Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059E24Rik |
C |
T |
19: 21,630,075 (GRCm39) |
|
probably benign |
Het |
Abcd4 |
C |
T |
12: 84,655,356 (GRCm39) |
W369* |
probably null |
Het |
Abcf3 |
A |
G |
16: 20,368,056 (GRCm39) |
E98G |
probably benign |
Het |
Acaca |
A |
T |
11: 84,262,410 (GRCm39) |
D2004V |
probably damaging |
Het |
Acot5 |
G |
C |
12: 84,116,630 (GRCm39) |
M130I |
|
Het |
Adamts3 |
C |
T |
5: 89,825,693 (GRCm39) |
E1049K |
probably benign |
Het |
Agfg2 |
A |
T |
5: 137,650,744 (GRCm39) |
L456Q |
probably damaging |
Het |
Agtr1b |
T |
A |
3: 20,370,343 (GRCm39) |
T88S |
possibly damaging |
Het |
Amer2 |
G |
C |
14: 60,617,376 (GRCm39) |
D524H |
probably damaging |
Het |
Ankrd61 |
T |
A |
5: 143,831,676 (GRCm39) |
T43S |
probably benign |
Het |
Apcs |
A |
G |
1: 172,721,776 (GRCm39) |
L190P |
probably benign |
Het |
Arsg |
A |
G |
11: 109,381,346 (GRCm39) |
K30E |
probably benign |
Het |
Banp |
A |
T |
8: 122,705,441 (GRCm39) |
M104L |
possibly damaging |
Het |
Caskin1 |
A |
G |
17: 24,718,111 (GRCm39) |
Q268R |
probably benign |
Het |
Ccdc112 |
A |
G |
18: 46,429,455 (GRCm39) |
V81A |
probably damaging |
Het |
Cfap44 |
T |
C |
16: 44,280,517 (GRCm39) |
I1432T |
probably damaging |
Het |
Chd2 |
A |
T |
7: 73,134,294 (GRCm39) |
N684K |
probably damaging |
Het |
Creb1 |
T |
C |
1: 64,605,478 (GRCm39) |
|
probably null |
Het |
Ctsc |
C |
T |
7: 87,927,502 (GRCm39) |
T31I |
probably damaging |
Het |
Cttnbp2 |
C |
A |
6: 18,434,430 (GRCm39) |
R476L |
probably damaging |
Het |
Cwf19l1 |
T |
C |
19: 44,111,653 (GRCm39) |
D260G |
possibly damaging |
Het |
Cyp24a1 |
A |
T |
2: 170,336,005 (GRCm39) |
S211T |
probably damaging |
Het |
Ddx3y |
T |
C |
Y: 1,282,919 (GRCm39) |
N46D |
probably damaging |
Het |
Dgkz |
G |
T |
2: 91,769,090 (GRCm39) |
H653Q |
probably benign |
Het |
Dnajc16 |
A |
T |
4: 141,491,945 (GRCm39) |
I626N |
possibly damaging |
Het |
Dsc2 |
T |
C |
18: 20,171,151 (GRCm39) |
D616G |
probably benign |
Het |
Dscam |
A |
T |
16: 96,602,580 (GRCm39) |
S621T |
probably damaging |
Het |
Dst |
T |
A |
1: 34,267,774 (GRCm39) |
V3058E |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,858,959 (GRCm39) |
C1125S |
unknown |
Het |
Glyatl3 |
G |
A |
17: 41,223,619 (GRCm39) |
Q41* |
probably null |
Het |
Gm7694 |
T |
G |
1: 170,128,927 (GRCm39) |
I201L |
probably damaging |
Het |
Gnal |
C |
T |
18: 67,221,830 (GRCm39) |
R78* |
probably null |
Het |
Gtf3c1 |
T |
C |
7: 125,303,069 (GRCm39) |
D122G |
probably benign |
Het |
Htt |
G |
T |
5: 34,975,095 (GRCm39) |
D622Y |
possibly damaging |
Het |
Igkv4-92 |
A |
G |
6: 68,732,081 (GRCm39) |
C98R |
probably benign |
Het |
Incenp |
G |
A |
19: 9,855,088 (GRCm39) |
R608* |
probably null |
Het |
Kics2 |
A |
G |
10: 121,586,501 (GRCm39) |
Y272C |
probably damaging |
Het |
Kif3c |
G |
A |
12: 3,451,706 (GRCm39) |
R679H |
probably damaging |
Het |
Kng1 |
T |
A |
16: 22,898,146 (GRCm39) |
H515Q |
probably damaging |
Het |
Lamb2 |
T |
C |
9: 108,361,370 (GRCm39) |
|
probably null |
Het |
Malrd1 |
A |
T |
2: 15,850,140 (GRCm39) |
N1253I |
unknown |
Het |
Map3k21 |
A |
T |
8: 126,637,471 (GRCm39) |
D19V |
|
Het |
Marchf2 |
G |
T |
17: 33,915,207 (GRCm39) |
P129Q |
probably damaging |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Ms4a4d |
T |
A |
19: 11,533,564 (GRCm39) |
D148E |
possibly damaging |
Het |
Myl4 |
A |
G |
11: 104,468,384 (GRCm39) |
D36G |
probably damaging |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or2a25 |
T |
C |
6: 42,889,170 (GRCm39) |
S238P |
probably damaging |
Het |
Or5ac24 |
A |
T |
16: 59,165,929 (GRCm39) |
I45N |
probably damaging |
Het |
Or5an11 |
A |
G |
19: 12,245,704 (GRCm39) |
T37A |
probably benign |
Het |
Pard3 |
G |
A |
8: 128,003,647 (GRCm39) |
S123N |
probably damaging |
Het |
Parp8 |
T |
C |
13: 117,013,126 (GRCm39) |
N638D |
probably benign |
Het |
Pgpep1l |
A |
T |
7: 67,887,406 (GRCm39) |
S65T |
probably damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,796,708 (GRCm39) |
V1068A |
probably benign |
Het |
Pramel20 |
G |
A |
4: 143,298,425 (GRCm39) |
D123N |
probably benign |
Het |
Prkd1 |
G |
A |
12: 50,430,185 (GRCm39) |
Q641* |
probably null |
Het |
Ptgr2 |
T |
C |
12: 84,344,873 (GRCm39) |
V82A |
possibly damaging |
Het |
Rbm34 |
G |
A |
8: 127,686,332 (GRCm39) |
P225S |
possibly damaging |
Het |
Rnps1 |
A |
T |
17: 24,637,496 (GRCm39) |
K46I |
unknown |
Het |
Shank1 |
T |
C |
7: 44,002,409 (GRCm39) |
V1376A |
probably benign |
Het |
Ski |
A |
T |
4: 155,306,317 (GRCm39) |
Y221N |
probably damaging |
Het |
Skint6 |
C |
A |
4: 113,095,347 (GRCm39) |
G104V |
probably damaging |
Het |
Slit2 |
G |
A |
5: 48,459,860 (GRCm39) |
C1380Y |
possibly damaging |
Het |
Smpd3 |
C |
T |
8: 106,984,058 (GRCm39) |
G554S |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Spdl1 |
C |
A |
11: 34,700,535 (GRCm39) |
C605F |
possibly damaging |
Het |
Syne1 |
C |
A |
10: 5,155,406 (GRCm39) |
D5568Y |
probably benign |
Het |
Tac1 |
C |
A |
6: 7,559,141 (GRCm39) |
A111D |
possibly damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tnfrsf1a |
T |
C |
6: 125,333,878 (GRCm39) |
C44R |
probably damaging |
Het |
Traf3ip3 |
T |
C |
1: 192,864,285 (GRCm39) |
Q366R |
probably benign |
Het |
Trip10 |
A |
G |
17: 57,569,416 (GRCm39) |
D479G |
probably damaging |
Het |
Trip11 |
T |
C |
12: 101,845,131 (GRCm39) |
T1536A |
probably benign |
Het |
Tstd3 |
G |
T |
4: 21,767,082 (GRCm39) |
A13E |
possibly damaging |
Het |
Urb1 |
T |
C |
16: 90,550,678 (GRCm39) |
K2058R |
probably benign |
Het |
Usp15 |
A |
T |
10: 122,982,703 (GRCm39) |
I304N |
possibly damaging |
Het |
Usp18 |
T |
G |
6: 121,229,529 (GRCm39) |
H49Q |
probably benign |
Het |
Vmn1r56 |
T |
A |
7: 5,199,389 (GRCm39) |
D76V |
probably damaging |
Het |
Zfp229 |
G |
A |
17: 21,965,731 (GRCm39) |
A654T |
possibly damaging |
Het |
Zfp977 |
C |
T |
7: 42,230,082 (GRCm39) |
V148I |
probably benign |
Het |
Znfx1 |
A |
T |
2: 166,880,656 (GRCm39) |
I1240N |
|
Het |
|
Other mutations in Wnk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00901:Wnk1
|
APN |
6 |
119,937,669 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01364:Wnk1
|
APN |
6 |
119,914,372 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01715:Wnk1
|
APN |
6 |
119,925,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Wnk1
|
APN |
6 |
119,940,446 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02043:Wnk1
|
APN |
6 |
119,926,039 (GRCm39) |
unclassified |
probably benign |
|
IGL02268:Wnk1
|
APN |
6 |
119,914,334 (GRCm39) |
nonsense |
probably null |
|
IGL02348:Wnk1
|
APN |
6 |
119,940,289 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02425:Wnk1
|
APN |
6 |
119,940,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02850:Wnk1
|
APN |
6 |
119,914,823 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03160:Wnk1
|
APN |
6 |
119,903,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03387:Wnk1
|
APN |
6 |
119,931,148 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL03405:Wnk1
|
APN |
6 |
119,930,856 (GRCm39) |
missense |
probably benign |
0.41 |
Actor
|
UTSW |
6 |
119,947,939 (GRCm39) |
missense |
probably damaging |
1.00 |
Bad
|
UTSW |
6 |
119,942,639 (GRCm39) |
intron |
probably benign |
|
Blink
|
UTSW |
6 |
119,979,234 (GRCm39) |
nonsense |
probably null |
|
Knock
|
UTSW |
6 |
119,920,839 (GRCm39) |
splice site |
probably null |
|
Narrow
|
UTSW |
6 |
119,969,369 (GRCm39) |
missense |
probably damaging |
1.00 |
nictitate
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
opportunity
|
UTSW |
6 |
119,928,029 (GRCm39) |
missense |
probably damaging |
1.00 |
path
|
UTSW |
6 |
120,014,110 (GRCm39) |
missense |
probably damaging |
0.99 |
Stormy
|
UTSW |
6 |
119,969,408 (GRCm39) |
missense |
probably damaging |
1.00 |
tear
|
UTSW |
6 |
119,940,431 (GRCm39) |
missense |
probably damaging |
0.98 |
Tic
|
UTSW |
6 |
119,927,044 (GRCm39) |
missense |
probably damaging |
1.00 |
Unforgiving
|
UTSW |
6 |
119,925,243 (GRCm39) |
missense |
probably damaging |
1.00 |
Window
|
UTSW |
6 |
119,969,414 (GRCm39) |
missense |
probably damaging |
1.00 |
Woke
|
UTSW |
6 |
119,939,916 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03052:Wnk1
|
UTSW |
6 |
119,921,760 (GRCm39) |
splice site |
probably benign |
|
PIT4480001:Wnk1
|
UTSW |
6 |
119,940,328 (GRCm39) |
nonsense |
probably null |
|
R0044:Wnk1
|
UTSW |
6 |
120,014,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R0207:Wnk1
|
UTSW |
6 |
119,929,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R0333:Wnk1
|
UTSW |
6 |
119,905,124 (GRCm39) |
intron |
probably benign |
|
R0453:Wnk1
|
UTSW |
6 |
119,940,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R0457:Wnk1
|
UTSW |
6 |
119,946,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R0501:Wnk1
|
UTSW |
6 |
119,939,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0525:Wnk1
|
UTSW |
6 |
119,903,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R0526:Wnk1
|
UTSW |
6 |
119,928,953 (GRCm39) |
missense |
probably damaging |
0.99 |
R0606:Wnk1
|
UTSW |
6 |
119,903,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Wnk1
|
UTSW |
6 |
119,925,466 (GRCm39) |
missense |
probably damaging |
0.98 |
R1148:Wnk1
|
UTSW |
6 |
119,928,967 (GRCm39) |
splice site |
probably benign |
|
R1188:Wnk1
|
UTSW |
6 |
119,925,670 (GRCm39) |
nonsense |
probably null |
|
R1245:Wnk1
|
UTSW |
6 |
119,925,418 (GRCm39) |
missense |
probably benign |
0.26 |
R1449:Wnk1
|
UTSW |
6 |
119,929,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Wnk1
|
UTSW |
6 |
119,927,645 (GRCm39) |
splice site |
probably benign |
|
R1869:Wnk1
|
UTSW |
6 |
119,928,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Wnk1
|
UTSW |
6 |
119,928,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Wnk1
|
UTSW |
6 |
119,929,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Wnk1
|
UTSW |
6 |
119,946,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R1961:Wnk1
|
UTSW |
6 |
119,946,208 (GRCm39) |
missense |
probably damaging |
0.98 |
R1964:Wnk1
|
UTSW |
6 |
119,911,343 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1983:Wnk1
|
UTSW |
6 |
119,914,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Wnk1
|
UTSW |
6 |
119,905,118 (GRCm39) |
splice site |
probably null |
|
R2144:Wnk1
|
UTSW |
6 |
119,925,949 (GRCm39) |
unclassified |
probably benign |
|
R2186:Wnk1
|
UTSW |
6 |
119,925,528 (GRCm39) |
missense |
probably benign |
0.26 |
R2281:Wnk1
|
UTSW |
6 |
119,940,601 (GRCm39) |
splice site |
probably null |
|
R2338:Wnk1
|
UTSW |
6 |
119,946,495 (GRCm39) |
missense |
probably benign |
0.42 |
R2420:Wnk1
|
UTSW |
6 |
119,913,328 (GRCm39) |
critical splice donor site |
probably null |
|
R3727:Wnk1
|
UTSW |
6 |
119,969,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Wnk1
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3836:Wnk1
|
UTSW |
6 |
119,927,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R3837:Wnk1
|
UTSW |
6 |
119,927,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Wnk1
|
UTSW |
6 |
119,946,315 (GRCm39) |
missense |
possibly damaging |
0.70 |
R3903:Wnk1
|
UTSW |
6 |
119,926,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R4031:Wnk1
|
UTSW |
6 |
119,928,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Wnk1
|
UTSW |
6 |
119,925,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4232:Wnk1
|
UTSW |
6 |
119,926,222 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4422:Wnk1
|
UTSW |
6 |
119,930,856 (GRCm39) |
missense |
probably benign |
0.41 |
R4423:Wnk1
|
UTSW |
6 |
119,903,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4572:Wnk1
|
UTSW |
6 |
119,928,872 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4704:Wnk1
|
UTSW |
6 |
119,942,705 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4755:Wnk1
|
UTSW |
6 |
119,940,431 (GRCm39) |
missense |
probably damaging |
0.98 |
R4812:Wnk1
|
UTSW |
6 |
119,929,732 (GRCm39) |
missense |
probably benign |
0.16 |
R4822:Wnk1
|
UTSW |
6 |
119,939,399 (GRCm39) |
missense |
probably benign |
0.02 |
R4879:Wnk1
|
UTSW |
6 |
119,926,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4970:Wnk1
|
UTSW |
6 |
119,942,696 (GRCm39) |
intron |
probably benign |
|
R5002:Wnk1
|
UTSW |
6 |
119,914,924 (GRCm39) |
missense |
probably benign |
0.13 |
R5037:Wnk1
|
UTSW |
6 |
119,942,696 (GRCm39) |
intron |
probably benign |
|
R5152:Wnk1
|
UTSW |
6 |
119,979,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5257:Wnk1
|
UTSW |
6 |
120,014,149 (GRCm39) |
missense |
probably benign |
0.00 |
R5354:Wnk1
|
UTSW |
6 |
119,945,484 (GRCm39) |
missense |
probably benign |
0.01 |
R5421:Wnk1
|
UTSW |
6 |
119,929,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5564:Wnk1
|
UTSW |
6 |
119,925,852 (GRCm39) |
unclassified |
probably benign |
|
R5600:Wnk1
|
UTSW |
6 |
119,926,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Wnk1
|
UTSW |
6 |
119,969,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R6083:Wnk1
|
UTSW |
6 |
120,014,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R6110:Wnk1
|
UTSW |
6 |
119,949,958 (GRCm39) |
intron |
probably benign |
|
R6128:Wnk1
|
UTSW |
6 |
119,940,747 (GRCm39) |
splice site |
probably null |
|
R6237:Wnk1
|
UTSW |
6 |
119,929,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Wnk1
|
UTSW |
6 |
119,925,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6467:Wnk1
|
UTSW |
6 |
119,939,916 (GRCm39) |
missense |
probably benign |
0.12 |
R6696:Wnk1
|
UTSW |
6 |
119,925,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Wnk1
|
UTSW |
6 |
119,925,742 (GRCm39) |
missense |
probably benign |
0.26 |
R6923:Wnk1
|
UTSW |
6 |
119,942,639 (GRCm39) |
intron |
probably benign |
|
R7024:Wnk1
|
UTSW |
6 |
119,942,687 (GRCm39) |
intron |
probably benign |
|
R7072:Wnk1
|
UTSW |
6 |
119,914,822 (GRCm39) |
missense |
unknown |
|
R7087:Wnk1
|
UTSW |
6 |
120,014,491 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7102:Wnk1
|
UTSW |
6 |
119,925,268 (GRCm39) |
missense |
unknown |
|
R7134:Wnk1
|
UTSW |
6 |
119,903,389 (GRCm39) |
missense |
unknown |
|
R7137:Wnk1
|
UTSW |
6 |
120,015,173 (GRCm39) |
unclassified |
probably benign |
|
R7142:Wnk1
|
UTSW |
6 |
119,926,240 (GRCm39) |
missense |
probably benign |
0.09 |
R7174:Wnk1
|
UTSW |
6 |
119,947,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Wnk1
|
UTSW |
6 |
119,920,839 (GRCm39) |
splice site |
probably null |
|
R7218:Wnk1
|
UTSW |
6 |
119,979,234 (GRCm39) |
nonsense |
probably null |
|
R7498:Wnk1
|
UTSW |
6 |
119,904,157 (GRCm39) |
missense |
unknown |
|
R7599:Wnk1
|
UTSW |
6 |
119,906,789 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7615:Wnk1
|
UTSW |
6 |
119,909,699 (GRCm39) |
missense |
probably benign |
0.27 |
R7799:Wnk1
|
UTSW |
6 |
119,926,137 (GRCm39) |
missense |
probably benign |
0.04 |
R7979:Wnk1
|
UTSW |
6 |
120,014,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Wnk1
|
UTSW |
6 |
119,909,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R8331:Wnk1
|
UTSW |
6 |
119,930,794 (GRCm39) |
missense |
probably benign |
0.09 |
R8343:Wnk1
|
UTSW |
6 |
119,940,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8348:Wnk1
|
UTSW |
6 |
119,906,960 (GRCm39) |
splice site |
probably null |
|
R8359:Wnk1
|
UTSW |
6 |
119,969,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Wnk1
|
UTSW |
6 |
119,911,388 (GRCm39) |
missense |
unknown |
|
R8519:Wnk1
|
UTSW |
6 |
119,927,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R8930:Wnk1
|
UTSW |
6 |
119,940,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R8932:Wnk1
|
UTSW |
6 |
119,940,226 (GRCm39) |
missense |
probably damaging |
0.99 |
R8933:Wnk1
|
UTSW |
6 |
120,013,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Wnk1
|
UTSW |
6 |
119,925,631 (GRCm39) |
missense |
unknown |
|
R9148:Wnk1
|
UTSW |
6 |
119,925,631 (GRCm39) |
missense |
unknown |
|
R9354:Wnk1
|
UTSW |
6 |
119,942,660 (GRCm39) |
missense |
unknown |
|
R9379:Wnk1
|
UTSW |
6 |
119,928,678 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Wnk1
|
UTSW |
6 |
120,013,993 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Wnk1
|
UTSW |
6 |
119,925,166 (GRCm39) |
missense |
unknown |
|
|