Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700016H13Rik |
T |
C |
5: 103,802,806 (GRCm39) |
K16R |
possibly damaging |
Het |
2810408A11Rik |
A |
G |
11: 69,790,112 (GRCm39) |
F210L |
probably benign |
Het |
Adam6a |
G |
T |
12: 113,509,078 (GRCm39) |
D484Y |
probably damaging |
Het |
B9d1 |
A |
G |
11: 61,397,192 (GRCm39) |
Y29C |
possibly damaging |
Het |
Cald1 |
T |
C |
6: 34,722,696 (GRCm39) |
F115L |
unknown |
Het |
Ccnd1 |
A |
T |
7: 144,491,718 (GRCm39) |
M107K |
probably damaging |
Het |
Ccnh |
G |
A |
13: 85,337,712 (GRCm39) |
A20T |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,126,369 (GRCm39) |
D181G |
probably benign |
Het |
Cep44 |
AACGC |
A |
8: 56,994,018 (GRCm39) |
|
probably null |
Het |
Ces2b |
A |
G |
8: 105,561,692 (GRCm39) |
D262G |
probably benign |
Het |
Cic |
A |
G |
7: 24,985,192 (GRCm39) |
Y1146C |
probably damaging |
Het |
Cmtm1 |
G |
A |
8: 105,036,108 (GRCm39) |
R174C |
possibly damaging |
Het |
Cobl |
G |
T |
11: 12,203,324 (GRCm39) |
P1126H |
probably damaging |
Het |
Col14a1 |
T |
A |
15: 55,245,876 (GRCm39) |
M460K |
unknown |
Het |
Cst11 |
G |
A |
2: 148,613,227 (GRCm39) |
R33W |
possibly damaging |
Het |
Cyp19a1 |
A |
T |
9: 54,079,089 (GRCm39) |
V340E |
probably benign |
Het |
Dbt |
A |
T |
3: 116,339,746 (GRCm39) |
Q378L |
possibly damaging |
Het |
Dchs1 |
A |
G |
7: 105,412,180 (GRCm39) |
V1312A |
probably benign |
Het |
Eif3l |
T |
C |
15: 78,973,779 (GRCm39) |
M398T |
probably benign |
Het |
Faxc |
A |
G |
4: 21,958,584 (GRCm39) |
H247R |
probably benign |
Het |
Fbxl17 |
T |
C |
17: 63,794,820 (GRCm39) |
R421G |
probably damaging |
Het |
Fbxo3 |
T |
A |
2: 103,890,337 (GRCm39) |
D450E |
unknown |
Het |
Fmn1 |
T |
C |
2: 113,359,810 (GRCm39) |
|
probably null |
Het |
Foxs1 |
T |
A |
2: 152,774,907 (GRCm39) |
M49L |
possibly damaging |
Het |
Gucy1a2 |
A |
G |
9: 3,634,766 (GRCm39) |
E270G |
probably benign |
Het |
Hspa4 |
G |
A |
11: 53,157,887 (GRCm39) |
A572V |
possibly damaging |
Het |
Ica1 |
T |
A |
6: 8,737,072 (GRCm39) |
D174V |
probably damaging |
Het |
Igfbp6 |
A |
T |
15: 102,056,352 (GRCm39) |
Q137L |
possibly damaging |
Het |
Il1r2 |
T |
C |
1: 40,144,628 (GRCm39) |
L105P |
probably damaging |
Het |
Iqca1 |
A |
T |
1: 89,987,337 (GRCm39) |
C72S |
|
Het |
Itgbl1 |
T |
C |
14: 124,209,645 (GRCm39) |
|
probably null |
Het |
Ivl |
T |
A |
3: 92,479,699 (GRCm39) |
Q122L |
possibly damaging |
Het |
Kdsr |
T |
C |
1: 106,671,415 (GRCm39) |
E198G |
probably damaging |
Het |
Lama2 |
T |
C |
10: 27,031,529 (GRCm39) |
T1510A |
probably benign |
Het |
Lrrc37a |
A |
T |
11: 103,391,931 (GRCm39) |
Y1165N |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,384,267 (GRCm39) |
|
probably null |
Het |
Myh3 |
A |
G |
11: 66,989,518 (GRCm39) |
E1546G |
probably damaging |
Het |
Nacad |
A |
T |
11: 6,551,031 (GRCm39) |
V720E |
probably benign |
Het |
Napa |
A |
G |
7: 15,849,559 (GRCm39) |
D257G |
possibly damaging |
Het |
Nif3l1 |
T |
C |
1: 58,487,042 (GRCm39) |
V76A |
probably damaging |
Het |
Nkapd1 |
A |
C |
9: 50,521,716 (GRCm39) |
S68R |
probably damaging |
Het |
Nphp4 |
G |
A |
4: 152,581,140 (GRCm39) |
S108N |
probably benign |
Het |
Npr1 |
A |
T |
3: 90,362,175 (GRCm39) |
L990H |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,224,372 (GRCm39) |
R322G |
unknown |
Het |
Or4a79 |
C |
A |
2: 89,552,309 (GRCm39) |
A49S |
probably benign |
Het |
Or4q3 |
G |
T |
14: 50,583,285 (GRCm39) |
Q174K |
probably benign |
Het |
Or52n2c |
T |
A |
7: 104,574,066 (GRCm39) |
I302F |
possibly damaging |
Het |
Or8c14-ps1 |
T |
G |
9: 38,101,777 (GRCm39) |
M252R |
unknown |
Het |
Or8c19-ps1 |
T |
A |
9: 38,220,817 (GRCm39) |
V242E |
unknown |
Het |
Ovch2 |
G |
T |
7: 107,393,298 (GRCm39) |
Q192K |
probably benign |
Het |
Pcca |
T |
A |
14: 122,800,384 (GRCm39) |
D91E |
probably benign |
Het |
Pole2 |
T |
C |
12: 69,251,032 (GRCm39) |
T444A |
probably damaging |
Het |
Ppip5k1 |
T |
C |
2: 121,173,276 (GRCm39) |
K466E |
probably benign |
Het |
Prr35 |
A |
T |
17: 26,167,458 (GRCm39) |
Y26* |
probably null |
Het |
Ptgfrn |
A |
T |
3: 100,968,126 (GRCm39) |
I489N |
probably damaging |
Het |
Rassf1 |
A |
G |
9: 107,438,744 (GRCm39) |
*341W |
probably null |
Het |
Ret |
G |
A |
6: 118,132,321 (GRCm39) |
P1040S |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rsf1 |
A |
AAGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
Slc6a17 |
A |
T |
3: 107,384,214 (GRCm39) |
Y377N |
possibly damaging |
Het |
Snrnp200 |
C |
A |
2: 127,078,754 (GRCm39) |
D1806E |
probably benign |
Het |
Synj2 |
G |
A |
17: 6,094,419 (GRCm39) |
R1215H |
unknown |
Het |
Tbc1d5 |
TTGCTGCTGGTGTTGCTGCTGCTGCTGCTG |
TTGCTGCTG |
17: 51,106,950 (GRCm39) |
|
probably benign |
Het |
Top2a |
A |
T |
11: 98,913,176 (GRCm39) |
D85E |
probably damaging |
Het |
Tram1l1 |
A |
T |
3: 124,115,353 (GRCm39) |
Q171L |
probably damaging |
Het |
Tram1l1 |
G |
T |
3: 124,115,354 (GRCm39) |
Q171H |
probably damaging |
Het |
Tspyl4 |
A |
G |
10: 34,174,267 (GRCm39) |
H253R |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,662,490 (GRCm39) |
I23V |
|
Het |
Ubr5 |
T |
C |
15: 37,981,150 (GRCm39) |
N2376D |
|
Het |
Ugt2b37 |
T |
C |
5: 87,398,489 (GRCm39) |
N316D |
probably benign |
Het |
Usp31 |
A |
C |
7: 121,247,679 (GRCm39) |
S1255A |
probably benign |
Het |
Usp31 |
A |
T |
7: 121,276,535 (GRCm39) |
V334E |
probably damaging |
Het |
Vmn2r108 |
A |
G |
17: 20,690,305 (GRCm39) |
|
probably null |
Het |
Vmn2r87 |
T |
A |
10: 130,333,095 (GRCm39) |
T52S |
probably benign |
Het |
Vrk2 |
C |
A |
11: 26,421,457 (GRCm39) |
L500F |
probably damaging |
Het |
Zan |
T |
A |
5: 137,435,064 (GRCm39) |
I2110F |
unknown |
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 |
R7583:Helz2
|
UTSW |
2 |
180,879,365 (GRCm39) |
missense |
probably benign |
0.06 |
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 |
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 |
|