Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009J06Rik |
T |
A |
6: 40,968,247 (GRCm38) |
V220D |
probably benign |
Het |
Ankrd1 |
T |
C |
19: 36,118,233 (GRCm38) |
E113G |
possibly damaging |
Het |
Aqp12 |
T |
C |
1: 93,011,996 (GRCm38) |
L249P |
probably damaging |
Het |
Atg4a-ps |
A |
G |
3: 103,645,980 (GRCm38) |
F15S |
possibly damaging |
Het |
Bub1 |
T |
A |
2: 127,829,527 (GRCm38) |
M46L |
probably benign |
Het |
C1ra |
G |
A |
6: 124,517,725 (GRCm38) |
E316K |
probably benign |
Het |
C2cd4d |
A |
G |
3: 94,363,493 (GRCm38) |
H22R |
probably benign |
Het |
Ccdc157 |
A |
G |
11: 4,144,586 (GRCm38) |
V480A |
probably benign |
Het |
Cdc42ep3 |
G |
A |
17: 79,335,523 (GRCm38) |
|
probably benign |
Het |
Cela1 |
T |
A |
15: 100,682,893 (GRCm38) |
T161S |
possibly damaging |
Het |
Chtf18 |
G |
T |
17: 25,721,126 (GRCm38) |
A697E |
possibly damaging |
Het |
Cr2 |
T |
C |
1: 195,151,610 (GRCm38) |
D957G |
possibly damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,807,619 (GRCm38) |
V60A |
probably damaging |
Het |
Dazl |
CCATGATGGCGGC |
CC |
17: 50,293,406 (GRCm38) |
|
probably null |
Het |
Dock2 |
T |
C |
11: 34,695,217 (GRCm38) |
Y546C |
probably benign |
Het |
Dock2 |
A |
T |
11: 34,227,684 (GRCm38) |
L1824Q |
probably benign |
Het |
Fam208a |
A |
T |
14: 27,461,651 (GRCm38) |
N689I |
probably damaging |
Het |
Focad |
G |
A |
4: 88,274,105 (GRCm38) |
C557Y |
unknown |
Het |
Ftmt |
T |
A |
18: 52,332,108 (GRCm38) |
N165K |
probably benign |
Het |
Gen1 |
A |
C |
12: 11,242,418 (GRCm38) |
S457A |
probably benign |
Het |
Gja1 |
T |
G |
10: 56,388,033 (GRCm38) |
S163A |
probably benign |
Het |
Gm8267 |
T |
C |
14: 44,722,024 (GRCm38) |
I194M |
probably damaging |
Het |
Golga3 |
T |
A |
5: 110,188,663 (GRCm38) |
S389R |
probably damaging |
Het |
Gpc5 |
C |
A |
14: 115,133,242 (GRCm38) |
Q87K |
possibly damaging |
Het |
Htt |
A |
G |
5: 34,821,723 (GRCm38) |
S817G |
probably null |
Het |
Hus1b |
C |
T |
13: 30,947,550 (GRCm38) |
C42Y |
possibly damaging |
Het |
Iars2 |
A |
G |
1: 185,289,367 (GRCm38) |
F913L |
probably benign |
Het |
Kcna4 |
A |
G |
2: 107,295,320 (GRCm38) |
E133G |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 119,876,797 (GRCm38) |
L597P |
probably benign |
Het |
Ltv1 |
T |
C |
10: 13,180,902 (GRCm38) |
E299G |
possibly damaging |
Het |
Mmp12 |
A |
G |
9: 7,357,840 (GRCm38) |
Y348C |
probably damaging |
Het |
Mmp12 |
G |
A |
9: 7,369,173 (GRCm38) |
V270I |
probably benign |
Het |
Mmp2 |
A |
G |
8: 92,831,705 (GRCm38) |
D134G |
probably damaging |
Het |
Mrpl15 |
A |
T |
1: 4,776,642 (GRCm38) |
M237K |
probably benign |
Het |
Ms4a6b |
G |
T |
19: 11,526,889 (GRCm38) |
V177F |
possibly damaging |
Het |
Muc16 |
A |
G |
9: 18,646,079 (GRCm38) |
S2973P |
unknown |
Het |
Olfr1219 |
A |
C |
2: 89,074,464 (GRCm38) |
I209S |
possibly damaging |
Het |
Olfr1445 |
A |
T |
19: 12,884,642 (GRCm38) |
I254F |
probably damaging |
Het |
Olfr1477 |
G |
T |
19: 13,502,879 (GRCm38) |
D179Y |
probably damaging |
Het |
Olfr390 |
A |
C |
11: 73,787,148 (GRCm38) |
D70A |
possibly damaging |
Het |
Olfr912 |
A |
T |
9: 38,581,754 (GRCm38) |
H159L |
probably damaging |
Het |
Pikfyve |
T |
A |
1: 65,247,205 (GRCm38) |
I1201K |
probably benign |
Het |
Plekhn1 |
T |
G |
4: 156,233,917 (GRCm38) |
M83L |
probably damaging |
Het |
Pnlip |
G |
T |
19: 58,676,263 (GRCm38) |
D212Y |
probably damaging |
Het |
Pomt2 |
T |
C |
12: 87,127,378 (GRCm38) |
N417S |
probably damaging |
Het |
Pxylp1 |
T |
A |
9: 96,825,050 (GRCm38) |
M360L |
probably benign |
Het |
Rbak |
G |
A |
5: 143,173,927 (GRCm38) |
T457I |
possibly damaging |
Het |
Runx2 |
A |
T |
17: 44,814,537 (GRCm38) |
W31R |
probably null |
Het |
Sec16a |
T |
A |
2: 26,425,265 (GRCm38) |
I1795F |
probably damaging |
Het |
Sik2 |
A |
T |
9: 50,998,561 (GRCm38) |
I64N |
probably damaging |
Het |
Slc26a8 |
T |
C |
17: 28,638,397 (GRCm38) |
E924G |
possibly damaging |
Het |
Slc30a2 |
G |
A |
4: 134,347,415 (GRCm38) |
R161Q |
probably damaging |
Het |
Slc45a4 |
C |
A |
15: 73,587,638 (GRCm38) |
D174Y |
probably damaging |
Het |
Slc6a6 |
A |
C |
6: 91,741,267 (GRCm38) |
E354A |
probably damaging |
Het |
Slc8a1 |
A |
T |
17: 81,649,095 (GRCm38) |
S171R |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,804,953 (GRCm38) |
I669M |
probably benign |
Het |
Stk39 |
C |
A |
2: 68,410,127 (GRCm38) |
A87S |
possibly damaging |
Het |
Tbx18 |
C |
A |
9: 87,705,264 (GRCm38) |
S600I |
possibly damaging |
Het |
Tesc |
A |
C |
5: 118,054,960 (GRCm38) |
K114Q |
probably damaging |
Het |
Tll1 |
T |
C |
8: 64,101,881 (GRCm38) |
D256G |
probably damaging |
Het |
Tmem35b |
T |
A |
4: 127,127,886 (GRCm38) |
I45K |
probably benign |
Het |
Tnks |
T |
C |
8: 34,840,014 (GRCm38) |
D1127G |
probably damaging |
Het |
Trpm8 |
A |
T |
1: 88,362,080 (GRCm38) |
D920V |
probably null |
Het |
U2af1 |
A |
T |
17: 31,648,857 (GRCm38) |
D79E |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,470,917 (GRCm38) |
D331G |
probably damaging |
Het |
Znrf3 |
G |
T |
11: 5,282,442 (GRCm38) |
P261Q |
probably benign |
Het |
Zscan4b |
A |
T |
7: 10,901,709 (GRCm38) |
C202* |
probably null |
Het |
|
Other mutations in Hmcn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Hmcn2
|
APN |
2 |
31,343,096 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00966:Hmcn2
|
APN |
2 |
31,428,994 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL00973:Hmcn2
|
APN |
2 |
31,383,821 (GRCm38) |
intron |
probably benign |
|
IGL01364:Hmcn2
|
APN |
2 |
31,361,814 (GRCm38) |
nonsense |
probably null |
|
IGL01486:Hmcn2
|
APN |
2 |
31,336,621 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01530:Hmcn2
|
APN |
2 |
31,354,264 (GRCm38) |
missense |
possibly damaging |
0.85 |
IGL01550:Hmcn2
|
APN |
2 |
31,424,252 (GRCm38) |
missense |
possibly damaging |
0.84 |
IGL01710:Hmcn2
|
APN |
2 |
31,343,102 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01764:Hmcn2
|
APN |
2 |
31,405,630 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL01924:Hmcn2
|
APN |
2 |
31,398,917 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02003:Hmcn2
|
APN |
2 |
31,428,982 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02117:Hmcn2
|
APN |
2 |
31,457,173 (GRCm38) |
missense |
possibly damaging |
0.75 |
IGL02205:Hmcn2
|
APN |
2 |
31,400,127 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02273:Hmcn2
|
APN |
2 |
31,424,377 (GRCm38) |
missense |
probably benign |
0.06 |
IGL02313:Hmcn2
|
APN |
2 |
31,453,605 (GRCm38) |
missense |
possibly damaging |
0.68 |
IGL02326:Hmcn2
|
APN |
2 |
31,450,952 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02486:Hmcn2
|
APN |
2 |
31,420,095 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02551:Hmcn2
|
APN |
2 |
31,454,811 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL02695:Hmcn2
|
APN |
2 |
31,408,973 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL02725:Hmcn2
|
APN |
2 |
31,405,528 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02792:Hmcn2
|
APN |
2 |
31,346,590 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02882:Hmcn2
|
APN |
2 |
31,413,367 (GRCm38) |
nonsense |
probably null |
|
IGL03003:Hmcn2
|
APN |
2 |
31,433,486 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03067:Hmcn2
|
APN |
2 |
31,346,630 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03137:Hmcn2
|
APN |
2 |
31,362,230 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03220:Hmcn2
|
APN |
2 |
31,346,621 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL03411:Hmcn2
|
APN |
2 |
31,346,637 (GRCm38) |
missense |
possibly damaging |
0.83 |
PIT4544001:Hmcn2
|
UTSW |
2 |
31,428,250 (GRCm38) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,412,508 (GRCm38) |
missense |
probably damaging |
0.98 |
R0044:Hmcn2
|
UTSW |
2 |
31,412,508 (GRCm38) |
missense |
probably damaging |
0.98 |
R0048:Hmcn2
|
UTSW |
2 |
31,428,237 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0048:Hmcn2
|
UTSW |
2 |
31,428,237 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0078:Hmcn2
|
UTSW |
2 |
31,388,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R0090:Hmcn2
|
UTSW |
2 |
31,426,198 (GRCm38) |
missense |
probably damaging |
1.00 |
R0173:Hmcn2
|
UTSW |
2 |
31,438,331 (GRCm38) |
critical splice donor site |
probably null |
|
R0257:Hmcn2
|
UTSW |
2 |
31,369,164 (GRCm38) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,445,353 (GRCm38) |
splice site |
probably benign |
|
R0266:Hmcn2
|
UTSW |
2 |
31,394,827 (GRCm38) |
missense |
probably benign |
0.03 |
R0326:Hmcn2
|
UTSW |
2 |
31,423,225 (GRCm38) |
nonsense |
probably null |
|
R0366:Hmcn2
|
UTSW |
2 |
31,424,206 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0400:Hmcn2
|
UTSW |
2 |
31,400,129 (GRCm38) |
missense |
probably damaging |
0.98 |
R0412:Hmcn2
|
UTSW |
2 |
31,388,247 (GRCm38) |
missense |
probably damaging |
0.98 |
R0436:Hmcn2
|
UTSW |
2 |
31,405,612 (GRCm38) |
missense |
probably damaging |
1.00 |
R0457:Hmcn2
|
UTSW |
2 |
31,415,284 (GRCm38) |
critical splice donor site |
probably null |
|
R0487:Hmcn2
|
UTSW |
2 |
31,386,677 (GRCm38) |
missense |
possibly damaging |
0.60 |
R0568:Hmcn2
|
UTSW |
2 |
31,415,236 (GRCm38) |
missense |
probably benign |
0.02 |
R0755:Hmcn2
|
UTSW |
2 |
31,453,160 (GRCm38) |
missense |
probably damaging |
0.99 |
R0811:Hmcn2
|
UTSW |
2 |
31,420,371 (GRCm38) |
missense |
probably damaging |
0.99 |
R0812:Hmcn2
|
UTSW |
2 |
31,420,371 (GRCm38) |
missense |
probably damaging |
0.99 |
R0964:Hmcn2
|
UTSW |
2 |
31,391,511 (GRCm38) |
missense |
probably benign |
0.23 |
R0988:Hmcn2
|
UTSW |
2 |
31,335,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R1484:Hmcn2
|
UTSW |
2 |
31,346,495 (GRCm38) |
missense |
probably damaging |
1.00 |
R1509:Hmcn2
|
UTSW |
2 |
31,314,479 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1535:Hmcn2
|
UTSW |
2 |
31,420,407 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1574:Hmcn2
|
UTSW |
2 |
31,404,887 (GRCm38) |
missense |
probably damaging |
0.97 |
R1574:Hmcn2
|
UTSW |
2 |
31,404,887 (GRCm38) |
missense |
probably damaging |
0.97 |
R1600:Hmcn2
|
UTSW |
2 |
31,430,787 (GRCm38) |
missense |
probably damaging |
0.98 |
R1623:Hmcn2
|
UTSW |
2 |
31,458,039 (GRCm38) |
missense |
possibly damaging |
0.84 |
R1692:Hmcn2
|
UTSW |
2 |
31,450,844 (GRCm38) |
missense |
possibly damaging |
0.47 |
R1719:Hmcn2
|
UTSW |
2 |
31,354,721 (GRCm38) |
missense |
probably damaging |
1.00 |
R1747:Hmcn2
|
UTSW |
2 |
31,457,985 (GRCm38) |
missense |
probably benign |
0.00 |
R1756:Hmcn2
|
UTSW |
2 |
31,396,120 (GRCm38) |
missense |
probably damaging |
0.99 |
R1763:Hmcn2
|
UTSW |
2 |
31,314,590 (GRCm38) |
missense |
probably damaging |
1.00 |
R1815:Hmcn2
|
UTSW |
2 |
31,393,043 (GRCm38) |
missense |
probably damaging |
0.97 |
R1822:Hmcn2
|
UTSW |
2 |
31,383,692 (GRCm38) |
missense |
probably damaging |
0.99 |
R1858:Hmcn2
|
UTSW |
2 |
31,415,283 (GRCm38) |
critical splice donor site |
probably null |
|
R1895:Hmcn2
|
UTSW |
2 |
31,405,635 (GRCm38) |
missense |
probably damaging |
0.99 |
R1908:Hmcn2
|
UTSW |
2 |
31,411,910 (GRCm38) |
critical splice donor site |
probably null |
|
R1946:Hmcn2
|
UTSW |
2 |
31,405,635 (GRCm38) |
missense |
probably damaging |
0.99 |
R1966:Hmcn2
|
UTSW |
2 |
31,389,329 (GRCm38) |
missense |
probably damaging |
0.99 |
R2007:Hmcn2
|
UTSW |
2 |
31,438,255 (GRCm38) |
missense |
possibly damaging |
0.91 |
R2050:Hmcn2
|
UTSW |
2 |
31,335,436 (GRCm38) |
missense |
probably damaging |
1.00 |
R2055:Hmcn2
|
UTSW |
2 |
31,378,282 (GRCm38) |
missense |
probably benign |
0.33 |
R2097:Hmcn2
|
UTSW |
2 |
31,380,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R2145:Hmcn2
|
UTSW |
2 |
31,333,931 (GRCm38) |
splice site |
probably benign |
|
R2155:Hmcn2
|
UTSW |
2 |
31,460,349 (GRCm38) |
missense |
possibly damaging |
0.68 |
R2170:Hmcn2
|
UTSW |
2 |
31,380,281 (GRCm38) |
missense |
probably benign |
0.08 |
R2188:Hmcn2
|
UTSW |
2 |
31,419,935 (GRCm38) |
missense |
probably benign |
0.14 |
R2208:Hmcn2
|
UTSW |
2 |
31,380,297 (GRCm38) |
missense |
probably damaging |
1.00 |
R2217:Hmcn2
|
UTSW |
2 |
31,350,574 (GRCm38) |
missense |
probably benign |
0.02 |
R2407:Hmcn2
|
UTSW |
2 |
31,335,412 (GRCm38) |
critical splice acceptor site |
probably null |
|
R2764:Hmcn2
|
UTSW |
2 |
31,388,298 (GRCm38) |
missense |
probably damaging |
0.98 |
R2913:Hmcn2
|
UTSW |
2 |
31,460,210 (GRCm38) |
missense |
possibly damaging |
0.68 |
R2986:Hmcn2
|
UTSW |
2 |
31,360,998 (GRCm38) |
missense |
probably damaging |
1.00 |
R3157:Hmcn2
|
UTSW |
2 |
31,400,255 (GRCm38) |
missense |
probably damaging |
0.99 |
R3406:Hmcn2
|
UTSW |
2 |
31,433,272 (GRCm38) |
splice site |
probably benign |
|
R3429:Hmcn2
|
UTSW |
2 |
31,409,144 (GRCm38) |
missense |
possibly damaging |
0.87 |
R3737:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R3739:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R3771:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3772:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3773:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably damaging |
0.99 |
R3804:Hmcn2
|
UTSW |
2 |
31,352,885 (GRCm38) |
splice site |
probably null |
|
R3837:Hmcn2
|
UTSW |
2 |
31,413,407 (GRCm38) |
missense |
probably damaging |
0.99 |
R3838:Hmcn2
|
UTSW |
2 |
31,413,407 (GRCm38) |
missense |
probably damaging |
0.99 |
R3846:Hmcn2
|
UTSW |
2 |
31,430,350 (GRCm38) |
missense |
possibly damaging |
0.51 |
R3925:Hmcn2
|
UTSW |
2 |
31,453,157 (GRCm38) |
missense |
probably benign |
0.00 |
R3934:Hmcn2
|
UTSW |
2 |
31,380,484 (GRCm38) |
critical splice donor site |
probably null |
|
R3946:Hmcn2
|
UTSW |
2 |
31,382,394 (GRCm38) |
missense |
possibly damaging |
0.91 |
R4035:Hmcn2
|
UTSW |
2 |
31,336,612 (GRCm38) |
nonsense |
probably null |
|
R4057:Hmcn2
|
UTSW |
2 |
31,400,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R4583:Hmcn2
|
UTSW |
2 |
31,413,265 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4623:Hmcn2
|
UTSW |
2 |
31,396,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R4647:Hmcn2
|
UTSW |
2 |
31,399,019 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4668:Hmcn2
|
UTSW |
2 |
31,435,792 (GRCm38) |
missense |
probably benign |
0.40 |
R4669:Hmcn2
|
UTSW |
2 |
31,435,792 (GRCm38) |
missense |
probably benign |
0.40 |
R4687:Hmcn2
|
UTSW |
2 |
31,438,285 (GRCm38) |
missense |
probably benign |
0.14 |
R4735:Hmcn2
|
UTSW |
2 |
31,383,775 (GRCm38) |
missense |
probably benign |
0.06 |
R4772:Hmcn2
|
UTSW |
2 |
31,445,314 (GRCm38) |
missense |
probably benign |
0.02 |
R4866:Hmcn2
|
UTSW |
2 |
31,389,391 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4916:Hmcn2
|
UTSW |
2 |
31,360,980 (GRCm38) |
missense |
probably damaging |
0.98 |
R4943:Hmcn2
|
UTSW |
2 |
31,335,492 (GRCm38) |
missense |
probably damaging |
1.00 |
R4967:Hmcn2
|
UTSW |
2 |
31,354,164 (GRCm38) |
critical splice acceptor site |
probably null |
|
R4973:Hmcn2
|
UTSW |
2 |
31,344,096 (GRCm38) |
missense |
probably benign |
0.15 |
R4975:Hmcn2
|
UTSW |
2 |
31,393,025 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4994:Hmcn2
|
UTSW |
2 |
31,458,055 (GRCm38) |
critical splice donor site |
probably null |
|
R4997:Hmcn2
|
UTSW |
2 |
31,401,708 (GRCm38) |
missense |
probably damaging |
1.00 |
R5045:Hmcn2
|
UTSW |
2 |
31,409,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R5117:Hmcn2
|
UTSW |
2 |
31,458,049 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5151:Hmcn2
|
UTSW |
2 |
31,389,443 (GRCm38) |
missense |
probably null |
|
R5232:Hmcn2
|
UTSW |
2 |
31,457,748 (GRCm38) |
missense |
probably damaging |
0.99 |
R5237:Hmcn2
|
UTSW |
2 |
31,414,716 (GRCm38) |
missense |
probably benign |
0.01 |
R5288:Hmcn2
|
UTSW |
2 |
31,460,321 (GRCm38) |
missense |
probably benign |
0.11 |
R5375:Hmcn2
|
UTSW |
2 |
31,430,441 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5379:Hmcn2
|
UTSW |
2 |
31,409,011 (GRCm38) |
missense |
probably damaging |
0.99 |
R5385:Hmcn2
|
UTSW |
2 |
31,460,321 (GRCm38) |
missense |
probably benign |
0.11 |
R5412:Hmcn2
|
UTSW |
2 |
31,346,617 (GRCm38) |
missense |
possibly damaging |
0.77 |
R5426:Hmcn2
|
UTSW |
2 |
31,336,544 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5434:Hmcn2
|
UTSW |
2 |
31,420,363 (GRCm38) |
missense |
probably damaging |
1.00 |
R5441:Hmcn2
|
UTSW |
2 |
31,406,416 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5484:Hmcn2
|
UTSW |
2 |
31,393,054 (GRCm38) |
nonsense |
probably null |
|
R5492:Hmcn2
|
UTSW |
2 |
31,420,306 (GRCm38) |
missense |
probably benign |
0.03 |
R5572:Hmcn2
|
UTSW |
2 |
31,414,526 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5572:Hmcn2
|
UTSW |
2 |
31,414,525 (GRCm38) |
critical splice acceptor site |
probably null |
|
R5591:Hmcn2
|
UTSW |
2 |
31,344,047 (GRCm38) |
missense |
probably damaging |
1.00 |
R5614:Hmcn2
|
UTSW |
2 |
31,428,303 (GRCm38) |
missense |
probably damaging |
0.99 |
R5634:Hmcn2
|
UTSW |
2 |
31,333,881 (GRCm38) |
missense |
probably damaging |
1.00 |
R5645:Hmcn2
|
UTSW |
2 |
31,420,812 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5716:Hmcn2
|
UTSW |
2 |
31,458,738 (GRCm38) |
missense |
possibly damaging |
0.68 |
R5716:Hmcn2
|
UTSW |
2 |
31,336,567 (GRCm38) |
missense |
probably damaging |
1.00 |
R5725:Hmcn2
|
UTSW |
2 |
31,383,815 (GRCm38) |
critical splice donor site |
probably null |
|
R5760:Hmcn2
|
UTSW |
2 |
31,414,568 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5774:Hmcn2
|
UTSW |
2 |
31,409,135 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5838:Hmcn2
|
UTSW |
2 |
31,457,807 (GRCm38) |
missense |
probably damaging |
0.99 |
R5899:Hmcn2
|
UTSW |
2 |
31,354,673 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5916:Hmcn2
|
UTSW |
2 |
31,396,139 (GRCm38) |
missense |
probably damaging |
1.00 |
R5973:Hmcn2
|
UTSW |
2 |
31,420,323 (GRCm38) |
missense |
probably damaging |
0.99 |
R6002:Hmcn2
|
UTSW |
2 |
31,420,309 (GRCm38) |
missense |
probably damaging |
0.99 |
R6018:Hmcn2
|
UTSW |
2 |
31,370,792 (GRCm38) |
missense |
probably benign |
0.13 |
R6063:Hmcn2
|
UTSW |
2 |
31,434,713 (GRCm38) |
missense |
probably benign |
0.06 |
R6161:Hmcn2
|
UTSW |
2 |
31,356,254 (GRCm38) |
missense |
probably benign |
|
R6166:Hmcn2
|
UTSW |
2 |
31,369,262 (GRCm38) |
missense |
probably damaging |
1.00 |
R6177:Hmcn2
|
UTSW |
2 |
31,420,106 (GRCm38) |
nonsense |
probably null |
|
R6191:Hmcn2
|
UTSW |
2 |
31,458,746 (GRCm38) |
missense |
probably damaging |
0.99 |
R6195:Hmcn2
|
UTSW |
2 |
31,384,115 (GRCm38) |
missense |
probably damaging |
0.96 |
R6273:Hmcn2
|
UTSW |
2 |
31,411,834 (GRCm38) |
missense |
probably damaging |
0.99 |
R6293:Hmcn2
|
UTSW |
2 |
31,335,451 (GRCm38) |
missense |
probably damaging |
1.00 |
R6349:Hmcn2
|
UTSW |
2 |
31,388,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R6395:Hmcn2
|
UTSW |
2 |
31,369,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R6448:Hmcn2
|
UTSW |
2 |
31,420,820 (GRCm38) |
missense |
probably benign |
0.02 |
R6450:Hmcn2
|
UTSW |
2 |
31,361,800 (GRCm38) |
missense |
probably benign |
0.11 |
R6479:Hmcn2
|
UTSW |
2 |
31,425,468 (GRCm38) |
missense |
probably damaging |
0.99 |
R6502:Hmcn2
|
UTSW |
2 |
31,382,478 (GRCm38) |
missense |
probably damaging |
0.99 |
R6511:Hmcn2
|
UTSW |
2 |
31,356,342 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6537:Hmcn2
|
UTSW |
2 |
31,415,268 (GRCm38) |
missense |
probably benign |
0.00 |
R6880:Hmcn2
|
UTSW |
2 |
31,343,056 (GRCm38) |
missense |
probably damaging |
1.00 |
R6924:Hmcn2
|
UTSW |
2 |
31,350,505 (GRCm38) |
splice site |
probably null |
|
R6971:Hmcn2
|
UTSW |
2 |
31,432,321 (GRCm38) |
missense |
probably benign |
0.02 |
R7141:Hmcn2
|
UTSW |
2 |
31,360,896 (GRCm38) |
missense |
probably benign |
0.17 |
R7268:Hmcn2
|
UTSW |
2 |
31,457,966 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7307:Hmcn2
|
UTSW |
2 |
31,343,081 (GRCm38) |
missense |
probably damaging |
0.96 |
R7322:Hmcn2
|
UTSW |
2 |
31,459,081 (GRCm38) |
missense |
probably damaging |
0.99 |
R7334:Hmcn2
|
UTSW |
2 |
31,453,135 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7334:Hmcn2
|
UTSW |
2 |
31,435,794 (GRCm38) |
missense |
probably damaging |
0.98 |
R7335:Hmcn2
|
UTSW |
2 |
31,392,157 (GRCm38) |
missense |
possibly damaging |
0.88 |
R7358:Hmcn2
|
UTSW |
2 |
31,416,812 (GRCm38) |
missense |
probably damaging |
1.00 |
R7359:Hmcn2
|
UTSW |
2 |
31,388,383 (GRCm38) |
missense |
probably benign |
0.13 |
R7488:Hmcn2
|
UTSW |
2 |
31,420,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R7498:Hmcn2
|
UTSW |
2 |
31,383,475 (GRCm38) |
splice site |
probably null |
|
R7560:Hmcn2
|
UTSW |
2 |
31,457,173 (GRCm38) |
missense |
probably benign |
|
R7566:Hmcn2
|
UTSW |
2 |
31,454,857 (GRCm38) |
missense |
probably damaging |
0.96 |
R7570:Hmcn2
|
UTSW |
2 |
31,423,911 (GRCm38) |
missense |
probably benign |
|
R7574:Hmcn2
|
UTSW |
2 |
31,455,519 (GRCm38) |
missense |
possibly damaging |
0.68 |
R7599:Hmcn2
|
UTSW |
2 |
31,356,286 (GRCm38) |
missense |
possibly damaging |
0.93 |
R7654:Hmcn2
|
UTSW |
2 |
31,346,569 (GRCm38) |
missense |
probably benign |
0.00 |
R7662:Hmcn2
|
UTSW |
2 |
31,382,345 (GRCm38) |
missense |
probably benign |
0.01 |
R7666:Hmcn2
|
UTSW |
2 |
31,380,233 (GRCm38) |
missense |
probably damaging |
1.00 |
R7698:Hmcn2
|
UTSW |
2 |
31,423,153 (GRCm38) |
missense |
probably damaging |
0.98 |
R7722:Hmcn2
|
UTSW |
2 |
31,382,500 (GRCm38) |
nonsense |
probably null |
|
R7739:Hmcn2
|
UTSW |
2 |
31,458,026 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7749:Hmcn2
|
UTSW |
2 |
31,453,033 (GRCm38) |
splice site |
probably null |
|
R7828:Hmcn2
|
UTSW |
2 |
31,405,875 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7912:Hmcn2
|
UTSW |
2 |
31,420,299 (GRCm38) |
missense |
probably benign |
0.00 |
R7978:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R8075:Hmcn2
|
UTSW |
2 |
31,389,391 (GRCm38) |
missense |
possibly damaging |
0.88 |
R8088:Hmcn2
|
UTSW |
2 |
31,426,903 (GRCm38) |
nonsense |
probably null |
|
R8101:Hmcn2
|
UTSW |
2 |
31,350,070 (GRCm38) |
missense |
probably benign |
0.08 |
R8124:Hmcn2
|
UTSW |
2 |
31,400,124 (GRCm38) |
missense |
probably benign |
0.01 |
R8145:Hmcn2
|
UTSW |
2 |
31,423,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R8230:Hmcn2
|
UTSW |
2 |
31,344,473 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8267:Hmcn2
|
UTSW |
2 |
31,459,179 (GRCm38) |
missense |
probably benign |
|
R8277:Hmcn2
|
UTSW |
2 |
31,369,177 (GRCm38) |
missense |
probably benign |
0.16 |
R8307:Hmcn2
|
UTSW |
2 |
31,396,115 (GRCm38) |
missense |
probably damaging |
0.99 |
R8353:Hmcn2
|
UTSW |
2 |
31,385,341 (GRCm38) |
splice site |
probably null |
|
R8415:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8416:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8437:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8438:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8440:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8442:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8497:Hmcn2
|
UTSW |
2 |
31,423,345 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8520:Hmcn2
|
UTSW |
2 |
31,354,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R8530:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8537:Hmcn2
|
UTSW |
2 |
31,391,076 (GRCm38) |
missense |
probably benign |
0.15 |
R8550:Hmcn2
|
UTSW |
2 |
31,350,642 (GRCm38) |
critical splice donor site |
probably null |
|
R8721:Hmcn2
|
UTSW |
2 |
31,425,177 (GRCm38) |
missense |
probably damaging |
1.00 |
R8795:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8802:Hmcn2
|
UTSW |
2 |
31,411,276 (GRCm38) |
missense |
probably damaging |
0.97 |
R8804:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8805:Hmcn2
|
UTSW |
2 |
31,425,381 (GRCm38) |
missense |
probably benign |
0.01 |
R8904:Hmcn2
|
UTSW |
2 |
31,433,392 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8937:Hmcn2
|
UTSW |
2 |
31,314,415 (GRCm38) |
start codon destroyed |
probably benign |
0.01 |
R8947:Hmcn2
|
UTSW |
2 |
31,388,208 (GRCm38) |
missense |
probably damaging |
0.99 |
R8948:Hmcn2
|
UTSW |
2 |
31,354,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R8950:Hmcn2
|
UTSW |
2 |
31,354,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R8959:Hmcn2
|
UTSW |
2 |
31,392,147 (GRCm38) |
missense |
probably damaging |
1.00 |
R9025:Hmcn2
|
UTSW |
2 |
31,457,955 (GRCm38) |
missense |
possibly damaging |
0.56 |
R9039:Hmcn2
|
UTSW |
2 |
31,354,634 (GRCm38) |
missense |
probably damaging |
0.97 |
R9068:Hmcn2
|
UTSW |
2 |
31,413,673 (GRCm38) |
missense |
probably benign |
0.01 |
R9161:Hmcn2
|
UTSW |
2 |
31,352,746 (GRCm38) |
missense |
probably benign |
0.02 |
R9178:Hmcn2
|
UTSW |
2 |
31,391,509 (GRCm38) |
missense |
possibly damaging |
0.77 |
R9204:Hmcn2
|
UTSW |
2 |
31,388,365 (GRCm38) |
missense |
probably damaging |
0.98 |
R9317:Hmcn2
|
UTSW |
2 |
31,460,316 (GRCm38) |
missense |
possibly damaging |
0.91 |
R9341:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R9343:Hmcn2
|
UTSW |
2 |
31,389,347 (GRCm38) |
missense |
probably benign |
0.40 |
R9355:Hmcn2
|
UTSW |
2 |
31,438,290 (GRCm38) |
missense |
probably benign |
0.18 |
R9371:Hmcn2
|
UTSW |
2 |
31,411,905 (GRCm38) |
missense |
probably damaging |
1.00 |
R9450:Hmcn2
|
UTSW |
2 |
31,426,833 (GRCm38) |
missense |
probably damaging |
1.00 |
R9477:Hmcn2
|
UTSW |
2 |
31,396,019 (GRCm38) |
critical splice acceptor site |
probably null |
|
R9483:Hmcn2
|
UTSW |
2 |
31,430,363 (GRCm38) |
missense |
|
|
R9536:Hmcn2
|
UTSW |
2 |
31,445,118 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9580:Hmcn2
|
UTSW |
2 |
31,404,863 (GRCm38) |
missense |
probably benign |
0.16 |
R9593:Hmcn2
|
UTSW |
2 |
31,354,730 (GRCm38) |
missense |
probably damaging |
0.99 |
R9649:Hmcn2
|
UTSW |
2 |
31,402,438 (GRCm38) |
missense |
possibly damaging |
0.95 |
R9706:Hmcn2
|
UTSW |
2 |
31,415,267 (GRCm38) |
missense |
probably benign |
0.00 |
X0066:Hmcn2
|
UTSW |
2 |
31,454,811 (GRCm38) |
missense |
possibly damaging |
0.83 |
X0067:Hmcn2
|
UTSW |
2 |
31,405,867 (GRCm38) |
missense |
possibly damaging |
0.82 |
Z1088:Hmcn2
|
UTSW |
2 |
31,459,064 (GRCm38) |
splice site |
probably null |
|
Z1088:Hmcn2
|
UTSW |
2 |
31,381,067 (GRCm38) |
missense |
probably benign |
0.01 |
Z1176:Hmcn2
|
UTSW |
2 |
31,429,091 (GRCm38) |
missense |
probably damaging |
0.97 |
Z1176:Hmcn2
|
UTSW |
2 |
31,425,416 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Hmcn2
|
UTSW |
2 |
31,344,029 (GRCm38) |
missense |
possibly damaging |
0.95 |
Z1177:Hmcn2
|
UTSW |
2 |
31,426,824 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Hmcn2
|
UTSW |
2 |
31,344,506 (GRCm38) |
missense |
probably damaging |
1.00 |
|