Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
T |
2: 68,569,670 (GRCm39) |
D462V |
probably damaging |
Het |
Abcc1 |
T |
C |
16: 14,221,902 (GRCm39) |
W222R |
probably damaging |
Het |
Adamts13 |
A |
G |
2: 26,863,965 (GRCm39) |
K48E |
probably benign |
Het |
Adgrd1 |
A |
C |
5: 129,256,652 (GRCm39) |
T674P |
probably benign |
Het |
Agbl4 |
A |
T |
4: 110,976,150 (GRCm39) |
Y169F |
possibly damaging |
Het |
Ahnak |
T |
A |
19: 8,983,457 (GRCm39) |
N1580K |
possibly damaging |
Het |
Angptl8 |
A |
C |
9: 21,747,210 (GRCm39) |
|
probably null |
Het |
Ap3d1 |
G |
A |
10: 80,545,292 (GRCm39) |
T1053I |
probably benign |
Het |
Atad2 |
T |
C |
15: 57,990,060 (GRCm39) |
T139A |
probably benign |
Het |
Bdp1 |
T |
A |
13: 100,186,320 (GRCm39) |
T1711S |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,991,133 (GRCm39) |
I141V |
probably damaging |
Het |
Cavin2 |
A |
T |
1: 51,328,777 (GRCm39) |
N78I |
possibly damaging |
Het |
Ccnb1 |
T |
C |
13: 100,916,262 (GRCm39) |
H406R |
probably benign |
Het |
Cd200r4 |
A |
G |
16: 44,653,784 (GRCm39) |
T194A |
probably damaging |
Het |
Cdt1 |
G |
A |
8: 123,296,995 (GRCm39) |
R263H |
probably damaging |
Het |
Cep85l |
A |
T |
10: 53,157,450 (GRCm39) |
I751N |
probably damaging |
Het |
Clasp2 |
A |
G |
9: 113,737,755 (GRCm39) |
D1043G |
probably benign |
Het |
Cmip |
A |
T |
8: 118,181,691 (GRCm39) |
N578I |
probably damaging |
Het |
Col2a1 |
T |
G |
15: 97,874,065 (GRCm39) |
K1440N |
unknown |
Het |
Cpne2 |
A |
T |
8: 95,282,209 (GRCm39) |
M252L |
probably benign |
Het |
Crb2 |
A |
G |
2: 37,680,607 (GRCm39) |
T512A |
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,048,833 (GRCm39) |
Y2290H |
probably damaging |
Het |
Ctnnd1 |
A |
T |
2: 84,442,405 (GRCm39) |
D642E |
probably damaging |
Het |
Ctns |
A |
G |
11: 73,079,296 (GRCm39) |
S141P |
probably benign |
Het |
Cwh43 |
A |
G |
5: 73,591,632 (GRCm39) |
Q575R |
probably benign |
Het |
Cyp2b19 |
C |
A |
7: 26,458,489 (GRCm39) |
T68K |
probably damaging |
Het |
Dcaf6 |
A |
G |
1: 165,160,879 (GRCm39) |
S849P |
probably damaging |
Het |
Dnm3 |
T |
A |
1: 162,305,343 (GRCm39) |
Q17L |
possibly damaging |
Het |
Enpp3 |
A |
T |
10: 24,711,990 (GRCm39) |
M1K |
probably null |
Het |
Fam124a |
T |
A |
14: 62,844,008 (GRCm39) |
C505* |
probably null |
Het |
Fhip2a |
T |
A |
19: 57,367,034 (GRCm39) |
D192E |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,805,585 (GRCm39) |
I635V |
probably benign |
Het |
Gm5878 |
A |
T |
6: 85,095,682 (GRCm39) |
|
probably null |
Het |
Gpld1 |
C |
A |
13: 25,159,743 (GRCm39) |
A437D |
probably damaging |
Het |
Grk5 |
G |
T |
19: 61,071,642 (GRCm39) |
V401L |
possibly damaging |
Het |
Gucy2g |
A |
T |
19: 55,224,047 (GRCm39) |
L259Q |
probably damaging |
Het |
Habp2 |
T |
A |
19: 56,300,236 (GRCm39) |
D191E |
probably benign |
Het |
Hgsnat |
A |
G |
8: 26,461,592 (GRCm39) |
|
probably null |
Het |
Hivep1 |
T |
A |
13: 42,317,716 (GRCm39) |
V2064E |
probably damaging |
Het |
Ikbke |
C |
T |
1: 131,204,216 (GRCm39) |
A26T |
probably damaging |
Het |
Ivd |
C |
A |
2: 118,692,612 (GRCm39) |
D37E |
probably damaging |
Het |
Kif26b |
G |
A |
1: 178,358,010 (GRCm39) |
W40* |
probably null |
Het |
Klrc2 |
A |
G |
6: 129,636,274 (GRCm39) |
S114P |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,068,616 (GRCm39) |
T772S |
|
Het |
Lamc1 |
T |
A |
1: 153,118,978 (GRCm39) |
K880N |
possibly damaging |
Het |
Lmf1 |
G |
A |
17: 25,874,423 (GRCm39) |
D12N |
|
Het |
Lpin2 |
G |
T |
17: 71,538,391 (GRCm39) |
E384* |
probably null |
Het |
Lrrc23 |
T |
C |
6: 124,756,541 (GRCm39) |
|
probably benign |
Het |
Lrrc31 |
T |
C |
3: 30,745,248 (GRCm39) |
|
probably null |
Het |
Luc7l2 |
A |
G |
6: 38,528,820 (GRCm39) |
Q13R |
probably damaging |
Het |
Ly6c1 |
G |
T |
15: 74,920,346 (GRCm39) |
H5Q |
probably damaging |
Het |
Lyst |
A |
T |
13: 13,810,472 (GRCm39) |
H714L |
probably damaging |
Het |
Man2a2 |
C |
T |
7: 80,016,692 (GRCm39) |
R374H |
probably damaging |
Het |
Mchr1 |
A |
T |
15: 81,121,642 (GRCm39) |
T131S |
probably benign |
Het |
Msto1 |
T |
C |
3: 88,820,236 (GRCm39) |
|
probably null |
Het |
Myh1 |
C |
T |
11: 67,111,739 (GRCm39) |
T1698I |
probably benign |
Het |
Ncapd3 |
G |
T |
9: 26,983,144 (GRCm39) |
C964F |
probably damaging |
Het |
Nefh |
T |
C |
11: 4,891,089 (GRCm39) |
E510G |
probably damaging |
Het |
Or10g3b |
T |
C |
14: 52,587,360 (GRCm39) |
T48A |
possibly damaging |
Het |
Or13a24 |
A |
G |
7: 140,154,123 (GRCm39) |
E19G |
probably benign |
Het |
Or1b1 |
A |
T |
2: 36,995,539 (GRCm39) |
L41* |
probably null |
Het |
Or1q1 |
A |
C |
2: 36,887,092 (GRCm39) |
K90T |
probably damaging |
Het |
Or4a73 |
A |
T |
2: 89,421,095 (GRCm39) |
Y121* |
probably null |
Het |
P4ha1 |
T |
A |
10: 59,205,462 (GRCm39) |
S497R |
probably benign |
Het |
Palb2 |
T |
C |
7: 121,726,565 (GRCm39) |
D435G |
probably benign |
Het |
Papola |
C |
T |
12: 105,777,304 (GRCm39) |
P282L |
probably damaging |
Het |
Pcdhgb1 |
A |
G |
18: 37,815,377 (GRCm39) |
R623G |
probably damaging |
Het |
Pcolce |
T |
G |
5: 137,605,707 (GRCm39) |
K229Q |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,431,760 (GRCm39) |
|
probably null |
Het |
Ppp6r3 |
T |
A |
19: 3,540,790 (GRCm39) |
T443S |
probably benign |
Het |
Pramel58 |
A |
T |
5: 94,830,753 (GRCm39) |
T84S |
possibly damaging |
Het |
Psg20 |
T |
A |
7: 18,416,408 (GRCm39) |
D236V |
probably damaging |
Het |
Ptgr2 |
T |
G |
12: 84,355,179 (GRCm39) |
S304R |
probably damaging |
Het |
Ptpn22 |
A |
T |
3: 103,809,430 (GRCm39) |
D681V |
probably benign |
Het |
Rab3gap1 |
T |
C |
1: 127,858,612 (GRCm39) |
S574P |
probably benign |
Het |
Slc36a1 |
A |
G |
11: 55,104,754 (GRCm39) |
|
probably null |
Het |
Slc9a5 |
A |
G |
8: 106,089,904 (GRCm39) |
S621G |
possibly damaging |
Het |
Sntg1 |
A |
G |
1: 8,515,249 (GRCm39) |
|
probably null |
Het |
Snx17 |
A |
G |
5: 31,353,877 (GRCm39) |
N222D |
possibly damaging |
Het |
Spata19 |
G |
T |
9: 27,311,729 (GRCm39) |
S116I |
possibly damaging |
Het |
Spn |
G |
A |
7: 126,736,234 (GRCm39) |
A91V |
probably damaging |
Het |
Srrm3 |
T |
C |
5: 135,881,135 (GRCm39) |
V145A |
probably benign |
Het |
St7 |
A |
T |
6: 17,942,753 (GRCm39) |
T575S |
possibly damaging |
Het |
Taf2 |
A |
T |
15: 54,928,072 (GRCm39) |
Y110* |
probably null |
Het |
Tcf20 |
T |
C |
15: 82,739,477 (GRCm39) |
E658G |
possibly damaging |
Het |
Tdrd6 |
G |
T |
17: 43,935,129 (GRCm39) |
A1973E |
probably benign |
Het |
Tg |
T |
G |
15: 66,636,267 (GRCm39) |
L2237W |
probably damaging |
Het |
Ticrr |
C |
A |
7: 79,346,487 (GRCm39) |
Y1882* |
probably null |
Het |
Trim45 |
T |
A |
3: 100,832,339 (GRCm39) |
C191S |
probably damaging |
Het |
Upf3a |
G |
A |
8: 13,835,889 (GRCm39) |
|
probably null |
Het |
Vmn2r42 |
A |
T |
7: 8,197,740 (GRCm39) |
L293* |
probably null |
Het |
Vmn2r62 |
T |
A |
7: 42,437,466 (GRCm39) |
Q339H |
possibly damaging |
Het |
Wdr24 |
A |
T |
17: 26,044,804 (GRCm39) |
R220W |
probably null |
Het |
Wdr5 |
T |
A |
2: 27,408,787 (GRCm39) |
S22T |
probably benign |
Het |
Zfp37 |
G |
A |
4: 62,110,253 (GRCm39) |
|
probably benign |
Het |
Zfp735 |
A |
T |
11: 73,601,933 (GRCm39) |
L292F |
possibly damaging |
Het |
Zfp985 |
T |
A |
4: 147,667,946 (GRCm39) |
C271* |
probably null |
Het |
Zranb1 |
G |
A |
7: 132,585,625 (GRCm39) |
R691Q |
probably benign |
Het |
|
Other mutations in Helz2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Helz2
|
APN |
2 |
180,871,495 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00515:Helz2
|
APN |
2 |
180,874,799 (GRCm39) |
nonsense |
probably null |
|
IGL00704:Helz2
|
APN |
2 |
180,876,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00847:Helz2
|
APN |
2 |
180,874,038 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01448:Helz2
|
APN |
2 |
180,875,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01783:Helz2
|
APN |
2 |
180,874,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01790:Helz2
|
APN |
2 |
180,880,274 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02116:Helz2
|
APN |
2 |
180,873,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02226:Helz2
|
APN |
2 |
180,873,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02402:Helz2
|
APN |
2 |
180,872,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02403:Helz2
|
APN |
2 |
180,872,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Helz2
|
APN |
2 |
180,876,819 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02869:Helz2
|
APN |
2 |
180,872,939 (GRCm39) |
intron |
probably benign |
|
IGL03003:Helz2
|
APN |
2 |
180,882,046 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03060:Helz2
|
APN |
2 |
180,871,015 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03310:Helz2
|
APN |
2 |
180,873,597 (GRCm39) |
missense |
probably benign |
0.00 |
Colby
|
UTSW |
2 |
180,874,995 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU74:Helz2
|
UTSW |
2 |
180,876,627 (GRCm39) |
missense |
probably benign |
0.03 |
R0013:Helz2
|
UTSW |
2 |
180,882,752 (GRCm39) |
missense |
probably benign |
|
R0013:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Helz2
|
UTSW |
2 |
180,882,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Helz2
|
UTSW |
2 |
180,882,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0018:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Helz2
|
UTSW |
2 |
180,870,614 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0055:Helz2
|
UTSW |
2 |
180,870,614 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0071:Helz2
|
UTSW |
2 |
180,878,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0071:Helz2
|
UTSW |
2 |
180,878,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Helz2
|
UTSW |
2 |
180,879,595 (GRCm39) |
missense |
probably benign |
0.30 |
R0117:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:Helz2
|
UTSW |
2 |
180,874,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Helz2
|
UTSW |
2 |
180,872,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Helz2
|
UTSW |
2 |
180,872,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Helz2
|
UTSW |
2 |
180,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Helz2
|
UTSW |
2 |
180,872,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Helz2
|
UTSW |
2 |
180,874,002 (GRCm39) |
missense |
probably damaging |
0.97 |
R0497:Helz2
|
UTSW |
2 |
180,871,449 (GRCm39) |
missense |
probably damaging |
0.97 |
R0517:Helz2
|
UTSW |
2 |
180,869,563 (GRCm39) |
missense |
probably benign |
0.00 |
R0541:Helz2
|
UTSW |
2 |
180,876,618 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0542:Helz2
|
UTSW |
2 |
180,873,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Helz2
|
UTSW |
2 |
180,873,909 (GRCm39) |
missense |
probably damaging |
0.96 |
R0692:Helz2
|
UTSW |
2 |
180,882,674 (GRCm39) |
missense |
probably benign |
|
R0826:Helz2
|
UTSW |
2 |
180,882,646 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0834:Helz2
|
UTSW |
2 |
180,872,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R0880:Helz2
|
UTSW |
2 |
180,877,928 (GRCm39) |
missense |
probably benign |
|
R1170:Helz2
|
UTSW |
2 |
180,871,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Helz2
|
UTSW |
2 |
180,872,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R1344:Helz2
|
UTSW |
2 |
180,879,389 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1358:Helz2
|
UTSW |
2 |
180,874,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Helz2
|
UTSW |
2 |
180,877,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R1464:Helz2
|
UTSW |
2 |
180,881,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Helz2
|
UTSW |
2 |
180,881,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Helz2
|
UTSW |
2 |
180,878,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Helz2
|
UTSW |
2 |
180,878,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1477:Helz2
|
UTSW |
2 |
180,874,597 (GRCm39) |
missense |
probably benign |
0.00 |
R1564:Helz2
|
UTSW |
2 |
180,875,021 (GRCm39) |
missense |
probably benign |
0.01 |
R1584:Helz2
|
UTSW |
2 |
180,878,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Helz2
|
UTSW |
2 |
180,875,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R1757:Helz2
|
UTSW |
2 |
180,878,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Helz2
|
UTSW |
2 |
180,880,252 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1779:Helz2
|
UTSW |
2 |
180,876,780 (GRCm39) |
missense |
probably benign |
|
R1837:Helz2
|
UTSW |
2 |
180,871,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R1845:Helz2
|
UTSW |
2 |
180,873,878 (GRCm39) |
missense |
probably benign |
0.02 |
R1894:Helz2
|
UTSW |
2 |
180,876,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Helz2
|
UTSW |
2 |
180,875,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Helz2
|
UTSW |
2 |
180,873,122 (GRCm39) |
missense |
probably benign |
0.45 |
R2034:Helz2
|
UTSW |
2 |
180,874,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Helz2
|
UTSW |
2 |
180,879,272 (GRCm39) |
missense |
probably benign |
0.03 |
R2061:Helz2
|
UTSW |
2 |
180,882,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R2088:Helz2
|
UTSW |
2 |
180,876,895 (GRCm39) |
missense |
probably benign |
0.07 |
R2142:Helz2
|
UTSW |
2 |
180,873,173 (GRCm39) |
missense |
probably benign |
|
R2180:Helz2
|
UTSW |
2 |
180,875,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Helz2
|
UTSW |
2 |
180,870,841 (GRCm39) |
nonsense |
probably null |
|
R2248:Helz2
|
UTSW |
2 |
180,875,226 (GRCm39) |
missense |
probably benign |
0.33 |
R2495:Helz2
|
UTSW |
2 |
180,874,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R2886:Helz2
|
UTSW |
2 |
180,882,535 (GRCm39) |
missense |
probably benign |
|
R3617:Helz2
|
UTSW |
2 |
180,874,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R3776:Helz2
|
UTSW |
2 |
180,882,182 (GRCm39) |
nonsense |
probably null |
|
R3803:Helz2
|
UTSW |
2 |
180,881,789 (GRCm39) |
missense |
probably damaging |
0.96 |
R4043:Helz2
|
UTSW |
2 |
180,871,503 (GRCm39) |
missense |
probably benign |
0.00 |
R4052:Helz2
|
UTSW |
2 |
180,882,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Helz2
|
UTSW |
2 |
180,871,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4521:Helz2
|
UTSW |
2 |
180,870,626 (GRCm39) |
missense |
probably benign |
|
R4624:Helz2
|
UTSW |
2 |
180,881,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R4720:Helz2
|
UTSW |
2 |
180,880,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4831:Helz2
|
UTSW |
2 |
180,879,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R4852:Helz2
|
UTSW |
2 |
180,871,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R4894:Helz2
|
UTSW |
2 |
180,877,940 (GRCm39) |
missense |
probably benign |
0.01 |
R4915:Helz2
|
UTSW |
2 |
180,874,231 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4965:Helz2
|
UTSW |
2 |
180,882,709 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5022:Helz2
|
UTSW |
2 |
180,882,362 (GRCm39) |
missense |
probably benign |
|
R5089:Helz2
|
UTSW |
2 |
180,876,942 (GRCm39) |
missense |
probably benign |
0.14 |
R5190:Helz2
|
UTSW |
2 |
180,872,550 (GRCm39) |
critical splice donor site |
probably null |
|
R5309:Helz2
|
UTSW |
2 |
180,876,639 (GRCm39) |
missense |
probably benign |
0.08 |
R5358:Helz2
|
UTSW |
2 |
180,877,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R5379:Helz2
|
UTSW |
2 |
180,876,862 (GRCm39) |
missense |
probably benign |
|
R5559:Helz2
|
UTSW |
2 |
180,871,919 (GRCm39) |
missense |
probably damaging |
0.98 |
R5591:Helz2
|
UTSW |
2 |
180,882,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R5596:Helz2
|
UTSW |
2 |
180,879,082 (GRCm39) |
intron |
probably benign |
|
R5805:Helz2
|
UTSW |
2 |
180,882,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5823:Helz2
|
UTSW |
2 |
180,878,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5825:Helz2
|
UTSW |
2 |
180,874,449 (GRCm39) |
missense |
probably benign |
0.02 |
R5873:Helz2
|
UTSW |
2 |
180,875,821 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5928:Helz2
|
UTSW |
2 |
180,872,177 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5936:Helz2
|
UTSW |
2 |
180,872,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R5975:Helz2
|
UTSW |
2 |
180,872,843 (GRCm39) |
missense |
probably benign |
0.08 |
R6045:Helz2
|
UTSW |
2 |
180,882,106 (GRCm39) |
missense |
probably benign |
0.03 |
R6077:Helz2
|
UTSW |
2 |
180,874,831 (GRCm39) |
missense |
probably benign |
0.41 |
R6218:Helz2
|
UTSW |
2 |
180,874,087 (GRCm39) |
missense |
probably benign |
0.03 |
R6218:Helz2
|
UTSW |
2 |
180,877,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6315:Helz2
|
UTSW |
2 |
180,874,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R6346:Helz2
|
UTSW |
2 |
180,875,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6371:Helz2
|
UTSW |
2 |
180,875,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Helz2
|
UTSW |
2 |
180,875,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6373:Helz2
|
UTSW |
2 |
180,875,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Helz2
|
UTSW |
2 |
180,875,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R6464:Helz2
|
UTSW |
2 |
180,876,862 (GRCm39) |
missense |
probably benign |
|
R6581:Helz2
|
UTSW |
2 |
180,871,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R6651:Helz2
|
UTSW |
2 |
180,881,350 (GRCm39) |
nonsense |
probably null |
|
R6964:Helz2
|
UTSW |
2 |
180,872,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Helz2
|
UTSW |
2 |
180,882,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R7153:Helz2
|
UTSW |
2 |
180,873,078 (GRCm39) |
missense |
probably benign |
0.00 |
R7372:Helz2
|
UTSW |
2 |
180,880,216 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7512:Helz2
|
UTSW |
2 |
180,877,393 (GRCm39) |
splice site |
probably null |
|
R7512:Helz2
|
UTSW |
2 |
180,872,647 (GRCm39) |
missense |
probably benign |
0.00 |
R7724:Helz2
|
UTSW |
2 |
180,873,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7733:Helz2
|
UTSW |
2 |
180,872,148 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7748:Helz2
|
UTSW |
2 |
180,876,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7774:Helz2
|
UTSW |
2 |
180,875,784 (GRCm39) |
missense |
probably benign |
|
R7799:Helz2
|
UTSW |
2 |
180,879,782 (GRCm39) |
missense |
probably benign |
0.15 |
R7841:Helz2
|
UTSW |
2 |
180,874,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R7939:Helz2
|
UTSW |
2 |
180,879,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R8026:Helz2
|
UTSW |
2 |
180,881,998 (GRCm39) |
missense |
probably benign |
0.34 |
R8030:Helz2
|
UTSW |
2 |
180,879,689 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8080:Helz2
|
UTSW |
2 |
180,880,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R8237:Helz2
|
UTSW |
2 |
180,871,124 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8245:Helz2
|
UTSW |
2 |
180,879,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Helz2
|
UTSW |
2 |
180,871,950 (GRCm39) |
missense |
probably benign |
0.03 |
R8486:Helz2
|
UTSW |
2 |
180,871,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R8556:Helz2
|
UTSW |
2 |
180,871,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R8878:Helz2
|
UTSW |
2 |
180,874,560 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8907:Helz2
|
UTSW |
2 |
180,874,920 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8911:Helz2
|
UTSW |
2 |
180,880,173 (GRCm39) |
missense |
|
|
R8953:Helz2
|
UTSW |
2 |
180,874,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Helz2
|
UTSW |
2 |
180,871,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R8969:Helz2
|
UTSW |
2 |
180,879,581 (GRCm39) |
missense |
probably benign |
0.19 |
R8976:Helz2
|
UTSW |
2 |
180,876,486 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9015:Helz2
|
UTSW |
2 |
180,870,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Helz2
|
UTSW |
2 |
180,874,261 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9052:Helz2
|
UTSW |
2 |
180,881,968 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9089:Helz2
|
UTSW |
2 |
180,881,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R9145:Helz2
|
UTSW |
2 |
180,881,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Helz2
|
UTSW |
2 |
180,871,883 (GRCm39) |
missense |
probably benign |
|
R9186:Helz2
|
UTSW |
2 |
180,876,457 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9373:Helz2
|
UTSW |
2 |
180,882,741 (GRCm39) |
missense |
probably benign |
|
R9407:Helz2
|
UTSW |
2 |
180,881,975 (GRCm39) |
missense |
probably benign |
0.01 |
R9465:Helz2
|
UTSW |
2 |
180,874,710 (GRCm39) |
missense |
probably benign |
0.01 |
R9502:Helz2
|
UTSW |
2 |
180,878,245 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9538:Helz2
|
UTSW |
2 |
180,882,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9554:Helz2
|
UTSW |
2 |
180,882,470 (GRCm39) |
missense |
probably damaging |
0.96 |
R9659:Helz2
|
UTSW |
2 |
180,882,025 (GRCm39) |
missense |
probably benign |
0.00 |
R9800:Helz2
|
UTSW |
2 |
180,882,616 (GRCm39) |
missense |
probably damaging |
0.99 |
X0064:Helz2
|
UTSW |
2 |
180,873,534 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Helz2
|
UTSW |
2 |
180,879,357 (GRCm39) |
missense |
probably benign |
0.39 |
Z1177:Helz2
|
UTSW |
2 |
180,877,754 (GRCm39) |
missense |
probably damaging |
1.00 |
|