Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam39 |
T |
C |
8: 41,278,106 (GRCm39) |
S166P |
probably damaging |
Het |
Appl1 |
T |
A |
14: 26,686,914 (GRCm39) |
T19S |
probably damaging |
Het |
Arid4b |
T |
A |
13: 14,344,594 (GRCm39) |
D557E |
probably benign |
Het |
Aven |
C |
T |
2: 112,390,120 (GRCm39) |
R8W |
probably benign |
Het |
C2cd2l |
T |
C |
9: 44,227,502 (GRCm39) |
E307G |
possibly damaging |
Het |
Cdh20 |
A |
C |
1: 110,027,832 (GRCm39) |
T526P |
probably benign |
Het |
Dchs1 |
C |
T |
7: 105,414,718 (GRCm39) |
V775M |
probably benign |
Het |
Dennd1b |
A |
G |
1: 138,969,673 (GRCm39) |
N63S |
probably benign |
Het |
Dtnb |
A |
T |
12: 3,694,056 (GRCm39) |
Y248F |
unknown |
Het |
Ehbp1l1 |
T |
A |
19: 5,770,089 (GRCm39) |
T405S |
possibly damaging |
Het |
Fam149a |
A |
G |
8: 45,803,490 (GRCm39) |
Y415H |
possibly damaging |
Het |
Fam186a |
A |
G |
15: 99,839,191 (GRCm39) |
L2351P |
unknown |
Het |
Fsip2 |
T |
G |
2: 82,819,687 (GRCm39) |
I5140S |
possibly damaging |
Het |
Gm8674 |
T |
C |
13: 50,054,262 (GRCm39) |
T749A |
noncoding transcript |
Het |
Kpna3 |
A |
T |
14: 61,624,919 (GRCm39) |
N141K |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,449,882 (GRCm39) |
G2067D |
probably damaging |
Het |
Lrp2 |
G |
T |
2: 69,311,611 (GRCm39) |
Y2622* |
probably null |
Het |
Lrtm2 |
A |
C |
6: 119,297,778 (GRCm39) |
F88V |
probably damaging |
Het |
Mboat1 |
T |
C |
13: 30,429,333 (GRCm39) |
S454P |
probably damaging |
Het |
Nkpd1 |
C |
T |
7: 19,253,753 (GRCm39) |
P40S |
probably benign |
Het |
Or2b7 |
T |
C |
13: 21,739,788 (GRCm39) |
I135V |
probably benign |
Het |
Or4a76 |
T |
A |
2: 89,460,907 (GRCm39) |
I112F |
probably damaging |
Het |
Or8b54 |
G |
A |
9: 38,686,577 (GRCm39) |
V9M |
noncoding transcript |
Het |
Or8k27 |
C |
A |
2: 86,275,473 (GRCm39) |
M284I |
noncoding transcript |
Het |
Patj |
A |
G |
4: 98,570,308 (GRCm39) |
E1711G |
possibly damaging |
Het |
Pcdha4 |
A |
T |
18: 37,086,128 (GRCm39) |
I104F |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Plekhg4 |
C |
T |
8: 106,107,546 (GRCm39) |
R990* |
probably null |
Het |
Pphln1 |
T |
C |
15: 93,386,930 (GRCm39) |
S343P |
probably benign |
Het |
Pram1 |
A |
T |
17: 33,860,241 (GRCm39) |
K269N |
probably damaging |
Het |
Psmd13 |
T |
A |
7: 140,466,450 (GRCm39) |
I79K |
probably damaging |
Het |
Ptprf |
T |
C |
4: 118,069,309 (GRCm39) |
D1586G |
possibly damaging |
Het |
Ptprh |
T |
A |
7: 4,584,090 (GRCm39) |
Q167H |
probably damaging |
Het |
Rbm46 |
C |
T |
3: 82,772,775 (GRCm39) |
R119Q |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,077,848 (GRCm39) |
M20T |
probably damaging |
Het |
Scrn2 |
T |
G |
11: 96,923,046 (GRCm39) |
L163R |
probably damaging |
Het |
Slc36a3 |
C |
T |
11: 55,022,433 (GRCm39) |
V254I |
probably benign |
Het |
Slc6a6 |
T |
C |
6: 91,701,951 (GRCm39) |
F120L |
probably benign |
Het |
Slc8a2 |
A |
T |
7: 15,879,230 (GRCm39) |
H572L |
probably benign |
Het |
Spats2 |
T |
A |
15: 99,106,776 (GRCm39) |
D357E |
probably damaging |
Het |
Speg |
A |
T |
1: 75,395,677 (GRCm39) |
N1816I |
probably damaging |
Het |
Sult2b1 |
A |
G |
7: 45,433,361 (GRCm39) |
V2A |
unknown |
Het |
Susd3 |
T |
C |
13: 49,384,731 (GRCm39) |
T231A |
probably benign |
Het |
Tamalin |
C |
T |
15: 101,128,902 (GRCm39) |
L217F |
probably damaging |
Het |
Tcp1 |
A |
G |
17: 13,139,738 (GRCm39) |
D261G |
probably benign |
Het |
Trpm2 |
C |
G |
10: 77,771,836 (GRCm39) |
S601T |
probably benign |
Het |
Ugt2b38 |
A |
T |
5: 87,571,659 (GRCm39) |
F124L |
probably benign |
Het |
Unc80 |
G |
T |
1: 66,693,178 (GRCm39) |
E2522D |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,396,750 (GRCm39) |
T2365A |
|
Het |
Vmn2r92 |
G |
T |
17: 18,405,278 (GRCm39) |
M807I |
probably benign |
Het |
Vps13b |
C |
A |
15: 35,597,550 (GRCm39) |
P1030Q |
probably damaging |
Het |
Wrn |
T |
G |
8: 33,819,213 (GRCm39) |
K246N |
probably damaging |
Het |
Zer1 |
T |
A |
2: 29,991,147 (GRCm39) |
|
probably null |
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 |
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 |
|
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 |
|