Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009J06Rik |
T |
A |
6: 40,945,181 (GRCm39) |
V220D |
probably benign |
Het |
Ankrd1 |
T |
C |
19: 36,095,633 (GRCm39) |
E113G |
possibly damaging |
Het |
Aqp12 |
T |
C |
1: 92,939,718 (GRCm39) |
L249P |
probably damaging |
Het |
Atg4a-ps |
A |
G |
3: 103,553,296 (GRCm39) |
F15S |
possibly damaging |
Het |
Bub1 |
T |
A |
2: 127,671,447 (GRCm39) |
M46L |
probably benign |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
C2cd4d |
A |
G |
3: 94,270,800 (GRCm39) |
H22R |
probably benign |
Het |
Ccdc157 |
A |
G |
11: 4,094,586 (GRCm39) |
V480A |
probably benign |
Het |
Cdc42ep3 |
G |
A |
17: 79,642,952 (GRCm39) |
|
probably benign |
Het |
Cela1 |
T |
A |
15: 100,580,774 (GRCm39) |
T161S |
possibly damaging |
Het |
Chtf18 |
G |
T |
17: 25,940,100 (GRCm39) |
A697E |
possibly damaging |
Het |
Cr2 |
T |
C |
1: 194,833,918 (GRCm39) |
D957G |
possibly damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,796,063 (GRCm39) |
V60A |
probably damaging |
Het |
Dazl |
CCATGATGGCGGC |
CC |
17: 50,600,434 (GRCm39) |
|
probably null |
Het |
Dock2 |
A |
T |
11: 34,177,684 (GRCm39) |
L1824Q |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,586,044 (GRCm39) |
Y546C |
probably benign |
Het |
Focad |
G |
A |
4: 88,192,342 (GRCm39) |
C557Y |
unknown |
Het |
Ftmt |
T |
A |
18: 52,465,180 (GRCm39) |
N165K |
probably benign |
Het |
Gen1 |
A |
C |
12: 11,292,419 (GRCm39) |
S457A |
probably benign |
Het |
Gja1 |
T |
G |
10: 56,264,129 (GRCm39) |
S163A |
probably benign |
Het |
Gm8267 |
T |
C |
14: 44,959,481 (GRCm39) |
I194M |
probably damaging |
Het |
Golga3 |
T |
A |
5: 110,336,529 (GRCm39) |
S389R |
probably damaging |
Het |
Gpc5 |
C |
A |
14: 115,370,654 (GRCm39) |
Q87K |
possibly damaging |
Het |
Htt |
A |
G |
5: 34,979,067 (GRCm39) |
S817G |
probably null |
Het |
Hus1b |
C |
T |
13: 31,131,533 (GRCm39) |
C42Y |
possibly damaging |
Het |
Iars2 |
A |
G |
1: 185,021,564 (GRCm39) |
F913L |
probably benign |
Het |
Kcna4 |
A |
G |
2: 107,125,665 (GRCm39) |
E133G |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 120,603,536 (GRCm39) |
L597P |
probably benign |
Het |
Ltv1 |
T |
C |
10: 13,056,646 (GRCm39) |
E299G |
possibly damaging |
Het |
Mmp12 |
A |
G |
9: 7,357,840 (GRCm39) |
Y348C |
probably damaging |
Het |
Mmp12 |
G |
A |
9: 7,369,173 (GRCm39) |
V270I |
probably benign |
Het |
Mmp2 |
A |
G |
8: 93,558,333 (GRCm39) |
D134G |
probably damaging |
Het |
Mrpl15 |
A |
T |
1: 4,846,865 (GRCm39) |
M237K |
probably benign |
Het |
Ms4a6b |
G |
T |
19: 11,504,253 (GRCm39) |
V177F |
possibly damaging |
Het |
Muc16 |
A |
G |
9: 18,557,375 (GRCm39) |
S2973P |
unknown |
Het |
Or1e30 |
A |
C |
11: 73,677,974 (GRCm39) |
D70A |
possibly damaging |
Het |
Or4c114 |
A |
C |
2: 88,904,808 (GRCm39) |
I209S |
possibly damaging |
Het |
Or5b120 |
G |
T |
19: 13,480,243 (GRCm39) |
D179Y |
probably damaging |
Het |
Or5b12b |
A |
T |
19: 12,862,006 (GRCm39) |
I254F |
probably damaging |
Het |
Or8b48 |
A |
T |
9: 38,493,050 (GRCm39) |
H159L |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,286,364 (GRCm39) |
I1201K |
probably benign |
Het |
Plekhn1 |
T |
G |
4: 156,318,374 (GRCm39) |
M83L |
probably damaging |
Het |
Pnlip |
G |
T |
19: 58,664,695 (GRCm39) |
D212Y |
probably damaging |
Het |
Pomt2 |
T |
C |
12: 87,174,152 (GRCm39) |
N417S |
probably damaging |
Het |
Pxylp1 |
T |
A |
9: 96,707,103 (GRCm39) |
M360L |
probably benign |
Het |
Rbak |
G |
A |
5: 143,159,682 (GRCm39) |
T457I |
possibly damaging |
Het |
Runx2 |
A |
T |
17: 45,125,424 (GRCm39) |
W31R |
probably null |
Het |
Sec16a |
T |
A |
2: 26,315,277 (GRCm39) |
I1795F |
probably damaging |
Het |
Sik2 |
A |
T |
9: 50,909,861 (GRCm39) |
I64N |
probably damaging |
Het |
Slc26a8 |
T |
C |
17: 28,857,371 (GRCm39) |
E924G |
possibly damaging |
Het |
Slc30a2 |
G |
A |
4: 134,074,726 (GRCm39) |
R161Q |
probably damaging |
Het |
Slc45a4 |
C |
A |
15: 73,459,487 (GRCm39) |
D174Y |
probably damaging |
Het |
Slc6a6 |
A |
C |
6: 91,718,248 (GRCm39) |
E354A |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,956,524 (GRCm39) |
S171R |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,640,858 (GRCm39) |
I669M |
probably benign |
Het |
Stk39 |
C |
A |
2: 68,240,471 (GRCm39) |
A87S |
possibly damaging |
Het |
Tasor |
A |
T |
14: 27,183,608 (GRCm39) |
N689I |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,587,317 (GRCm39) |
S600I |
possibly damaging |
Het |
Tesc |
A |
C |
5: 118,193,025 (GRCm39) |
K114Q |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,554,915 (GRCm39) |
D256G |
probably damaging |
Het |
Tmem35b |
T |
A |
4: 127,021,679 (GRCm39) |
I45K |
probably benign |
Het |
Tnks |
T |
C |
8: 35,307,168 (GRCm39) |
D1127G |
probably damaging |
Het |
Trpm8 |
A |
T |
1: 88,289,802 (GRCm39) |
D920V |
probably null |
Het |
U2af1 |
A |
T |
17: 31,867,831 (GRCm39) |
D79E |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,535,977 (GRCm39) |
D331G |
probably damaging |
Het |
Znrf3 |
G |
T |
11: 5,232,442 (GRCm39) |
P261Q |
probably benign |
Het |
Zscan4b |
A |
T |
7: 10,635,636 (GRCm39) |
C202* |
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 |
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 |
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 |
|