Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
A |
4: 88,786,480 (GRCm39) |
D46V |
unknown |
Het |
Abcb9 |
A |
G |
5: 124,215,358 (GRCm39) |
V461A |
probably damaging |
Het |
Ackr4 |
T |
A |
9: 103,976,679 (GRCm39) |
L89F |
probably benign |
Het |
Acsf2 |
T |
C |
11: 94,452,196 (GRCm39) |
T449A |
probably benign |
Het |
Acsl4 |
C |
G |
X: 141,116,714 (GRCm39) |
G489R |
probably damaging |
Het |
Actl6a |
T |
A |
3: 32,779,469 (GRCm39) |
I399N |
probably damaging |
Het |
Adamts19 |
G |
A |
18: 59,144,220 (GRCm39) |
C934Y |
probably null |
Het |
Adsl |
A |
G |
15: 80,845,561 (GRCm39) |
E40G |
possibly damaging |
Het |
Alppl2 |
T |
G |
1: 87,016,465 (GRCm39) |
D203A |
probably damaging |
Het |
Asb10 |
C |
A |
5: 24,742,930 (GRCm39) |
A268S |
probably benign |
Het |
Atp9a |
T |
C |
2: 168,485,805 (GRCm39) |
S832G |
probably benign |
Het |
Bckdha |
A |
T |
7: 25,330,875 (GRCm39) |
I297N |
probably damaging |
Het |
Blm |
G |
A |
7: 80,114,694 (GRCm39) |
|
probably benign |
Het |
C9orf72 |
T |
A |
4: 35,197,207 (GRCm39) |
D122V |
probably damaging |
Het |
Cacna1h |
A |
G |
17: 25,599,898 (GRCm39) |
|
probably benign |
Het |
Camsap2 |
G |
A |
1: 136,220,686 (GRCm39) |
Q298* |
probably null |
Het |
Ccdc38 |
A |
T |
10: 93,401,774 (GRCm39) |
K145* |
probably null |
Het |
Cfap45 |
C |
T |
1: 172,368,894 (GRCm39) |
T434M |
probably benign |
Het |
Cfap54 |
A |
T |
10: 92,870,524 (GRCm39) |
|
probably benign |
Het |
Clcn6 |
G |
A |
4: 148,097,213 (GRCm39) |
P618L |
probably damaging |
Het |
Copg1 |
T |
C |
6: 87,881,179 (GRCm39) |
|
probably benign |
Het |
Dctd |
T |
A |
8: 48,565,113 (GRCm39) |
N79K |
probably benign |
Het |
Dgkq |
A |
G |
5: 108,802,510 (GRCm39) |
|
probably benign |
Het |
Dntt |
A |
T |
19: 41,027,409 (GRCm39) |
T159S |
possibly damaging |
Het |
Doc2g |
G |
A |
19: 4,053,656 (GRCm39) |
R29Q |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,673,199 (GRCm39) |
T957A |
probably damaging |
Het |
Eif3c |
T |
A |
7: 126,157,795 (GRCm39) |
|
probably benign |
Het |
Ephb3 |
T |
A |
16: 21,036,859 (GRCm39) |
D107E |
probably benign |
Het |
Esrrb |
A |
T |
12: 86,517,255 (GRCm39) |
D108V |
probably damaging |
Het |
Exo1 |
A |
G |
1: 175,719,596 (GRCm39) |
K214E |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,839,644 (GRCm39) |
T2200I |
possibly damaging |
Het |
Fam227a |
C |
T |
15: 79,524,870 (GRCm39) |
W194* |
probably null |
Het |
Foxn4 |
A |
G |
5: 114,397,809 (GRCm39) |
|
probably null |
Het |
Gabbr2 |
T |
C |
4: 46,787,565 (GRCm39) |
K366R |
possibly damaging |
Het |
Garem2 |
T |
A |
5: 30,318,928 (GRCm39) |
V130E |
probably damaging |
Het |
Grin2b |
A |
G |
6: 135,756,303 (GRCm39) |
F474S |
probably damaging |
Het |
H2-M10.6 |
G |
T |
17: 37,124,934 (GRCm39) |
V284F |
probably damaging |
Het |
Hivep1 |
G |
T |
13: 42,308,911 (GRCm39) |
V384F |
probably damaging |
Het |
Hmox1 |
A |
G |
8: 75,823,736 (GRCm39) |
T135A |
probably damaging |
Het |
Hpse |
T |
C |
5: 100,867,378 (GRCm39) |
D28G |
probably benign |
Het |
Itm2b |
G |
T |
14: 73,602,058 (GRCm39) |
D213E |
probably benign |
Het |
Jakmip1 |
T |
A |
5: 37,291,627 (GRCm39) |
M692K |
possibly damaging |
Het |
Kdm3a |
T |
C |
6: 71,601,578 (GRCm39) |
Q151R |
probably null |
Het |
Limch1 |
C |
A |
5: 67,156,616 (GRCm39) |
A517E |
probably benign |
Het |
Lrit1 |
T |
A |
14: 36,783,677 (GRCm39) |
L335Q |
probably damaging |
Het |
Lrrc37a |
A |
G |
11: 103,390,616 (GRCm39) |
V1603A |
possibly damaging |
Het |
Mbtps1 |
T |
A |
8: 120,262,108 (GRCm39) |
N347I |
probably damaging |
Het |
Mier1 |
A |
T |
4: 102,996,716 (GRCm39) |
|
probably null |
Het |
Mt2 |
A |
T |
8: 94,899,476 (GRCm39) |
M1L |
probably damaging |
Het |
Mug1 |
A |
T |
6: 121,817,066 (GRCm39) |
E45V |
probably damaging |
Het |
Mybphl |
A |
G |
3: 108,281,484 (GRCm39) |
K67E |
probably benign |
Het |
Myh4 |
A |
G |
11: 67,143,162 (GRCm39) |
K1030R |
probably damaging |
Het |
Myl3 |
T |
A |
9: 110,598,189 (GRCm39) |
D176E |
probably benign |
Het |
Ncapg2 |
A |
G |
12: 116,384,303 (GRCm39) |
|
probably null |
Het |
Ndor1 |
T |
C |
2: 25,138,718 (GRCm39) |
|
probably null |
Het |
Nedd4 |
T |
G |
9: 72,577,335 (GRCm39) |
N53K |
possibly damaging |
Het |
Nek11 |
C |
A |
9: 105,270,151 (GRCm39) |
A24S |
probably benign |
Het |
Nudt19 |
G |
T |
7: 35,250,939 (GRCm39) |
P267T |
probably benign |
Het |
Olfml2b |
T |
C |
1: 170,508,684 (GRCm39) |
M514T |
possibly damaging |
Het |
Or14a258 |
A |
T |
7: 86,035,582 (GRCm39) |
C95* |
probably null |
Het |
Or2ag17 |
C |
A |
7: 106,390,030 (GRCm39) |
M59I |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,406 (GRCm39) |
D93G |
probably benign |
Het |
Or6k4 |
A |
T |
1: 173,964,327 (GRCm39) |
T6S |
probably benign |
Het |
P3h1 |
T |
A |
4: 119,095,149 (GRCm39) |
F302Y |
probably damaging |
Het |
Pappa2 |
T |
A |
1: 158,592,671 (GRCm39) |
|
probably benign |
Het |
Pex2 |
A |
C |
3: 5,626,424 (GRCm39) |
H128Q |
probably benign |
Het |
Phf11d |
A |
C |
14: 59,590,180 (GRCm39) |
L214R |
probably damaging |
Het |
Plcg2 |
G |
A |
8: 118,300,136 (GRCm39) |
|
probably benign |
Het |
Ppargc1b |
A |
C |
18: 61,441,016 (GRCm39) |
L634R |
possibly damaging |
Het |
Prune1 |
A |
T |
3: 95,169,671 (GRCm39) |
I177N |
probably damaging |
Het |
Puf60 |
T |
C |
15: 75,942,334 (GRCm39) |
D496G |
probably damaging |
Het |
Rasl11b |
A |
G |
5: 74,356,824 (GRCm39) |
|
probably null |
Het |
Sdr42e1 |
A |
T |
8: 118,389,848 (GRCm39) |
F264L |
probably damaging |
Het |
Sec24b |
A |
T |
3: 129,777,814 (GRCm39) |
|
probably null |
Het |
Sgta |
G |
T |
10: 80,886,893 (GRCm39) |
P79T |
probably benign |
Het |
Shisa9 |
C |
T |
16: 11,802,818 (GRCm39) |
T125M |
probably damaging |
Het |
Shoc1 |
T |
A |
4: 59,066,534 (GRCm39) |
|
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,063,283 (GRCm39) |
D921G |
probably damaging |
Het |
Slc13a5 |
C |
T |
11: 72,136,059 (GRCm39) |
V494I |
probably benign |
Het |
Slc13a5 |
T |
A |
11: 72,152,956 (GRCm39) |
I42L |
possibly damaging |
Het |
Spire2 |
G |
A |
8: 124,089,750 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
G |
A |
7: 27,104,336 (GRCm39) |
R962C |
probably benign |
Het |
St8sia5 |
G |
A |
18: 77,342,420 (GRCm39) |
V377I |
probably benign |
Het |
Stag2 |
T |
G |
X: 41,295,014 (GRCm39) |
|
probably benign |
Het |
Syne1 |
C |
A |
10: 5,374,311 (GRCm39) |
M165I |
probably benign |
Het |
Synm |
C |
A |
7: 67,384,672 (GRCm39) |
V997L |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,392 (GRCm39) |
S279P |
probably benign |
Het |
Tbc1d10a |
T |
C |
11: 4,162,901 (GRCm39) |
|
probably null |
Het |
Tbc1d19 |
A |
G |
5: 54,017,498 (GRCm39) |
T302A |
probably damaging |
Het |
Tecpr1 |
A |
C |
5: 144,155,335 (GRCm39) |
N74K |
probably damaging |
Het |
Tmem120a |
T |
C |
5: 135,771,252 (GRCm39) |
E28G |
possibly damaging |
Het |
Tnfrsf1b |
A |
T |
4: 144,951,382 (GRCm39) |
I186N |
probably benign |
Het |
Trim55 |
A |
G |
3: 19,716,025 (GRCm39) |
D195G |
probably benign |
Het |
Trpm3 |
G |
T |
19: 22,692,720 (GRCm39) |
|
probably null |
Het |
Ttc39a |
T |
A |
4: 109,301,376 (GRCm39) |
S571T |
probably benign |
Het |
Vwf |
T |
G |
6: 125,620,260 (GRCm39) |
I1646S |
probably benign |
Het |
Wbp2nl |
T |
C |
15: 82,198,483 (GRCm39) |
F340S |
possibly damaging |
Het |
Yeats2 |
T |
C |
16: 19,971,719 (GRCm39) |
M1T |
probably null |
Het |
Zfp236 |
T |
A |
18: 82,675,112 (GRCm39) |
E460V |
probably damaging |
Het |
Zfp277 |
G |
A |
12: 40,428,876 (GRCm39) |
|
probably benign |
Het |
Zfp975 |
T |
A |
7: 42,311,916 (GRCm39) |
K232N |
probably benign |
Het |
Zxdc |
T |
C |
6: 90,349,519 (GRCm39) |
|
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 |
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 |
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 |
|