Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
T |
A |
5: 81,935,296 (GRCm39) |
N1276K |
probably damaging |
Het |
Als2cl |
A |
G |
9: 110,713,128 (GRCm39) |
E6G |
probably damaging |
Het |
Ankrd12 |
A |
T |
17: 66,293,269 (GRCm39) |
D721E |
probably benign |
Het |
Anpep |
A |
G |
7: 79,488,155 (GRCm39) |
|
probably null |
Het |
Apob |
A |
T |
12: 8,040,839 (GRCm39) |
I655L |
possibly damaging |
Het |
Atp2b1 |
T |
A |
10: 98,832,810 (GRCm39) |
L437Q |
probably damaging |
Het |
Cacna2d3 |
T |
A |
14: 29,073,779 (GRCm39) |
R222S |
probably damaging |
Het |
Cenpf |
C |
T |
1: 189,384,910 (GRCm39) |
D2457N |
probably damaging |
Het |
Cenpo |
A |
T |
12: 4,265,433 (GRCm39) |
|
probably null |
Het |
Ces2b |
G |
T |
8: 105,562,521 (GRCm39) |
A284S |
probably benign |
Het |
Clock |
T |
C |
5: 76,390,679 (GRCm39) |
D311G |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,559,257 (GRCm39) |
|
probably null |
Het |
D430041D05Rik |
GTGATGATGATGATGATGATG |
GTGATGATGATGATGATG |
2: 104,051,553 (GRCm39) |
|
probably benign |
Het |
Dbil5 |
A |
G |
11: 76,109,308 (GRCm39) |
M71V |
probably benign |
Het |
Ddhd1 |
A |
C |
14: 45,833,004 (GRCm39) |
L864R |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,024,052 (GRCm39) |
C1900R |
probably damaging |
Het |
Dnah2 |
A |
G |
11: 69,405,514 (GRCm39) |
V666A |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,252,569 (GRCm39) |
M754K |
probably benign |
Het |
Dnajc15 |
A |
T |
14: 78,063,854 (GRCm39) |
S145T |
probably benign |
Het |
Drap1 |
A |
G |
19: 5,474,285 (GRCm39) |
F25S |
probably damaging |
Het |
Fam83e |
G |
A |
7: 45,376,135 (GRCm39) |
E283K |
probably damaging |
Het |
Fbxo48 |
G |
T |
11: 16,903,368 (GRCm39) |
|
probably benign |
Het |
Fndc3a |
A |
T |
14: 72,793,997 (GRCm39) |
I892N |
probably damaging |
Het |
Gcn1 |
A |
G |
5: 115,753,611 (GRCm39) |
T2321A |
probably benign |
Het |
Greb1l |
A |
G |
18: 10,554,997 (GRCm39) |
D1681G |
possibly damaging |
Het |
Iqcd |
A |
T |
5: 120,738,300 (GRCm39) |
K39N |
probably damaging |
Het |
Kank2 |
A |
G |
9: 21,685,871 (GRCm39) |
S668P |
probably damaging |
Het |
Kcng1 |
T |
A |
2: 168,110,961 (GRCm39) |
N68Y |
probably damaging |
Het |
Kmt5b |
T |
A |
19: 3,836,633 (GRCm39) |
|
probably null |
Het |
Lama2 |
T |
A |
10: 27,200,750 (GRCm39) |
I533F |
possibly damaging |
Het |
Lcmt1 |
T |
A |
7: 123,002,131 (GRCm39) |
I132N |
probably damaging |
Het |
Mcph1 |
T |
C |
8: 18,851,428 (GRCm39) |
I807T |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,722,315 (GRCm39) |
I2366V |
probably benign |
Het |
Moxd1 |
T |
C |
10: 24,176,217 (GRCm39) |
W558R |
probably damaging |
Het |
Mtus2 |
A |
C |
5: 148,013,362 (GRCm39) |
K52Q |
probably benign |
Het |
Myrf |
T |
C |
19: 10,202,851 (GRCm39) |
D141G |
probably damaging |
Het |
Naca |
G |
T |
10: 127,876,267 (GRCm39) |
|
probably benign |
Het |
Ncoa7 |
T |
C |
10: 30,570,097 (GRCm39) |
I249M |
probably damaging |
Het |
Obox5 |
T |
C |
7: 15,492,558 (GRCm39) |
V171A |
probably damaging |
Het |
Or13e8 |
A |
T |
4: 43,697,134 (GRCm39) |
V13D |
possibly damaging |
Het |
Or13p3 |
T |
A |
4: 118,566,751 (GRCm39) |
I49N |
probably damaging |
Het |
Or2c1 |
T |
C |
16: 3,657,521 (GRCm39) |
I228T |
probably damaging |
Het |
Or5ak20 |
A |
T |
2: 85,184,243 (GRCm39) |
V9E |
probably damaging |
Het |
Or6c219 |
A |
G |
10: 129,781,379 (GRCm39) |
L69P |
probably damaging |
Het |
Or7a36 |
C |
A |
10: 78,819,820 (GRCm39) |
N32K |
probably damaging |
Het |
Parp4 |
A |
G |
14: 56,839,752 (GRCm39) |
T487A |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,729,845 (GRCm39) |
|
probably benign |
Het |
Pcnx2 |
G |
A |
8: 126,500,669 (GRCm39) |
R1474C |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,341,445 (GRCm39) |
I99M |
unknown |
Het |
Ruvbl1 |
T |
C |
6: 88,456,136 (GRCm39) |
V70A |
probably damaging |
Het |
Sart1 |
G |
A |
19: 5,430,287 (GRCm39) |
P788L |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,984,634 (GRCm39) |
T740A |
probably benign |
Het |
Serpinb1c |
T |
C |
13: 33,072,979 (GRCm39) |
D61G |
possibly damaging |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Slc24a5 |
G |
A |
2: 124,922,782 (GRCm39) |
G152S |
probably damaging |
Het |
Slc6a4 |
A |
T |
11: 76,910,022 (GRCm39) |
I426F |
possibly damaging |
Het |
Srsf4 |
T |
A |
4: 131,625,006 (GRCm39) |
D134E |
probably damaging |
Het |
Stk33 |
C |
T |
7: 108,879,027 (GRCm39) |
V441I |
probably benign |
Het |
Sult1c2 |
A |
G |
17: 54,143,927 (GRCm39) |
|
probably null |
Het |
Tdpoz4 |
T |
A |
3: 93,703,835 (GRCm39) |
V44E |
probably benign |
Het |
Tdrd6 |
G |
A |
17: 43,936,515 (GRCm39) |
S1511L |
probably damaging |
Het |
Tmprss13 |
C |
A |
9: 45,254,529 (GRCm39) |
T432K |
probably damaging |
Het |
Traf7 |
A |
G |
17: 24,729,527 (GRCm39) |
L428P |
probably damaging |
Het |
Tubb1 |
T |
C |
2: 174,299,215 (GRCm39) |
I299T |
probably benign |
Het |
Vmn1r158 |
A |
T |
7: 22,489,772 (GRCm39) |
W146R |
probably damaging |
Het |
Vmn1r42 |
A |
G |
6: 89,822,059 (GRCm39) |
I170T |
possibly damaging |
Het |
Vmn1r42 |
C |
T |
6: 89,822,363 (GRCm39) |
G69S |
probably damaging |
Het |
Vmn2r116 |
A |
T |
17: 23,606,063 (GRCm39) |
H325L |
probably damaging |
Het |
Zfp516 |
T |
A |
18: 83,011,300 (GRCm39) |
L1111H |
possibly damaging |
Het |
Zfp61 |
C |
G |
7: 23,990,635 (GRCm39) |
K505N |
probably damaging |
Het |
Zfp653 |
C |
A |
9: 21,969,274 (GRCm39) |
E331* |
probably null |
Het |
Zfp949 |
A |
T |
9: 88,451,830 (GRCm39) |
K467* |
probably null |
Het |
|
Other mutations in Hmcn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Hmcn2
|
APN |
2 |
31,233,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00966:Hmcn2
|
APN |
2 |
31,319,006 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00973:Hmcn2
|
APN |
2 |
31,273,833 (GRCm39) |
intron |
probably benign |
|
IGL01364:Hmcn2
|
APN |
2 |
31,251,826 (GRCm39) |
nonsense |
probably null |
|
IGL01486:Hmcn2
|
APN |
2 |
31,226,633 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Hmcn2
|
APN |
2 |
31,244,276 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01550:Hmcn2
|
APN |
2 |
31,314,264 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01710:Hmcn2
|
APN |
2 |
31,233,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01764:Hmcn2
|
APN |
2 |
31,295,642 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01924:Hmcn2
|
APN |
2 |
31,288,929 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02003:Hmcn2
|
APN |
2 |
31,318,994 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02117:Hmcn2
|
APN |
2 |
31,347,185 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02205:Hmcn2
|
APN |
2 |
31,290,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02273:Hmcn2
|
APN |
2 |
31,314,389 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02313:Hmcn2
|
APN |
2 |
31,343,617 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02326:Hmcn2
|
APN |
2 |
31,340,964 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02486:Hmcn2
|
APN |
2 |
31,310,107 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02551:Hmcn2
|
APN |
2 |
31,344,823 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02695:Hmcn2
|
APN |
2 |
31,298,985 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02725:Hmcn2
|
APN |
2 |
31,295,540 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02792:Hmcn2
|
APN |
2 |
31,236,602 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02882:Hmcn2
|
APN |
2 |
31,303,379 (GRCm39) |
nonsense |
probably null |
|
IGL03003:Hmcn2
|
APN |
2 |
31,323,498 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03067:Hmcn2
|
APN |
2 |
31,236,642 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03137:Hmcn2
|
APN |
2 |
31,252,242 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03220:Hmcn2
|
APN |
2 |
31,236,633 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03411:Hmcn2
|
APN |
2 |
31,236,649 (GRCm39) |
missense |
possibly damaging |
0.83 |
PIT4544001:Hmcn2
|
UTSW |
2 |
31,318,262 (GRCm39) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,302,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,302,520 (GRCm39) |
missense |
probably damaging |
0.98 |
R0048:Hmcn2
|
UTSW |
2 |
31,318,249 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0048:Hmcn2
|
UTSW |
2 |
31,318,249 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0078:Hmcn2
|
UTSW |
2 |
31,278,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Hmcn2
|
UTSW |
2 |
31,316,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R0173:Hmcn2
|
UTSW |
2 |
31,328,343 (GRCm39) |
critical splice donor site |
probably null |
|
R0257:Hmcn2
|
UTSW |
2 |
31,259,176 (GRCm39) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,335,365 (GRCm39) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,284,839 (GRCm39) |
missense |
probably benign |
0.03 |
R0326:Hmcn2
|
UTSW |
2 |
31,313,237 (GRCm39) |
nonsense |
probably null |
|
R0366:Hmcn2
|
UTSW |
2 |
31,314,218 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0400:Hmcn2
|
UTSW |
2 |
31,290,141 (GRCm39) |
missense |
probably damaging |
0.98 |
R0412:Hmcn2
|
UTSW |
2 |
31,278,259 (GRCm39) |
missense |
probably damaging |
0.98 |
R0436:Hmcn2
|
UTSW |
2 |
31,295,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Hmcn2
|
UTSW |
2 |
31,305,296 (GRCm39) |
critical splice donor site |
probably null |
|
R0487:Hmcn2
|
UTSW |
2 |
31,276,689 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0568:Hmcn2
|
UTSW |
2 |
31,305,248 (GRCm39) |
missense |
probably benign |
0.02 |
R0755:Hmcn2
|
UTSW |
2 |
31,343,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R0811:Hmcn2
|
UTSW |
2 |
31,310,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R0812:Hmcn2
|
UTSW |
2 |
31,310,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R0964:Hmcn2
|
UTSW |
2 |
31,281,523 (GRCm39) |
missense |
probably benign |
0.23 |
R0988:Hmcn2
|
UTSW |
2 |
31,225,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Hmcn2
|
UTSW |
2 |
31,236,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Hmcn2
|
UTSW |
2 |
31,204,491 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1535:Hmcn2
|
UTSW |
2 |
31,310,419 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1574:Hmcn2
|
UTSW |
2 |
31,294,899 (GRCm39) |
missense |
probably damaging |
0.97 |
R1600:Hmcn2
|
UTSW |
2 |
31,320,799 (GRCm39) |
missense |
probably damaging |
0.98 |
R1623:Hmcn2
|
UTSW |
2 |
31,348,051 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1692:Hmcn2
|
UTSW |
2 |
31,340,856 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1719:Hmcn2
|
UTSW |
2 |
31,244,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1747:Hmcn2
|
UTSW |
2 |
31,347,997 (GRCm39) |
missense |
probably benign |
0.00 |
R1756:Hmcn2
|
UTSW |
2 |
31,286,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R1763:Hmcn2
|
UTSW |
2 |
31,204,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R1815:Hmcn2
|
UTSW |
2 |
31,283,055 (GRCm39) |
missense |
probably damaging |
0.97 |
R1822:Hmcn2
|
UTSW |
2 |
31,273,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R1858:Hmcn2
|
UTSW |
2 |
31,305,295 (GRCm39) |
critical splice donor site |
probably null |
|
R1895:Hmcn2
|
UTSW |
2 |
31,295,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R1908:Hmcn2
|
UTSW |
2 |
31,301,922 (GRCm39) |
critical splice donor site |
probably null |
|
R1946:Hmcn2
|
UTSW |
2 |
31,295,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R1966:Hmcn2
|
UTSW |
2 |
31,279,341 (GRCm39) |
missense |
probably damaging |
0.99 |
R2007:Hmcn2
|
UTSW |
2 |
31,328,267 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2050:Hmcn2
|
UTSW |
2 |
31,225,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Hmcn2
|
UTSW |
2 |
31,268,294 (GRCm39) |
missense |
probably benign |
0.33 |
R2097:Hmcn2
|
UTSW |
2 |
31,270,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Hmcn2
|
UTSW |
2 |
31,223,943 (GRCm39) |
splice site |
probably benign |
|
R2155:Hmcn2
|
UTSW |
2 |
31,350,361 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2170:Hmcn2
|
UTSW |
2 |
31,270,293 (GRCm39) |
missense |
probably benign |
0.08 |
R2188:Hmcn2
|
UTSW |
2 |
31,309,947 (GRCm39) |
missense |
probably benign |
0.14 |
R2208:Hmcn2
|
UTSW |
2 |
31,270,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R2217:Hmcn2
|
UTSW |
2 |
31,240,586 (GRCm39) |
missense |
probably benign |
0.02 |
R2407:Hmcn2
|
UTSW |
2 |
31,225,424 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2764:Hmcn2
|
UTSW |
2 |
31,278,310 (GRCm39) |
missense |
probably damaging |
0.98 |
R2913:Hmcn2
|
UTSW |
2 |
31,350,222 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2986:Hmcn2
|
UTSW |
2 |
31,251,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R3157:Hmcn2
|
UTSW |
2 |
31,290,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R3406:Hmcn2
|
UTSW |
2 |
31,323,284 (GRCm39) |
splice site |
probably benign |
|
R3429:Hmcn2
|
UTSW |
2 |
31,299,156 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3737:Hmcn2
|
UTSW |
2 |
31,226,624 (GRCm39) |
nonsense |
probably null |
|
R3739:Hmcn2
|
UTSW |
2 |
31,226,624 (GRCm39) |
nonsense |
probably null |
|
R3771:Hmcn2
|
UTSW |
2 |
31,250,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R3772:Hmcn2
|
UTSW |
2 |
31,250,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R3773:Hmcn2
|
UTSW |
2 |
31,250,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R3804:Hmcn2
|
UTSW |
2 |
31,242,897 (GRCm39) |
splice site |
probably null |
|
R3837:Hmcn2
|
UTSW |
2 |
31,303,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R3838:Hmcn2
|
UTSW |
2 |
31,303,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R3846:Hmcn2
|
UTSW |
2 |
31,320,362 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3925:Hmcn2
|
UTSW |
2 |
31,343,169 (GRCm39) |
missense |
probably benign |
0.00 |
R3934:Hmcn2
|
UTSW |
2 |
31,270,496 (GRCm39) |
critical splice donor site |
probably null |
|
R3946:Hmcn2
|
UTSW |
2 |
31,272,406 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4035:Hmcn2
|
UTSW |
2 |
31,226,624 (GRCm39) |
nonsense |
probably null |
|
R4057:Hmcn2
|
UTSW |
2 |
31,290,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4583:Hmcn2
|
UTSW |
2 |
31,303,277 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4623:Hmcn2
|
UTSW |
2 |
31,286,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Hmcn2
|
UTSW |
2 |
31,289,031 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4668:Hmcn2
|
UTSW |
2 |
31,325,804 (GRCm39) |
missense |
probably benign |
0.40 |
R4669:Hmcn2
|
UTSW |
2 |
31,325,804 (GRCm39) |
missense |
probably benign |
0.40 |
R4687:Hmcn2
|
UTSW |
2 |
31,328,297 (GRCm39) |
missense |
probably benign |
0.14 |
R4735:Hmcn2
|
UTSW |
2 |
31,273,787 (GRCm39) |
missense |
probably benign |
0.06 |
R4772:Hmcn2
|
UTSW |
2 |
31,335,326 (GRCm39) |
missense |
probably benign |
0.02 |
R4866:Hmcn2
|
UTSW |
2 |
31,279,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4916:Hmcn2
|
UTSW |
2 |
31,250,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R4943:Hmcn2
|
UTSW |
2 |
31,225,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Hmcn2
|
UTSW |
2 |
31,244,176 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4973:Hmcn2
|
UTSW |
2 |
31,234,108 (GRCm39) |
missense |
probably benign |
0.15 |
R4975:Hmcn2
|
UTSW |
2 |
31,283,037 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4994:Hmcn2
|
UTSW |
2 |
31,348,067 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Hmcn2
|
UTSW |
2 |
31,291,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Hmcn2
|
UTSW |
2 |
31,299,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5117:Hmcn2
|
UTSW |
2 |
31,348,061 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5151:Hmcn2
|
UTSW |
2 |
31,279,455 (GRCm39) |
missense |
probably null |
|
R5232:Hmcn2
|
UTSW |
2 |
31,347,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R5237:Hmcn2
|
UTSW |
2 |
31,304,728 (GRCm39) |
missense |
probably benign |
0.01 |
R5288:Hmcn2
|
UTSW |
2 |
31,350,333 (GRCm39) |
missense |
probably benign |
0.11 |
R5375:Hmcn2
|
UTSW |
2 |
31,320,453 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5379:Hmcn2
|
UTSW |
2 |
31,299,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R5385:Hmcn2
|
UTSW |
2 |
31,350,333 (GRCm39) |
missense |
probably benign |
0.11 |
R5412:Hmcn2
|
UTSW |
2 |
31,236,629 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5426:Hmcn2
|
UTSW |
2 |
31,226,556 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5434:Hmcn2
|
UTSW |
2 |
31,310,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Hmcn2
|
UTSW |
2 |
31,296,428 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5484:Hmcn2
|
UTSW |
2 |
31,283,066 (GRCm39) |
nonsense |
probably null |
|
R5492:Hmcn2
|
UTSW |
2 |
31,310,318 (GRCm39) |
missense |
probably benign |
0.03 |
R5572:Hmcn2
|
UTSW |
2 |
31,304,538 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5572:Hmcn2
|
UTSW |
2 |
31,304,537 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5591:Hmcn2
|
UTSW |
2 |
31,234,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5614:Hmcn2
|
UTSW |
2 |
31,318,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R5634:Hmcn2
|
UTSW |
2 |
31,223,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Hmcn2
|
UTSW |
2 |
31,310,824 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5716:Hmcn2
|
UTSW |
2 |
31,348,750 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5716:Hmcn2
|
UTSW |
2 |
31,226,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Hmcn2
|
UTSW |
2 |
31,273,827 (GRCm39) |
critical splice donor site |
probably null |
|
R5760:Hmcn2
|
UTSW |
2 |
31,304,580 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5774:Hmcn2
|
UTSW |
2 |
31,299,147 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5838:Hmcn2
|
UTSW |
2 |
31,347,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R5899:Hmcn2
|
UTSW |
2 |
31,244,685 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5916:Hmcn2
|
UTSW |
2 |
31,286,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Hmcn2
|
UTSW |
2 |
31,310,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R6002:Hmcn2
|
UTSW |
2 |
31,310,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R6018:Hmcn2
|
UTSW |
2 |
31,260,804 (GRCm39) |
missense |
probably benign |
0.13 |
R6063:Hmcn2
|
UTSW |
2 |
31,324,725 (GRCm39) |
missense |
probably benign |
0.06 |
R6161:Hmcn2
|
UTSW |
2 |
31,246,266 (GRCm39) |
missense |
probably benign |
|
R6166:Hmcn2
|
UTSW |
2 |
31,259,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Hmcn2
|
UTSW |
2 |
31,310,118 (GRCm39) |
nonsense |
probably null |
|
R6191:Hmcn2
|
UTSW |
2 |
31,348,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R6195:Hmcn2
|
UTSW |
2 |
31,274,127 (GRCm39) |
missense |
probably damaging |
0.96 |
R6273:Hmcn2
|
UTSW |
2 |
31,301,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R6293:Hmcn2
|
UTSW |
2 |
31,225,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Hmcn2
|
UTSW |
2 |
31,278,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Hmcn2
|
UTSW |
2 |
31,259,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Hmcn2
|
UTSW |
2 |
31,310,832 (GRCm39) |
missense |
probably benign |
0.02 |
R6450:Hmcn2
|
UTSW |
2 |
31,251,812 (GRCm39) |
missense |
probably benign |
0.11 |
R6479:Hmcn2
|
UTSW |
2 |
31,315,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R6502:Hmcn2
|
UTSW |
2 |
31,272,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6511:Hmcn2
|
UTSW |
2 |
31,246,354 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6537:Hmcn2
|
UTSW |
2 |
31,305,280 (GRCm39) |
missense |
probably benign |
0.00 |
R6880:Hmcn2
|
UTSW |
2 |
31,233,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Hmcn2
|
UTSW |
2 |
31,240,517 (GRCm39) |
splice site |
probably null |
|
R6971:Hmcn2
|
UTSW |
2 |
31,322,333 (GRCm39) |
missense |
probably benign |
0.02 |
R7057:Hmcn2
|
UTSW |
2 |
31,312,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R7141:Hmcn2
|
UTSW |
2 |
31,250,908 (GRCm39) |
missense |
probably benign |
0.17 |
R7268:Hmcn2
|
UTSW |
2 |
31,347,978 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7307:Hmcn2
|
UTSW |
2 |
31,233,093 (GRCm39) |
missense |
probably damaging |
0.96 |
R7322:Hmcn2
|
UTSW |
2 |
31,349,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R7334:Hmcn2
|
UTSW |
2 |
31,343,147 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7334:Hmcn2
|
UTSW |
2 |
31,325,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R7335:Hmcn2
|
UTSW |
2 |
31,282,169 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7358:Hmcn2
|
UTSW |
2 |
31,306,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Hmcn2
|
UTSW |
2 |
31,278,395 (GRCm39) |
missense |
probably benign |
0.13 |
R7488:Hmcn2
|
UTSW |
2 |
31,310,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Hmcn2
|
UTSW |
2 |
31,273,487 (GRCm39) |
splice site |
probably null |
|
R7560:Hmcn2
|
UTSW |
2 |
31,347,185 (GRCm39) |
missense |
probably benign |
|
R7566:Hmcn2
|
UTSW |
2 |
31,344,869 (GRCm39) |
missense |
probably damaging |
0.96 |
R7570:Hmcn2
|
UTSW |
2 |
31,313,923 (GRCm39) |
missense |
probably benign |
|
R7574:Hmcn2
|
UTSW |
2 |
31,345,531 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7599:Hmcn2
|
UTSW |
2 |
31,246,298 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7654:Hmcn2
|
UTSW |
2 |
31,236,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7662:Hmcn2
|
UTSW |
2 |
31,272,357 (GRCm39) |
missense |
probably benign |
0.01 |
R7666:Hmcn2
|
UTSW |
2 |
31,270,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Hmcn2
|
UTSW |
2 |
31,313,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R7722:Hmcn2
|
UTSW |
2 |
31,272,512 (GRCm39) |
nonsense |
probably null |
|
R7739:Hmcn2
|
UTSW |
2 |
31,348,038 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7749:Hmcn2
|
UTSW |
2 |
31,343,045 (GRCm39) |
splice site |
probably null |
|
R7828:Hmcn2
|
UTSW |
2 |
31,295,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7912:Hmcn2
|
UTSW |
2 |
31,310,311 (GRCm39) |
missense |
probably benign |
0.00 |
R7978:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R8075:Hmcn2
|
UTSW |
2 |
31,279,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8088:Hmcn2
|
UTSW |
2 |
31,316,915 (GRCm39) |
nonsense |
probably null |
|
R8101:Hmcn2
|
UTSW |
2 |
31,240,082 (GRCm39) |
missense |
probably benign |
0.08 |
R8124:Hmcn2
|
UTSW |
2 |
31,290,136 (GRCm39) |
missense |
probably benign |
0.01 |
R8145:Hmcn2
|
UTSW |
2 |
31,313,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8230:Hmcn2
|
UTSW |
2 |
31,234,485 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8267:Hmcn2
|
UTSW |
2 |
31,349,191 (GRCm39) |
missense |
probably benign |
|
R8277:Hmcn2
|
UTSW |
2 |
31,259,189 (GRCm39) |
missense |
probably benign |
0.16 |
R8307:Hmcn2
|
UTSW |
2 |
31,286,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R8353:Hmcn2
|
UTSW |
2 |
31,275,353 (GRCm39) |
splice site |
probably null |
|
R8415:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8416:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8437:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8438:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8440:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8442:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8497:Hmcn2
|
UTSW |
2 |
31,313,357 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8520:Hmcn2
|
UTSW |
2 |
31,244,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8530:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8537:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8550:Hmcn2
|
UTSW |
2 |
31,240,654 (GRCm39) |
critical splice donor site |
probably null |
|
R8721:Hmcn2
|
UTSW |
2 |
31,315,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8802:Hmcn2
|
UTSW |
2 |
31,301,288 (GRCm39) |
missense |
probably damaging |
0.97 |
R8804:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8805:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8904:Hmcn2
|
UTSW |
2 |
31,323,404 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8937:Hmcn2
|
UTSW |
2 |
31,204,427 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R8947:Hmcn2
|
UTSW |
2 |
31,278,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R8948:Hmcn2
|
UTSW |
2 |
31,244,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Hmcn2
|
UTSW |
2 |
31,244,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8959:Hmcn2
|
UTSW |
2 |
31,282,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R9025:Hmcn2
|
UTSW |
2 |
31,347,967 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9039:Hmcn2
|
UTSW |
2 |
31,244,646 (GRCm39) |
missense |
probably damaging |
0.97 |
R9068:Hmcn2
|
UTSW |
2 |
31,303,685 (GRCm39) |
missense |
probably benign |
0.01 |
R9161:Hmcn2
|
UTSW |
2 |
31,242,758 (GRCm39) |
missense |
probably benign |
0.02 |
R9178:Hmcn2
|
UTSW |
2 |
31,281,521 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9204:Hmcn2
|
UTSW |
2 |
31,278,377 (GRCm39) |
missense |
probably damaging |
0.98 |
R9317:Hmcn2
|
UTSW |
2 |
31,350,328 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9341:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R9343:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R9355:Hmcn2
|
UTSW |
2 |
31,328,302 (GRCm39) |
missense |
probably benign |
0.18 |
R9371:Hmcn2
|
UTSW |
2 |
31,301,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Hmcn2
|
UTSW |
2 |
31,316,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Hmcn2
|
UTSW |
2 |
31,286,031 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9483:Hmcn2
|
UTSW |
2 |
31,320,375 (GRCm39) |
missense |
|
|
R9536:Hmcn2
|
UTSW |
2 |
31,335,130 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9580:Hmcn2
|
UTSW |
2 |
31,294,875 (GRCm39) |
missense |
probably benign |
0.16 |
R9593:Hmcn2
|
UTSW |
2 |
31,244,742 (GRCm39) |
missense |
probably damaging |
0.99 |
R9649:Hmcn2
|
UTSW |
2 |
31,292,450 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9706:Hmcn2
|
UTSW |
2 |
31,305,279 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Hmcn2
|
UTSW |
2 |
31,344,823 (GRCm39) |
missense |
possibly damaging |
0.83 |
X0067:Hmcn2
|
UTSW |
2 |
31,295,879 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1088:Hmcn2
|
UTSW |
2 |
31,349,076 (GRCm39) |
splice site |
probably null |
|
Z1088:Hmcn2
|
UTSW |
2 |
31,271,079 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Hmcn2
|
UTSW |
2 |
31,319,103 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Hmcn2
|
UTSW |
2 |
31,315,428 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Hmcn2
|
UTSW |
2 |
31,234,041 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Hmcn2
|
UTSW |
2 |
31,316,836 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Hmcn2
|
UTSW |
2 |
31,234,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|