Other mutations in this stock |
Total: 130 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc1 |
T |
C |
16: 14,214,257 (GRCm39) |
Y191H |
probably damaging |
Het |
Aco1 |
T |
C |
4: 40,167,193 (GRCm39) |
|
probably null |
Het |
Adap1 |
A |
G |
5: 139,259,096 (GRCm39) |
Y364H |
probably benign |
Het |
Add2 |
T |
C |
6: 86,073,738 (GRCm39) |
F209S |
probably damaging |
Het |
Adgb |
A |
T |
10: 10,270,993 (GRCm39) |
D883E |
probably benign |
Het |
Anapc1 |
C |
A |
2: 128,475,335 (GRCm39) |
R1381S |
probably benign |
Het |
Aoah |
A |
G |
13: 20,978,564 (GRCm39) |
M1V |
probably null |
Het |
Arap1 |
C |
A |
7: 101,022,222 (GRCm39) |
A8E |
probably damaging |
Het |
Arhgap10 |
A |
G |
8: 78,136,255 (GRCm39) |
F319S |
possibly damaging |
Het |
Btrc |
T |
G |
19: 45,515,782 (GRCm39) |
I480S |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,570,924 (GRCm39) |
V784E |
possibly damaging |
Het |
Card9 |
T |
A |
2: 26,244,885 (GRCm39) |
|
probably null |
Het |
Cdk18 |
A |
G |
1: 132,045,559 (GRCm39) |
I238T |
possibly damaging |
Het |
Clec12a |
A |
C |
6: 129,327,444 (GRCm39) |
T21P |
possibly damaging |
Het |
Commd3 |
A |
T |
2: 18,678,774 (GRCm39) |
I70F |
probably benign |
Het |
Cspg5 |
G |
A |
9: 110,080,094 (GRCm39) |
V340M |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,937,902 (GRCm39) |
S307N |
possibly damaging |
Het |
Cyp26c1 |
T |
A |
19: 37,675,825 (GRCm39) |
F230I |
probably damaging |
Het |
Ddx11 |
A |
G |
17: 66,437,723 (GRCm39) |
M150V |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,176,080 (GRCm39) |
Y190C |
probably damaging |
Het |
Det1 |
A |
G |
7: 78,493,191 (GRCm39) |
V271A |
probably benign |
Het |
Dgkd |
C |
A |
1: 87,857,549 (GRCm39) |
P754T |
possibly damaging |
Het |
Dhx36 |
T |
C |
3: 62,386,806 (GRCm39) |
S649G |
probably benign |
Het |
Dlgap5 |
A |
G |
14: 47,653,843 (GRCm39) |
I62T |
possibly damaging |
Het |
Dmgdh |
A |
G |
13: 93,857,067 (GRCm39) |
M724V |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,724,142 (GRCm39) |
S108P |
probably benign |
Het |
Dock4 |
A |
T |
12: 40,760,797 (GRCm39) |
K495M |
probably damaging |
Het |
Dse |
A |
G |
10: 34,036,202 (GRCm39) |
Y225H |
probably damaging |
Het |
Emx1 |
G |
A |
6: 85,180,916 (GRCm39) |
R211K |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,100,852 (GRCm39) |
|
probably null |
Het |
Fbxo27 |
G |
A |
7: 28,397,797 (GRCm39) |
C277Y |
possibly damaging |
Het |
Fcrl1 |
T |
C |
3: 87,283,827 (GRCm39) |
I9T |
possibly damaging |
Het |
Fjx1 |
T |
C |
2: 102,281,152 (GRCm39) |
E261G |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,698,437 (GRCm39) |
V327D |
possibly damaging |
Het |
Flnb |
C |
T |
14: 7,884,735 (GRCm38) |
Q445* |
probably null |
Het |
Flrt2 |
G |
A |
12: 95,747,074 (GRCm39) |
V471I |
probably benign |
Het |
Frmd4a |
G |
A |
2: 4,539,997 (GRCm39) |
V210M |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,821,894 (GRCm39) |
K5876E |
probably benign |
Het |
Galnt10 |
T |
C |
11: 57,656,443 (GRCm39) |
L209P |
probably damaging |
Het |
Gata5 |
A |
T |
2: 179,968,729 (GRCm39) |
S382T |
possibly damaging |
Het |
Glt6d1 |
C |
A |
2: 25,684,425 (GRCm39) |
V194L |
probably damaging |
Het |
Gm10803 |
T |
G |
2: 93,394,288 (GRCm39) |
V20G |
unknown |
Het |
Gm44511 |
T |
G |
6: 128,797,234 (GRCm39) |
T52P |
probably damaging |
Het |
Gpat4 |
A |
T |
8: 23,672,952 (GRCm39) |
L88Q |
possibly damaging |
Het |
Gpr15 |
T |
A |
16: 58,538,370 (GRCm39) |
I240L |
probably benign |
Het |
Hivep2 |
A |
T |
10: 14,008,453 (GRCm39) |
I1684F |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,525,427 (GRCm39) |
T3366A |
probably benign |
Het |
Hnmt |
A |
G |
2: 23,893,894 (GRCm39) |
V200A |
possibly damaging |
Het |
Hps6 |
A |
T |
19: 45,992,774 (GRCm39) |
H237L |
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,292,206 (GRCm39) |
P4033S |
probably damaging |
Het |
Ift70b |
C |
T |
2: 75,767,443 (GRCm39) |
E437K |
probably benign |
Het |
Irf9 |
T |
A |
14: 55,845,174 (GRCm39) |
S297T |
possibly damaging |
Het |
Kdm3b |
T |
C |
18: 34,945,448 (GRCm39) |
V753A |
possibly damaging |
Het |
Kif27 |
T |
G |
13: 58,440,937 (GRCm39) |
R1159S |
probably benign |
Het |
Krtap4-16 |
A |
G |
11: 99,742,373 (GRCm39) |
V9A |
unknown |
Het |
Lama2 |
G |
T |
10: 27,298,614 (GRCm39) |
P161T |
probably damaging |
Het |
Ltbp4 |
G |
A |
7: 27,028,443 (GRCm39) |
P273L |
unknown |
Het |
Lvrn |
T |
A |
18: 47,027,784 (GRCm39) |
S866R |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,189,805 (GRCm39) |
Y1035H |
probably damaging |
Het |
Mertk |
T |
A |
2: 128,601,010 (GRCm39) |
N331K |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,437 (GRCm39) |
F211Y |
probably benign |
Het |
Mpeg1 |
G |
A |
19: 12,440,275 (GRCm39) |
V578M |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,453,764 (GRCm39) |
S183T |
possibly damaging |
Het |
Mrto4 |
A |
T |
4: 139,076,949 (GRCm39) |
I56N |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,416,374 (GRCm39) |
C3107R |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,230,476 (GRCm39) |
Y1023H |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,330,737 (GRCm39) |
E553G |
probably damaging |
Het |
Nlrp6 |
GAGAAGAAGAAGAAGAAGAAGA |
GAGAAGAAGAAGAAGAAGA |
7: 140,504,026 (GRCm39) |
|
probably benign |
Het |
Nr2f1 |
T |
C |
13: 78,337,935 (GRCm39) |
T237A |
probably damaging |
Het |
Nup205 |
C |
A |
6: 35,210,301 (GRCm39) |
Q1621K |
probably benign |
Het |
Nup50l |
A |
G |
6: 96,142,250 (GRCm39) |
S265P |
possibly damaging |
Het |
Nxpe2 |
T |
A |
9: 48,231,026 (GRCm39) |
S448C |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,296,638 (GRCm39) |
C498S |
possibly damaging |
Het |
Oplah |
G |
A |
15: 76,181,664 (GRCm39) |
T1119I |
probably damaging |
Het |
Or14a256 |
A |
T |
7: 86,265,639 (GRCm39) |
F71L |
probably benign |
Het |
Or2ag15 |
T |
C |
7: 106,340,601 (GRCm39) |
E180G |
probably damaging |
Het |
Or2d2 |
A |
T |
7: 106,727,717 (GRCm39) |
D294E |
possibly damaging |
Het |
Or5ak24 |
T |
C |
2: 85,260,963 (GRCm39) |
D70G |
probably damaging |
Het |
Or5d46 |
T |
C |
2: 88,170,545 (GRCm39) |
L212P |
probably damaging |
Het |
Or6p1 |
A |
T |
1: 174,258,471 (GRCm39) |
K159M |
probably damaging |
Het |
Or8s8 |
T |
C |
15: 98,354,634 (GRCm39) |
S148P |
probably damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,536,369 (GRCm39) |
Y788N |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,410,782 (GRCm39) |
D1870G |
unknown |
Het |
Pde6g |
A |
G |
11: 120,338,962 (GRCm39) |
L76P |
probably damaging |
Het |
Peak1 |
A |
T |
9: 56,114,073 (GRCm39) |
Y593N |
probably damaging |
Het |
Pfas |
C |
T |
11: 68,885,110 (GRCm39) |
G16R |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,769,970 (GRCm39) |
|
probably null |
Het |
Pla2g3 |
C |
T |
11: 3,440,983 (GRCm39) |
T316I |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,530,788 (GRCm39) |
I489F |
probably damaging |
Het |
Rere |
T |
G |
4: 150,553,247 (GRCm39) |
H146Q |
probably benign |
Het |
Rundc1 |
A |
T |
11: 101,322,322 (GRCm39) |
Q272L |
probably damaging |
Het |
Scml4 |
T |
C |
10: 42,832,017 (GRCm39) |
L305P |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,320,144 (GRCm39) |
H1431Q |
probably benign |
Het |
Serpina1a |
G |
A |
12: 103,820,059 (GRCm39) |
Q373* |
probably null |
Het |
Shank1 |
A |
T |
7: 43,974,801 (GRCm39) |
N377I |
unknown |
Het |
Shc2 |
T |
C |
10: 79,462,625 (GRCm39) |
|
probably null |
Het |
Slc22a29 |
C |
A |
19: 8,146,557 (GRCm39) |
R415M |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 41,368,002 (GRCm39) |
I589F |
probably damaging |
Het |
Smim8 |
C |
T |
4: 34,771,316 (GRCm39) |
R26Q |
probably damaging |
Het |
Smox |
C |
A |
2: 131,362,384 (GRCm39) |
A221D |
probably damaging |
Het |
Sox5 |
A |
G |
6: 143,819,831 (GRCm39) |
S62P |
possibly damaging |
Het |
Spg21 |
A |
C |
9: 65,391,774 (GRCm39) |
K240N |
probably damaging |
Het |
Sv2c |
C |
T |
13: 96,113,153 (GRCm39) |
V599M |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,801,121 (GRCm39) |
H1112Q |
probably damaging |
Het |
Tbata |
T |
C |
10: 61,011,623 (GRCm39) |
I58T |
possibly damaging |
Het |
Tbc1d2 |
T |
G |
4: 46,606,419 (GRCm39) |
Y842S |
probably benign |
Het |
Tctn1 |
A |
T |
5: 122,379,903 (GRCm39) |
|
probably null |
Het |
Tenm1 |
T |
C |
X: 41,916,078 (GRCm39) |
D402G |
probably benign |
Het |
Tfcp2l1 |
T |
C |
1: 118,597,119 (GRCm39) |
V400A |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,363,576 (GRCm39) |
L99I |
probably benign |
Het |
Top2a |
T |
C |
11: 98,886,803 (GRCm39) |
|
probably null |
Het |
Traf7 |
C |
A |
17: 24,732,255 (GRCm39) |
G191C |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 63,879,978 (GRCm39) |
L661Q |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,580,967 (GRCm39) |
I23309V |
probably benign |
Het |
Usp50 |
T |
C |
2: 126,619,881 (GRCm39) |
K199E |
possibly damaging |
Het |
Vmn1r218 |
T |
C |
13: 23,320,683 (GRCm39) |
F10S |
probably damaging |
Het |
Vmn2r89 |
C |
A |
14: 51,694,897 (GRCm39) |
T459K |
probably benign |
Het |
Vps13a |
T |
G |
19: 16,655,302 (GRCm39) |
S1909R |
possibly damaging |
Het |
Vwa5b2 |
T |
C |
16: 20,420,941 (GRCm39) |
|
probably null |
Het |
Vwa8 |
A |
G |
14: 79,219,800 (GRCm39) |
H516R |
possibly damaging |
Het |
Wnk1 |
T |
C |
6: 119,946,208 (GRCm39) |
I648M |
probably damaging |
Het |
Zfat |
G |
C |
15: 68,018,392 (GRCm39) |
P974R |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,259,158 (GRCm39) |
I1601K |
probably benign |
Het |
Zfp239 |
A |
G |
6: 117,848,778 (GRCm39) |
K172R |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,736,722 (GRCm39) |
G971D |
probably damaging |
Het |
Zfp532 |
A |
T |
18: 65,757,563 (GRCm39) |
I499F |
probably damaging |
Het |
Zfp647 |
T |
C |
15: 76,795,314 (GRCm39) |
T449A |
possibly damaging |
Het |
Zfp938 |
C |
T |
10: 82,061,465 (GRCm39) |
G385D |
probably damaging |
Het |
Zfp959 |
T |
G |
17: 56,204,404 (GRCm39) |
V147G |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 166,892,270 (GRCm39) |
C649S |
probably damaging |
Het |
|
Other mutations in Kif21a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00539:Kif21a
|
APN |
15 |
90,821,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01476:Kif21a
|
APN |
15 |
90,828,067 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01617:Kif21a
|
APN |
15 |
90,879,840 (GRCm39) |
splice site |
probably benign |
|
IGL01736:Kif21a
|
APN |
15 |
90,843,948 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01923:Kif21a
|
APN |
15 |
90,840,633 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01985:Kif21a
|
APN |
15 |
90,875,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02304:Kif21a
|
APN |
15 |
90,849,738 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02589:Kif21a
|
APN |
15 |
90,869,489 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Kif21a
|
APN |
15 |
90,869,598 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03211:Kif21a
|
APN |
15 |
90,882,166 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03372:Kif21a
|
APN |
15 |
90,840,579 (GRCm39) |
missense |
probably benign |
0.38 |
reflex
|
UTSW |
15 |
90,852,561 (GRCm39) |
missense |
probably null |
1.00 |
R0052:Kif21a
|
UTSW |
15 |
90,855,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R0052:Kif21a
|
UTSW |
15 |
90,855,060 (GRCm39) |
missense |
probably damaging |
0.98 |
R0304:Kif21a
|
UTSW |
15 |
90,860,724 (GRCm39) |
splice site |
probably null |
|
R0378:Kif21a
|
UTSW |
15 |
90,853,977 (GRCm39) |
splice site |
probably null |
|
R0420:Kif21a
|
UTSW |
15 |
90,852,257 (GRCm39) |
unclassified |
probably benign |
|
R0536:Kif21a
|
UTSW |
15 |
90,843,886 (GRCm39) |
splice site |
probably benign |
|
R0826:Kif21a
|
UTSW |
15 |
90,881,744 (GRCm39) |
critical splice donor site |
probably null |
|
R0971:Kif21a
|
UTSW |
15 |
90,824,784 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1052:Kif21a
|
UTSW |
15 |
90,819,853 (GRCm39) |
missense |
probably benign |
0.17 |
R1168:Kif21a
|
UTSW |
15 |
90,877,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1324:Kif21a
|
UTSW |
15 |
90,832,525 (GRCm39) |
critical splice donor site |
probably null |
|
R1471:Kif21a
|
UTSW |
15 |
90,840,622 (GRCm39) |
missense |
probably benign |
0.04 |
R1625:Kif21a
|
UTSW |
15 |
90,826,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Kif21a
|
UTSW |
15 |
90,869,008 (GRCm39) |
splice site |
probably benign |
|
R1647:Kif21a
|
UTSW |
15 |
90,878,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1648:Kif21a
|
UTSW |
15 |
90,878,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Kif21a
|
UTSW |
15 |
90,843,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R1703:Kif21a
|
UTSW |
15 |
90,833,250 (GRCm39) |
splice site |
probably null |
|
R1795:Kif21a
|
UTSW |
15 |
90,856,930 (GRCm39) |
splice site |
probably null |
|
R1812:Kif21a
|
UTSW |
15 |
90,855,969 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1960:Kif21a
|
UTSW |
15 |
90,855,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R1961:Kif21a
|
UTSW |
15 |
90,855,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R1996:Kif21a
|
UTSW |
15 |
90,878,574 (GRCm39) |
nonsense |
probably null |
|
R2230:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2231:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2232:Kif21a
|
UTSW |
15 |
90,869,565 (GRCm39) |
nonsense |
probably null |
|
R2424:Kif21a
|
UTSW |
15 |
90,855,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R2429:Kif21a
|
UTSW |
15 |
90,882,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R2513:Kif21a
|
UTSW |
15 |
90,878,594 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2846:Kif21a
|
UTSW |
15 |
90,818,667 (GRCm39) |
missense |
probably benign |
|
R3027:Kif21a
|
UTSW |
15 |
90,856,845 (GRCm39) |
missense |
probably damaging |
0.99 |
R3624:Kif21a
|
UTSW |
15 |
90,849,798 (GRCm39) |
missense |
probably damaging |
0.99 |
R3820:Kif21a
|
UTSW |
15 |
90,852,277 (GRCm39) |
missense |
probably benign |
0.17 |
R3923:Kif21a
|
UTSW |
15 |
90,821,497 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3962:Kif21a
|
UTSW |
15 |
90,869,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4355:Kif21a
|
UTSW |
15 |
90,855,036 (GRCm39) |
missense |
probably benign |
0.17 |
R4516:Kif21a
|
UTSW |
15 |
90,855,345 (GRCm39) |
missense |
probably benign |
0.38 |
R4530:Kif21a
|
UTSW |
15 |
90,852,292 (GRCm39) |
splice site |
probably null |
|
R4612:Kif21a
|
UTSW |
15 |
90,852,426 (GRCm39) |
splice site |
probably null |
|
R4674:Kif21a
|
UTSW |
15 |
90,824,748 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4675:Kif21a
|
UTSW |
15 |
90,824,748 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4698:Kif21a
|
UTSW |
15 |
90,840,508 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4712:Kif21a
|
UTSW |
15 |
90,868,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Kif21a
|
UTSW |
15 |
90,821,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Kif21a
|
UTSW |
15 |
90,833,213 (GRCm39) |
missense |
probably benign |
0.16 |
R5034:Kif21a
|
UTSW |
15 |
90,852,561 (GRCm39) |
missense |
probably null |
1.00 |
R5165:Kif21a
|
UTSW |
15 |
90,840,579 (GRCm39) |
missense |
probably benign |
0.38 |
R5464:Kif21a
|
UTSW |
15 |
90,878,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Kif21a
|
UTSW |
15 |
90,852,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R5757:Kif21a
|
UTSW |
15 |
90,835,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5936:Kif21a
|
UTSW |
15 |
90,819,850 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5976:Kif21a
|
UTSW |
15 |
90,820,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R6074:Kif21a
|
UTSW |
15 |
90,865,095 (GRCm39) |
missense |
probably benign |
|
R6638:Kif21a
|
UTSW |
15 |
90,850,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6723:Kif21a
|
UTSW |
15 |
90,824,649 (GRCm39) |
missense |
probably damaging |
0.97 |
R6785:Kif21a
|
UTSW |
15 |
90,819,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R6977:Kif21a
|
UTSW |
15 |
90,865,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Kif21a
|
UTSW |
15 |
90,833,106 (GRCm39) |
splice site |
probably null |
|
R7147:Kif21a
|
UTSW |
15 |
90,865,086 (GRCm39) |
missense |
probably benign |
0.13 |
R7290:Kif21a
|
UTSW |
15 |
90,851,432 (GRCm39) |
nonsense |
probably null |
|
R7438:Kif21a
|
UTSW |
15 |
90,877,999 (GRCm39) |
missense |
probably benign |
0.37 |
R7593:Kif21a
|
UTSW |
15 |
90,828,064 (GRCm39) |
missense |
probably benign |
0.03 |
R7661:Kif21a
|
UTSW |
15 |
90,865,122 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7891:Kif21a
|
UTSW |
15 |
90,840,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Kif21a
|
UTSW |
15 |
90,852,645 (GRCm39) |
missense |
probably benign |
|
R8182:Kif21a
|
UTSW |
15 |
90,819,964 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8303:Kif21a
|
UTSW |
15 |
90,855,399 (GRCm39) |
missense |
probably damaging |
0.99 |
R8388:Kif21a
|
UTSW |
15 |
90,843,327 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8867:Kif21a
|
UTSW |
15 |
90,852,382 (GRCm39) |
missense |
probably damaging |
0.96 |
R8921:Kif21a
|
UTSW |
15 |
90,855,930 (GRCm39) |
missense |
probably benign |
0.04 |
R8984:Kif21a
|
UTSW |
15 |
90,840,559 (GRCm39) |
missense |
probably benign |
0.00 |
R9024:Kif21a
|
UTSW |
15 |
90,821,399 (GRCm39) |
nonsense |
probably null |
|
R9254:Kif21a
|
UTSW |
15 |
90,854,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9366:Kif21a
|
UTSW |
15 |
90,843,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Kif21a
|
UTSW |
15 |
90,854,030 (GRCm39) |
missense |
probably damaging |
0.99 |
R9393:Kif21a
|
UTSW |
15 |
90,853,981 (GRCm39) |
missense |
probably benign |
0.00 |
R9518:Kif21a
|
UTSW |
15 |
90,840,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R9712:Kif21a
|
UTSW |
15 |
90,879,715 (GRCm39) |
missense |
probably benign |
0.13 |
R9712:Kif21a
|
UTSW |
15 |
90,869,528 (GRCm39) |
missense |
probably damaging |
0.98 |
R9721:Kif21a
|
UTSW |
15 |
90,855,330 (GRCm39) |
missense |
probably damaging |
0.99 |
|