Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
T |
9: 46,218,120 (GRCm39) |
I206N |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,947,248 (GRCm39) |
D315E |
probably damaging |
Het |
Abcc8 |
A |
G |
7: 45,773,330 (GRCm39) |
F800L |
probably benign |
Het |
Adamts16 |
C |
A |
13: 70,877,029 (GRCm39) |
C1204F |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 89,038,856 (GRCm39) |
T291A |
possibly damaging |
Het |
AI182371 |
G |
T |
2: 34,976,134 (GRCm39) |
Q255K |
possibly damaging |
Het |
Aig1 |
A |
T |
10: 13,677,528 (GRCm39) |
|
probably benign |
Het |
Ak5 |
T |
C |
3: 152,321,589 (GRCm39) |
D266G |
probably damaging |
Het |
Ank1 |
A |
T |
8: 23,630,220 (GRCm39) |
E93D |
probably damaging |
Het |
Bop1 |
T |
C |
15: 76,340,117 (GRCm39) |
D153G |
probably damaging |
Het |
Bub1 |
G |
T |
2: 127,661,142 (GRCm39) |
N316K |
probably benign |
Het |
Capn1 |
T |
C |
19: 6,047,827 (GRCm39) |
N412S |
probably benign |
Het |
Cdca4 |
A |
G |
12: 112,785,339 (GRCm39) |
S130P |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,264,158 (GRCm39) |
D663E |
probably damaging |
Het |
Clca3a1 |
T |
C |
3: 144,455,403 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
C |
T |
4: 128,091,178 (GRCm39) |
P239L |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 91,646,579 (GRCm39) |
|
probably benign |
Het |
Dnpep |
C |
T |
1: 75,288,635 (GRCm39) |
|
probably null |
Het |
Dscam |
C |
T |
16: 96,622,120 (GRCm39) |
D444N |
probably damaging |
Het |
Emc9 |
C |
T |
14: 55,819,569 (GRCm39) |
|
probably null |
Het |
Ero1b |
T |
A |
13: 12,615,207 (GRCm39) |
I346N |
probably damaging |
Het |
Etv3 |
A |
G |
3: 87,442,850 (GRCm39) |
T145A |
probably benign |
Het |
Fam170a |
T |
A |
18: 50,415,321 (GRCm39) |
|
probably null |
Het |
Fap |
A |
T |
2: 62,374,700 (GRCm39) |
I261N |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,178,409 (GRCm39) |
N1943S |
probably damaging |
Het |
Glb1l3 |
A |
T |
9: 26,737,679 (GRCm39) |
V466E |
probably damaging |
Het |
Gm10521 |
A |
T |
1: 171,724,070 (GRCm39) |
H127L |
unknown |
Het |
Gm8186 |
G |
T |
17: 26,318,130 (GRCm39) |
N22K |
probably damaging |
Het |
Gpr132 |
A |
C |
12: 112,815,717 (GRCm39) |
L370V |
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,845,537 (GRCm39) |
H449Q |
probably damaging |
Het |
Hook3 |
A |
G |
8: 26,534,306 (GRCm39) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,311,345 (GRCm39) |
D1180G |
probably benign |
Het |
Isoc2b |
A |
T |
7: 4,852,577 (GRCm39) |
|
probably null |
Het |
Itga4 |
C |
T |
2: 79,153,000 (GRCm39) |
H896Y |
probably benign |
Het |
Itga7 |
T |
C |
10: 128,778,850 (GRCm39) |
Y326H |
probably damaging |
Het |
Itpr3 |
A |
T |
17: 27,336,867 (GRCm39) |
E2397V |
probably damaging |
Het |
Jtb |
T |
G |
3: 90,142,884 (GRCm39) |
|
probably null |
Het |
Klk15 |
A |
G |
7: 43,588,183 (GRCm39) |
T164A |
probably benign |
Het |
Kmt2e |
C |
A |
5: 23,669,704 (GRCm39) |
H64N |
probably damaging |
Het |
Lamtor3 |
T |
A |
3: 137,633,054 (GRCm39) |
|
probably benign |
Het |
Laptm4b |
A |
G |
15: 34,258,830 (GRCm39) |
I35V |
possibly damaging |
Het |
Lrrc1 |
A |
C |
9: 77,341,379 (GRCm39) |
L393R |
probably damaging |
Het |
Ltn1 |
A |
G |
16: 87,178,391 (GRCm39) |
S1613P |
possibly damaging |
Het |
Mtmr4 |
T |
A |
11: 87,502,876 (GRCm39) |
W920R |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,267,950 (GRCm39) |
|
probably benign |
Het |
Nup133 |
A |
G |
8: 124,643,038 (GRCm39) |
Y761H |
possibly damaging |
Het |
Nwd2 |
T |
A |
5: 63,963,326 (GRCm39) |
V970D |
probably damaging |
Het |
Or4c126 |
A |
G |
2: 89,824,301 (GRCm39) |
H188R |
probably benign |
Het |
Or6n1 |
T |
C |
1: 173,916,785 (GRCm39) |
Y60H |
probably benign |
Het |
Or8k24 |
A |
T |
2: 86,216,218 (GRCm39) |
S181R |
probably damaging |
Het |
Osbp |
C |
T |
19: 11,951,240 (GRCm39) |
L262F |
probably damaging |
Het |
Phf8-ps |
G |
T |
17: 33,285,124 (GRCm39) |
D559E |
probably benign |
Het |
Phldb2 |
G |
T |
16: 45,645,551 (GRCm39) |
D343E |
probably damaging |
Het |
Phrf1 |
T |
A |
7: 140,840,453 (GRCm39) |
M1216K |
possibly damaging |
Het |
Phyh |
A |
T |
2: 4,935,462 (GRCm39) |
|
probably null |
Het |
Plekhf1 |
A |
T |
7: 37,921,594 (GRCm39) |
|
probably null |
Het |
Rars1 |
T |
C |
11: 35,719,475 (GRCm39) |
N116D |
probably damaging |
Het |
Rnf44 |
T |
A |
13: 54,830,621 (GRCm39) |
Q181L |
possibly damaging |
Het |
Rpe65 |
T |
C |
3: 159,321,319 (GRCm39) |
|
probably null |
Het |
Scaf1 |
A |
G |
7: 44,663,016 (GRCm39) |
|
probably benign |
Het |
Serpinb11 |
A |
T |
1: 107,299,919 (GRCm39) |
R88S |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,616,560 (GRCm39) |
N174S |
probably damaging |
Het |
Slc9a5 |
T |
C |
8: 106,083,807 (GRCm39) |
|
probably null |
Het |
Slfn1 |
C |
A |
11: 83,012,002 (GRCm39) |
N39K |
possibly damaging |
Het |
Snx20 |
G |
A |
8: 89,353,923 (GRCm39) |
A269V |
possibly damaging |
Het |
Snx6 |
A |
G |
12: 54,801,104 (GRCm39) |
Y298H |
probably damaging |
Het |
Stk32c |
C |
T |
7: 138,700,590 (GRCm39) |
R213Q |
probably benign |
Het |
Tgfbr1 |
A |
T |
4: 47,396,555 (GRCm39) |
I190F |
probably damaging |
Het |
Ube2d2b |
T |
A |
5: 107,978,498 (GRCm39) |
F50I |
probably damaging |
Het |
Ubl5 |
G |
A |
9: 20,557,830 (GRCm39) |
|
probably benign |
Het |
Ubqln5 |
T |
G |
7: 103,777,781 (GRCm39) |
T348P |
possibly damaging |
Het |
Usp46 |
T |
C |
5: 74,197,746 (GRCm39) |
D22G |
probably benign |
Het |
Vars1 |
A |
G |
17: 35,231,352 (GRCm39) |
N655S |
probably damaging |
Het |
Vmn2r103 |
A |
C |
17: 20,032,715 (GRCm39) |
I830L |
possibly damaging |
Het |
Vmn2r26 |
T |
A |
6: 124,016,830 (GRCm39) |
N431K |
probably benign |
Het |
Vmn2r4 |
G |
T |
3: 64,298,487 (GRCm39) |
P547Q |
probably damaging |
Het |
Yy1 |
T |
A |
12: 108,772,354 (GRCm39) |
|
probably benign |
Het |
Zbtb2 |
A |
T |
10: 4,318,592 (GRCm39) |
L478Q |
possibly damaging |
Het |
Zfp12 |
T |
C |
5: 143,225,743 (GRCm39) |
F17S |
probably damaging |
Het |
Zfp219 |
T |
A |
14: 52,244,606 (GRCm39) |
|
probably null |
Het |
Zfp629 |
G |
A |
7: 127,209,542 (GRCm39) |
H756Y |
probably damaging |
Het |
Zfp748 |
T |
C |
13: 67,689,292 (GRCm39) |
K656R |
possibly damaging |
Het |
Zfp958 |
T |
A |
8: 4,679,072 (GRCm39) |
Y366N |
probably benign |
Het |
Zp3 |
C |
T |
5: 136,017,377 (GRCm39) |
T396I |
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 |
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 |
R7894:Dop1b
|
UTSW |
16 |
93,607,092 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|