Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adra1d |
A |
T |
2: 131,403,289 (GRCm39) |
M267K |
probably damaging |
Het |
Aen |
T |
C |
7: 78,555,793 (GRCm39) |
|
probably null |
Het |
Ano2 |
A |
G |
6: 125,992,502 (GRCm39) |
D825G |
probably damaging |
Het |
Bdh2 |
T |
C |
3: 135,001,025 (GRCm39) |
S142P |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,800,924 (GRCm39) |
L2507P |
possibly damaging |
Het |
Ces3a |
T |
C |
8: 105,782,212 (GRCm39) |
F308S |
probably benign |
Het |
Cfap47 |
C |
T |
X: 78,454,218 (GRCm39) |
R1646Q |
probably damaging |
Het |
Chd4 |
T |
A |
6: 125,082,320 (GRCm39) |
M603K |
probably damaging |
Het |
Cit |
T |
C |
5: 116,106,068 (GRCm39) |
V984A |
probably benign |
Het |
Clstn3 |
A |
T |
6: 124,436,166 (GRCm39) |
D194E |
probably damaging |
Het |
Ctdp1 |
T |
C |
18: 80,492,696 (GRCm39) |
R600G |
probably benign |
Het |
Ctnnd1 |
C |
T |
2: 84,439,907 (GRCm39) |
G801D |
probably damaging |
Het |
Dgkg |
A |
G |
16: 22,407,049 (GRCm39) |
F179L |
probably damaging |
Het |
Dlg3 |
G |
A |
X: 99,817,827 (GRCm39) |
D379N |
probably damaging |
Het |
Drd2 |
G |
T |
9: 49,314,571 (GRCm39) |
R267S |
probably benign |
Het |
Dsg1b |
T |
C |
18: 20,542,675 (GRCm39) |
*1061Q |
probably null |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Edc3 |
T |
C |
9: 57,620,826 (GRCm39) |
V49A |
probably damaging |
Het |
Ern1 |
G |
A |
11: 106,300,750 (GRCm39) |
T548I |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,838,192 (GRCm39) |
D2684G |
possibly damaging |
Het |
Fam20a |
A |
G |
11: 109,565,449 (GRCm39) |
M454T |
probably benign |
Het |
Fbp2 |
A |
G |
13: 63,006,056 (GRCm39) |
M19T |
possibly damaging |
Het |
Frmd4b |
A |
T |
6: 97,464,577 (GRCm39) |
C47S |
probably damaging |
Het |
Gtf2h1 |
T |
A |
7: 46,464,747 (GRCm39) |
I388N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,453,206 (GRCm39) |
V571A |
possibly damaging |
Het |
Helz2 |
T |
A |
2: 180,870,841 (GRCm39) |
K2832* |
probably null |
Het |
Herc1 |
T |
A |
9: 66,372,688 (GRCm39) |
D3081E |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,591,566 (GRCm39) |
S1878T |
probably damaging |
Het |
Iars1 |
A |
G |
13: 49,841,605 (GRCm39) |
|
probably null |
Het |
Il17rd |
A |
T |
14: 26,816,835 (GRCm39) |
K180M |
probably damaging |
Het |
Ints6l |
T |
A |
X: 55,550,110 (GRCm39) |
H678Q |
probably benign |
Het |
Khdrbs1 |
A |
G |
4: 129,613,830 (GRCm39) |
|
probably null |
Het |
Lce3a |
A |
C |
3: 92,832,837 (GRCm39) |
S88A |
unknown |
Het |
Lgals12 |
C |
T |
19: 7,578,606 (GRCm39) |
|
probably null |
Het |
Lnpk |
T |
C |
2: 74,399,373 (GRCm39) |
T57A |
probably benign |
Het |
Lrp2bp |
C |
T |
8: 46,466,206 (GRCm39) |
T105I |
probably benign |
Het |
Lrrc4c |
C |
G |
2: 97,459,657 (GRCm39) |
N94K |
possibly damaging |
Het |
Mag |
A |
T |
7: 30,600,066 (GRCm39) |
Y571* |
probably null |
Het |
Mbd1 |
T |
A |
18: 74,410,449 (GRCm39) |
D583E |
probably damaging |
Het |
Mill1 |
T |
A |
7: 17,998,544 (GRCm39) |
Y251* |
probably null |
Het |
Mllt10 |
T |
C |
2: 18,211,871 (GRCm39) |
I928T |
probably benign |
Het |
Ms4a18 |
T |
C |
19: 10,991,029 (GRCm39) |
T22A |
probably benign |
Het |
Mtmr14 |
T |
C |
6: 113,257,700 (GRCm39) |
F250L |
probably damaging |
Het |
Mtmr3 |
A |
T |
11: 4,449,032 (GRCm39) |
W244R |
probably damaging |
Het |
Myorg |
A |
G |
4: 41,497,704 (GRCm39) |
I642T |
probably damaging |
Het |
Nat10 |
C |
A |
2: 103,556,522 (GRCm39) |
E885D |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,321,054 (GRCm39) |
L2055H |
probably damaging |
Het |
Necab3 |
T |
A |
2: 154,388,999 (GRCm39) |
I192F |
possibly damaging |
Het |
Nedd4 |
T |
A |
9: 72,650,000 (GRCm39) |
N783K |
probably damaging |
Het |
Nf2 |
A |
T |
11: 4,749,899 (GRCm39) |
W61R |
probably damaging |
Het |
Nox4 |
T |
A |
7: 87,023,588 (GRCm39) |
F491L |
probably benign |
Het |
Omt2b |
G |
A |
9: 78,235,457 (GRCm39) |
|
probably benign |
Het |
Or4c125 |
A |
T |
2: 89,170,009 (GRCm39) |
Y212* |
probably null |
Het |
Or4c127 |
T |
A |
2: 89,832,774 (GRCm39) |
I8N |
probably damaging |
Het |
Or8i2 |
A |
G |
2: 86,852,855 (GRCm39) |
V11A |
probably benign |
Het |
Osbpl5 |
A |
T |
7: 143,247,596 (GRCm39) |
Y723* |
probably null |
Het |
Otop2 |
T |
C |
11: 115,217,757 (GRCm39) |
S198P |
possibly damaging |
Het |
Pgam5 |
T |
G |
5: 110,413,785 (GRCm39) |
H126P |
probably damaging |
Het |
Phip |
A |
T |
9: 82,753,868 (GRCm39) |
N1625K |
probably damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,451 (GRCm39) |
Y202* |
probably null |
Het |
Pkd1l3 |
T |
A |
8: 110,347,156 (GRCm39) |
H176Q |
unknown |
Het |
Plxdc2 |
A |
G |
2: 16,570,147 (GRCm39) |
R109G |
probably damaging |
Het |
Prorsd1 |
T |
C |
11: 29,463,592 (GRCm39) |
K57E |
probably benign |
Het |
Rnf150 |
A |
T |
8: 83,591,020 (GRCm39) |
R128W |
probably damaging |
Het |
Samm50 |
G |
A |
15: 84,084,625 (GRCm39) |
|
probably null |
Het |
Skint6 |
A |
T |
4: 112,722,909 (GRCm39) |
Y889* |
probably null |
Het |
Slc35b1 |
T |
C |
11: 95,276,640 (GRCm39) |
Y40H |
probably damaging |
Het |
Speg |
A |
G |
1: 75,394,371 (GRCm39) |
H1722R |
probably damaging |
Het |
Suz12 |
T |
C |
11: 79,913,024 (GRCm39) |
L356P |
probably damaging |
Het |
Tln2 |
T |
G |
9: 67,262,503 (GRCm39) |
I585L |
probably damaging |
Het |
Trim2 |
G |
A |
3: 84,098,225 (GRCm39) |
Q359* |
probably null |
Het |
Ttn |
C |
T |
2: 76,543,549 (GRCm39) |
E33146K |
probably damaging |
Het |
Vcp |
G |
T |
4: 42,982,547 (GRCm39) |
T715K |
probably benign |
Het |
Vmn1r230 |
T |
A |
17: 21,067,355 (GRCm39) |
N181K |
probably benign |
Het |
Vmn2r17 |
T |
A |
5: 109,582,144 (GRCm39) |
M511K |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 102,055,408 (GRCm39) |
R1554Q |
possibly damaging |
Het |
Zfp112 |
A |
T |
7: 23,824,863 (GRCm39) |
Q277L |
probably damaging |
Het |
Zfp850 |
T |
C |
7: 27,684,620 (GRCm39) |
E42G |
probably damaging |
Het |
Zfp976 |
G |
A |
7: 42,262,695 (GRCm39) |
P381S |
probably damaging |
Het |
Zzef1 |
A |
T |
11: 72,800,982 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ttc28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Ttc28
|
APN |
5 |
111,373,554 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00963:Ttc28
|
APN |
5 |
111,434,255 (GRCm39) |
nonsense |
probably null |
|
IGL00969:Ttc28
|
APN |
5 |
111,373,606 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01366:Ttc28
|
APN |
5 |
111,233,037 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01528:Ttc28
|
APN |
5 |
111,249,826 (GRCm39) |
splice site |
probably benign |
|
IGL01558:Ttc28
|
APN |
5 |
111,431,828 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01973:Ttc28
|
APN |
5 |
111,372,101 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02040:Ttc28
|
APN |
5 |
111,040,802 (GRCm39) |
nonsense |
probably null |
|
IGL02432:Ttc28
|
APN |
5 |
111,371,101 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02531:Ttc28
|
APN |
5 |
111,373,716 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02819:Ttc28
|
APN |
5 |
111,414,449 (GRCm39) |
missense |
probably benign |
|
IGL02830:Ttc28
|
APN |
5 |
111,434,105 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02893:Ttc28
|
APN |
5 |
111,433,251 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03387:Ttc28
|
APN |
5 |
111,381,208 (GRCm39) |
missense |
probably benign |
0.07 |
PIT4131001:Ttc28
|
UTSW |
5 |
111,040,719 (GRCm39) |
missense |
probably benign |
0.00 |
R0142:Ttc28
|
UTSW |
5 |
111,425,323 (GRCm39) |
missense |
probably benign |
0.40 |
R0166:Ttc28
|
UTSW |
5 |
111,373,500 (GRCm39) |
missense |
probably benign |
0.01 |
R0328:Ttc28
|
UTSW |
5 |
111,431,933 (GRCm39) |
splice site |
probably benign |
|
R0582:Ttc28
|
UTSW |
5 |
111,331,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Ttc28
|
UTSW |
5 |
111,378,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R0811:Ttc28
|
UTSW |
5 |
111,383,366 (GRCm39) |
missense |
probably benign |
0.24 |
R0812:Ttc28
|
UTSW |
5 |
111,383,366 (GRCm39) |
missense |
probably benign |
0.24 |
R0828:Ttc28
|
UTSW |
5 |
111,371,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Ttc28
|
UTSW |
5 |
111,378,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1013:Ttc28
|
UTSW |
5 |
111,424,831 (GRCm39) |
missense |
probably benign |
0.01 |
R1168:Ttc28
|
UTSW |
5 |
111,378,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R1194:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1196:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Ttc28
|
UTSW |
5 |
111,433,635 (GRCm39) |
missense |
probably benign |
0.04 |
R1386:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Ttc28
|
UTSW |
5 |
111,433,254 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Ttc28
|
UTSW |
5 |
111,433,254 (GRCm39) |
missense |
probably benign |
0.00 |
R1537:Ttc28
|
UTSW |
5 |
111,433,184 (GRCm39) |
missense |
probably damaging |
0.96 |
R1539:Ttc28
|
UTSW |
5 |
111,248,677 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1558:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1560:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1561:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1566:Ttc28
|
UTSW |
5 |
111,373,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Ttc28
|
UTSW |
5 |
111,425,034 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1775:Ttc28
|
UTSW |
5 |
111,424,677 (GRCm39) |
missense |
probably benign |
0.00 |
R1909:Ttc28
|
UTSW |
5 |
111,431,920 (GRCm39) |
critical splice donor site |
probably null |
|
R1911:Ttc28
|
UTSW |
5 |
111,428,616 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1970:Ttc28
|
UTSW |
5 |
111,383,501 (GRCm39) |
missense |
probably benign |
0.00 |
R1990:Ttc28
|
UTSW |
5 |
111,424,188 (GRCm39) |
missense |
probably benign |
0.37 |
R1992:Ttc28
|
UTSW |
5 |
111,424,188 (GRCm39) |
missense |
probably benign |
0.37 |
R2066:Ttc28
|
UTSW |
5 |
111,373,799 (GRCm39) |
missense |
probably benign |
0.01 |
R2112:Ttc28
|
UTSW |
5 |
111,424,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R2158:Ttc28
|
UTSW |
5 |
111,325,483 (GRCm39) |
intron |
probably benign |
|
R2267:Ttc28
|
UTSW |
5 |
111,373,869 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2384:Ttc28
|
UTSW |
5 |
111,424,074 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2989:Ttc28
|
UTSW |
5 |
111,371,881 (GRCm39) |
missense |
probably benign |
0.29 |
R3881:Ttc28
|
UTSW |
5 |
111,331,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R3919:Ttc28
|
UTSW |
5 |
111,433,245 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4455:Ttc28
|
UTSW |
5 |
111,371,924 (GRCm39) |
frame shift |
probably null |
|
R4456:Ttc28
|
UTSW |
5 |
111,371,924 (GRCm39) |
frame shift |
probably null |
|
R4522:Ttc28
|
UTSW |
5 |
111,428,038 (GRCm39) |
missense |
probably benign |
0.01 |
R4548:Ttc28
|
UTSW |
5 |
111,419,090 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4591:Ttc28
|
UTSW |
5 |
111,371,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Ttc28
|
UTSW |
5 |
111,371,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Ttc28
|
UTSW |
5 |
111,424,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4714:Ttc28
|
UTSW |
5 |
111,433,095 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4790:Ttc28
|
UTSW |
5 |
111,372,083 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4803:Ttc28
|
UTSW |
5 |
111,425,329 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4840:Ttc28
|
UTSW |
5 |
111,433,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4969:Ttc28
|
UTSW |
5 |
111,424,121 (GRCm39) |
missense |
probably damaging |
0.96 |
R5019:Ttc28
|
UTSW |
5 |
111,249,930 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5130:Ttc28
|
UTSW |
5 |
111,040,722 (GRCm39) |
missense |
probably benign |
|
R5150:Ttc28
|
UTSW |
5 |
111,373,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Ttc28
|
UTSW |
5 |
111,325,489 (GRCm39) |
intron |
probably benign |
|
R5254:Ttc28
|
UTSW |
5 |
111,419,104 (GRCm39) |
missense |
probably benign |
0.01 |
R5518:Ttc28
|
UTSW |
5 |
111,373,794 (GRCm39) |
missense |
probably benign |
0.17 |
R5851:Ttc28
|
UTSW |
5 |
111,383,335 (GRCm39) |
splice site |
probably benign |
|
R5931:Ttc28
|
UTSW |
5 |
111,232,975 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6011:Ttc28
|
UTSW |
5 |
111,434,309 (GRCm39) |
missense |
probably benign |
|
R6176:Ttc28
|
UTSW |
5 |
111,371,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R6221:Ttc28
|
UTSW |
5 |
111,419,114 (GRCm39) |
missense |
probably benign |
0.00 |
R6398:Ttc28
|
UTSW |
5 |
111,424,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R6717:Ttc28
|
UTSW |
5 |
111,433,302 (GRCm39) |
missense |
probably benign |
|
R6770:Ttc28
|
UTSW |
5 |
111,434,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Ttc28
|
UTSW |
5 |
111,424,891 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7038:Ttc28
|
UTSW |
5 |
111,414,445 (GRCm39) |
missense |
probably benign |
0.09 |
R7073:Ttc28
|
UTSW |
5 |
111,371,282 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7101:Ttc28
|
UTSW |
5 |
111,232,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Ttc28
|
UTSW |
5 |
111,427,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R7350:Ttc28
|
UTSW |
5 |
111,373,903 (GRCm39) |
missense |
probably damaging |
0.97 |
R7454:Ttc28
|
UTSW |
5 |
111,433,350 (GRCm39) |
missense |
probably benign |
0.19 |
R7461:Ttc28
|
UTSW |
5 |
111,371,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7596:Ttc28
|
UTSW |
5 |
111,427,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R7613:Ttc28
|
UTSW |
5 |
111,371,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Ttc28
|
UTSW |
5 |
111,433,085 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7648:Ttc28
|
UTSW |
5 |
111,331,258 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7735:Ttc28
|
UTSW |
5 |
111,414,544 (GRCm39) |
splice site |
probably null |
|
R8030:Ttc28
|
UTSW |
5 |
111,433,922 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8205:Ttc28
|
UTSW |
5 |
111,373,596 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8246:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8247:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8269:Ttc28
|
UTSW |
5 |
111,425,325 (GRCm39) |
missense |
probably benign |
0.09 |
R8292:Ttc28
|
UTSW |
5 |
111,371,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8356:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8423:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8424:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8426:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8441:Ttc28
|
UTSW |
5 |
111,325,507 (GRCm39) |
nonsense |
probably null |
|
R8494:Ttc28
|
UTSW |
5 |
111,383,506 (GRCm39) |
missense |
probably damaging |
0.96 |
R8508:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8510:Ttc28
|
UTSW |
5 |
111,381,207 (GRCm39) |
missense |
probably benign |
0.33 |
R8729:Ttc28
|
UTSW |
5 |
111,383,509 (GRCm39) |
critical splice donor site |
probably null |
|
R8845:Ttc28
|
UTSW |
5 |
111,372,041 (GRCm39) |
missense |
probably benign |
0.11 |
R9003:Ttc28
|
UTSW |
5 |
111,424,896 (GRCm39) |
missense |
probably benign |
0.00 |
R9185:Ttc28
|
UTSW |
5 |
111,371,342 (GRCm39) |
missense |
probably benign |
0.03 |
R9187:Ttc28
|
UTSW |
5 |
111,249,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Ttc28
|
UTSW |
5 |
111,325,525 (GRCm39) |
missense |
unknown |
|
R9251:Ttc28
|
UTSW |
5 |
111,040,698 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9372:Ttc28
|
UTSW |
5 |
111,331,073 (GRCm39) |
missense |
probably benign |
0.25 |
R9466:Ttc28
|
UTSW |
5 |
111,330,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R9563:Ttc28
|
UTSW |
5 |
111,371,092 (GRCm39) |
missense |
probably benign |
0.22 |
R9606:Ttc28
|
UTSW |
5 |
111,433,140 (GRCm39) |
missense |
probably benign |
0.00 |
R9691:Ttc28
|
UTSW |
5 |
111,431,879 (GRCm39) |
missense |
probably benign |
0.01 |
R9709:Ttc28
|
UTSW |
5 |
111,433,637 (GRCm39) |
missense |
probably damaging |
0.97 |
V8831:Ttc28
|
UTSW |
5 |
111,248,578 (GRCm39) |
missense |
probably benign |
0.11 |
Z1088:Ttc28
|
UTSW |
5 |
111,434,181 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Ttc28
|
UTSW |
5 |
111,414,432 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1177:Ttc28
|
UTSW |
5 |
111,433,605 (GRCm39) |
missense |
probably benign |
0.10 |
Z1177:Ttc28
|
UTSW |
5 |
111,426,452 (GRCm39) |
missense |
probably damaging |
1.00 |
|