Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot12 |
A |
G |
13: 91,932,510 (GRCm39) |
D502G |
probably benign |
Het |
Adrb1 |
T |
C |
19: 56,711,120 (GRCm39) |
V106A |
probably damaging |
Het |
Ahcyl2 |
G |
T |
6: 29,886,139 (GRCm39) |
G352W |
probably damaging |
Het |
Ahnak2 |
T |
G |
12: 112,745,851 (GRCm39) |
D446A |
|
Het |
Arhgap42 |
T |
C |
9: 9,035,532 (GRCm39) |
D270G |
probably benign |
Het |
Atp2a1 |
A |
G |
7: 126,058,828 (GRCm39) |
V129A |
possibly damaging |
Het |
B9d2 |
G |
A |
7: 25,380,784 (GRCm39) |
|
probably benign |
Het |
Bace1 |
A |
T |
9: 45,767,437 (GRCm39) |
I207F |
possibly damaging |
Het |
Blnk |
T |
A |
19: 40,940,834 (GRCm39) |
I190F |
possibly damaging |
Het |
Bmp7 |
C |
T |
2: 172,781,757 (GRCm39) |
E36K |
possibly damaging |
Het |
Brsk2 |
A |
G |
7: 141,554,597 (GRCm39) |
E654G |
probably benign |
Het |
Cacna2d3 |
T |
C |
14: 28,780,378 (GRCm39) |
H661R |
probably benign |
Het |
Cdh4 |
T |
C |
2: 179,532,695 (GRCm39) |
V719A |
probably benign |
Het |
Cdkn2d |
G |
T |
9: 21,200,540 (GRCm39) |
P77H |
probably damaging |
Het |
Chd3 |
A |
G |
11: 69,247,096 (GRCm39) |
V1024A |
probably damaging |
Het |
Chsy1 |
T |
A |
7: 65,820,992 (GRCm39) |
M409K |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,319 (GRCm39) |
L518P |
probably damaging |
Het |
Cic |
G |
A |
7: 24,972,278 (GRCm39) |
V670M |
probably damaging |
Het |
Clock |
A |
T |
5: 76,390,738 (GRCm39) |
|
probably null |
Het |
Coro1a |
C |
A |
7: 126,302,306 (GRCm39) |
V14L |
probably damaging |
Het |
Ctcfl |
C |
A |
2: 172,960,199 (GRCm39) |
C128F |
probably damaging |
Het |
Cyb5b |
A |
G |
8: 107,896,491 (GRCm39) |
T71A |
probably damaging |
Het |
Cyp2c40 |
C |
G |
19: 39,795,658 (GRCm39) |
V174L |
possibly damaging |
Het |
D630045J12Rik |
T |
A |
6: 38,173,562 (GRCm39) |
Q202L |
possibly damaging |
Het |
Dgkz |
T |
C |
2: 91,773,160 (GRCm39) |
|
probably benign |
Het |
Dlgap2 |
T |
C |
8: 14,872,697 (GRCm39) |
|
probably null |
Het |
Dnah1 |
T |
C |
14: 31,026,940 (GRCm39) |
I695V |
probably benign |
Het |
Dst |
T |
A |
1: 34,221,532 (GRCm39) |
S2445R |
possibly damaging |
Het |
Elob |
T |
C |
17: 24,043,950 (GRCm39) |
D83G |
probably benign |
Het |
Elp4 |
T |
A |
2: 105,624,933 (GRCm39) |
D320V |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,530,886 (GRCm39) |
Y45C |
probably damaging |
Het |
Exph5 |
A |
G |
9: 53,287,073 (GRCm39) |
I1385V |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,138 (GRCm39) |
D2621E |
probably damaging |
Het |
Fbxl6 |
G |
T |
15: 76,422,669 (GRCm39) |
A83D |
probably benign |
Het |
Fmo2 |
A |
G |
1: 162,716,318 (GRCm39) |
Y90H |
probably damaging |
Het |
Fzd4 |
T |
A |
7: 89,056,761 (GRCm39) |
Y269* |
probably null |
Het |
Grik5 |
T |
A |
7: 24,757,951 (GRCm39) |
I377F |
probably damaging |
Het |
Havcr2 |
C |
A |
11: 46,349,889 (GRCm39) |
P137Q |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,392,405 (GRCm39) |
N223S |
possibly damaging |
Het |
Hps3 |
T |
G |
3: 20,084,616 (GRCm39) |
I191L |
probably benign |
Het |
Ica1l |
T |
A |
1: 60,049,369 (GRCm39) |
K195* |
probably null |
Het |
Idh2 |
TCCCAGGGCC |
TCC |
7: 79,748,079 (GRCm39) |
|
probably null |
Het |
Ift140 |
A |
G |
17: 25,311,315 (GRCm39) |
D1170G |
probably benign |
Het |
Igflr1 |
T |
C |
7: 30,266,776 (GRCm39) |
F208S |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 23,580,310 (GRCm39) |
T313A |
probably benign |
Het |
Krt6a |
T |
A |
15: 101,598,994 (GRCm39) |
I524F |
unknown |
Het |
Lce1d |
G |
T |
3: 92,593,148 (GRCm39) |
H88Q |
unknown |
Het |
Lrmda |
A |
G |
14: 22,878,770 (GRCm39) |
E177G |
probably benign |
Het |
Lrrn3 |
T |
A |
12: 41,502,712 (GRCm39) |
N535I |
possibly damaging |
Het |
Map2k4 |
T |
A |
11: 65,666,583 (GRCm39) |
I40L |
unknown |
Het |
Map7d1 |
A |
G |
4: 126,130,429 (GRCm39) |
L459P |
probably damaging |
Het |
Mipol1 |
A |
T |
12: 57,352,859 (GRCm39) |
N66I |
possibly damaging |
Het |
Mycn |
A |
C |
12: 12,990,292 (GRCm39) |
F35V |
probably benign |
Het |
Mzt2 |
A |
C |
16: 15,680,669 (GRCm39) |
M40R |
possibly damaging |
Het |
N4bp2 |
T |
G |
5: 65,948,458 (GRCm39) |
L363V |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,097,221 (GRCm39) |
M1532K |
probably benign |
Het |
Notch1 |
G |
A |
2: 26,350,177 (GRCm39) |
T2321M |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,334,123 (GRCm39) |
D89G |
probably benign |
Het |
Nsun4 |
G |
A |
4: 115,908,691 (GRCm39) |
T623I |
possibly damaging |
Het |
Nup155 |
T |
C |
15: 8,184,531 (GRCm39) |
S1309P |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,851 (GRCm39) |
N205S |
probably damaging |
Het |
Or51f5 |
T |
C |
7: 102,430,889 (GRCm39) |
S69P |
probably damaging |
Het |
Or8h10 |
T |
C |
2: 86,809,122 (GRCm39) |
Y6C |
probably benign |
Het |
Pcsk5 |
A |
G |
19: 17,814,336 (GRCm39) |
F61L |
probably benign |
Het |
Phrf1 |
A |
T |
7: 140,811,138 (GRCm39) |
|
probably null |
Het |
Pkd1 |
G |
A |
17: 24,792,605 (GRCm39) |
E1431K |
probably benign |
Het |
Pkd2 |
T |
A |
5: 104,628,219 (GRCm39) |
I431N |
probably damaging |
Het |
Plcb2 |
A |
G |
2: 118,546,124 (GRCm39) |
L557P |
probably damaging |
Het |
Poteg |
A |
G |
8: 27,984,988 (GRCm39) |
N449S |
probably benign |
Het |
Ppargc1b |
C |
A |
18: 61,445,281 (GRCm39) |
G192W |
probably damaging |
Het |
Rab13 |
T |
C |
3: 90,132,206 (GRCm39) |
S178P |
probably benign |
Het |
Ralgds |
A |
G |
2: 28,437,607 (GRCm39) |
D571G |
probably damaging |
Het |
Ror2 |
A |
G |
13: 53,264,849 (GRCm39) |
S748P |
probably benign |
Het |
Sart1 |
A |
T |
19: 5,434,905 (GRCm39) |
L167Q |
probably damaging |
Het |
Septin12 |
A |
G |
16: 4,810,055 (GRCm39) |
V160A |
possibly damaging |
Het |
Sgo1 |
T |
C |
17: 53,986,295 (GRCm39) |
S299G |
probably benign |
Het |
Shoc1 |
T |
C |
4: 59,076,140 (GRCm39) |
N601S |
possibly damaging |
Het |
Slc35b4 |
T |
A |
6: 34,140,296 (GRCm39) |
D152V |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,120,449 (GRCm39) |
Y4187C |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,019,235 (GRCm39) |
|
probably null |
Het |
Synj1 |
G |
A |
16: 90,737,371 (GRCm39) |
T1308I |
probably benign |
Het |
Thap12 |
T |
G |
7: 98,359,438 (GRCm39) |
L106V |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,057,916 (GRCm39) |
M1501T |
possibly damaging |
Het |
Top2a |
G |
T |
11: 98,891,663 (GRCm39) |
N1153K |
probably benign |
Het |
Trpm5 |
A |
G |
7: 142,634,723 (GRCm39) |
L658P |
probably damaging |
Het |
Ttc21b |
G |
A |
2: 66,047,548 (GRCm39) |
A849V |
possibly damaging |
Het |
Vcf1 |
C |
T |
11: 113,554,215 (GRCm39) |
G160D |
probably damaging |
Het |
Vmn1r80 |
A |
T |
7: 11,927,750 (GRCm39) |
I287F |
probably damaging |
Het |
Vmn1r87 |
T |
C |
7: 12,865,745 (GRCm39) |
S181G |
probably damaging |
Het |
Vmn2r71 |
A |
T |
7: 85,273,115 (GRCm39) |
H643L |
probably benign |
Het |
Washc5 |
G |
A |
15: 59,238,041 (GRCm39) |
R228C |
probably damaging |
Het |
Wdr72 |
T |
C |
9: 74,117,408 (GRCm39) |
S719P |
probably damaging |
Het |
Xrcc3 |
G |
T |
12: 111,774,336 (GRCm39) |
D164E |
probably benign |
Het |
Zc2hc1b |
G |
A |
10: 13,044,529 (GRCm39) |
R45C |
probably damaging |
Het |
Zfp335 |
A |
G |
2: 164,737,912 (GRCm39) |
Y900H |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,228,875 (GRCm39) |
R697C |
probably damaging |
Het |
Zfp60 |
T |
C |
7: 27,448,561 (GRCm39) |
Y410H |
probably damaging |
Het |
Zfp60 |
T |
A |
7: 27,448,696 (GRCm39) |
C455S |
probably damaging |
Het |
Zfp605 |
C |
T |
5: 110,275,157 (GRCm39) |
Q92* |
probably null |
Het |
Zfp64 |
C |
T |
2: 168,767,585 (GRCm39) |
D676N |
probably damaging |
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 |
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 |
|
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 |
|