Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
G |
17: 24,537,165 (GRCm39) |
F473L |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,401,691 (GRCm39) |
I1449V |
probably benign |
Het |
Aox4 |
T |
A |
1: 58,293,477 (GRCm39) |
L943* |
probably null |
Het |
Arap1 |
G |
A |
7: 101,053,240 (GRCm39) |
V1257M |
probably damaging |
Het |
B3gnt9 |
T |
C |
8: 105,981,230 (GRCm39) |
S53G |
probably benign |
Het |
Baiap3 |
A |
T |
17: 25,467,444 (GRCm39) |
|
probably benign |
Het |
Canx |
T |
C |
11: 50,187,946 (GRCm39) |
D554G |
possibly damaging |
Het |
Cbfa2t2 |
T |
C |
2: 154,352,501 (GRCm39) |
V165A |
probably damaging |
Het |
Ccdc17 |
C |
T |
4: 116,457,145 (GRCm39) |
|
probably null |
Het |
Cdcp1 |
A |
G |
9: 123,014,396 (GRCm39) |
I126T |
probably benign |
Het |
Cdk13 |
A |
T |
13: 17,895,800 (GRCm39) |
D1036E |
probably damaging |
Het |
Cfap157 |
A |
G |
2: 32,669,863 (GRCm39) |
L240P |
probably damaging |
Het |
Clec18a |
C |
A |
8: 111,805,448 (GRCm39) |
E218* |
probably null |
Het |
Col3a1 |
T |
C |
1: 45,384,173 (GRCm39) |
|
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,794,227 (GRCm39) |
E682G |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,494,052 (GRCm39) |
V1736A |
possibly damaging |
Het |
Dpep2 |
T |
A |
8: 106,717,270 (GRCm39) |
D162V |
possibly damaging |
Het |
Drd3 |
C |
A |
16: 43,641,646 (GRCm39) |
P321T |
probably benign |
Het |
Egfr |
A |
G |
11: 16,861,554 (GRCm39) |
H1111R |
probably benign |
Het |
Entpd1 |
T |
C |
19: 40,708,928 (GRCm39) |
S58P |
probably damaging |
Het |
Epha3 |
C |
A |
16: 63,423,967 (GRCm39) |
V541L |
possibly damaging |
Het |
Eri3 |
T |
A |
4: 117,421,825 (GRCm39) |
D34E |
probably damaging |
Het |
Eya1 |
T |
C |
1: 14,353,374 (GRCm39) |
D58G |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,833,975 (GRCm39) |
S26C |
probably null |
Het |
Fgl1 |
T |
C |
8: 41,653,548 (GRCm39) |
D115G |
probably damaging |
Het |
Fitm2 |
T |
C |
2: 163,312,036 (GRCm39) |
Y59C |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,912,725 (GRCm39) |
I3343N |
probably damaging |
Het |
Gba2 |
C |
A |
4: 43,568,330 (GRCm39) |
C679F |
probably damaging |
Het |
Glis2 |
G |
A |
16: 4,431,603 (GRCm39) |
|
probably benign |
Het |
Gm5150 |
T |
A |
3: 16,044,917 (GRCm39) |
I103F |
probably damaging |
Het |
Hhipl2 |
T |
C |
1: 183,204,965 (GRCm39) |
S313P |
possibly damaging |
Het |
Hmgcs1 |
A |
G |
13: 120,166,995 (GRCm39) |
D474G |
probably benign |
Het |
Homer3 |
C |
T |
8: 70,744,076 (GRCm39) |
Q267* |
probably null |
Het |
Hsd17b8 |
A |
G |
17: 34,246,429 (GRCm39) |
L118P |
probably damaging |
Het |
Igkv8-28 |
C |
T |
6: 70,120,673 (GRCm39) |
G90D |
probably damaging |
Het |
Krt4 |
A |
G |
15: 101,831,194 (GRCm39) |
|
probably null |
Het |
Lamb2 |
T |
A |
9: 108,364,811 (GRCm39) |
C1188* |
probably null |
Het |
Lsr |
A |
T |
7: 30,658,042 (GRCm39) |
M355K |
probably damaging |
Het |
Map3k11 |
T |
G |
19: 5,747,430 (GRCm39) |
D555E |
probably benign |
Het |
Myocd |
A |
G |
11: 65,087,082 (GRCm39) |
Y282H |
probably damaging |
Het |
Nae1 |
T |
C |
8: 105,261,176 (GRCm39) |
I7M |
probably benign |
Het |
Nprl3 |
G |
T |
11: 32,205,453 (GRCm39) |
H102N |
possibly damaging |
Het |
Nup62 |
T |
A |
7: 44,478,464 (GRCm39) |
F160I |
possibly damaging |
Het |
Or10w1 |
C |
A |
19: 13,631,871 (GRCm39) |
P26Q |
possibly damaging |
Het |
Or2d3c |
A |
T |
7: 106,525,896 (GRCm39) |
F257I |
probably benign |
Het |
Or2r2 |
T |
A |
6: 42,463,588 (GRCm39) |
T180S |
possibly damaging |
Het |
Or5p76 |
A |
G |
7: 108,122,945 (GRCm39) |
S71P |
probably benign |
Het |
Or6c35 |
C |
A |
10: 129,169,071 (GRCm39) |
T107K |
possibly damaging |
Het |
Osbpl10 |
T |
C |
9: 114,896,383 (GRCm39) |
|
probably null |
Het |
Pcdh9 |
C |
T |
14: 94,123,282 (GRCm39) |
V963I |
probably benign |
Het |
Phf12 |
A |
G |
11: 77,909,044 (GRCm39) |
R375G |
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,233,008 (GRCm39) |
T108M |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,779,635 (GRCm39) |
Q269L |
probably benign |
Het |
Pomgnt1 |
T |
A |
4: 116,008,799 (GRCm39) |
N11K |
possibly damaging |
Het |
Pramel22 |
T |
A |
4: 143,382,222 (GRCm39) |
D158V |
probably damaging |
Het |
Prkd1 |
A |
T |
12: 50,413,083 (GRCm39) |
|
probably null |
Het |
Prpf40a |
T |
C |
2: 53,049,293 (GRCm39) |
T190A |
probably benign |
Het |
Prrc2b |
A |
C |
2: 32,102,297 (GRCm39) |
H790P |
possibly damaging |
Het |
Rest |
T |
G |
5: 77,429,027 (GRCm39) |
V482G |
probably benign |
Het |
Ros1 |
T |
A |
10: 52,039,999 (GRCm39) |
I322L |
probably benign |
Het |
Rpl18 |
G |
A |
7: 45,369,554 (GRCm39) |
|
probably benign |
Het |
Rsad2 |
G |
A |
12: 26,500,577 (GRCm39) |
H237Y |
probably benign |
Het |
Sbf2 |
A |
G |
7: 110,040,741 (GRCm39) |
L362S |
probably damaging |
Het |
Sgsm3 |
A |
G |
15: 80,893,464 (GRCm39) |
T409A |
probably benign |
Het |
Slc16a14 |
T |
C |
1: 84,890,430 (GRCm39) |
T292A |
possibly damaging |
Het |
Spg11 |
T |
G |
2: 121,927,837 (GRCm39) |
K649T |
probably damaging |
Het |
Srprb |
T |
A |
9: 103,067,415 (GRCm39) |
I268F |
possibly damaging |
Het |
Tap2 |
G |
A |
17: 34,433,683 (GRCm39) |
G566S |
probably damaging |
Het |
Tecpr2 |
T |
C |
12: 110,885,325 (GRCm39) |
V168A |
possibly damaging |
Het |
Tln1 |
G |
C |
4: 43,555,052 (GRCm39) |
F259L |
probably damaging |
Het |
Tmem181a |
T |
A |
17: 6,330,890 (GRCm39) |
L50H |
probably damaging |
Het |
Tshz1 |
A |
G |
18: 84,032,194 (GRCm39) |
I738T |
probably damaging |
Het |
Tspan12 |
T |
C |
6: 21,772,637 (GRCm39) |
E304G |
probably benign |
Het |
Urb1 |
C |
T |
16: 90,559,271 (GRCm39) |
G1671S |
probably damaging |
Het |
Vmn2r2 |
T |
C |
3: 64,024,782 (GRCm39) |
S600G |
possibly damaging |
Het |
Wnt3 |
C |
A |
11: 103,699,000 (GRCm39) |
Y35* |
probably null |
Het |
Xpo7 |
T |
C |
14: 70,921,159 (GRCm39) |
Y603C |
possibly damaging |
Het |
Zfp457 |
G |
A |
13: 67,442,015 (GRCm39) |
H91Y |
probably damaging |
Het |
Zfp664 |
T |
A |
5: 124,963,250 (GRCm39) |
C215S |
unknown |
Het |
Zfp882 |
G |
A |
8: 72,668,349 (GRCm39) |
G392D |
probably benign |
Het |
|
Other mutations in Kalrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01361:Kalrn
|
APN |
16 |
33,996,092 (GRCm39) |
splice site |
probably benign |
|
IGL01364:Kalrn
|
APN |
16 |
34,082,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01510:Kalrn
|
APN |
16 |
34,055,700 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01664:Kalrn
|
APN |
16 |
34,114,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Kalrn
|
APN |
16 |
34,018,882 (GRCm39) |
splice site |
probably null |
|
IGL02059:Kalrn
|
APN |
16 |
34,072,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02102:Kalrn
|
APN |
16 |
34,040,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Kalrn
|
APN |
16 |
34,130,897 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02328:Kalrn
|
APN |
16 |
34,152,594 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02532:Kalrn
|
APN |
16 |
34,181,216 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Kalrn
|
APN |
16 |
34,334,329 (GRCm39) |
nonsense |
probably null |
|
IGL02696:Kalrn
|
APN |
16 |
34,040,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Kalrn
|
APN |
16 |
34,212,420 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02937:Kalrn
|
APN |
16 |
34,040,500 (GRCm39) |
nonsense |
probably null |
|
IGL03188:Kalrn
|
APN |
16 |
34,134,562 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03289:Kalrn
|
APN |
16 |
34,205,667 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03408:Kalrn
|
APN |
16 |
34,134,546 (GRCm39) |
missense |
probably damaging |
0.99 |
breeze
|
UTSW |
16 |
33,834,045 (GRCm39) |
missense |
|
|
ethereal
|
UTSW |
16 |
33,795,805 (GRCm39) |
utr 3 prime |
probably benign |
|
Feather
|
UTSW |
16 |
34,134,579 (GRCm39) |
missense |
probably damaging |
0.99 |
Hidden
|
UTSW |
16 |
33,848,346 (GRCm39) |
missense |
probably damaging |
1.00 |
Soulful
|
UTSW |
16 |
34,007,854 (GRCm39) |
nonsense |
probably null |
|
G1Funyon:Kalrn
|
UTSW |
16 |
34,177,470 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4498001:Kalrn
|
UTSW |
16 |
33,851,952 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0019:Kalrn
|
UTSW |
16 |
34,018,884 (GRCm39) |
splice site |
probably benign |
|
R0043:Kalrn
|
UTSW |
16 |
33,875,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Kalrn
|
UTSW |
16 |
34,177,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Kalrn
|
UTSW |
16 |
34,024,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Kalrn
|
UTSW |
16 |
33,795,989 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0098:Kalrn
|
UTSW |
16 |
33,795,989 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0111:Kalrn
|
UTSW |
16 |
33,851,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Kalrn
|
UTSW |
16 |
33,870,306 (GRCm39) |
intron |
probably benign |
|
R0183:Kalrn
|
UTSW |
16 |
33,991,749 (GRCm39) |
splice site |
probably null |
|
R0422:Kalrn
|
UTSW |
16 |
34,134,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R0498:Kalrn
|
UTSW |
16 |
33,875,261 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0614:Kalrn
|
UTSW |
16 |
33,814,040 (GRCm39) |
splice site |
probably benign |
|
R0656:Kalrn
|
UTSW |
16 |
33,852,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Kalrn
|
UTSW |
16 |
33,936,778 (GRCm39) |
missense |
probably benign |
0.04 |
R0707:Kalrn
|
UTSW |
16 |
33,830,951 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0709:Kalrn
|
UTSW |
16 |
33,855,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R0834:Kalrn
|
UTSW |
16 |
33,870,289 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0976:Kalrn
|
UTSW |
16 |
34,205,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Kalrn
|
UTSW |
16 |
33,836,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R1355:Kalrn
|
UTSW |
16 |
33,795,954 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1370:Kalrn
|
UTSW |
16 |
33,795,954 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1389:Kalrn
|
UTSW |
16 |
33,809,173 (GRCm39) |
missense |
probably benign |
0.01 |
R1398:Kalrn
|
UTSW |
16 |
34,033,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1427:Kalrn
|
UTSW |
16 |
33,796,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Kalrn
|
UTSW |
16 |
33,994,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Kalrn
|
UTSW |
16 |
34,007,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Kalrn
|
UTSW |
16 |
34,007,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R1557:Kalrn
|
UTSW |
16 |
34,134,648 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1559:Kalrn
|
UTSW |
16 |
33,830,918 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1654:Kalrn
|
UTSW |
16 |
33,796,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Kalrn
|
UTSW |
16 |
34,025,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Kalrn
|
UTSW |
16 |
34,181,320 (GRCm39) |
missense |
probably damaging |
0.97 |
R1764:Kalrn
|
UTSW |
16 |
34,033,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Kalrn
|
UTSW |
16 |
34,114,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Kalrn
|
UTSW |
16 |
34,177,331 (GRCm39) |
missense |
probably damaging |
0.99 |
R1850:Kalrn
|
UTSW |
16 |
33,796,293 (GRCm39) |
missense |
probably damaging |
0.98 |
R1921:Kalrn
|
UTSW |
16 |
34,212,463 (GRCm39) |
missense |
probably benign |
0.02 |
R1922:Kalrn
|
UTSW |
16 |
34,212,463 (GRCm39) |
missense |
probably benign |
0.02 |
R1970:Kalrn
|
UTSW |
16 |
33,797,894 (GRCm39) |
critical splice donor site |
probably null |
|
R1991:Kalrn
|
UTSW |
16 |
33,796,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Kalrn
|
UTSW |
16 |
33,796,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2001:Kalrn
|
UTSW |
16 |
33,848,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R2025:Kalrn
|
UTSW |
16 |
34,010,106 (GRCm39) |
missense |
probably damaging |
0.96 |
R2048:Kalrn
|
UTSW |
16 |
34,072,680 (GRCm39) |
missense |
probably benign |
0.18 |
R2076:Kalrn
|
UTSW |
16 |
34,152,513 (GRCm39) |
missense |
probably benign |
0.15 |
R2118:Kalrn
|
UTSW |
16 |
34,152,600 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2136:Kalrn
|
UTSW |
16 |
34,128,094 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2145:Kalrn
|
UTSW |
16 |
33,829,632 (GRCm39) |
unclassified |
probably benign |
|
R2193:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2195:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2234:Kalrn
|
UTSW |
16 |
33,996,632 (GRCm39) |
splice site |
probably null |
|
R2404:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2405:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2408:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2411:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2570:Kalrn
|
UTSW |
16 |
34,130,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R2903:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2904:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2924:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3411:Kalrn
|
UTSW |
16 |
34,032,642 (GRCm39) |
missense |
probably benign |
0.07 |
R3693:Kalrn
|
UTSW |
16 |
34,177,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R3709:Kalrn
|
UTSW |
16 |
34,212,400 (GRCm39) |
splice site |
probably null |
|
R3788:Kalrn
|
UTSW |
16 |
34,040,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R3833:Kalrn
|
UTSW |
16 |
33,860,259 (GRCm39) |
nonsense |
probably null |
|
R3871:Kalrn
|
UTSW |
16 |
34,024,226 (GRCm39) |
splice site |
probably null |
|
R3934:Kalrn
|
UTSW |
16 |
34,130,901 (GRCm39) |
missense |
probably benign |
0.34 |
R4033:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4056:Kalrn
|
UTSW |
16 |
34,134,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R4057:Kalrn
|
UTSW |
16 |
34,134,579 (GRCm39) |
missense |
probably damaging |
0.99 |
R4303:Kalrn
|
UTSW |
16 |
34,055,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4402:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4444:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4482:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4487:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4558:Kalrn
|
UTSW |
16 |
33,807,578 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4572:Kalrn
|
UTSW |
16 |
34,212,412 (GRCm39) |
missense |
probably damaging |
0.98 |
R4583:Kalrn
|
UTSW |
16 |
34,055,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R4604:Kalrn
|
UTSW |
16 |
34,334,296 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4620:Kalrn
|
UTSW |
16 |
33,849,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R4651:Kalrn
|
UTSW |
16 |
33,996,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R4703:Kalrn
|
UTSW |
16 |
34,024,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kalrn
|
UTSW |
16 |
34,024,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4705:Kalrn
|
UTSW |
16 |
34,024,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Kalrn
|
UTSW |
16 |
34,018,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4794:Kalrn
|
UTSW |
16 |
33,810,180 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4811:Kalrn
|
UTSW |
16 |
34,177,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4816:Kalrn
|
UTSW |
16 |
34,334,389 (GRCm39) |
unclassified |
probably benign |
|
R4888:Kalrn
|
UTSW |
16 |
33,991,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Kalrn
|
UTSW |
16 |
34,177,785 (GRCm39) |
splice site |
probably null |
|
R5030:Kalrn
|
UTSW |
16 |
33,796,112 (GRCm39) |
missense |
probably benign |
0.00 |
R5045:Kalrn
|
UTSW |
16 |
34,134,722 (GRCm39) |
nonsense |
probably null |
|
R5117:Kalrn
|
UTSW |
16 |
33,853,971 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5289:Kalrn
|
UTSW |
16 |
34,072,711 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5426:Kalrn
|
UTSW |
16 |
34,083,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5432:Kalrn
|
UTSW |
16 |
33,873,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5611:Kalrn
|
UTSW |
16 |
33,996,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Kalrn
|
UTSW |
16 |
33,860,304 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5635:Kalrn
|
UTSW |
16 |
33,834,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R5713:Kalrn
|
UTSW |
16 |
33,836,949 (GRCm39) |
missense |
probably benign |
|
R5716:Kalrn
|
UTSW |
16 |
33,807,546 (GRCm39) |
missense |
probably benign |
0.01 |
R5772:Kalrn
|
UTSW |
16 |
33,796,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Kalrn
|
UTSW |
16 |
34,032,619 (GRCm39) |
missense |
probably damaging |
0.98 |
R5835:Kalrn
|
UTSW |
16 |
33,807,461 (GRCm39) |
missense |
probably benign |
0.28 |
R5895:Kalrn
|
UTSW |
16 |
33,795,805 (GRCm39) |
utr 3 prime |
probably benign |
|
R5924:Kalrn
|
UTSW |
16 |
34,064,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R5999:Kalrn
|
UTSW |
16 |
34,177,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Kalrn
|
UTSW |
16 |
33,830,950 (GRCm39) |
missense |
probably benign |
0.06 |
R6122:Kalrn
|
UTSW |
16 |
33,805,561 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6128:Kalrn
|
UTSW |
16 |
34,033,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R6136:Kalrn
|
UTSW |
16 |
34,177,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Kalrn
|
UTSW |
16 |
33,874,009 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6229:Kalrn
|
UTSW |
16 |
33,875,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Kalrn
|
UTSW |
16 |
33,796,361 (GRCm39) |
missense |
probably benign |
|
R6397:Kalrn
|
UTSW |
16 |
33,813,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R6429:Kalrn
|
UTSW |
16 |
34,152,534 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6473:Kalrn
|
UTSW |
16 |
34,025,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Kalrn
|
UTSW |
16 |
34,181,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:Kalrn
|
UTSW |
16 |
34,003,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Kalrn
|
UTSW |
16 |
34,038,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6808:Kalrn
|
UTSW |
16 |
33,848,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Kalrn
|
UTSW |
16 |
33,796,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R6955:Kalrn
|
UTSW |
16 |
34,040,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R7060:Kalrn
|
UTSW |
16 |
34,177,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R7064:Kalrn
|
UTSW |
16 |
34,038,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Kalrn
|
UTSW |
16 |
34,076,597 (GRCm39) |
missense |
unknown |
|
R7154:Kalrn
|
UTSW |
16 |
34,032,527 (GRCm39) |
critical splice donor site |
probably null |
|
R7181:Kalrn
|
UTSW |
16 |
33,983,447 (GRCm39) |
missense |
probably benign |
0.00 |
R7234:Kalrn
|
UTSW |
16 |
33,996,792 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7235:Kalrn
|
UTSW |
16 |
33,996,131 (GRCm39) |
missense |
probably benign |
0.18 |
R7504:Kalrn
|
UTSW |
16 |
34,076,603 (GRCm39) |
missense |
unknown |
|
R7563:Kalrn
|
UTSW |
16 |
34,212,464 (GRCm39) |
missense |
probably damaging |
0.97 |
R7612:Kalrn
|
UTSW |
16 |
34,134,582 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7772:Kalrn
|
UTSW |
16 |
33,851,952 (GRCm39) |
missense |
probably benign |
0.04 |
R7796:Kalrn
|
UTSW |
16 |
34,007,854 (GRCm39) |
nonsense |
probably null |
|
R7867:Kalrn
|
UTSW |
16 |
33,810,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7869:Kalrn
|
UTSW |
16 |
33,809,217 (GRCm39) |
missense |
probably damaging |
0.98 |
R7914:Kalrn
|
UTSW |
16 |
33,849,122 (GRCm39) |
missense |
probably benign |
|
R8080:Kalrn
|
UTSW |
16 |
33,796,038 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8147:Kalrn
|
UTSW |
16 |
33,875,414 (GRCm39) |
missense |
probably benign |
|
R8239:Kalrn
|
UTSW |
16 |
33,870,153 (GRCm39) |
missense |
noncoding transcript |
|
R8281:Kalrn
|
UTSW |
16 |
33,855,431 (GRCm39) |
nonsense |
probably null |
|
R8294:Kalrn
|
UTSW |
16 |
33,853,954 (GRCm39) |
missense |
probably benign |
0.12 |
R8301:Kalrn
|
UTSW |
16 |
34,177,470 (GRCm39) |
missense |
probably benign |
0.05 |
R8686:Kalrn
|
UTSW |
16 |
34,181,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Kalrn
|
UTSW |
16 |
33,854,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8798:Kalrn
|
UTSW |
16 |
33,803,225 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8878:Kalrn
|
UTSW |
16 |
34,025,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Kalrn
|
UTSW |
16 |
34,018,830 (GRCm39) |
missense |
probably benign |
0.05 |
R8880:Kalrn
|
UTSW |
16 |
34,038,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8883:Kalrn
|
UTSW |
16 |
33,814,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Kalrn
|
UTSW |
16 |
34,047,496 (GRCm39) |
missense |
probably benign |
0.22 |
R9048:Kalrn
|
UTSW |
16 |
33,854,854 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9111:Kalrn
|
UTSW |
16 |
34,181,371 (GRCm39) |
missense |
probably damaging |
0.96 |
R9317:Kalrn
|
UTSW |
16 |
33,834,045 (GRCm39) |
missense |
|
|
R9424:Kalrn
|
UTSW |
16 |
33,809,188 (GRCm39) |
missense |
probably benign |
0.06 |
R9442:Kalrn
|
UTSW |
16 |
33,916,249 (GRCm39) |
start codon destroyed |
probably null |
0.56 |
R9445:Kalrn
|
UTSW |
16 |
33,805,600 (GRCm39) |
missense |
probably benign |
0.13 |
R9515:Kalrn
|
UTSW |
16 |
33,854,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R9516:Kalrn
|
UTSW |
16 |
33,854,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R9625:Kalrn
|
UTSW |
16 |
33,849,197 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9645:Kalrn
|
UTSW |
16 |
34,032,583 (GRCm39) |
missense |
probably benign |
0.01 |
RF014:Kalrn
|
UTSW |
16 |
33,860,303 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Kalrn
|
UTSW |
16 |
33,855,876 (GRCm39) |
missense |
probably damaging |
1.00 |
|