Other mutations in this stock |
Total: 121 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
A |
T |
17: 24,526,549 (GRCm39) |
H578Q |
probably benign |
Het |
Abcc12 |
A |
G |
8: 87,253,910 (GRCm39) |
I958T |
probably benign |
Het |
Abcg5 |
AATCATTTG |
AG |
17: 84,981,030 (GRCm39) |
|
probably null |
Het |
Acap2 |
A |
G |
16: 30,952,345 (GRCm39) |
|
probably null |
Het |
Adgrb1 |
T |
C |
15: 74,411,726 (GRCm39) |
|
probably benign |
Het |
Akap6 |
T |
A |
12: 52,985,258 (GRCm39) |
V897E |
probably damaging |
Het |
Als2 |
A |
T |
1: 59,254,328 (GRCm39) |
L343Q |
probably benign |
Het |
Arhgap5 |
A |
G |
12: 52,589,376 (GRCm39) |
I1275M |
probably damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Bglap3 |
C |
T |
3: 88,284,300 (GRCm39) |
|
probably benign |
Het |
Blnk |
T |
C |
19: 40,928,609 (GRCm39) |
|
probably benign |
Het |
C1qtnf4 |
T |
C |
2: 90,720,003 (GRCm39) |
M92T |
probably damaging |
Het |
Ccdc177 |
G |
A |
12: 80,805,486 (GRCm39) |
R263C |
unknown |
Het |
Ccdc83 |
T |
A |
7: 89,893,362 (GRCm39) |
S132C |
probably damaging |
Het |
Cdc7 |
A |
G |
5: 107,120,940 (GRCm39) |
|
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,632,817 (GRCm39) |
N178I |
probably benign |
Het |
Col27a1 |
C |
T |
4: 63,191,354 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
A |
T |
2: 27,876,766 (GRCm39) |
M822L |
unknown |
Het |
Coro7 |
T |
C |
16: 4,451,620 (GRCm39) |
I451V |
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,536,927 (GRCm39) |
T92A |
probably damaging |
Het |
Ddc |
A |
G |
11: 11,765,292 (GRCm39) |
V460A |
possibly damaging |
Het |
Ddx4 |
C |
T |
13: 112,736,547 (GRCm39) |
V608I |
probably damaging |
Het |
Ddx60 |
A |
T |
8: 62,425,240 (GRCm39) |
H676L |
possibly damaging |
Het |
Dmtf1 |
T |
C |
5: 9,198,989 (GRCm39) |
E48G |
probably benign |
Het |
Dpf3 |
T |
A |
12: 83,371,809 (GRCm39) |
|
probably null |
Het |
Dydc2 |
A |
G |
14: 40,783,860 (GRCm39) |
C88R |
probably benign |
Het |
Elovl4 |
A |
G |
9: 83,662,772 (GRCm39) |
Y163H |
probably damaging |
Het |
Enpp2 |
T |
C |
15: 54,746,378 (GRCm39) |
D296G |
probably damaging |
Het |
Fam83h |
G |
T |
15: 75,878,419 (GRCm39) |
|
probably benign |
Het |
Fbf1 |
T |
A |
11: 116,042,317 (GRCm39) |
Q511L |
possibly damaging |
Het |
Fhdc1 |
A |
T |
3: 84,362,158 (GRCm39) |
L323Q |
probably damaging |
Het |
Fmnl2 |
T |
A |
2: 52,995,588 (GRCm39) |
V437D |
possibly damaging |
Het |
Foxo3 |
A |
G |
10: 42,073,258 (GRCm39) |
S420P |
probably benign |
Het |
Foxp4 |
C |
T |
17: 48,186,796 (GRCm39) |
R378Q |
unknown |
Het |
Garem2 |
G |
T |
5: 30,322,172 (GRCm39) |
G844* |
probably null |
Het |
Glmp |
T |
C |
3: 88,235,177 (GRCm39) |
L269S |
probably damaging |
Het |
Gm9915 |
T |
C |
1: 42,269,881 (GRCm39) |
|
noncoding transcript |
Het |
Gnb4 |
A |
T |
3: 32,652,290 (GRCm39) |
D27E |
probably damaging |
Het |
Gnb5 |
A |
G |
9: 75,251,932 (GRCm39) |
|
probably null |
Het |
Gpr161 |
T |
G |
1: 165,133,927 (GRCm39) |
V63G |
probably damaging |
Het |
Gsk3a |
T |
A |
7: 24,929,146 (GRCm39) |
|
probably benign |
Het |
Hapln2 |
T |
C |
3: 87,931,427 (GRCm39) |
|
probably null |
Het |
Incenp |
G |
T |
19: 9,862,851 (GRCm39) |
T401N |
unknown |
Het |
Kcnq3 |
A |
G |
15: 65,900,472 (GRCm39) |
|
probably null |
Het |
Kif21b |
T |
C |
1: 136,098,894 (GRCm39) |
V1394A |
probably damaging |
Het |
Klhl23 |
T |
C |
2: 69,664,030 (GRCm39) |
C460R |
probably damaging |
Het |
L3mbtl1 |
G |
A |
2: 162,801,492 (GRCm39) |
A291T |
probably damaging |
Het |
Lcp1 |
T |
C |
14: 75,437,946 (GRCm39) |
S119P |
probably damaging |
Het |
Ldhc |
A |
G |
7: 46,519,175 (GRCm39) |
I133V |
probably benign |
Het |
Lmntd2 |
G |
A |
7: 140,791,972 (GRCm39) |
|
probably benign |
Het |
Lpl |
A |
T |
8: 69,349,454 (GRCm39) |
K327* |
probably null |
Het |
Lrp1b |
T |
C |
2: 40,765,081 (GRCm39) |
D2801G |
probably damaging |
Het |
Mppe1 |
C |
A |
18: 67,362,843 (GRCm39) |
A131S |
probably benign |
Het |
Msh3 |
T |
A |
13: 92,386,328 (GRCm39) |
|
probably benign |
Het |
Msh5 |
A |
G |
17: 35,252,576 (GRCm39) |
I377T |
probably damaging |
Het |
Myo1e |
T |
C |
9: 70,276,055 (GRCm39) |
F757L |
probably benign |
Het |
Myof |
A |
T |
19: 37,934,082 (GRCm39) |
D955E |
probably damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,115,982 (GRCm39) |
D858G |
probably damaging |
Het |
Neb |
A |
T |
2: 52,153,917 (GRCm39) |
V2398D |
possibly damaging |
Het |
Nefl |
C |
G |
14: 68,324,121 (GRCm39) |
T453R |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,444,787 (GRCm39) |
N371D |
probably benign |
Het |
Nhsl3 |
A |
G |
4: 129,119,810 (GRCm39) |
|
probably benign |
Het |
Nlrp4f |
T |
C |
13: 65,341,905 (GRCm39) |
Y580C |
probably damaging |
Het |
Nme8 |
A |
C |
13: 19,836,492 (GRCm39) |
L228R |
probably damaging |
Het |
Numa1 |
C |
T |
7: 101,658,529 (GRCm39) |
A1605V |
probably damaging |
Het |
Ofd1 |
T |
C |
X: 165,210,210 (GRCm39) |
Y205C |
probably benign |
Het |
Or2ag12 |
T |
A |
7: 106,276,877 (GRCm39) |
N272I |
probably damaging |
Het |
Or2d3b |
G |
A |
7: 106,513,453 (GRCm39) |
G16D |
probably damaging |
Het |
Or4k77 |
C |
T |
2: 111,199,421 (GRCm39) |
S148L |
probably benign |
Het |
Or8g55 |
T |
A |
9: 39,785,234 (GRCm39) |
I221N |
probably damaging |
Het |
Or8k3 |
T |
A |
2: 86,058,596 (GRCm39) |
T240S |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,763,487 (GRCm39) |
T3987A |
unknown |
Het |
Pdgfrb |
G |
A |
18: 61,199,566 (GRCm39) |
|
probably benign |
Het |
Pdxk |
G |
A |
10: 78,276,988 (GRCm39) |
T270I |
probably damaging |
Het |
Pex5 |
T |
C |
6: 124,391,364 (GRCm39) |
E10G |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,846,112 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
A |
1: 20,451,747 (GRCm39) |
I2183F |
probably damaging |
Het |
Plppr2 |
T |
C |
9: 21,852,422 (GRCm39) |
V102A |
probably damaging |
Het |
Plxnd1 |
T |
C |
6: 115,939,478 (GRCm39) |
T1449A |
probably damaging |
Het |
Pnkd |
T |
A |
1: 74,325,069 (GRCm39) |
|
probably null |
Het |
Pom121l2 |
A |
G |
13: 22,167,642 (GRCm39) |
I638V |
probably damaging |
Het |
Prag1 |
A |
G |
8: 36,596,314 (GRCm39) |
|
probably null |
Het |
Ranbp10 |
A |
G |
8: 106,513,340 (GRCm39) |
F191L |
probably damaging |
Het |
Rapgef1 |
T |
C |
2: 29,623,723 (GRCm39) |
L824P |
probably damaging |
Het |
Rec8 |
T |
C |
14: 55,861,599 (GRCm39) |
L418P |
probably damaging |
Het |
Rimbp2 |
T |
A |
5: 128,874,305 (GRCm39) |
N429Y |
probably damaging |
Het |
Rpe65 |
C |
A |
3: 159,321,307 (GRCm39) |
T373K |
probably benign |
Het |
Rpl35rt |
T |
G |
1: 156,194,017 (GRCm39) |
*124G |
probably null |
Het |
Rrn3 |
T |
C |
16: 13,606,938 (GRCm39) |
S151P |
probably damaging |
Het |
Scn7a |
A |
G |
2: 66,514,633 (GRCm39) |
V1047A |
possibly damaging |
Het |
Scn9a |
G |
T |
2: 66,345,724 (GRCm39) |
P1123Q |
probably damaging |
Het |
Secisbp2l |
T |
C |
2: 125,589,430 (GRCm39) |
D706G |
probably damaging |
Het |
Serpina5 |
A |
T |
12: 104,070,116 (GRCm39) |
T338S |
probably benign |
Het |
Sez6 |
G |
A |
11: 77,844,894 (GRCm39) |
|
probably null |
Het |
Shisa4 |
C |
T |
1: 135,300,012 (GRCm39) |
G157D |
probably damaging |
Het |
Slc1a7 |
G |
T |
4: 107,825,782 (GRCm39) |
D14Y |
probably benign |
Het |
Slc25a11 |
A |
C |
11: 70,536,999 (GRCm39) |
L51V |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,521,668 (GRCm39) |
|
probably null |
Het |
Spata13 |
G |
T |
14: 60,928,912 (GRCm39) |
G157W |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,067,933 (GRCm39) |
V2120A |
possibly damaging |
Het |
Srpra |
T |
C |
9: 35,124,834 (GRCm39) |
|
probably null |
Het |
Syt6 |
A |
G |
3: 103,494,736 (GRCm39) |
I234V |
probably benign |
Het |
Thada |
G |
T |
17: 84,617,470 (GRCm39) |
P1349T |
probably damaging |
Het |
Tmem161a |
C |
T |
8: 70,629,559 (GRCm39) |
R58W |
probably damaging |
Het |
Top3b |
A |
G |
16: 16,701,383 (GRCm39) |
I232V |
probably damaging |
Het |
Tspan1 |
T |
A |
4: 116,020,826 (GRCm39) |
Q197L |
possibly damaging |
Het |
Ttc28 |
A |
C |
5: 111,383,501 (GRCm39) |
Y1334S |
probably benign |
Het |
Ubxn6 |
G |
T |
17: 56,380,077 (GRCm39) |
N28K |
possibly damaging |
Het |
Uggt1 |
T |
C |
1: 36,190,862 (GRCm39) |
D1366G |
probably damaging |
Het |
Ugp2 |
A |
G |
11: 21,278,942 (GRCm39) |
S415P |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,837,157 (GRCm39) |
S2796T |
probably damaging |
Het |
Vipr2 |
T |
C |
12: 116,099,826 (GRCm39) |
V231A |
probably benign |
Het |
Vmn1r176 |
T |
C |
7: 23,534,373 (GRCm39) |
N260S |
probably benign |
Het |
Vmn1r59 |
A |
T |
7: 5,457,038 (GRCm39) |
Y241N |
probably damaging |
Het |
Vmn2r67 |
A |
T |
7: 84,801,013 (GRCm39) |
Y308N |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,797,470 (GRCm39) |
M781K |
probably damaging |
Het |
Vwa3a |
A |
T |
7: 120,379,394 (GRCm39) |
I500F |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,702,559 (GRCm39) |
V31A |
probably damaging |
Het |
Zfp689 |
G |
T |
7: 127,043,959 (GRCm39) |
Q224K |
probably damaging |
Het |
Zfp81 |
A |
T |
17: 33,554,475 (GRCm39) |
L113H |
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 |
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 |
R6052:Kalrn
|
UTSW |
16 |
34,181,255 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|