Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
T |
C |
1: 138,781,380 (GRCm39) |
T90A |
probably damaging |
Het |
A930011G23Rik |
T |
C |
5: 99,381,784 (GRCm39) |
D326G |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,795,581 (GRCm39) |
I446F |
probably damaging |
Het |
Adam34l |
T |
C |
8: 44,080,176 (GRCm39) |
K16R |
probably benign |
Het |
Adamts14 |
A |
G |
10: 61,034,439 (GRCm39) |
Y1150H |
probably benign |
Het |
Adgrl2 |
A |
G |
3: 148,522,880 (GRCm39) |
I217T |
possibly damaging |
Het |
Afap1l1 |
A |
T |
18: 61,874,842 (GRCm39) |
Y446* |
probably null |
Het |
Aimp2 |
G |
A |
5: 143,843,548 (GRCm39) |
A14V |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,535,586 (GRCm39) |
H143Y |
probably damaging |
Het |
Aldh2 |
A |
T |
5: 121,714,026 (GRCm39) |
V207E |
possibly damaging |
Het |
Aoc1l2 |
T |
A |
6: 48,907,703 (GRCm39) |
H234Q |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,986,861 (GRCm39) |
E230G |
probably damaging |
Het |
Arrdc3 |
G |
A |
13: 81,031,808 (GRCm39) |
D14N |
probably damaging |
Het |
Atn1 |
A |
G |
6: 124,722,291 (GRCm39) |
|
probably benign |
Het |
Atxn7l1 |
G |
A |
12: 33,408,743 (GRCm39) |
D302N |
probably damaging |
Het |
Bbs1 |
T |
A |
19: 4,941,736 (GRCm39) |
H518L |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,054,181 (GRCm39) |
H3100L |
probably benign |
Het |
Bmpr1a |
C |
A |
14: 34,147,050 (GRCm39) |
G241C |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Calcrl |
T |
C |
2: 84,200,855 (GRCm39) |
Y63C |
probably damaging |
Het |
Cand2 |
A |
G |
6: 115,762,093 (GRCm39) |
H173R |
possibly damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Card14 |
A |
T |
11: 119,212,647 (GRCm39) |
|
probably null |
Het |
Cd3d |
T |
A |
9: 44,896,299 (GRCm39) |
Y29* |
probably null |
Het |
Cd4 |
A |
G |
6: 124,844,651 (GRCm39) |
V378A |
possibly damaging |
Het |
Cluh |
A |
T |
11: 74,550,828 (GRCm39) |
H318L |
probably damaging |
Het |
Clvs1 |
T |
A |
4: 9,281,899 (GRCm39) |
D114E |
probably benign |
Het |
Cnot4 |
T |
A |
6: 35,000,344 (GRCm39) |
T548S |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crebbp |
A |
T |
16: 3,946,561 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
G |
1: 53,621,835 (GRCm39) |
K1097Q |
possibly damaging |
Het |
Doc2a |
T |
A |
7: 126,450,979 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
T |
1: 123,832,833 (GRCm39) |
V48E |
probably null |
Het |
Dsg2 |
A |
G |
18: 20,734,530 (GRCm39) |
K836R |
probably damaging |
Het |
Egr2 |
T |
C |
10: 67,375,857 (GRCm39) |
V164A |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,970,221 (GRCm39) |
S1132T |
probably benign |
Het |
Espn |
T |
A |
4: 152,213,012 (GRCm39) |
|
probably null |
Het |
Fam83b |
A |
G |
9: 76,399,304 (GRCm39) |
S600P |
probably benign |
Het |
Fanca |
A |
T |
8: 124,024,551 (GRCm39) |
N425K |
possibly damaging |
Het |
Flot2 |
C |
T |
11: 77,949,445 (GRCm39) |
L294F |
probably damaging |
Het |
Frs2 |
A |
G |
10: 116,910,459 (GRCm39) |
V301A |
probably benign |
Het |
Fv1 |
T |
A |
4: 147,953,618 (GRCm39) |
N61K |
possibly damaging |
Het |
Fxr2 |
A |
G |
11: 69,540,659 (GRCm39) |
E339G |
possibly damaging |
Het |
Gck |
T |
C |
11: 5,856,515 (GRCm39) |
Y214C |
probably damaging |
Het |
Golga3 |
C |
G |
5: 110,340,839 (GRCm39) |
T551R |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,625 (GRCm39) |
S59P |
probably damaging |
Het |
Gsdme |
C |
T |
6: 50,185,102 (GRCm39) |
V451M |
probably damaging |
Het |
H2-T13 |
A |
C |
17: 36,391,938 (GRCm39) |
I216S |
probably damaging |
Het |
Herc4 |
T |
A |
10: 63,081,743 (GRCm39) |
V22E |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
A |
T |
6: 52,141,576 (GRCm39) |
S17T |
probably damaging |
Het |
Hs3st5 |
A |
G |
10: 36,708,882 (GRCm39) |
Y139C |
probably damaging |
Het |
Ism1 |
G |
A |
2: 139,587,937 (GRCm39) |
V221I |
probably benign |
Het |
Katnip |
A |
G |
7: 125,419,261 (GRCm39) |
N476S |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,261,631 (GRCm39) |
D602G |
possibly damaging |
Het |
Ktn1 |
A |
G |
14: 47,932,978 (GRCm39) |
K711E |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Macf1 |
A |
G |
4: 123,350,488 (GRCm39) |
S3792P |
probably damaging |
Het |
Maml3 |
C |
T |
3: 51,598,178 (GRCm39) |
M189I |
probably benign |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mep1a |
T |
G |
17: 43,813,573 (GRCm39) |
I13L |
probably benign |
Het |
Mkrn2 |
G |
T |
6: 115,586,562 (GRCm39) |
C16F |
probably damaging |
Het |
Mlh1 |
C |
T |
9: 111,057,631 (GRCm39) |
A727T |
probably damaging |
Het |
Muc21 |
A |
T |
17: 35,929,600 (GRCm39) |
S1529T |
probably benign |
Het |
Naa16 |
T |
C |
14: 79,593,931 (GRCm39) |
Y344C |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,752,628 (GRCm39) |
Y585F |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,587,753 (GRCm39) |
K149R |
probably damaging |
Het |
Nufip1 |
T |
A |
14: 76,372,287 (GRCm39) |
I467N |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,632,960 (GRCm39) |
I1057T |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,886,653 (GRCm39) |
|
probably benign |
Het |
Or10ag52 |
T |
A |
2: 87,043,588 (GRCm39) |
C117* |
probably null |
Het |
Or5k1 |
A |
G |
16: 58,617,309 (GRCm39) |
V300A |
probably benign |
Het |
Or5k14 |
A |
C |
16: 58,692,874 (GRCm39) |
I213R |
probably benign |
Het |
Pi4k2a |
A |
T |
19: 42,104,377 (GRCm39) |
I380F |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pik3cg |
A |
T |
12: 32,254,024 (GRCm39) |
D654E |
possibly damaging |
Het |
Poli |
G |
T |
18: 70,642,058 (GRCm39) |
P714Q |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,378,230 (GRCm39) |
N201D |
probably benign |
Het |
Prorp |
A |
G |
12: 55,384,991 (GRCm39) |
D89G |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,747 (GRCm39) |
K81N |
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,271,948 (GRCm39) |
|
probably null |
Het |
Sec24a |
C |
T |
11: 51,627,190 (GRCm39) |
V241I |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,950,567 (GRCm39) |
T160A |
possibly damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,375 (GRCm39) |
I497T |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,532 (GRCm39) |
D512V |
probably damaging |
Het |
Slc43a3 |
C |
T |
2: 84,788,084 (GRCm39) |
R489C |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,452,089 (GRCm39) |
F327L |
probably benign |
Het |
Slitrk3 |
A |
G |
3: 72,957,104 (GRCm39) |
V556A |
possibly damaging |
Het |
Spata6l |
A |
G |
19: 28,926,024 (GRCm39) |
F130L |
probably damaging |
Het |
Spib |
T |
C |
7: 44,178,281 (GRCm39) |
E180G |
probably benign |
Het |
Spint2 |
T |
A |
7: 28,958,833 (GRCm39) |
N128Y |
probably damaging |
Het |
Spx |
G |
A |
6: 142,364,245 (GRCm39) |
G102E |
probably benign |
Het |
Spz1 |
T |
A |
13: 92,712,166 (GRCm39) |
E103D |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,495 (GRCm39) |
I138T |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,000,448 (GRCm39) |
I206N |
possibly damaging |
Het |
Tcaf2 |
T |
C |
6: 42,606,791 (GRCm39) |
T388A |
probably benign |
Het |
Tdpoz8 |
G |
T |
3: 92,981,344 (GRCm39) |
A121S |
probably benign |
Het |
Thap12 |
T |
C |
7: 98,365,572 (GRCm39) |
V580A |
possibly damaging |
Het |
Tlr5 |
T |
A |
1: 182,801,912 (GRCm39) |
D405E |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,890,878 (GRCm39) |
V407A |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim43a |
T |
G |
9: 88,466,312 (GRCm39) |
L211R |
probably damaging |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Ttll8 |
T |
C |
15: 88,798,654 (GRCm39) |
T694A |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,953,535 (GRCm39) |
A823V |
probably damaging |
Het |
Ubqln5 |
C |
A |
7: 103,778,741 (GRCm39) |
V28F |
probably damaging |
Het |
Ulk1 |
T |
A |
5: 110,935,017 (GRCm39) |
Q972L |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,994,062 (GRCm39) |
Y398H |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,531 (GRCm39) |
D615G |
probably benign |
Het |
Utp15 |
A |
G |
13: 98,387,420 (GRCm39) |
C385R |
probably benign |
Het |
Vmn2r91 |
T |
A |
17: 18,356,142 (GRCm39) |
V603D |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Yjefn3 |
A |
T |
8: 70,341,645 (GRCm39) |
|
probably null |
Het |
Ywhab |
A |
T |
2: 163,853,807 (GRCm39) |
I95F |
probably damaging |
Het |
Zfp143 |
C |
T |
7: 109,660,489 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
C |
G |
7: 27,401,949 (GRCm39) |
T135R |
possibly damaging |
Het |
Zfp970 |
A |
G |
2: 177,166,663 (GRCm39) |
Q79R |
possibly damaging |
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 |
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 |
|