Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
C |
T |
8: 120,872,284 (GRCm39) |
R71C |
probably damaging |
Het |
Aanat |
A |
T |
11: 116,486,455 (GRCm39) |
|
probably benign |
Het |
Ahrr |
G |
T |
13: 74,405,664 (GRCm39) |
S91* |
probably null |
Het |
Ampd1 |
A |
T |
3: 102,995,758 (GRCm39) |
N223Y |
probably benign |
Het |
Ankar |
T |
G |
1: 72,719,217 (GRCm39) |
N544T |
probably damaging |
Het |
Ankk1 |
A |
G |
9: 49,330,050 (GRCm39) |
S302P |
possibly damaging |
Het |
Bcr |
T |
C |
10: 74,992,932 (GRCm39) |
V809A |
probably benign |
Het |
Bpifb2 |
A |
G |
2: 153,732,460 (GRCm39) |
N353S |
possibly damaging |
Het |
Cyth1 |
A |
T |
11: 118,074,835 (GRCm39) |
|
probably null |
Het |
Ddx5 |
A |
T |
11: 106,673,006 (GRCm39) |
N506K |
probably benign |
Het |
Dnaja1 |
A |
T |
4: 40,730,244 (GRCm39) |
I239F |
probably benign |
Het |
Ethe1 |
C |
T |
7: 24,305,676 (GRCm39) |
T141I |
probably damaging |
Het |
Fhip2b |
T |
C |
14: 70,831,447 (GRCm39) |
H29R |
probably damaging |
Het |
Gdap2 |
A |
T |
3: 100,109,382 (GRCm39) |
I36F |
unknown |
Het |
Gm13030 |
A |
T |
4: 138,598,577 (GRCm39) |
D115E |
unknown |
Het |
Gm17019 |
A |
T |
5: 15,079,386 (GRCm39) |
L227Q |
probably damaging |
Het |
Gm9195 |
T |
A |
14: 72,673,217 (GRCm39) |
E2517D |
possibly damaging |
Het |
Gramd2a |
T |
A |
9: 59,615,354 (GRCm39) |
V39D |
possibly damaging |
Het |
Hmcn1 |
C |
T |
1: 150,506,017 (GRCm39) |
W3836* |
probably null |
Het |
Hspa14 |
C |
T |
2: 3,490,078 (GRCm39) |
D494N |
possibly damaging |
Het |
Ifit2 |
A |
G |
19: 34,550,598 (GRCm39) |
N46S |
probably benign |
Het |
Ifna6 |
A |
T |
4: 88,746,044 (GRCm39) |
E131V |
possibly damaging |
Het |
Ift140 |
T |
C |
17: 25,256,010 (GRCm39) |
V504A |
possibly damaging |
Het |
Irgc |
T |
C |
7: 24,131,653 (GRCm39) |
N388S |
probably damaging |
Het |
Itgal |
T |
A |
7: 126,916,537 (GRCm39) |
V743E |
probably benign |
Het |
Itih5 |
T |
C |
2: 10,250,448 (GRCm39) |
S716P |
probably damaging |
Het |
Kcnab1 |
A |
T |
3: 65,173,924 (GRCm39) |
K78N |
possibly damaging |
Het |
Kif1a |
A |
T |
1: 92,982,039 (GRCm39) |
V787E |
possibly damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Krt39 |
A |
T |
11: 99,408,917 (GRCm39) |
V293E |
probably damaging |
Het |
Lrrn4 |
A |
G |
2: 132,711,663 (GRCm39) |
F720S |
possibly damaging |
Het |
Map2 |
G |
A |
1: 66,453,983 (GRCm39) |
A958T |
possibly damaging |
Het |
Map3k9 |
A |
G |
12: 81,770,871 (GRCm39) |
S906P |
probably benign |
Het |
Mdc1 |
T |
C |
17: 36,164,201 (GRCm39) |
S1250P |
probably benign |
Het |
Meltf |
G |
A |
16: 31,703,764 (GRCm39) |
V164I |
probably damaging |
Het |
Mtap |
T |
G |
4: 89,097,699 (GRCm39) |
|
probably null |
Het |
Mtus1 |
C |
A |
8: 41,475,443 (GRCm39) |
V184F |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,104,489 (GRCm39) |
D1015V |
probably damaging |
Het |
Ndrg1 |
T |
C |
15: 66,816,787 (GRCm39) |
|
probably null |
Het |
Nkd1 |
G |
T |
8: 89,311,803 (GRCm39) |
V130L |
probably benign |
Het |
Nsfl1c |
A |
G |
2: 151,342,673 (GRCm39) |
D81G |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,431,391 (GRCm39) |
|
probably null |
Het |
Nucb1 |
T |
C |
7: 45,148,202 (GRCm39) |
K204E |
possibly damaging |
Het |
Nwd1 |
T |
G |
8: 73,401,801 (GRCm39) |
M774R |
possibly damaging |
Het |
Or2m13 |
A |
T |
16: 19,225,944 (GRCm39) |
V274E |
probably damaging |
Het |
Or52u1 |
G |
C |
7: 104,237,907 (GRCm39) |
E299Q |
probably damaging |
Het |
Or5an1c |
A |
T |
19: 12,218,318 (GRCm39) |
S236T |
possibly damaging |
Het |
Pan3 |
T |
A |
5: 147,473,082 (GRCm39) |
|
probably null |
Het |
Pcdh15 |
A |
T |
10: 74,342,317 (GRCm39) |
T1135S |
probably benign |
Het |
Pfas |
A |
G |
11: 68,890,918 (GRCm39) |
I331T |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,488,647 (GRCm39) |
I1641N |
probably damaging |
Het |
Pramel27 |
C |
T |
4: 143,579,779 (GRCm39) |
P455S |
probably benign |
Het |
Ptar1 |
A |
T |
19: 23,695,465 (GRCm39) |
R311W |
probably damaging |
Het |
Ranbp2 |
T |
G |
10: 58,315,016 (GRCm39) |
M1912R |
probably damaging |
Het |
Rbm12 |
A |
G |
2: 155,939,223 (GRCm39) |
F350L |
possibly damaging |
Het |
Sdhaf1 |
T |
C |
7: 30,021,468 (GRCm39) |
D96G |
probably benign |
Het |
Serpinb6b |
T |
A |
13: 33,152,650 (GRCm39) |
M53K |
probably damaging |
Het |
Sh2d6 |
A |
T |
6: 72,494,147 (GRCm39) |
L147Q |
probably benign |
Het |
Slc19a2 |
T |
A |
1: 164,088,445 (GRCm39) |
C298S |
probably benign |
Het |
St8sia2 |
T |
A |
7: 73,610,650 (GRCm39) |
Q211L |
possibly damaging |
Het |
Sult2a2 |
T |
C |
7: 13,468,822 (GRCm39) |
I96T |
possibly damaging |
Het |
Tab2 |
G |
T |
10: 7,783,247 (GRCm39) |
H678Q |
probably damaging |
Het |
Tnfaip6 |
A |
G |
2: 51,928,228 (GRCm39) |
E14G |
probably benign |
Het |
Trip11 |
A |
T |
12: 101,851,457 (GRCm39) |
L869H |
probably damaging |
Het |
Tslp |
T |
C |
18: 32,952,133 (GRCm39) |
Y133H |
not run |
Het |
Ttn |
T |
C |
2: 76,571,334 (GRCm39) |
I26520V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,762,487 (GRCm39) |
V3374A |
unknown |
Het |
Tubgcp2 |
T |
A |
7: 139,587,837 (GRCm39) |
I263F |
possibly damaging |
Het |
Uaca |
A |
G |
9: 60,777,392 (GRCm39) |
E593G |
probably damaging |
Het |
Unc13b |
C |
T |
4: 43,172,235 (GRCm39) |
T1021I |
unknown |
Het |
Ush1c |
T |
A |
7: 45,874,979 (GRCm39) |
I131F |
probably benign |
Het |
Usp24 |
C |
A |
4: 106,236,304 (GRCm39) |
D997E |
probably benign |
Het |
Usp54 |
T |
C |
14: 20,627,108 (GRCm39) |
T517A |
probably benign |
Het |
Vmn1r151 |
A |
T |
7: 22,198,505 (GRCm39) |
M200K |
possibly damaging |
Het |
Vmn2r43 |
T |
C |
7: 8,258,328 (GRCm39) |
D295G |
probably damaging |
Het |
Vmn2r70 |
G |
A |
7: 85,213,076 (GRCm39) |
P444S |
probably damaging |
Het |
Vmn2r85 |
G |
T |
10: 130,254,849 (GRCm39) |
P612T |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,875,317 (GRCm39) |
V1736D |
|
Het |
Zbtb11 |
A |
T |
16: 55,810,850 (GRCm39) |
H336L |
probably benign |
Het |
|
Other mutations in Son |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Son
|
APN |
16 |
91,461,210 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01024:Son
|
APN |
16 |
91,452,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Son
|
APN |
16 |
91,457,024 (GRCm39) |
intron |
probably benign |
|
IGL01083:Son
|
APN |
16 |
91,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01115:Son
|
APN |
16 |
91,456,346 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01467:Son
|
APN |
16 |
91,454,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01506:Son
|
APN |
16 |
91,454,174 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:Son
|
APN |
16 |
91,454,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Son
|
APN |
16 |
91,452,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02473:Son
|
APN |
16 |
91,455,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02498:Son
|
APN |
16 |
91,453,713 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Son
|
APN |
16 |
91,452,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02530:Son
|
APN |
16 |
91,455,359 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02865:Son
|
APN |
16 |
91,448,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Son
|
APN |
16 |
91,453,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Son
|
UTSW |
16 |
91,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Son
|
UTSW |
16 |
91,457,054 (GRCm39) |
intron |
probably benign |
|
R0037:Son
|
UTSW |
16 |
91,461,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Son
|
UTSW |
16 |
91,456,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0056:Son
|
UTSW |
16 |
91,475,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0227:Son
|
UTSW |
16 |
91,453,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R0256:Son
|
UTSW |
16 |
91,453,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0302:Son
|
UTSW |
16 |
91,453,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Son
|
UTSW |
16 |
91,452,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Son
|
UTSW |
16 |
91,454,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Son
|
UTSW |
16 |
91,461,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Son
|
UTSW |
16 |
91,453,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Son
|
UTSW |
16 |
91,452,230 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1535:Son
|
UTSW |
16 |
91,456,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Son
|
UTSW |
16 |
91,456,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Son
|
UTSW |
16 |
91,454,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Son
|
UTSW |
16 |
91,457,114 (GRCm39) |
intron |
probably benign |
|
R2138:Son
|
UTSW |
16 |
91,456,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2245:Son
|
UTSW |
16 |
91,444,848 (GRCm39) |
splice site |
probably null |
|
R2351:Son
|
UTSW |
16 |
91,454,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2434:Son
|
UTSW |
16 |
91,451,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2871:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2872:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2889:Son
|
UTSW |
16 |
91,456,787 (GRCm39) |
unclassified |
probably benign |
|
R3712:Son
|
UTSW |
16 |
91,453,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R3913:Son
|
UTSW |
16 |
91,456,999 (GRCm39) |
intron |
probably benign |
|
R4172:Son
|
UTSW |
16 |
91,456,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4302:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4770:Son
|
UTSW |
16 |
91,455,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4881:Son
|
UTSW |
16 |
91,472,397 (GRCm39) |
missense |
probably benign |
0.31 |
R5020:Son
|
UTSW |
16 |
91,453,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Son
|
UTSW |
16 |
91,452,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Son
|
UTSW |
16 |
91,451,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5215:Son
|
UTSW |
16 |
91,453,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5243:Son
|
UTSW |
16 |
91,451,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Son
|
UTSW |
16 |
91,452,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5529:Son
|
UTSW |
16 |
91,452,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Son
|
UTSW |
16 |
91,468,301 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5763:Son
|
UTSW |
16 |
91,454,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Son
|
UTSW |
16 |
91,461,875 (GRCm39) |
intron |
probably benign |
|
R5788:Son
|
UTSW |
16 |
91,456,940 (GRCm39) |
intron |
probably benign |
|
R5992:Son
|
UTSW |
16 |
91,455,792 (GRCm39) |
missense |
probably benign |
0.04 |
R6314:Son
|
UTSW |
16 |
91,457,298 (GRCm39) |
intron |
probably benign |
|
R6371:Son
|
UTSW |
16 |
91,471,629 (GRCm39) |
|
|
|
R6429:Son
|
UTSW |
16 |
91,455,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6451:Son
|
UTSW |
16 |
91,454,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6489:Son
|
UTSW |
16 |
91,452,044 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6513:Son
|
UTSW |
16 |
91,456,835 (GRCm39) |
intron |
probably benign |
|
R6753:Son
|
UTSW |
16 |
91,454,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Son
|
UTSW |
16 |
91,451,673 (GRCm39) |
missense |
probably damaging |
0.97 |
R7070:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7079:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7110:Son
|
UTSW |
16 |
91,453,406 (GRCm39) |
missense |
probably benign |
0.01 |
R7120:Son
|
UTSW |
16 |
91,467,414 (GRCm39) |
missense |
unknown |
|
R7120:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7167:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7205:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7208:Son
|
UTSW |
16 |
91,458,990 (GRCm39) |
missense |
unknown |
|
R7219:Son
|
UTSW |
16 |
91,461,889 (GRCm39) |
missense |
unknown |
|
R7249:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7328:Son
|
UTSW |
16 |
91,455,278 (GRCm39) |
missense |
probably benign |
0.33 |
R7330:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7374:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7405:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7420:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7464:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7514:Son
|
UTSW |
16 |
91,451,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R7555:Son
|
UTSW |
16 |
91,455,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7716:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7718:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7778:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7824:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7856:Son
|
UTSW |
16 |
91,456,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7928:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7978:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8000:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8192:Son
|
UTSW |
16 |
91,452,437 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8221:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8233:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8255:Son
|
UTSW |
16 |
91,461,824 (GRCm39) |
missense |
unknown |
|
R8292:Son
|
UTSW |
16 |
91,453,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8407:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8468:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8495:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R8772:Son
|
UTSW |
16 |
91,454,826 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8796:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8862:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Son
|
UTSW |
16 |
91,455,057 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8991:Son
|
UTSW |
16 |
91,453,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Son
|
UTSW |
16 |
91,453,366 (GRCm39) |
missense |
probably benign |
0.04 |
R9086:Son
|
UTSW |
16 |
91,467,418 (GRCm39) |
missense |
unknown |
|
R9138:Son
|
UTSW |
16 |
91,452,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9232:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9241:Son
|
UTSW |
16 |
91,454,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R9258:Son
|
UTSW |
16 |
91,474,570 (GRCm39) |
missense |
unknown |
|
R9328:Son
|
UTSW |
16 |
91,452,645 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9420:Son
|
UTSW |
16 |
91,454,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Son
|
UTSW |
16 |
91,454,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9500:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9516:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9595:Son
|
UTSW |
16 |
91,454,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9679:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9719:Son
|
UTSW |
16 |
91,456,440 (GRCm39) |
missense |
probably damaging |
0.96 |
R9749:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9772:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9782:Son
|
UTSW |
16 |
91,444,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Son
|
UTSW |
16 |
91,453,699 (GRCm39) |
unclassified |
probably benign |
|
RF007:Son
|
UTSW |
16 |
91,456,257 (GRCm39) |
missense |
possibly damaging |
0.53 |
RF041:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Son
|
UTSW |
16 |
91,452,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
|