Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
C |
3: 59,840,161 (GRCm39) |
T78P |
probably damaging |
Het |
Abcc8 |
T |
C |
7: 45,800,291 (GRCm39) |
K497R |
probably damaging |
Het |
Aldh1a3 |
C |
T |
7: 66,068,927 (GRCm39) |
R19Q |
possibly damaging |
Het |
Bmp2k |
A |
G |
5: 97,234,944 (GRCm39) |
|
probably benign |
Het |
Ccni |
A |
T |
5: 93,335,553 (GRCm39) |
L195Q |
possibly damaging |
Het |
Cdkl4 |
C |
A |
17: 80,832,764 (GRCm39) |
G327* |
probably null |
Het |
Cdsn |
T |
C |
17: 35,866,326 (GRCm39) |
V285A |
possibly damaging |
Het |
Cfap20dc |
A |
G |
14: 8,518,736 (GRCm38) |
V240A |
probably benign |
Het |
Chtf18 |
T |
C |
17: 25,943,540 (GRCm39) |
E352G |
possibly damaging |
Het |
Clasp2 |
T |
A |
9: 113,732,984 (GRCm39) |
I961N |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,949,752 (GRCm39) |
Q128R |
probably damaging |
Het |
Cttnbp2 |
C |
A |
6: 18,406,525 (GRCm39) |
Q1055H |
possibly damaging |
Het |
Cyld |
T |
G |
8: 89,433,860 (GRCm39) |
F216L |
probably benign |
Het |
Cyp3a41a |
A |
G |
5: 145,656,858 (GRCm39) |
M1T |
probably null |
Het |
Disp3 |
C |
T |
4: 148,328,673 (GRCm39) |
R1097H |
possibly damaging |
Het |
Dmap1 |
T |
C |
4: 117,538,233 (GRCm39) |
D67G |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,875,959 (GRCm39) |
F529L |
probably benign |
Het |
Ergic3 |
T |
C |
2: 155,859,638 (GRCm39) |
|
probably null |
Het |
Fkbp14 |
A |
G |
6: 54,569,943 (GRCm39) |
I29T |
probably benign |
Het |
Gm4845 |
T |
A |
1: 141,184,623 (GRCm39) |
|
noncoding transcript |
Het |
Gm7135 |
A |
T |
1: 97,281,801 (GRCm39) |
|
noncoding transcript |
Het |
Gpbar1 |
TACCAC |
TAC |
1: 74,318,704 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,424,481 (GRCm39) |
I57F |
probably damaging |
Het |
Hectd1 |
A |
G |
12: 51,809,280 (GRCm39) |
V1722A |
probably benign |
Het |
Il21 |
C |
A |
3: 37,286,653 (GRCm39) |
S21I |
probably damaging |
Het |
Itih4 |
T |
A |
14: 30,614,244 (GRCm39) |
I398N |
probably damaging |
Het |
Kansl1 |
A |
T |
11: 104,226,390 (GRCm39) |
S922R |
probably damaging |
Het |
Krt27 |
G |
A |
11: 99,237,722 (GRCm39) |
Q339* |
probably null |
Het |
Lama1 |
C |
A |
17: 68,045,829 (GRCm39) |
L245I |
possibly damaging |
Het |
Lmo2 |
T |
A |
2: 103,806,488 (GRCm39) |
C60* |
probably null |
Het |
Med16 |
A |
G |
10: 79,738,839 (GRCm39) |
S316P |
possibly damaging |
Het |
Mia3 |
T |
C |
1: 183,111,970 (GRCm39) |
N529S |
probably benign |
Het |
Msi2 |
T |
C |
11: 88,285,481 (GRCm39) |
K188E |
probably damaging |
Het |
Myh7 |
T |
C |
14: 55,209,128 (GRCm39) |
K1870R |
probably damaging |
Het |
Nhlrc1 |
A |
G |
13: 47,167,216 (GRCm39) |
V347A |
probably benign |
Het |
Nol6 |
C |
T |
4: 41,120,167 (GRCm39) |
R487H |
probably benign |
Het |
Or4c117 |
T |
C |
2: 88,955,682 (GRCm39) |
Y131C |
probably damaging |
Het |
Or4k41 |
T |
C |
2: 111,280,028 (GRCm39) |
I181T |
probably benign |
Het |
Or52h1 |
A |
T |
7: 103,828,736 (GRCm39) |
V293D |
probably damaging |
Het |
Or5d18 |
T |
C |
2: 87,865,005 (GRCm39) |
I159M |
probably benign |
Het |
Or6c205 |
T |
C |
10: 129,087,141 (GRCm39) |
I246T |
probably damaging |
Het |
Otog |
T |
C |
7: 45,937,415 (GRCm39) |
V1708A |
probably benign |
Het |
Ptprv |
A |
G |
1: 135,046,586 (GRCm39) |
|
noncoding transcript |
Het |
Pus7l |
A |
G |
15: 94,427,369 (GRCm39) |
V471A |
possibly damaging |
Het |
Rab11fip4 |
A |
G |
11: 79,510,497 (GRCm39) |
R68G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,277,428 (GRCm39) |
D264G |
possibly damaging |
Het |
Reln |
A |
G |
5: 22,165,424 (GRCm39) |
S2045P |
probably damaging |
Het |
Rgs22 |
A |
C |
15: 36,055,022 (GRCm39) |
Y593* |
probably null |
Het |
Ror2 |
C |
T |
13: 53,285,954 (GRCm39) |
D87N |
probably damaging |
Het |
Rps6ka4 |
A |
T |
19: 6,817,678 (GRCm39) |
|
probably null |
Het |
Rttn |
T |
A |
18: 89,082,209 (GRCm39) |
|
probably null |
Het |
Runx3 |
A |
G |
4: 134,898,446 (GRCm39) |
T206A |
probably benign |
Het |
Setx |
A |
G |
2: 29,054,562 (GRCm39) |
E2158G |
probably damaging |
Het |
Siglece |
C |
T |
7: 43,308,396 (GRCm39) |
|
probably null |
Het |
Slco1a8 |
T |
C |
6: 141,926,599 (GRCm39) |
S576G |
probably benign |
Het |
Snx1 |
A |
T |
9: 66,012,187 (GRCm39) |
L96* |
probably null |
Het |
Srrm1 |
A |
G |
4: 135,074,031 (GRCm39) |
|
probably benign |
Het |
Stk39 |
A |
T |
2: 68,051,336 (GRCm39) |
|
probably benign |
Het |
Sun3 |
G |
A |
11: 8,988,311 (GRCm39) |
R4* |
probably null |
Het |
Svil |
A |
G |
18: 5,054,025 (GRCm39) |
K347E |
possibly damaging |
Het |
Sybu |
T |
A |
15: 44,541,063 (GRCm39) |
E333V |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,192,520 (GRCm39) |
|
probably benign |
Het |
Tfip11 |
G |
T |
5: 112,483,613 (GRCm39) |
|
probably benign |
Het |
Tmc1 |
A |
C |
19: 20,884,319 (GRCm39) |
D40E |
probably damaging |
Het |
Twf2 |
G |
T |
9: 106,089,539 (GRCm39) |
G121W |
probably damaging |
Het |
Vpreb3 |
A |
G |
10: 75,775,636 (GRCm39) |
V50A |
probably damaging |
Het |
Vps8 |
T |
A |
16: 21,285,219 (GRCm39) |
L400Q |
probably damaging |
Het |
Xylt1 |
A |
T |
7: 117,266,565 (GRCm39) |
Y861F |
probably damaging |
Het |
Zfp608 |
T |
G |
18: 55,022,962 (GRCm39) |
T1485P |
probably damaging |
Het |
Zfp619 |
T |
G |
7: 39,186,504 (GRCm39) |
S845A |
possibly damaging |
Het |
Zscan4d |
A |
T |
7: 10,899,274 (GRCm39) |
M1K |
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 |
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 |
|