39) |
T256K |
probably damaging |
Het |
Zfp729b |
A |
G |
13: 67,740,022 (GRCm39) |
Y748H |
probably damaging |
Het |
Zfp777 |
T |
C |
6: 48,001,903 (GRCm39) |
E773G |
probably damaging |
Het |
|
Other mutations in Kif14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00159:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00160:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00164:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00310:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00330:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00335:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00434:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00468:Kif14
|
APN |
1 |
136,396,756 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01330:Kif14
|
APN |
1 |
136,404,112 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01530:Kif14
|
APN |
1 |
136,406,157 (GRCm39) |
splice site |
probably benign |
|
IGL01622:Kif14
|
APN |
1 |
136,425,094 (GRCm39) |
splice site |
probably benign |
|
IGL01689:Kif14
|
APN |
1 |
136,447,380 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02115:Kif14
|
APN |
1 |
136,424,305 (GRCm39) |
splice site |
probably benign |
|
IGL02252:Kif14
|
APN |
1 |
136,406,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02259:Kif14
|
APN |
1 |
136,427,840 (GRCm39) |
missense |
probably benign |
|
IGL02439:Kif14
|
APN |
1 |
136,417,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Kif14
|
APN |
1 |
136,423,742 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02606:Kif14
|
APN |
1 |
136,424,331 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03253:Kif14
|
APN |
1 |
136,415,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0106:Kif14
|
UTSW |
1 |
136,407,662 (GRCm39) |
splice site |
probably benign |
|
R0193:Kif14
|
UTSW |
1 |
136,396,176 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0239:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0239:Kif14
|
UTSW |
1 |
136,455,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R0329:Kif14
|
UTSW |
1 |
136,423,764 (GRCm39) |
splice site |
probably benign |
|
R0346:Kif14
|
UTSW |
1 |
136,395,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R0393:Kif14
|
UTSW |
1 |
136,410,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Kif14
|
UTSW |
1 |
136,396,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Kif14
|
UTSW |
1 |
136,410,210 (GRCm39) |
missense |
probably damaging |
0.97 |
R0633:Kif14
|
UTSW |
1 |
136,455,043 (GRCm39) |
missense |
probably damaging |
0.96 |
R0657:Kif14
|
UTSW |
1 |
136,396,840 (GRCm39) |
missense |
probably benign |
0.07 |
R0831:Kif14
|
UTSW |
1 |
136,453,609 (GRCm39) |
splice site |
probably benign |
|
R0971:Kif14
|
UTSW |
1 |
136,447,392 (GRCm39) |
missense |
probably damaging |
0.98 |
R1018:Kif14
|
UTSW |
1 |
136,423,579 (GRCm39) |
splice site |
probably benign |
|
R1520:Kif14
|
UTSW |
1 |
136,431,062 (GRCm39) |
missense |
probably benign |
0.00 |
R1713:Kif14
|
UTSW |
1 |
136,455,202 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1728:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1728:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1728:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1728:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1728:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1729:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1729:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1729:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1729:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1730:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1730:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1730:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1730:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1730:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1739:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1739:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1739:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1762:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1762:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1762:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1762:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1762:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1783:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1783:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1783:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1783:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1783:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1784:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1784:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1784:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1784:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1784:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1785:Kif14
|
UTSW |
1 |
136,396,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Kif14
|
UTSW |
1 |
136,418,070 (GRCm39) |
missense |
probably benign |
|
R1785:Kif14
|
UTSW |
1 |
136,431,169 (GRCm39) |
missense |
probably benign |
0.10 |
R1785:Kif14
|
UTSW |
1 |
136,443,699 (GRCm39) |
missense |
probably benign |
0.04 |
R1785:Kif14
|
UTSW |
1 |
136,453,521 (GRCm39) |
missense |
probably benign |
0.03 |
R1785:Kif14
|
UTSW |
1 |
136,396,017 (GRCm39) |
missense |
probably benign |
|
R1872:Kif14
|
UTSW |
1 |
136,414,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Kif14
|
UTSW |
1 |
136,414,818 (GRCm39) |
missense |
probably benign |
|
R2049:Kif14
|
UTSW |
1 |
136,437,905 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2268:Kif14
|
UTSW |
1 |
136,447,486 (GRCm39) |
nonsense |
probably null |
|
R2373:Kif14
|
UTSW |
1 |
136,407,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R3076:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3077:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3078:Kif14
|
UTSW |
1 |
136,447,383 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4232:Kif14
|
UTSW |
1 |
136,444,101 (GRCm39) |
nonsense |
probably null |
|
R4246:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4247:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4250:Kif14
|
UTSW |
1 |
136,401,126 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4672:Kif14
|
UTSW |
1 |
136,449,016 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Kif14
|
UTSW |
1 |
136,449,017 (GRCm39) |
missense |
probably benign |
|
R4890:Kif14
|
UTSW |
1 |
136,414,868 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4994:Kif14
|
UTSW |
1 |
136,410,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5102:Kif14
|
UTSW |
1 |
136,444,141 (GRCm39) |
missense |
probably benign |
0.00 |
R5185:Kif14
|
UTSW |
1 |
136,455,207 (GRCm39) |
nonsense |
probably null |
|
R5201:Kif14
|
UTSW |
1 |
136,431,145 (GRCm39) |
missense |
probably benign |
0.00 |
R5399:Kif14
|
UTSW |
1 |
136,431,062 (GRCm39) |
missense |
probably benign |
0.00 |
R5431:Kif14
|
UTSW |
1 |
136,424,433 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5932:Kif14
|
UTSW |
1 |
136,444,128 (GRCm39) |
missense |
probably benign |
0.23 |
R6027:Kif14
|
UTSW |
1 |
136,410,797 (GRCm39) |
splice site |
probably null |
|
R6246:Kif14
|
UTSW |
1 |
136,404,162 (GRCm39) |
nonsense |
probably null |
|
R6331:Kif14
|
UTSW |
1 |
136,443,724 (GRCm39) |
missense |
probably null |
1.00 |
R6448:Kif14
|
UTSW |
1 |
136,431,085 (GRCm39) |
missense |
probably damaging |
0.99 |
R6453:Kif14
|
UTSW |
1 |
136,410,042 (GRCm39) |
splice site |
probably null |
|
R6475:Kif14
|
UTSW |
1 |
136,455,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Kif14
|
UTSW |
1 |
136,443,697 (GRCm39) |
missense |
probably benign |
0.39 |
R6713:Kif14
|
UTSW |
1 |
136,453,544 (GRCm39) |
missense |
probably benign |
|
R7173:Kif14
|
UTSW |
1 |
136,406,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R7174:Kif14
|
UTSW |
1 |
136,448,995 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7241:Kif14
|
UTSW |
1 |
136,396,491 (GRCm39) |
missense |
probably benign |
0.41 |
R7674:Kif14
|
UTSW |
1 |
136,396,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R7688:Kif14
|
UTSW |
1 |
136,422,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Kif14
|
UTSW |
1 |
136,399,191 (GRCm39) |
missense |
probably benign |
0.10 |
R7722:Kif14
|
UTSW |
1 |
136,396,033 (GRCm39) |
missense |
probably benign |
0.00 |
R7763:Kif14
|
UTSW |
1 |
136,444,121 (GRCm39) |
missense |
probably benign |
0.00 |
R7882:Kif14
|
UTSW |
1 |
136,443,763 (GRCm39) |
missense |
probably benign |
0.43 |
R7882:Kif14
|
UTSW |
1 |
136,399,314 (GRCm39) |
critical splice donor site |
probably null |
|
R8077:Kif14
|
UTSW |
1 |
136,399,186 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8101:Kif14
|
UTSW |
1 |
136,404,090 (GRCm39) |
missense |
probably benign |
0.14 |
R8308:Kif14
|
UTSW |
1 |
136,443,651 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8338:Kif14
|
UTSW |
1 |
136,422,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R8527:Kif14
|
UTSW |
1 |
136,396,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8542:Kif14
|
UTSW |
1 |
136,396,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8884:Kif14
|
UTSW |
1 |
136,414,089 (GRCm39) |
missense |
|
|
R9435:Kif14
|
UTSW |
1 |
136,401,174 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9499:Kif14
|
UTSW |
1 |
136,455,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R9551:Kif14
|
UTSW |
1 |
136,455,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R9577:Kif14
|
UTSW |
1 |
136,399,138 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:Kif14
|
UTSW |
1 |
136,418,014 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kif14
|
UTSW |
1 |
136,427,754 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Kif14
|
UTSW |
1 |
136,424,391 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Kif14
|
UTSW |
1 |
136,406,103 (GRCm39) |
missense |
probably benign |
|
|