Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 109,997,415 (GRCm39) |
M1551T |
possibly damaging |
Het |
Abcc9 |
A |
G |
6: 142,539,733 (GRCm39) |
*1547Q |
probably null |
Het |
Adamts20 |
A |
C |
15: 94,249,641 (GRCm39) |
C459G |
probably damaging |
Het |
Adamts5 |
C |
T |
16: 85,674,808 (GRCm39) |
W452* |
probably null |
Het |
Adcy8 |
G |
T |
15: 64,792,054 (GRCm39) |
Q301K |
possibly damaging |
Het |
Adgrv1 |
A |
C |
13: 81,715,570 (GRCm39) |
C873G |
probably benign |
Het |
Ak9 |
A |
G |
10: 41,296,535 (GRCm39) |
D1427G |
unknown |
Het |
Amy2a1 |
T |
A |
3: 113,324,190 (GRCm39) |
M117L |
possibly damaging |
Het |
Ap5z1 |
G |
T |
5: 142,452,039 (GRCm39) |
R23L |
probably benign |
Het |
Ap5z1 |
C |
T |
5: 142,456,191 (GRCm39) |
Q337* |
probably null |
Het |
Astn1 |
C |
A |
1: 158,429,508 (GRCm39) |
Q759K |
probably damaging |
Het |
Cd276 |
T |
A |
9: 58,444,762 (GRCm39) |
T70S |
possibly damaging |
Het |
Cd38 |
C |
T |
5: 44,057,746 (GRCm39) |
T106I |
probably damaging |
Het |
Cdon |
C |
G |
9: 35,388,244 (GRCm39) |
R740G |
probably damaging |
Het |
Clk2 |
C |
T |
3: 89,076,201 (GRCm39) |
R124W |
possibly damaging |
Het |
Cyp1b1 |
C |
T |
17: 80,021,644 (GRCm39) |
V33M |
possibly damaging |
Het |
Dab1 |
T |
A |
4: 104,589,335 (GRCm39) |
D547E |
probably benign |
Het |
Degs1 |
A |
T |
1: 182,104,416 (GRCm39) |
Y290N |
probably damaging |
Het |
Degs1 |
G |
C |
1: 182,104,417 (GRCm39) |
H289Q |
probably benign |
Het |
Ecpas |
T |
C |
4: 58,853,708 (GRCm39) |
N361S |
probably damaging |
Het |
Ehd4 |
A |
C |
2: 119,932,909 (GRCm39) |
Y172* |
probably null |
Het |
Erc2 |
A |
G |
14: 27,499,165 (GRCm39) |
D347G |
probably damaging |
Het |
Espl1 |
T |
G |
15: 102,212,460 (GRCm39) |
V522G |
probably damaging |
Het |
Fabp9 |
T |
A |
3: 10,262,227 (GRCm39) |
T10S |
probably benign |
Het |
Fam193a |
T |
C |
5: 34,597,877 (GRCm39) |
I558T |
possibly damaging |
Het |
Fhod1 |
T |
C |
8: 106,057,789 (GRCm39) |
E912G |
probably damaging |
Het |
Gja1 |
T |
C |
10: 56,264,645 (GRCm39) |
F335L |
possibly damaging |
Het |
Gm29106 |
A |
G |
1: 118,127,265 (GRCm39) |
H319R |
probably damaging |
Het |
Hunk |
C |
T |
16: 90,269,353 (GRCm39) |
S299F |
probably damaging |
Het |
Hydin |
C |
T |
8: 111,239,642 (GRCm39) |
T1974M |
possibly damaging |
Het |
Ighv10-1 |
T |
A |
12: 114,442,650 (GRCm39) |
T112S |
probably damaging |
Het |
Ireb2 |
T |
A |
9: 54,789,620 (GRCm39) |
V98E |
probably damaging |
Het |
Irf4 |
A |
C |
13: 30,937,435 (GRCm39) |
H167P |
probably benign |
Het |
Irf6 |
C |
T |
1: 192,845,021 (GRCm39) |
P164L |
probably benign |
Het |
Josd1 |
A |
G |
15: 79,561,451 (GRCm39) |
I119T |
probably damaging |
Het |
Kcna5 |
G |
T |
6: 126,512,011 (GRCm39) |
T39K |
probably damaging |
Het |
Klhl24 |
A |
G |
16: 19,941,750 (GRCm39) |
D566G |
probably damaging |
Het |
Kmt2a |
T |
A |
9: 44,761,154 (GRCm39) |
K232* |
probably null |
Het |
Krt36 |
A |
G |
11: 99,996,061 (GRCm39) |
L121P |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,595,864 (GRCm39) |
H931L |
probably benign |
Het |
Lamp3 |
A |
T |
16: 19,474,141 (GRCm39) |
I411N |
probably damaging |
Het |
Lingo3 |
C |
T |
10: 80,670,610 (GRCm39) |
W440* |
probably null |
Het |
Mia2 |
T |
C |
12: 59,236,433 (GRCm39) |
Y712H |
probably damaging |
Het |
Mlh1 |
T |
A |
9: 111,059,145 (GRCm39) |
|
probably null |
Het |
Mta3 |
T |
A |
17: 84,070,363 (GRCm39) |
S174T |
probably benign |
Het |
Myo15a |
A |
G |
11: 60,381,963 (GRCm39) |
T347A |
|
Het |
Naaladl2 |
C |
T |
3: 23,900,718 (GRCm39) |
R704H |
possibly damaging |
Het |
Nfib |
T |
C |
4: 82,246,030 (GRCm39) |
N394S |
probably benign |
Het |
Nr2f2 |
A |
G |
7: 70,009,681 (GRCm39) |
Y133H |
probably damaging |
Het |
Or2ak7 |
C |
T |
11: 58,575,500 (GRCm39) |
S267F |
possibly damaging |
Het |
Or2i1 |
C |
T |
17: 37,508,047 (GRCm39) |
E196K |
probably damaging |
Het |
Or4c115 |
A |
G |
2: 88,927,932 (GRCm39) |
V113A |
possibly damaging |
Het |
Or4f61 |
A |
T |
2: 111,922,822 (GRCm39) |
C75S |
probably benign |
Het |
Or5p62 |
T |
A |
7: 107,771,391 (GRCm39) |
M187L |
probably benign |
Het |
Phgdh |
C |
A |
3: 98,247,124 (GRCm39) |
V9L |
probably damaging |
Het |
Pkd2 |
T |
A |
5: 104,628,103 (GRCm39) |
D392E |
probably damaging |
Het |
Plekhm3 |
A |
G |
1: 64,960,874 (GRCm39) |
S461P |
probably benign |
Het |
Prss39 |
A |
G |
1: 34,539,308 (GRCm39) |
T183A |
probably benign |
Het |
Pter |
T |
A |
2: 12,999,566 (GRCm39) |
I235K |
probably damaging |
Het |
Ptp4a3 |
T |
C |
15: 73,628,756 (GRCm39) |
V172A |
probably benign |
Het |
Rasa2 |
T |
C |
9: 96,484,780 (GRCm39) |
N145D |
probably benign |
Het |
Rasal2 |
A |
T |
1: 157,071,218 (GRCm39) |
H45Q |
probably benign |
Het |
Rbm43 |
A |
G |
2: 51,815,909 (GRCm39) |
V104A |
probably damaging |
Het |
Rhbdd2 |
C |
A |
5: 135,667,969 (GRCm39) |
|
probably null |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rimbp2 |
T |
A |
5: 128,838,528 (GRCm39) |
N1023I |
probably damaging |
Het |
Rtl1 |
A |
T |
12: 109,561,031 (GRCm39) |
D269E |
possibly damaging |
Het |
Sbp |
A |
G |
17: 24,161,163 (GRCm39) |
|
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,316,020 (GRCm39) |
T374S |
probably benign |
Het |
Tgs1 |
A |
T |
4: 3,598,652 (GRCm39) |
K655I |
probably benign |
Het |
Thsd1 |
A |
C |
8: 22,749,585 (GRCm39) |
T819P |
probably damaging |
Het |
Tmprss11c |
C |
T |
5: 86,379,655 (GRCm39) |
V418M |
probably damaging |
Het |
Top2a |
A |
T |
11: 98,900,431 (GRCm39) |
D645E |
probably damaging |
Het |
Top2b |
G |
A |
14: 16,413,081 (GRCm38) |
V997I |
possibly damaging |
Het |
Ttc34 |
A |
G |
4: 154,943,840 (GRCm39) |
D118G |
probably damaging |
Het |
Ttll5 |
A |
G |
12: 85,935,948 (GRCm39) |
D353G |
probably damaging |
Het |
Uba6 |
A |
T |
5: 86,265,924 (GRCm39) |
Y994* |
probably null |
Het |
Vinac1 |
A |
C |
2: 128,879,049 (GRCm39) |
V959G |
unknown |
Het |
Vmn1r189 |
A |
T |
13: 22,285,906 (GRCm39) |
Y310* |
probably null |
Het |
Vps13c |
T |
A |
9: 67,834,265 (GRCm39) |
I1644N |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,821 (GRCm39) |
D73G |
possibly damaging |
Het |
Zfp951 |
A |
T |
5: 104,962,838 (GRCm39) |
C243S |
probably benign |
Het |
|
Other mutations in Dop1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Dop1b
|
APN |
16 |
93,596,914 (GRCm39) |
unclassified |
probably benign |
|
IGL00492:Dop1b
|
APN |
16 |
93,577,670 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00753:Dop1b
|
APN |
16 |
93,566,512 (GRCm39) |
missense |
probably benign |
|
IGL00832:Dop1b
|
APN |
16 |
93,560,289 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00939:Dop1b
|
APN |
16 |
93,570,971 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01019:Dop1b
|
APN |
16 |
93,607,117 (GRCm39) |
missense |
probably benign |
0.32 |
IGL01288:Dop1b
|
APN |
16 |
93,536,181 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01505:Dop1b
|
APN |
16 |
93,554,004 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01535:Dop1b
|
APN |
16 |
93,566,846 (GRCm39) |
nonsense |
probably null |
|
IGL01696:Dop1b
|
APN |
16 |
93,567,128 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Dop1b
|
APN |
16 |
93,577,648 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02163:Dop1b
|
APN |
16 |
93,559,315 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02234:Dop1b
|
APN |
16 |
93,549,039 (GRCm39) |
missense |
probably benign |
|
IGL02302:Dop1b
|
APN |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02485:Dop1b
|
APN |
16 |
93,567,710 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02563:Dop1b
|
APN |
16 |
93,574,293 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02733:Dop1b
|
APN |
16 |
93,536,079 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02792:Dop1b
|
APN |
16 |
93,598,460 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02941:Dop1b
|
APN |
16 |
93,552,361 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03143:Dop1b
|
APN |
16 |
93,556,543 (GRCm39) |
missense |
probably benign |
|
PIT4519001:Dop1b
|
UTSW |
16 |
93,558,942 (GRCm39) |
missense |
probably benign |
|
R0320:Dop1b
|
UTSW |
16 |
93,607,035 (GRCm39) |
missense |
probably benign |
0.02 |
R0499:Dop1b
|
UTSW |
16 |
93,567,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0501:Dop1b
|
UTSW |
16 |
93,549,750 (GRCm39) |
missense |
probably benign |
0.00 |
R0534:Dop1b
|
UTSW |
16 |
93,559,393 (GRCm39) |
missense |
probably benign |
0.04 |
R0583:Dop1b
|
UTSW |
16 |
93,552,374 (GRCm39) |
missense |
probably benign |
0.30 |
R0626:Dop1b
|
UTSW |
16 |
93,560,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R0724:Dop1b
|
UTSW |
16 |
93,559,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0907:Dop1b
|
UTSW |
16 |
93,598,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Dop1b
|
UTSW |
16 |
93,574,274 (GRCm39) |
missense |
probably benign |
|
R1378:Dop1b
|
UTSW |
16 |
93,567,280 (GRCm39) |
missense |
probably benign |
|
R1572:Dop1b
|
UTSW |
16 |
93,567,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R1604:Dop1b
|
UTSW |
16 |
93,559,458 (GRCm39) |
missense |
probably benign |
|
R1642:Dop1b
|
UTSW |
16 |
93,559,203 (GRCm39) |
missense |
probably benign |
0.00 |
R1668:Dop1b
|
UTSW |
16 |
93,562,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Dop1b
|
UTSW |
16 |
93,566,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Dop1b
|
UTSW |
16 |
93,544,509 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1711:Dop1b
|
UTSW |
16 |
93,596,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1917:Dop1b
|
UTSW |
16 |
93,513,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Dop1b
|
UTSW |
16 |
93,579,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R1988:Dop1b
|
UTSW |
16 |
93,563,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Dop1b
|
UTSW |
16 |
93,566,323 (GRCm39) |
missense |
probably benign |
0.36 |
R2139:Dop1b
|
UTSW |
16 |
93,567,895 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2355:Dop1b
|
UTSW |
16 |
93,567,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R3609:Dop1b
|
UTSW |
16 |
93,536,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R3792:Dop1b
|
UTSW |
16 |
93,568,734 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4364:Dop1b
|
UTSW |
16 |
93,567,812 (GRCm39) |
missense |
probably benign |
0.00 |
R4380:Dop1b
|
UTSW |
16 |
93,513,120 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4455:Dop1b
|
UTSW |
16 |
93,563,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R4779:Dop1b
|
UTSW |
16 |
93,553,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Dop1b
|
UTSW |
16 |
93,589,978 (GRCm39) |
missense |
probably benign |
0.00 |
R4834:Dop1b
|
UTSW |
16 |
93,536,892 (GRCm39) |
start codon destroyed |
probably null |
0.70 |
R4866:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R4882:Dop1b
|
UTSW |
16 |
93,549,802 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4900:Dop1b
|
UTSW |
16 |
93,560,318 (GRCm39) |
critical splice donor site |
probably null |
|
R5153:Dop1b
|
UTSW |
16 |
93,570,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R5176:Dop1b
|
UTSW |
16 |
93,536,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5206:Dop1b
|
UTSW |
16 |
93,598,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Dop1b
|
UTSW |
16 |
93,536,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Dop1b
|
UTSW |
16 |
93,567,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Dop1b
|
UTSW |
16 |
93,560,298 (GRCm39) |
missense |
probably damaging |
0.96 |
R5476:Dop1b
|
UTSW |
16 |
93,570,801 (GRCm39) |
splice site |
probably null |
|
R5502:Dop1b
|
UTSW |
16 |
93,590,114 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:Dop1b
|
UTSW |
16 |
93,595,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R5557:Dop1b
|
UTSW |
16 |
93,560,819 (GRCm39) |
missense |
probably damaging |
0.96 |
R5901:Dop1b
|
UTSW |
16 |
93,566,639 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5907:Dop1b
|
UTSW |
16 |
93,598,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Dop1b
|
UTSW |
16 |
93,563,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R6256:Dop1b
|
UTSW |
16 |
93,604,102 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6383:Dop1b
|
UTSW |
16 |
93,579,136 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6525:Dop1b
|
UTSW |
16 |
93,606,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6554:Dop1b
|
UTSW |
16 |
93,557,346 (GRCm39) |
missense |
probably benign |
0.22 |
R6823:Dop1b
|
UTSW |
16 |
93,552,373 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7036:Dop1b
|
UTSW |
16 |
93,574,378 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Dop1b
|
UTSW |
16 |
93,573,878 (GRCm39) |
missense |
probably benign |
0.00 |
R7061:Dop1b
|
UTSW |
16 |
93,558,951 (GRCm39) |
missense |
probably benign |
0.00 |
R7209:Dop1b
|
UTSW |
16 |
93,566,733 (GRCm39) |
missense |
probably benign |
|
R7214:Dop1b
|
UTSW |
16 |
93,607,023 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7232:Dop1b
|
UTSW |
16 |
93,557,373 (GRCm39) |
critical splice donor site |
probably null |
|
R7255:Dop1b
|
UTSW |
16 |
93,567,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R7335:Dop1b
|
UTSW |
16 |
93,544,396 (GRCm39) |
missense |
probably benign |
0.04 |
R7535:Dop1b
|
UTSW |
16 |
93,603,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Dop1b
|
UTSW |
16 |
93,595,649 (GRCm39) |
splice site |
probably null |
|
R7763:Dop1b
|
UTSW |
16 |
93,552,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7814:Dop1b
|
UTSW |
16 |
93,596,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7839:Dop1b
|
UTSW |
16 |
93,560,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R7862:Dop1b
|
UTSW |
16 |
93,546,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7952:Dop1b
|
UTSW |
16 |
93,546,848 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7956:Dop1b
|
UTSW |
16 |
93,567,916 (GRCm39) |
critical splice donor site |
probably null |
|
R8033:Dop1b
|
UTSW |
16 |
93,566,371 (GRCm39) |
missense |
probably benign |
|
R8061:Dop1b
|
UTSW |
16 |
93,546,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R8067:Dop1b
|
UTSW |
16 |
93,562,336 (GRCm39) |
nonsense |
probably null |
|
R8146:Dop1b
|
UTSW |
16 |
93,546,827 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8184:Dop1b
|
UTSW |
16 |
93,573,881 (GRCm39) |
missense |
probably benign |
0.13 |
R8221:Dop1b
|
UTSW |
16 |
93,546,847 (GRCm39) |
missense |
probably benign |
0.01 |
R8263:Dop1b
|
UTSW |
16 |
93,559,083 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8329:Dop1b
|
UTSW |
16 |
93,568,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Dop1b
|
UTSW |
16 |
93,568,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Dop1b
|
UTSW |
16 |
93,570,809 (GRCm39) |
missense |
probably benign |
|
R8683:Dop1b
|
UTSW |
16 |
93,568,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R8716:Dop1b
|
UTSW |
16 |
93,577,673 (GRCm39) |
nonsense |
probably null |
|
R8807:Dop1b
|
UTSW |
16 |
93,558,973 (GRCm39) |
missense |
probably benign |
0.03 |
R8840:Dop1b
|
UTSW |
16 |
93,607,005 (GRCm39) |
missense |
probably benign |
0.08 |
R8851:Dop1b
|
UTSW |
16 |
93,559,398 (GRCm39) |
missense |
probably benign |
0.39 |
R8884:Dop1b
|
UTSW |
16 |
93,556,550 (GRCm39) |
missense |
probably benign |
|
R8976:Dop1b
|
UTSW |
16 |
93,558,969 (GRCm39) |
missense |
probably benign |
0.01 |
R9219:Dop1b
|
UTSW |
16 |
93,567,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Dop1b
|
UTSW |
16 |
93,546,018 (GRCm39) |
missense |
probably benign |
0.14 |
R9284:Dop1b
|
UTSW |
16 |
93,557,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Dop1b
|
UTSW |
16 |
93,568,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R9298:Dop1b
|
UTSW |
16 |
93,597,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R9338:Dop1b
|
UTSW |
16 |
93,600,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Dop1b
|
UTSW |
16 |
93,577,702 (GRCm39) |
critical splice donor site |
probably null |
|
R9444:Dop1b
|
UTSW |
16 |
93,607,127 (GRCm39) |
missense |
probably benign |
0.00 |
R9500:Dop1b
|
UTSW |
16 |
93,607,171 (GRCm39) |
missense |
probably benign |
|
R9601:Dop1b
|
UTSW |
16 |
93,544,531 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9793:Dop1b
|
UTSW |
16 |
93,598,503 (GRCm39) |
missense |
probably benign |
0.30 |
Z1088:Dop1b
|
UTSW |
16 |
93,560,214 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,604,756 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1176:Dop1b
|
UTSW |
16 |
93,600,434 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dop1b
|
UTSW |
16 |
93,566,469 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dop1b
|
UTSW |
16 |
93,560,783 (GRCm39) |
missense |
probably damaging |
1.00 |
|