Other mutations in this stock |
Total: 119 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022A10Rik |
T |
C |
7: 27,274,017 (GRCm39) |
L86P |
unknown |
Het |
Aimp1 |
C |
T |
3: 132,382,808 (GRCm39) |
E23K |
probably damaging |
Het |
Ap2b1 |
A |
T |
11: 83,288,605 (GRCm39) |
N884I |
probably benign |
Het |
Apoe |
G |
T |
7: 19,431,423 (GRCm39) |
Q65K |
possibly damaging |
Het |
Arhgef1 |
T |
A |
7: 24,611,996 (GRCm39) |
D93E |
probably benign |
Het |
Arhgef12 |
G |
T |
9: 42,888,958 (GRCm39) |
T1085K |
probably damaging |
Het |
Arid5a |
T |
C |
1: 36,356,745 (GRCm39) |
|
probably null |
Het |
Atp9a |
A |
T |
2: 168,531,280 (GRCm39) |
|
probably null |
Het |
Baz1a |
T |
C |
12: 54,969,325 (GRCm39) |
I635V |
probably damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Cckar |
T |
A |
5: 53,857,124 (GRCm39) |
M429L |
probably benign |
Het |
Ccl3 |
A |
T |
11: 83,539,164 (GRCm39) |
L65Q |
probably benign |
Het |
Ccr3 |
A |
G |
9: 123,829,477 (GRCm39) |
T271A |
probably benign |
Het |
Cd8b1 |
T |
A |
6: 71,303,081 (GRCm39) |
I52N |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,591,767 (GRCm39) |
E551K |
probably damaging |
Het |
Cdh17 |
A |
G |
4: 11,810,466 (GRCm39) |
K719R |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,825,655 (GRCm39) |
R38G |
probably null |
Het |
Chd6 |
T |
C |
2: 160,856,114 (GRCm39) |
E715G |
probably damaging |
Het |
Cldn34b2 |
T |
A |
X: 153,908,625 (GRCm39) |
R68* |
probably null |
Het |
Col19a1 |
T |
G |
1: 24,600,410 (GRCm39) |
D44A |
unknown |
Het |
Colgalt2 |
C |
T |
1: 152,382,627 (GRCm39) |
S493F |
probably damaging |
Het |
Cr1l |
T |
C |
1: 194,812,139 (GRCm39) |
I99M |
probably damaging |
Het |
Crybg1 |
T |
C |
10: 43,873,616 (GRCm39) |
E1164G |
probably damaging |
Het |
Cym |
G |
T |
3: 107,118,718 (GRCm39) |
D367E |
probably damaging |
Het |
Dennd2a |
G |
T |
6: 39,499,776 (GRCm39) |
T263K |
probably damaging |
Het |
Dhx9 |
T |
A |
1: 153,336,049 (GRCm39) |
M869L |
probably damaging |
Het |
Dnm2 |
A |
G |
9: 21,415,742 (GRCm39) |
H692R |
probably damaging |
Het |
Ern1 |
A |
T |
11: 106,298,031 (GRCm39) |
S697T |
probably damaging |
Het |
F12 |
G |
A |
13: 55,568,943 (GRCm39) |
T273I |
probably benign |
Het |
Fam151b |
A |
T |
13: 92,604,617 (GRCm39) |
L124Q |
probably damaging |
Het |
Fancg |
A |
G |
4: 43,002,991 (GRCm39) |
V622A |
probably benign |
Het |
Fbxo2 |
T |
A |
4: 148,249,356 (GRCm39) |
N159K |
possibly damaging |
Het |
Fgd2 |
C |
A |
17: 29,586,052 (GRCm39) |
T212K |
possibly damaging |
Het |
Fhl3 |
T |
A |
4: 124,601,342 (GRCm39) |
D178E |
probably benign |
Het |
Filip1 |
G |
T |
9: 79,723,091 (GRCm39) |
A1176D |
possibly damaging |
Het |
Fndc1 |
T |
C |
17: 7,958,081 (GRCm39) |
Y1722C |
probably damaging |
Het |
Frem3 |
T |
C |
8: 81,340,143 (GRCm39) |
V812A |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,809,017 (GRCm39) |
I1779V |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,769,798 (GRCm39) |
V585I |
probably benign |
Het |
Gm15056 |
C |
G |
8: 21,390,697 (GRCm39) |
S80T |
probably benign |
Het |
Gm5145 |
A |
G |
17: 20,790,715 (GRCm39) |
E31G |
probably benign |
Het |
Gmfg |
A |
G |
7: 28,145,369 (GRCm39) |
Y71C |
probably damaging |
Het |
Grk1 |
A |
G |
8: 13,459,322 (GRCm39) |
E291G |
probably damaging |
Het |
Gtpbp1 |
A |
G |
15: 79,600,152 (GRCm39) |
E393G |
possibly damaging |
Het |
Gtpbp2 |
A |
G |
17: 46,472,071 (GRCm39) |
D2G |
probably damaging |
Het |
Hc |
A |
T |
2: 34,918,189 (GRCm39) |
V698E |
probably benign |
Het |
Helz |
G |
A |
11: 107,536,895 (GRCm39) |
R249H |
probably damaging |
Het |
Hnrnpa3 |
A |
G |
2: 75,493,950 (GRCm39) |
R286G |
probably benign |
Het |
Hus1b |
A |
T |
13: 31,131,501 (GRCm39) |
W53R |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,321,857 (GRCm39) |
T4503I |
probably benign |
Het |
Ighmbp2 |
G |
C |
19: 3,315,324 (GRCm39) |
P699A |
probably benign |
Het |
Igkv1-122 |
A |
T |
6: 67,994,442 (GRCm39) |
Y110F |
probably benign |
Het |
Igkv8-28 |
T |
C |
6: 70,120,604 (GRCm39) |
Y113C |
probably damaging |
Het |
Iigp1c |
T |
C |
18: 60,379,152 (GRCm39) |
I229T |
possibly damaging |
Het |
Il16 |
A |
G |
7: 83,332,107 (GRCm39) |
S158P |
probably damaging |
Het |
Kalrn |
T |
A |
16: 34,055,637 (GRCm39) |
H876L |
probably damaging |
Het |
Kdm5d |
T |
A |
Y: 914,134 (GRCm39) |
L357H |
probably damaging |
Het |
Krt78 |
T |
C |
15: 101,855,055 (GRCm39) |
T919A |
possibly damaging |
Het |
L3mbtl2 |
T |
C |
15: 81,569,107 (GRCm39) |
C594R |
probably damaging |
Het |
Lcorl |
A |
T |
5: 45,890,931 (GRCm39) |
L474* |
probably null |
Het |
Lgals3 |
A |
T |
14: 47,619,144 (GRCm39) |
|
probably null |
Het |
Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
Lpcat3 |
T |
G |
6: 124,680,286 (GRCm39) |
W429G |
possibly damaging |
Het |
Lrp1 |
T |
C |
10: 127,377,241 (GRCm39) |
T4149A |
probably benign |
Het |
Memo1 |
G |
A |
17: 74,565,456 (GRCm39) |
Q36* |
probably null |
Het |
Mical2 |
A |
G |
7: 112,012,154 (GRCm39) |
N668S |
probably benign |
Het |
Ms4a10 |
A |
T |
19: 10,945,553 (GRCm39) |
I76N |
possibly damaging |
Het |
Mthfr |
T |
G |
4: 148,136,329 (GRCm39) |
L362V |
possibly damaging |
Het |
Myh3 |
T |
A |
11: 66,987,279 (GRCm39) |
Y1376* |
probably null |
Het |
Mymk |
C |
A |
2: 26,952,292 (GRCm39) |
V192F |
probably benign |
Het |
Myo1c |
A |
G |
11: 75,562,688 (GRCm39) |
D966G |
possibly damaging |
Het |
Ncam2 |
A |
G |
16: 81,314,445 (GRCm39) |
N474D |
probably damaging |
Het |
Nmnat1 |
T |
C |
4: 149,553,608 (GRCm39) |
N168S |
possibly damaging |
Het |
Nmur1 |
C |
T |
1: 86,314,367 (GRCm39) |
V323M |
possibly damaging |
Het |
Npr2 |
C |
A |
4: 43,633,522 (GRCm39) |
|
probably null |
Het |
Nsd3 |
T |
A |
8: 26,200,703 (GRCm39) |
M1265K |
probably benign |
Het |
Or13c7 |
A |
G |
4: 43,855,262 (GRCm39) |
T318A |
probably benign |
Het |
Or1e34 |
T |
C |
11: 73,778,629 (GRCm39) |
T190A |
probably damaging |
Het |
Or1j16 |
A |
C |
2: 36,530,626 (GRCm39) |
T192P |
probably damaging |
Het |
Or4c107 |
T |
A |
2: 88,789,556 (GRCm39) |
F249I |
probably damaging |
Het |
Or4c11 |
G |
T |
2: 88,695,838 (GRCm39) |
M296I |
probably benign |
Het |
Or5b108 |
T |
A |
19: 13,168,062 (GRCm39) |
F10L |
probably damaging |
Het |
Or5i1 |
T |
C |
2: 87,613,565 (GRCm39) |
V227A |
possibly damaging |
Het |
Or6c216 |
T |
C |
10: 129,678,344 (GRCm39) |
D189G |
probably damaging |
Het |
Otub1 |
G |
A |
19: 7,181,801 (GRCm39) |
A25V |
possibly damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
Patl2 |
A |
G |
2: 121,957,226 (GRCm39) |
S103P |
probably benign |
Het |
Pcdhb15 |
A |
T |
18: 37,608,628 (GRCm39) |
H620L |
possibly damaging |
Het |
Pdgfc |
A |
T |
3: 81,048,835 (GRCm39) |
D81V |
possibly damaging |
Het |
Pdia2 |
T |
C |
17: 26,415,476 (GRCm39) |
D447G |
probably damaging |
Het |
Pold1 |
C |
A |
7: 44,188,337 (GRCm39) |
A514S |
probably damaging |
Het |
Pomgnt1 |
C |
T |
4: 116,015,691 (GRCm39) |
T552I |
probably benign |
Het |
Ppl |
T |
C |
16: 4,922,400 (GRCm39) |
E294G |
probably benign |
Het |
Pramel12 |
A |
G |
4: 143,143,324 (GRCm39) |
Y30C |
probably damaging |
Het |
Prkcb |
A |
G |
7: 122,056,447 (GRCm39) |
S100G |
probably benign |
Het |
Psg16 |
T |
G |
7: 16,829,097 (GRCm39) |
I227S |
probably benign |
Het |
Rbbp6 |
AAAGAAGAAGAAGAAGAAG |
AAAGAAGAAGAAGAAG |
7: 122,601,175 (GRCm39) |
|
probably benign |
Het |
Reck |
T |
C |
4: 43,931,062 (GRCm39) |
|
probably null |
Het |
Rrbp1 |
C |
T |
2: 143,830,671 (GRCm39) |
G499S |
probably benign |
Het |
Sema6d |
G |
T |
2: 124,506,082 (GRCm39) |
R630L |
probably damaging |
Het |
Slc29a1 |
A |
G |
17: 45,900,882 (GRCm39) |
V94A |
possibly damaging |
Het |
Slc35a1 |
T |
A |
4: 34,664,146 (GRCm39) |
Q324L |
probably benign |
Het |
Slc35c1 |
A |
T |
2: 92,289,266 (GRCm39) |
L80Q |
probably damaging |
Het |
Slc7a10 |
G |
T |
7: 34,897,377 (GRCm39) |
|
probably null |
Het |
Srrm2 |
C |
T |
17: 24,038,593 (GRCm39) |
|
probably benign |
Het |
Stk38 |
T |
G |
17: 29,201,130 (GRCm39) |
D182A |
probably damaging |
Het |
Tas2r104 |
C |
T |
6: 131,662,398 (GRCm39) |
G104S |
probably benign |
Het |
Tmem121b |
T |
C |
6: 120,469,055 (GRCm39) |
E554G |
probably damaging |
Het |
Tor1aip2 |
A |
G |
1: 155,940,888 (GRCm39) |
H398R |
probably benign |
Het |
Tram2 |
C |
T |
1: 21,083,673 (GRCm39) |
V83I |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,935,811 (GRCm39) |
T565I |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,108,164 (GRCm39) |
V56A |
possibly damaging |
Het |
Vmn1r128 |
T |
C |
7: 21,083,644 (GRCm39) |
V116A |
possibly damaging |
Het |
Vmn1r170 |
C |
T |
7: 23,306,087 (GRCm39) |
T163I |
probably benign |
Het |
Vmn2r75 |
T |
A |
7: 85,813,290 (GRCm39) |
D504V |
possibly damaging |
Het |
Vps36 |
G |
A |
8: 22,708,436 (GRCm39) |
M363I |
probably benign |
Het |
Wdsub1 |
A |
G |
2: 59,708,661 (GRCm39) |
S71P |
probably damaging |
Het |
Zdhhc12 |
A |
G |
2: 29,981,496 (GRCm39) |
F189L |
probably benign |
Het |
Zfp521 |
T |
C |
18: 13,977,387 (GRCm39) |
M1009V |
probably benign |
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 |
R4623:Hmcn2
|
UTSW |
2 |
31,286,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Hmcn2
|
UTSW |
2 |
31,289,031 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4668:Hmcn2
|
UTSW |
2 |
31,325,804 (GRCm39) |
missense |
probably benign |
0.40 |
R4669:Hmcn2
|
UTSW |
2 |
31,325,804 (GRCm39) |
missense |
probably benign |
0.40 |
R4687:Hmcn2
|
UTSW |
2 |
31,328,297 (GRCm39) |
missense |
probably benign |
0.14 |
R4735:Hmcn2
|
UTSW |
2 |
31,273,787 (GRCm39) |
missense |
probably benign |
0.06 |
R4772:Hmcn2
|
UTSW |
2 |
31,335,326 (GRCm39) |
missense |
probably benign |
0.02 |
R4866:Hmcn2
|
UTSW |
2 |
31,279,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4916:Hmcn2
|
UTSW |
2 |
31,250,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R4943:Hmcn2
|
UTSW |
2 |
31,225,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Hmcn2
|
UTSW |
2 |
31,244,176 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4973:Hmcn2
|
UTSW |
2 |
31,234,108 (GRCm39) |
missense |
probably benign |
0.15 |
R4975:Hmcn2
|
UTSW |
2 |
31,283,037 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4994:Hmcn2
|
UTSW |
2 |
31,348,067 (GRCm39) |
critical splice donor site |
probably null |
|
R4997:Hmcn2
|
UTSW |
2 |
31,291,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Hmcn2
|
UTSW |
2 |
31,299,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5117:Hmcn2
|
UTSW |
2 |
31,348,061 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5151:Hmcn2
|
UTSW |
2 |
31,279,455 (GRCm39) |
missense |
probably null |
|
R5232:Hmcn2
|
UTSW |
2 |
31,347,760 (GRCm39) |
missense |
probably damaging |
0.99 |
R5237:Hmcn2
|
UTSW |
2 |
31,304,728 (GRCm39) |
missense |
probably benign |
0.01 |
R5288:Hmcn2
|
UTSW |
2 |
31,350,333 (GRCm39) |
missense |
probably benign |
0.11 |
R5375:Hmcn2
|
UTSW |
2 |
31,320,453 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5379:Hmcn2
|
UTSW |
2 |
31,299,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R5385:Hmcn2
|
UTSW |
2 |
31,350,333 (GRCm39) |
missense |
probably benign |
0.11 |
R5412:Hmcn2
|
UTSW |
2 |
31,236,629 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5426:Hmcn2
|
UTSW |
2 |
31,226,556 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5434:Hmcn2
|
UTSW |
2 |
31,310,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Hmcn2
|
UTSW |
2 |
31,296,428 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5484:Hmcn2
|
UTSW |
2 |
31,283,066 (GRCm39) |
nonsense |
probably null |
|
R5492:Hmcn2
|
UTSW |
2 |
31,310,318 (GRCm39) |
missense |
probably benign |
0.03 |
R5572:Hmcn2
|
UTSW |
2 |
31,304,538 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5572:Hmcn2
|
UTSW |
2 |
31,304,537 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5591:Hmcn2
|
UTSW |
2 |
31,234,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5614:Hmcn2
|
UTSW |
2 |
31,318,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R5634:Hmcn2
|
UTSW |
2 |
31,223,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Hmcn2
|
UTSW |
2 |
31,310,824 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5716:Hmcn2
|
UTSW |
2 |
31,348,750 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5716:Hmcn2
|
UTSW |
2 |
31,226,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5725:Hmcn2
|
UTSW |
2 |
31,273,827 (GRCm39) |
critical splice donor site |
probably null |
|
R5760:Hmcn2
|
UTSW |
2 |
31,304,580 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5774:Hmcn2
|
UTSW |
2 |
31,299,147 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5838:Hmcn2
|
UTSW |
2 |
31,347,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R5899:Hmcn2
|
UTSW |
2 |
31,244,685 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5916:Hmcn2
|
UTSW |
2 |
31,286,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Hmcn2
|
UTSW |
2 |
31,310,335 (GRCm39) |
missense |
probably damaging |
0.99 |
R6002:Hmcn2
|
UTSW |
2 |
31,310,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R6018:Hmcn2
|
UTSW |
2 |
31,260,804 (GRCm39) |
missense |
probably benign |
0.13 |
R6063:Hmcn2
|
UTSW |
2 |
31,324,725 (GRCm39) |
missense |
probably benign |
0.06 |
R6161:Hmcn2
|
UTSW |
2 |
31,246,266 (GRCm39) |
missense |
probably benign |
|
R6166:Hmcn2
|
UTSW |
2 |
31,259,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Hmcn2
|
UTSW |
2 |
31,310,118 (GRCm39) |
nonsense |
probably null |
|
R6191:Hmcn2
|
UTSW |
2 |
31,348,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R6195:Hmcn2
|
UTSW |
2 |
31,274,127 (GRCm39) |
missense |
probably damaging |
0.96 |
R6273:Hmcn2
|
UTSW |
2 |
31,301,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R6293:Hmcn2
|
UTSW |
2 |
31,225,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Hmcn2
|
UTSW |
2 |
31,278,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Hmcn2
|
UTSW |
2 |
31,259,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Hmcn2
|
UTSW |
2 |
31,310,832 (GRCm39) |
missense |
probably benign |
0.02 |
R6450:Hmcn2
|
UTSW |
2 |
31,251,812 (GRCm39) |
missense |
probably benign |
0.11 |
R6479:Hmcn2
|
UTSW |
2 |
31,315,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R6502:Hmcn2
|
UTSW |
2 |
31,272,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6511:Hmcn2
|
UTSW |
2 |
31,246,354 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6537:Hmcn2
|
UTSW |
2 |
31,305,280 (GRCm39) |
missense |
probably benign |
0.00 |
R6880:Hmcn2
|
UTSW |
2 |
31,233,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Hmcn2
|
UTSW |
2 |
31,240,517 (GRCm39) |
splice site |
probably null |
|
R6971:Hmcn2
|
UTSW |
2 |
31,322,333 (GRCm39) |
missense |
probably benign |
0.02 |
R7057:Hmcn2
|
UTSW |
2 |
31,312,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R7141:Hmcn2
|
UTSW |
2 |
31,250,908 (GRCm39) |
missense |
probably benign |
0.17 |
R7268:Hmcn2
|
UTSW |
2 |
31,347,978 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7307:Hmcn2
|
UTSW |
2 |
31,233,093 (GRCm39) |
missense |
probably damaging |
0.96 |
R7322:Hmcn2
|
UTSW |
2 |
31,349,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R7334:Hmcn2
|
UTSW |
2 |
31,343,147 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7334:Hmcn2
|
UTSW |
2 |
31,325,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R7335:Hmcn2
|
UTSW |
2 |
31,282,169 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7358:Hmcn2
|
UTSW |
2 |
31,306,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R7359:Hmcn2
|
UTSW |
2 |
31,278,395 (GRCm39) |
missense |
probably benign |
0.13 |
R7488:Hmcn2
|
UTSW |
2 |
31,310,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Hmcn2
|
UTSW |
2 |
31,273,487 (GRCm39) |
splice site |
probably null |
|
R7560:Hmcn2
|
UTSW |
2 |
31,347,185 (GRCm39) |
missense |
probably benign |
|
R7566:Hmcn2
|
UTSW |
2 |
31,344,869 (GRCm39) |
missense |
probably damaging |
0.96 |
R7570:Hmcn2
|
UTSW |
2 |
31,313,923 (GRCm39) |
missense |
probably benign |
|
R7574:Hmcn2
|
UTSW |
2 |
31,345,531 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7599:Hmcn2
|
UTSW |
2 |
31,246,298 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7654:Hmcn2
|
UTSW |
2 |
31,236,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7662:Hmcn2
|
UTSW |
2 |
31,272,357 (GRCm39) |
missense |
probably benign |
0.01 |
R7666:Hmcn2
|
UTSW |
2 |
31,270,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Hmcn2
|
UTSW |
2 |
31,313,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R7722:Hmcn2
|
UTSW |
2 |
31,272,512 (GRCm39) |
nonsense |
probably null |
|
R7739:Hmcn2
|
UTSW |
2 |
31,348,038 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7749:Hmcn2
|
UTSW |
2 |
31,343,045 (GRCm39) |
splice site |
probably null |
|
R7828:Hmcn2
|
UTSW |
2 |
31,295,887 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7912:Hmcn2
|
UTSW |
2 |
31,310,311 (GRCm39) |
missense |
probably benign |
0.00 |
R7978:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R8075:Hmcn2
|
UTSW |
2 |
31,279,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8088:Hmcn2
|
UTSW |
2 |
31,316,915 (GRCm39) |
nonsense |
probably null |
|
R8101:Hmcn2
|
UTSW |
2 |
31,240,082 (GRCm39) |
missense |
probably benign |
0.08 |
R8124:Hmcn2
|
UTSW |
2 |
31,290,136 (GRCm39) |
missense |
probably benign |
0.01 |
R8145:Hmcn2
|
UTSW |
2 |
31,313,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8230:Hmcn2
|
UTSW |
2 |
31,234,485 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8267:Hmcn2
|
UTSW |
2 |
31,349,191 (GRCm39) |
missense |
probably benign |
|
R8277:Hmcn2
|
UTSW |
2 |
31,259,189 (GRCm39) |
missense |
probably benign |
0.16 |
R8307:Hmcn2
|
UTSW |
2 |
31,286,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R8353:Hmcn2
|
UTSW |
2 |
31,275,353 (GRCm39) |
splice site |
probably null |
|
R8415:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8416:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8437:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8438:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8440:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8442:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8497:Hmcn2
|
UTSW |
2 |
31,313,357 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8520:Hmcn2
|
UTSW |
2 |
31,244,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R8530:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8537:Hmcn2
|
UTSW |
2 |
31,281,088 (GRCm39) |
missense |
probably benign |
0.15 |
R8550:Hmcn2
|
UTSW |
2 |
31,240,654 (GRCm39) |
critical splice donor site |
probably null |
|
R8721:Hmcn2
|
UTSW |
2 |
31,315,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8802:Hmcn2
|
UTSW |
2 |
31,301,288 (GRCm39) |
missense |
probably damaging |
0.97 |
R8804:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8805:Hmcn2
|
UTSW |
2 |
31,315,393 (GRCm39) |
missense |
probably benign |
0.01 |
R8904:Hmcn2
|
UTSW |
2 |
31,323,404 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8937:Hmcn2
|
UTSW |
2 |
31,204,427 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R8947:Hmcn2
|
UTSW |
2 |
31,278,220 (GRCm39) |
missense |
probably damaging |
0.99 |
R8948:Hmcn2
|
UTSW |
2 |
31,244,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Hmcn2
|
UTSW |
2 |
31,244,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8959:Hmcn2
|
UTSW |
2 |
31,282,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R9025:Hmcn2
|
UTSW |
2 |
31,347,967 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9039:Hmcn2
|
UTSW |
2 |
31,244,646 (GRCm39) |
missense |
probably damaging |
0.97 |
R9068:Hmcn2
|
UTSW |
2 |
31,303,685 (GRCm39) |
missense |
probably benign |
0.01 |
R9161:Hmcn2
|
UTSW |
2 |
31,242,758 (GRCm39) |
missense |
probably benign |
0.02 |
R9178:Hmcn2
|
UTSW |
2 |
31,281,521 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9204:Hmcn2
|
UTSW |
2 |
31,278,377 (GRCm39) |
missense |
probably damaging |
0.98 |
R9317:Hmcn2
|
UTSW |
2 |
31,350,328 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9341:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R9343:Hmcn2
|
UTSW |
2 |
31,279,359 (GRCm39) |
missense |
probably benign |
0.40 |
R9355:Hmcn2
|
UTSW |
2 |
31,328,302 (GRCm39) |
missense |
probably benign |
0.18 |
R9371:Hmcn2
|
UTSW |
2 |
31,301,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9450:Hmcn2
|
UTSW |
2 |
31,316,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Hmcn2
|
UTSW |
2 |
31,286,031 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9483:Hmcn2
|
UTSW |
2 |
31,320,375 (GRCm39) |
missense |
|
|
R9536:Hmcn2
|
UTSW |
2 |
31,335,130 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9580:Hmcn2
|
UTSW |
2 |
31,294,875 (GRCm39) |
missense |
probably benign |
0.16 |
R9593:Hmcn2
|
UTSW |
2 |
31,244,742 (GRCm39) |
missense |
probably damaging |
0.99 |
R9649:Hmcn2
|
UTSW |
2 |
31,292,450 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9706:Hmcn2
|
UTSW |
2 |
31,305,279 (GRCm39) |
missense |
probably benign |
0.00 |
X0066:Hmcn2
|
UTSW |
2 |
31,344,823 (GRCm39) |
missense |
possibly damaging |
0.83 |
X0067:Hmcn2
|
UTSW |
2 |
31,295,879 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1088:Hmcn2
|
UTSW |
2 |
31,349,076 (GRCm39) |
splice site |
probably null |
|
Z1088:Hmcn2
|
UTSW |
2 |
31,271,079 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Hmcn2
|
UTSW |
2 |
31,319,103 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Hmcn2
|
UTSW |
2 |
31,315,428 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Hmcn2
|
UTSW |
2 |
31,234,041 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Hmcn2
|
UTSW |
2 |
31,316,836 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Hmcn2
|
UTSW |
2 |
31,234,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|