Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,471,525 (GRCm39) |
S977C |
possibly damaging |
Het |
Abca8a |
T |
A |
11: 109,960,305 (GRCm39) |
D646V |
probably damaging |
Het |
Adss2 |
T |
A |
1: 177,597,526 (GRCm39) |
Y378F |
probably damaging |
Het |
Akap6 |
C |
T |
12: 53,188,319 (GRCm39) |
A1911V |
probably benign |
Het |
Alg2 |
T |
C |
4: 47,474,159 (GRCm39) |
Y43C |
probably benign |
Het |
Alk |
A |
C |
17: 72,202,758 (GRCm39) |
V1159G |
probably damaging |
Het |
Alx3 |
A |
T |
3: 107,508,010 (GRCm39) |
Q173L |
probably damaging |
Het |
Aqp9 |
A |
G |
9: 71,069,593 (GRCm39) |
|
probably benign |
Het |
Atf7ip |
C |
A |
6: 136,564,141 (GRCm39) |
L787I |
probably benign |
Het |
Bbs9 |
A |
T |
9: 22,590,234 (GRCm39) |
E657D |
possibly damaging |
Het |
Bean1 |
G |
A |
8: 104,908,752 (GRCm39) |
|
probably null |
Het |
Cactin |
G |
T |
10: 81,157,082 (GRCm39) |
R13L |
unknown |
Het |
Ccdc178 |
T |
C |
18: 22,200,721 (GRCm39) |
E412G |
probably damaging |
Het |
Ccdc30 |
A |
G |
4: 119,181,759 (GRCm39) |
I583T |
probably damaging |
Het |
Ccl8 |
T |
C |
11: 82,006,933 (GRCm39) |
Y49H |
probably damaging |
Het |
Clptm1 |
T |
A |
7: 19,372,932 (GRCm39) |
K199N |
probably damaging |
Het |
Cnbp |
G |
A |
6: 87,822,646 (GRCm39) |
S39L |
probably benign |
Het |
Cnih3 |
T |
A |
1: 181,237,437 (GRCm39) |
|
probably benign |
Het |
Cnksr3 |
A |
T |
10: 7,090,201 (GRCm39) |
|
probably benign |
Het |
Cntn1 |
A |
G |
15: 92,159,380 (GRCm39) |
I512V |
probably benign |
Het |
Col20a1 |
A |
G |
2: 180,640,296 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
A |
T |
6: 8,127,360 (GRCm39) |
|
probably benign |
Het |
Col6a2 |
A |
T |
10: 76,450,741 (GRCm39) |
Y63* |
probably null |
Het |
Copa |
T |
G |
1: 171,925,312 (GRCm39) |
F190V |
probably damaging |
Het |
Crisp4 |
A |
C |
1: 18,207,148 (GRCm39) |
|
probably benign |
Het |
Cxcl2 |
C |
T |
5: 91,052,085 (GRCm39) |
Q64* |
probably null |
Het |
Cxcr5 |
T |
C |
9: 44,425,549 (GRCm39) |
D36G |
probably benign |
Het |
Cyp20a1 |
T |
A |
1: 60,411,765 (GRCm39) |
V271E |
possibly damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,071,538 (GRCm39) |
Y570C |
probably damaging |
Het |
Ddi1 |
T |
G |
9: 6,266,198 (GRCm39) |
D57A |
probably benign |
Het |
Ddx11 |
T |
A |
17: 66,450,460 (GRCm39) |
S492T |
probably benign |
Het |
Dhx34 |
C |
T |
7: 15,950,376 (GRCm39) |
R264H |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,561,375 (GRCm39) |
I328F |
|
Het |
Dnah5 |
C |
T |
15: 28,327,886 (GRCm39) |
R2087C |
probably damaging |
Het |
Dnah8 |
C |
G |
17: 30,927,286 (GRCm39) |
S1314W |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,260,396 (GRCm39) |
N982D |
probably benign |
Het |
Dync1h1 |
A |
G |
12: 110,583,172 (GRCm39) |
D423G |
probably damaging |
Het |
Ect2l |
A |
C |
10: 18,048,583 (GRCm39) |
L213V |
probably damaging |
Het |
Fam210a |
T |
C |
18: 68,409,215 (GRCm39) |
I32V |
probably benign |
Het |
Fancg |
A |
G |
4: 43,007,266 (GRCm39) |
|
probably null |
Het |
Fastkd5 |
T |
C |
2: 130,457,111 (GRCm39) |
E493G |
probably benign |
Het |
Fbxo38 |
T |
C |
18: 62,659,272 (GRCm39) |
M342V |
probably damaging |
Het |
Flnc |
A |
C |
6: 29,455,410 (GRCm39) |
K2020Q |
probably damaging |
Het |
Flt4 |
A |
G |
11: 49,527,160 (GRCm39) |
|
probably benign |
Het |
Frmd4b |
G |
T |
6: 97,389,480 (GRCm39) |
P129T |
probably benign |
Het |
Galnt13 |
C |
A |
2: 54,770,138 (GRCm39) |
A310E |
probably benign |
Het |
Gm4884 |
T |
A |
7: 40,694,108 (GRCm39) |
Y692* |
probably null |
Het |
Gm6309 |
T |
A |
5: 146,105,103 (GRCm39) |
D270V |
probably damaging |
Het |
Grip1 |
G |
T |
10: 119,290,192 (GRCm39) |
|
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kdf1 |
G |
T |
4: 133,255,505 (GRCm39) |
C74F |
probably damaging |
Het |
Kdm1b |
T |
A |
13: 47,207,184 (GRCm39) |
C169* |
probably null |
Het |
Lama1 |
G |
A |
17: 68,080,779 (GRCm39) |
G1269E |
|
Het |
Lamb3 |
C |
T |
1: 193,017,182 (GRCm39) |
A791V |
probably benign |
Het |
Leng9 |
G |
T |
7: 4,151,774 (GRCm39) |
R301S |
possibly damaging |
Het |
Lgr6 |
C |
A |
1: 134,915,342 (GRCm39) |
V746L |
probably benign |
Het |
Lrp5 |
T |
A |
19: 3,702,170 (GRCm39) |
S216C |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,178,433 (GRCm39) |
T1599A |
probably damaging |
Het |
Map2k1 |
G |
T |
9: 64,094,606 (GRCm39) |
N345K |
probably damaging |
Het |
Map4k1 |
T |
A |
7: 28,688,862 (GRCm39) |
D304E |
probably benign |
Het |
Mcpt1 |
C |
T |
14: 56,256,522 (GRCm39) |
T86I |
probably damaging |
Het |
Mcpt9 |
T |
C |
14: 56,265,153 (GRCm39) |
K116R |
probably benign |
Het |
Morc2a |
G |
T |
11: 3,628,584 (GRCm39) |
A346S |
probably damaging |
Het |
Mybpc3 |
A |
T |
2: 90,954,237 (GRCm39) |
Q370L |
probably benign |
Het |
Nars2 |
T |
C |
7: 96,652,095 (GRCm39) |
S229P |
probably damaging |
Het |
Ndufa10 |
A |
T |
1: 92,397,693 (GRCm39) |
Y118N |
probably damaging |
Het |
Nek11 |
A |
T |
9: 105,172,571 (GRCm39) |
|
probably null |
Het |
Notch4 |
T |
C |
17: 34,803,470 (GRCm39) |
V1463A |
possibly damaging |
Het |
Nrcam |
T |
C |
12: 44,610,908 (GRCm39) |
I536T |
probably benign |
Het |
Or6c202 |
T |
C |
10: 128,996,334 (GRCm39) |
Y173C |
probably benign |
Het |
Pbld1 |
A |
T |
10: 62,912,226 (GRCm39) |
T285S |
probably benign |
Het |
Pcdhgb8 |
A |
T |
18: 37,896,177 (GRCm39) |
T416S |
possibly damaging |
Het |
Plekhg6 |
T |
C |
6: 125,351,523 (GRCm39) |
D242G |
probably damaging |
Het |
Pnmt |
T |
A |
11: 98,278,580 (GRCm39) |
V182D |
probably benign |
Het |
Ppp1r13b |
G |
T |
12: 111,799,871 (GRCm39) |
N758K |
probably damaging |
Het |
Prex2 |
A |
G |
1: 11,240,799 (GRCm39) |
|
probably benign |
Het |
Prss3 |
A |
T |
6: 41,354,512 (GRCm39) |
L7Q |
probably damaging |
Het |
Prss43 |
T |
A |
9: 110,660,046 (GRCm39) |
L370Q |
probably damaging |
Het |
Rac1 |
A |
T |
5: 143,493,885 (GRCm39) |
V104E |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,166,449 (GRCm39) |
Y107C |
probably damaging |
Het |
Rnase13 |
C |
T |
14: 52,159,940 (GRCm39) |
W66* |
probably null |
Het |
Rrp1b |
G |
A |
17: 32,270,688 (GRCm39) |
V216I |
possibly damaging |
Het |
Serinc1 |
A |
G |
10: 57,395,864 (GRCm39) |
S309P |
probably benign |
Het |
Serpine3 |
T |
A |
14: 62,902,587 (GRCm39) |
L66Q |
probably damaging |
Het |
Smc5 |
C |
T |
19: 23,191,234 (GRCm39) |
V924M |
probably damaging |
Het |
Spmip4 |
A |
T |
6: 50,551,028 (GRCm39) |
Y474N |
possibly damaging |
Het |
Srgap1 |
A |
T |
10: 121,761,545 (GRCm39) |
|
probably benign |
Het |
Stab1 |
T |
C |
14: 30,883,771 (GRCm39) |
E262G |
possibly damaging |
Het |
Ston2 |
A |
G |
12: 91,606,498 (GRCm39) |
*896R |
probably null |
Het |
Syt6 |
A |
G |
3: 103,532,941 (GRCm39) |
M442V |
probably benign |
Het |
Tap1 |
T |
C |
17: 34,408,536 (GRCm39) |
|
probably null |
Het |
Tbx3 |
A |
C |
5: 119,818,624 (GRCm39) |
S420R |
probably benign |
Het |
Tespa1 |
A |
T |
10: 130,198,316 (GRCm39) |
Q446L |
probably benign |
Het |
Tifab |
T |
C |
13: 56,324,108 (GRCm39) |
M112V |
probably benign |
Het |
Trpv5 |
A |
T |
6: 41,630,192 (GRCm39) |
S633T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,684,236 (GRCm39) |
K838R |
unknown |
Het |
Ttn |
A |
T |
2: 76,744,810 (GRCm39) |
V5413E |
probably damaging |
Het |
Tub |
C |
A |
7: 108,628,793 (GRCm39) |
N415K |
|
Het |
Vmn2r3 |
T |
C |
3: 64,182,383 (GRCm39) |
M439V |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,850,736 (GRCm39) |
D2231G |
probably benign |
Het |
Wbp1 |
C |
T |
6: 83,096,913 (GRCm39) |
C118Y |
unknown |
Het |
Zdhhc20 |
C |
T |
14: 58,127,671 (GRCm39) |
|
probably benign |
Het |
Zfp217 |
T |
A |
2: 169,956,391 (GRCm39) |
N869I |
probably benign |
Het |
Zfp677 |
T |
C |
17: 21,618,350 (GRCm39) |
I469T |
probably benign |
Het |
Zmym2 |
T |
A |
14: 57,185,329 (GRCm39) |
|
probably benign |
Het |
Zzef1 |
T |
G |
11: 72,687,402 (GRCm39) |
S94A |
probably benign |
Het |
|
Other mutations in Kmt2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00436:Kmt2c
|
APN |
5 |
25,486,259 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00694:Kmt2c
|
APN |
5 |
25,498,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00780:Kmt2c
|
APN |
5 |
25,516,049 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00811:Kmt2c
|
APN |
5 |
25,579,531 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL00885:Kmt2c
|
APN |
5 |
25,614,169 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL00948:Kmt2c
|
APN |
5 |
25,582,159 (GRCm39) |
missense |
probably benign |
0.08 |
IGL00959:Kmt2c
|
APN |
5 |
25,481,227 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01022:Kmt2c
|
APN |
5 |
25,507,699 (GRCm39) |
unclassified |
probably benign |
|
IGL01146:Kmt2c
|
APN |
5 |
25,513,510 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01154:Kmt2c
|
APN |
5 |
25,489,397 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01434:Kmt2c
|
APN |
5 |
25,614,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01464:Kmt2c
|
APN |
5 |
25,557,242 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01525:Kmt2c
|
APN |
5 |
25,534,439 (GRCm39) |
splice site |
probably benign |
|
IGL01530:Kmt2c
|
APN |
5 |
25,518,498 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01550:Kmt2c
|
APN |
5 |
25,486,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01598:Kmt2c
|
APN |
5 |
25,478,664 (GRCm39) |
makesense |
probably null |
|
IGL01598:Kmt2c
|
APN |
5 |
25,559,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Kmt2c
|
APN |
5 |
25,559,809 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01663:Kmt2c
|
APN |
5 |
25,515,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Kmt2c
|
APN |
5 |
25,505,096 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01714:Kmt2c
|
APN |
5 |
25,518,398 (GRCm39) |
missense |
probably benign |
|
IGL01784:Kmt2c
|
APN |
5 |
25,518,524 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Kmt2c
|
APN |
5 |
25,495,802 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01825:Kmt2c
|
APN |
5 |
25,515,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Kmt2c
|
APN |
5 |
25,600,453 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02072:Kmt2c
|
APN |
5 |
25,610,430 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02159:Kmt2c
|
APN |
5 |
25,516,341 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02303:Kmt2c
|
APN |
5 |
25,515,155 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02417:Kmt2c
|
APN |
5 |
25,578,018 (GRCm39) |
missense |
probably benign |
|
IGL02578:Kmt2c
|
APN |
5 |
25,571,198 (GRCm39) |
intron |
probably benign |
|
IGL02811:Kmt2c
|
APN |
5 |
25,520,026 (GRCm39) |
nonsense |
probably null |
|
IGL02943:Kmt2c
|
APN |
5 |
25,495,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Kmt2c
|
APN |
5 |
25,489,170 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Kmt2c
|
APN |
5 |
25,515,350 (GRCm39) |
missense |
probably benign |
|
IGL03076:Kmt2c
|
APN |
5 |
25,504,149 (GRCm39) |
nonsense |
probably null |
|
IGL03088:Kmt2c
|
APN |
5 |
25,504,802 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03131:Kmt2c
|
APN |
5 |
25,520,359 (GRCm39) |
missense |
probably benign |
0.00 |
FR4304:Kmt2c
|
UTSW |
5 |
25,520,764 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Kmt2c
|
UTSW |
5 |
25,520,761 (GRCm39) |
small insertion |
probably benign |
|
PIT4520001:Kmt2c
|
UTSW |
5 |
25,520,664 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4585001:Kmt2c
|
UTSW |
5 |
25,520,104 (GRCm39) |
missense |
probably benign |
0.21 |
R0313:Kmt2c
|
UTSW |
5 |
25,549,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Kmt2c
|
UTSW |
5 |
25,514,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Kmt2c
|
UTSW |
5 |
25,580,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Kmt2c
|
UTSW |
5 |
25,520,662 (GRCm39) |
missense |
probably benign |
|
R0453:Kmt2c
|
UTSW |
5 |
25,559,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Kmt2c
|
UTSW |
5 |
25,504,250 (GRCm39) |
missense |
probably benign |
|
R0619:Kmt2c
|
UTSW |
5 |
25,503,914 (GRCm39) |
missense |
probably benign |
0.21 |
R0671:Kmt2c
|
UTSW |
5 |
25,609,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R0736:Kmt2c
|
UTSW |
5 |
25,500,432 (GRCm39) |
missense |
probably benign |
|
R0745:Kmt2c
|
UTSW |
5 |
25,564,696 (GRCm39) |
splice site |
probably null |
|
R0760:Kmt2c
|
UTSW |
5 |
25,558,315 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0784:Kmt2c
|
UTSW |
5 |
25,515,893 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Kmt2c
|
UTSW |
5 |
25,500,605 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0893:Kmt2c
|
UTSW |
5 |
25,556,268 (GRCm39) |
splice site |
probably benign |
|
R0942:Kmt2c
|
UTSW |
5 |
25,520,301 (GRCm39) |
missense |
probably benign |
0.10 |
R1110:Kmt2c
|
UTSW |
5 |
25,519,360 (GRCm39) |
missense |
probably benign |
0.01 |
R1137:Kmt2c
|
UTSW |
5 |
25,515,981 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1255:Kmt2c
|
UTSW |
5 |
25,556,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Kmt2c
|
UTSW |
5 |
25,610,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R1497:Kmt2c
|
UTSW |
5 |
25,519,513 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1594:Kmt2c
|
UTSW |
5 |
25,519,876 (GRCm39) |
missense |
probably benign |
0.01 |
R1611:Kmt2c
|
UTSW |
5 |
25,564,309 (GRCm39) |
critical splice donor site |
probably null |
|
R1617:Kmt2c
|
UTSW |
5 |
25,580,925 (GRCm39) |
missense |
probably benign |
0.01 |
R1720:Kmt2c
|
UTSW |
5 |
25,504,182 (GRCm39) |
missense |
probably benign |
0.05 |
R1723:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Kmt2c
|
UTSW |
5 |
25,520,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Kmt2c
|
UTSW |
5 |
25,495,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Kmt2c
|
UTSW |
5 |
25,577,972 (GRCm39) |
missense |
probably benign |
0.02 |
R1809:Kmt2c
|
UTSW |
5 |
25,489,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Kmt2c
|
UTSW |
5 |
25,578,434 (GRCm39) |
missense |
probably benign |
0.45 |
R1895:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1946:Kmt2c
|
UTSW |
5 |
25,520,152 (GRCm39) |
missense |
probably benign |
0.34 |
R1989:Kmt2c
|
UTSW |
5 |
25,703,542 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2039:Kmt2c
|
UTSW |
5 |
25,534,038 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2049:Kmt2c
|
UTSW |
5 |
25,490,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2079:Kmt2c
|
UTSW |
5 |
25,557,278 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2080:Kmt2c
|
UTSW |
5 |
25,559,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Kmt2c
|
UTSW |
5 |
25,514,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2186:Kmt2c
|
UTSW |
5 |
25,492,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R2395:Kmt2c
|
UTSW |
5 |
25,520,150 (GRCm39) |
missense |
probably benign |
|
R2983:Kmt2c
|
UTSW |
5 |
25,520,755 (GRCm39) |
small deletion |
probably benign |
|
R3109:Kmt2c
|
UTSW |
5 |
25,480,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3500:Kmt2c
|
UTSW |
5 |
25,504,477 (GRCm39) |
missense |
probably benign |
0.02 |
R3738:Kmt2c
|
UTSW |
5 |
25,610,381 (GRCm39) |
missense |
probably benign |
0.41 |
R3809:Kmt2c
|
UTSW |
5 |
25,614,136 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4088:Kmt2c
|
UTSW |
5 |
25,492,711 (GRCm39) |
missense |
probably benign |
|
R4107:Kmt2c
|
UTSW |
5 |
25,503,918 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4212:Kmt2c
|
UTSW |
5 |
25,552,357 (GRCm39) |
critical splice donor site |
probably null |
|
R4376:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4377:Kmt2c
|
UTSW |
5 |
25,520,324 (GRCm39) |
missense |
probably benign |
0.00 |
R4383:Kmt2c
|
UTSW |
5 |
25,556,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4435:Kmt2c
|
UTSW |
5 |
25,519,875 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4456:Kmt2c
|
UTSW |
5 |
25,515,210 (GRCm39) |
missense |
probably benign |
|
R4461:Kmt2c
|
UTSW |
5 |
25,504,874 (GRCm39) |
missense |
probably benign |
0.00 |
R4519:Kmt2c
|
UTSW |
5 |
25,568,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4550:Kmt2c
|
UTSW |
5 |
25,505,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R4557:Kmt2c
|
UTSW |
5 |
25,505,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Kmt2c
|
UTSW |
5 |
25,559,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Kmt2c
|
UTSW |
5 |
25,571,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Kmt2c
|
UTSW |
5 |
25,519,025 (GRCm39) |
nonsense |
probably null |
|
R4781:Kmt2c
|
UTSW |
5 |
25,648,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Kmt2c
|
UTSW |
5 |
25,520,111 (GRCm39) |
missense |
probably benign |
|
R4855:Kmt2c
|
UTSW |
5 |
25,519,555 (GRCm39) |
missense |
probably benign |
0.00 |
R4919:Kmt2c
|
UTSW |
5 |
25,519,393 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4971:Kmt2c
|
UTSW |
5 |
25,515,870 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Kmt2c
|
UTSW |
5 |
25,500,509 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5012:Kmt2c
|
UTSW |
5 |
25,504,710 (GRCm39) |
nonsense |
probably null |
|
R5033:Kmt2c
|
UTSW |
5 |
25,519,706 (GRCm39) |
missense |
probably benign |
0.03 |
R5093:Kmt2c
|
UTSW |
5 |
25,614,205 (GRCm39) |
missense |
probably benign |
0.17 |
R5125:Kmt2c
|
UTSW |
5 |
25,489,379 (GRCm39) |
missense |
probably damaging |
0.99 |
R5231:Kmt2c
|
UTSW |
5 |
25,520,471 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5254:Kmt2c
|
UTSW |
5 |
25,519,592 (GRCm39) |
missense |
probably benign |
0.01 |
R5396:Kmt2c
|
UTSW |
5 |
25,499,732 (GRCm39) |
splice site |
probably null |
|
R5415:Kmt2c
|
UTSW |
5 |
25,519,699 (GRCm39) |
missense |
probably benign |
0.21 |
R5523:Kmt2c
|
UTSW |
5 |
25,504,337 (GRCm39) |
missense |
probably benign |
0.00 |
R5554:Kmt2c
|
UTSW |
5 |
25,499,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R5701:Kmt2c
|
UTSW |
5 |
25,519,015 (GRCm39) |
missense |
probably benign |
0.16 |
R5762:Kmt2c
|
UTSW |
5 |
25,515,455 (GRCm39) |
missense |
probably benign |
0.01 |
R5819:Kmt2c
|
UTSW |
5 |
25,614,130 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Kmt2c
|
UTSW |
5 |
25,489,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R5912:Kmt2c
|
UTSW |
5 |
25,552,467 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5951:Kmt2c
|
UTSW |
5 |
25,535,801 (GRCm39) |
missense |
probably benign |
0.15 |
R5988:Kmt2c
|
UTSW |
5 |
25,516,118 (GRCm39) |
missense |
probably benign |
0.02 |
R5999:Kmt2c
|
UTSW |
5 |
25,489,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6104:Kmt2c
|
UTSW |
5 |
25,504,127 (GRCm39) |
missense |
probably benign |
|
R6254:Kmt2c
|
UTSW |
5 |
25,554,872 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6311:Kmt2c
|
UTSW |
5 |
25,648,816 (GRCm39) |
critical splice donor site |
probably null |
|
R6329:Kmt2c
|
UTSW |
5 |
25,520,600 (GRCm39) |
missense |
probably benign |
0.01 |
R6347:Kmt2c
|
UTSW |
5 |
25,515,833 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6364:Kmt2c
|
UTSW |
5 |
25,514,634 (GRCm39) |
missense |
probably null |
0.99 |
R6379:Kmt2c
|
UTSW |
5 |
25,564,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R6588:Kmt2c
|
UTSW |
5 |
25,528,787 (GRCm39) |
missense |
probably damaging |
0.99 |
R6628:Kmt2c
|
UTSW |
5 |
25,503,926 (GRCm39) |
missense |
probably benign |
|
R6733:Kmt2c
|
UTSW |
5 |
25,614,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R6787:Kmt2c
|
UTSW |
5 |
25,480,737 (GRCm39) |
splice site |
probably null |
|
R6816:Kmt2c
|
UTSW |
5 |
25,610,530 (GRCm39) |
splice site |
probably null |
|
R6862:Kmt2c
|
UTSW |
5 |
25,515,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7150:Kmt2c
|
UTSW |
5 |
25,505,360 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7220:Kmt2c
|
UTSW |
5 |
25,549,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,514,805 (GRCm39) |
missense |
probably benign |
0.00 |
R7250:Kmt2c
|
UTSW |
5 |
25,504,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Kmt2c
|
UTSW |
5 |
25,600,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7465:Kmt2c
|
UTSW |
5 |
25,507,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R7467:Kmt2c
|
UTSW |
5 |
25,513,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R7491:Kmt2c
|
UTSW |
5 |
25,489,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R7549:Kmt2c
|
UTSW |
5 |
25,619,968 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7637:Kmt2c
|
UTSW |
5 |
25,520,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R7652:Kmt2c
|
UTSW |
5 |
25,520,717 (GRCm39) |
missense |
probably benign |
0.01 |
R7714:Kmt2c
|
UTSW |
5 |
25,580,364 (GRCm39) |
missense |
probably benign |
|
R7838:Kmt2c
|
UTSW |
5 |
25,499,697 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7891:Kmt2c
|
UTSW |
5 |
25,505,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7892:Kmt2c
|
UTSW |
5 |
25,504,814 (GRCm39) |
missense |
probably benign |
0.18 |
R7895:Kmt2c
|
UTSW |
5 |
25,578,174 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7960:Kmt2c
|
UTSW |
5 |
25,520,194 (GRCm39) |
missense |
probably benign |
0.01 |
R7974:Kmt2c
|
UTSW |
5 |
25,505,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R7978:Kmt2c
|
UTSW |
5 |
25,564,676 (GRCm39) |
missense |
probably benign |
0.00 |
R8011:Kmt2c
|
UTSW |
5 |
25,556,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R8021:Kmt2c
|
UTSW |
5 |
25,492,117 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8022:Kmt2c
|
UTSW |
5 |
25,486,678 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8079:Kmt2c
|
UTSW |
5 |
25,507,730 (GRCm39) |
missense |
probably damaging |
0.98 |
R8087:Kmt2c
|
UTSW |
5 |
25,534,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8109:Kmt2c
|
UTSW |
5 |
25,486,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Kmt2c
|
UTSW |
5 |
25,579,562 (GRCm39) |
missense |
probably benign |
0.00 |
R8169:Kmt2c
|
UTSW |
5 |
25,559,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Kmt2c
|
UTSW |
5 |
25,519,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R8218:Kmt2c
|
UTSW |
5 |
25,488,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Kmt2c
|
UTSW |
5 |
25,529,216 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8260:Kmt2c
|
UTSW |
5 |
25,610,514 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8330:Kmt2c
|
UTSW |
5 |
25,509,692 (GRCm39) |
missense |
probably null |
1.00 |
R8355:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8455:Kmt2c
|
UTSW |
5 |
25,559,499 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8508:Kmt2c
|
UTSW |
5 |
25,519,120 (GRCm39) |
missense |
probably benign |
0.34 |
R8907:Kmt2c
|
UTSW |
5 |
25,514,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Kmt2c
|
UTSW |
5 |
25,503,885 (GRCm39) |
missense |
probably benign |
|
R8969:Kmt2c
|
UTSW |
5 |
25,519,387 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9019:Kmt2c
|
UTSW |
5 |
25,488,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Kmt2c
|
UTSW |
5 |
25,524,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Kmt2c
|
UTSW |
5 |
25,489,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Kmt2c
|
UTSW |
5 |
25,489,194 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9130:Kmt2c
|
UTSW |
5 |
25,516,102 (GRCm39) |
missense |
probably benign |
0.01 |
R9171:Kmt2c
|
UTSW |
5 |
25,486,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R9235:Kmt2c
|
UTSW |
5 |
25,504,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9288:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Kmt2c
|
UTSW |
5 |
25,614,165 (GRCm39) |
missense |
probably benign |
0.06 |
R9443:Kmt2c
|
UTSW |
5 |
25,515,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,497,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Kmt2c
|
UTSW |
5 |
25,554,860 (GRCm39) |
missense |
probably benign |
0.34 |
R9526:Kmt2c
|
UTSW |
5 |
25,486,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9653:Kmt2c
|
UTSW |
5 |
25,507,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Kmt2c
|
UTSW |
5 |
25,489,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9731:Kmt2c
|
UTSW |
5 |
25,577,956 (GRCm39) |
missense |
probably benign |
0.18 |
R9784:Kmt2c
|
UTSW |
5 |
25,549,959 (GRCm39) |
missense |
probably damaging |
1.00 |
RF001:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF006:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF011:Kmt2c
|
UTSW |
5 |
25,543,457 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Kmt2c
|
UTSW |
5 |
25,520,773 (GRCm39) |
small insertion |
probably benign |
|
RF047:Kmt2c
|
UTSW |
5 |
25,520,758 (GRCm39) |
small insertion |
probably benign |
|
RF051:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF055:Kmt2c
|
UTSW |
5 |
25,520,770 (GRCm39) |
small insertion |
probably benign |
|
RF059:Kmt2c
|
UTSW |
5 |
25,518,477 (GRCm39) |
unclassified |
probably benign |
|
RF063:Kmt2c
|
UTSW |
5 |
25,520,762 (GRCm39) |
small insertion |
probably benign |
|
X0024:Kmt2c
|
UTSW |
5 |
25,610,483 (GRCm39) |
missense |
probably benign |
0.26 |
X0027:Kmt2c
|
UTSW |
5 |
25,535,885 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Kmt2c
|
UTSW |
5 |
25,559,411 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,571,195 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Kmt2c
|
UTSW |
5 |
25,505,001 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Kmt2c
|
UTSW |
5 |
25,500,395 (GRCm39) |
critical splice donor site |
probably null |
|
|