Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
C |
A |
5: 144,981,627 (GRCm39) |
A154E |
probably benign |
Het |
Adamts1 |
C |
A |
16: 85,596,060 (GRCm39) |
A419S |
probably benign |
Het |
Arap2 |
C |
G |
5: 62,761,621 (GRCm39) |
V1702L |
probably benign |
Het |
Arpc1a |
C |
T |
5: 145,034,087 (GRCm39) |
P152S |
probably benign |
Het |
Bbs10 |
T |
A |
10: 111,136,628 (GRCm39) |
C580* |
probably null |
Het |
Bcam |
A |
G |
7: 19,499,376 (GRCm39) |
Y216H |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,081,405 (GRCm39) |
S1016P |
|
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cd86 |
CA |
CAA |
16: 36,426,917 (GRCm39) |
|
probably null |
Het |
Ceacam5 |
T |
A |
7: 17,491,839 (GRCm39) |
|
probably null |
Het |
Cfap57 |
A |
G |
4: 118,446,264 (GRCm39) |
V666A |
probably benign |
Het |
Cntn3 |
A |
G |
6: 102,142,305 (GRCm39) |
F1021L |
probably benign |
Het |
Cr1l |
C |
T |
1: 194,811,497 (GRCm39) |
G119D |
probably benign |
Het |
Fgf10 |
A |
T |
13: 118,851,942 (GRCm39) |
H8L |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,903,436 (GRCm39) |
|
probably null |
Het |
Frem1 |
G |
T |
4: 82,840,493 (GRCm39) |
T1811N |
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,298,356 (GRCm39) |
Q227L |
probably benign |
Het |
Galk2 |
A |
G |
2: 125,738,621 (GRCm39) |
I138M |
probably damaging |
Het |
Igkv8-30 |
A |
G |
6: 70,094,582 (GRCm39) |
V7A |
possibly damaging |
Het |
Katnb1 |
G |
A |
8: 95,824,069 (GRCm39) |
A450T |
probably benign |
Het |
Klra3 |
A |
T |
6: 130,312,941 (GRCm39) |
|
probably null |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lepr |
A |
G |
4: 101,607,535 (GRCm39) |
N251S |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,263,416 (GRCm39) |
M4379V |
probably benign |
Het |
Lrriq1 |
T |
C |
10: 103,060,826 (GRCm39) |
N92S |
probably benign |
Het |
Map3k13 |
A |
G |
16: 21,745,006 (GRCm39) |
N855S |
probably damaging |
Het |
Marf1 |
T |
A |
16: 13,954,817 (GRCm39) |
D900V |
probably damaging |
Het |
Nckap5l |
A |
T |
15: 99,321,884 (GRCm39) |
M1087K |
probably benign |
Het |
Nlrp9c |
T |
C |
7: 26,084,722 (GRCm39) |
N286D |
probably benign |
Het |
Or12j4 |
T |
C |
7: 140,047,076 (GRCm39) |
*321Q |
probably null |
Het |
Or13c7d |
C |
T |
4: 43,770,691 (GRCm39) |
A107T |
not run |
Het |
Or4k2 |
T |
C |
14: 50,424,153 (GRCm39) |
I175V |
probably benign |
Het |
Or51ah3 |
A |
T |
7: 103,210,598 (GRCm39) |
R305* |
probably null |
Het |
Or5g9 |
C |
T |
2: 85,552,297 (GRCm39) |
P183S |
possibly damaging |
Het |
Or5p72 |
T |
A |
7: 108,022,367 (GRCm39) |
S196R |
probably benign |
Het |
Pcdhga3 |
A |
G |
18: 37,808,980 (GRCm39) |
T478A |
probably benign |
Het |
Pdgfrb |
T |
C |
18: 61,199,587 (GRCm39) |
I385T |
probably benign |
Het |
Poteg |
C |
T |
8: 27,943,305 (GRCm39) |
R192W |
probably benign |
Het |
Prmt2 |
G |
T |
10: 76,061,173 (GRCm39) |
D104E |
probably benign |
Het |
Rgl2 |
T |
C |
17: 34,153,964 (GRCm39) |
F457L |
possibly damaging |
Het |
Rlbp1 |
T |
C |
7: 79,027,090 (GRCm39) |
N190S |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,816,063 (GRCm39) |
D641G |
possibly damaging |
Het |
Sh3gl1 |
A |
T |
17: 56,324,846 (GRCm39) |
M303K |
probably benign |
Het |
Slc26a5 |
A |
G |
5: 22,018,892 (GRCm39) |
V649A |
probably damaging |
Het |
Slco4c1 |
T |
C |
1: 96,765,323 (GRCm39) |
N376D |
possibly damaging |
Het |
Socs3 |
A |
T |
11: 117,858,553 (GRCm39) |
Y168* |
probably null |
Het |
Spata31d1d |
A |
T |
13: 59,876,394 (GRCm39) |
N380K |
possibly damaging |
Het |
Speer1c |
T |
C |
5: 10,295,237 (GRCm39) |
K56E |
probably damaging |
Het |
Ssbp3 |
A |
G |
4: 106,894,843 (GRCm39) |
N254S |
probably benign |
Het |
Stard10 |
C |
T |
7: 100,995,226 (GRCm39) |
S326L |
probably damaging |
Het |
Taf2 |
T |
C |
15: 54,912,135 (GRCm39) |
D524G |
possibly damaging |
Het |
Taf7 |
A |
T |
18: 37,776,053 (GRCm39) |
S171R |
probably damaging |
Het |
Tchh |
C |
T |
3: 93,353,478 (GRCm39) |
R973C |
unknown |
Het |
Tmem67 |
T |
C |
4: 12,077,337 (GRCm39) |
R172G |
possibly damaging |
Het |
Top2a |
C |
A |
11: 98,914,922 (GRCm39) |
|
probably benign |
Het |
Ttc8 |
T |
A |
12: 98,940,960 (GRCm39) |
N323K |
possibly damaging |
Het |
Txnl1 |
T |
C |
18: 63,804,667 (GRCm39) |
N276D |
probably benign |
Het |
Usp24 |
T |
G |
4: 106,219,878 (GRCm39) |
|
probably null |
Het |
Vmn1r18 |
A |
C |
6: 57,366,609 (GRCm39) |
|
probably null |
Het |
Vmn2r53 |
A |
T |
7: 12,315,628 (GRCm39) |
H730Q |
probably benign |
Het |
Wnk1 |
A |
C |
6: 119,947,939 (GRCm39) |
I500M |
probably damaging |
Het |
Zfp335 |
A |
T |
2: 164,744,423 (GRCm39) |
Y451N |
probably damaging |
Het |
Zfp683 |
T |
A |
4: 133,783,064 (GRCm39) |
I176N |
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 |
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 |
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 |
|
|