Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406C07Rik |
G |
A |
9: 15,196,214 (GRCm39) |
T283M |
probably damaging |
Het |
Abca9 |
A |
G |
11: 110,056,817 (GRCm39) |
M1T |
probably null |
Het |
Ackr1 |
T |
C |
1: 173,159,952 (GRCm39) |
Y189C |
probably damaging |
Het |
Acsm4 |
A |
G |
7: 119,304,264 (GRCm39) |
D303G |
probably benign |
Het |
Arfgef2 |
A |
T |
2: 166,708,867 (GRCm39) |
M1060L |
probably benign |
Het |
Arhgef40 |
T |
A |
14: 52,238,414 (GRCm39) |
F1298I |
probably damaging |
Het |
Atg2a |
T |
C |
19: 6,306,674 (GRCm39) |
I1453T |
probably benign |
Het |
B4galnt1 |
A |
T |
10: 127,007,584 (GRCm39) |
D495V |
probably benign |
Het |
Brpf3 |
T |
A |
17: 29,040,214 (GRCm39) |
D878E |
probably benign |
Het |
C3 |
A |
G |
17: 57,511,015 (GRCm39) |
*1664R |
probably null |
Het |
Cap2 |
A |
G |
13: 46,684,548 (GRCm39) |
T73A |
probably benign |
Het |
Ccr6 |
A |
T |
17: 8,475,394 (GRCm39) |
I200F |
probably damaging |
Het |
Cdc42bpb |
C |
T |
12: 111,274,221 (GRCm39) |
G1021R |
probably benign |
Het |
Cidea |
C |
A |
18: 67,499,485 (GRCm39) |
S124* |
probably null |
Het |
Cnst |
C |
A |
1: 179,420,274 (GRCm39) |
T135K |
probably benign |
Het |
Crebbp |
A |
T |
16: 3,936,952 (GRCm39) |
M805K |
probably benign |
Het |
Crybb1 |
A |
G |
5: 112,411,439 (GRCm39) |
Y119C |
probably damaging |
Het |
Cux1 |
G |
T |
5: 136,402,220 (GRCm39) |
T121K |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 118,049,384 (GRCm39) |
|
probably null |
Het |
Dnmbp |
T |
C |
19: 43,900,677 (GRCm39) |
T48A |
probably damaging |
Het |
Dysf |
G |
A |
6: 84,171,353 (GRCm39) |
G1787E |
probably damaging |
Het |
Gcm2 |
T |
A |
13: 41,258,096 (GRCm39) |
R177S |
probably benign |
Het |
Gdf6 |
G |
T |
4: 9,859,429 (GRCm39) |
R170S |
probably damaging |
Het |
Gm16686 |
A |
T |
4: 88,673,775 (GRCm39) |
M18K |
unknown |
Het |
Gm36864 |
C |
T |
7: 43,886,304 (GRCm39) |
Q179* |
probably null |
Het |
Golgb1 |
A |
G |
16: 36,736,675 (GRCm39) |
D2015G |
probably damaging |
Het |
Gtf2i |
A |
G |
5: 134,324,374 (GRCm39) |
L30P |
probably damaging |
Het |
Herc2 |
A |
G |
7: 55,798,402 (GRCm39) |
E1955G |
possibly damaging |
Het |
Hes3 |
A |
T |
4: 152,372,132 (GRCm39) |
D37E |
probably damaging |
Het |
Igha |
A |
G |
12: 113,223,144 (GRCm39) |
V161A |
probably damaging |
Het |
Isl2 |
T |
G |
9: 55,452,722 (GRCm39) |
S327A |
probably benign |
Het |
Itk |
A |
G |
11: 46,231,539 (GRCm39) |
L339P |
probably damaging |
Het |
Kcnb2 |
T |
C |
1: 15,780,648 (GRCm39) |
S507P |
probably benign |
Het |
Lgals4 |
C |
T |
7: 28,540,921 (GRCm39) |
R282C |
probably damaging |
Het |
Lhfpl4 |
C |
A |
6: 113,171,034 (GRCm39) |
V51L |
possibly damaging |
Het |
Lhpp |
A |
G |
7: 132,243,261 (GRCm39) |
Y159C |
probably damaging |
Het |
Lrwd1 |
C |
A |
5: 136,162,257 (GRCm39) |
E159* |
probably null |
Het |
Map3k13 |
A |
G |
16: 21,745,008 (GRCm39) |
T856A |
probably damaging |
Het |
Mcm8 |
A |
G |
2: 132,665,141 (GRCm39) |
T206A |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,352,436 (GRCm39) |
K1265R |
probably benign |
Het |
Mrgprb2 |
A |
G |
7: 48,202,648 (GRCm39) |
Y26H |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,817,208 (GRCm39) |
|
probably benign |
Het |
Mysm1 |
C |
T |
4: 94,856,196 (GRCm39) |
G134S |
probably damaging |
Het |
Nlrp3 |
A |
C |
11: 59,440,216 (GRCm39) |
I598L |
probably benign |
Het |
Npas2 |
A |
T |
1: 39,331,797 (GRCm39) |
I71F |
possibly damaging |
Het |
Nr1h5 |
A |
G |
3: 102,862,015 (GRCm39) |
S85P |
probably benign |
Het |
Nrcam |
T |
A |
12: 44,619,075 (GRCm39) |
V868D |
possibly damaging |
Het |
Oas1a |
A |
G |
5: 121,040,019 (GRCm39) |
F191L |
probably damaging |
Het |
Or14j8 |
A |
T |
17: 38,263,673 (GRCm39) |
Y81N |
possibly damaging |
Het |
Orc3 |
A |
T |
4: 34,599,778 (GRCm39) |
L125H |
possibly damaging |
Het |
Osbpl7 |
A |
G |
11: 96,946,903 (GRCm39) |
E402G |
possibly damaging |
Het |
Phlda2 |
A |
C |
7: 143,055,959 (GRCm39) |
I90S |
probably damaging |
Het |
Plin3 |
C |
T |
17: 56,593,490 (GRCm39) |
V75I |
probably benign |
Het |
Pms1 |
A |
T |
1: 53,321,195 (GRCm39) |
S13T |
possibly damaging |
Het |
Ppm1d |
A |
G |
11: 85,236,732 (GRCm39) |
K504E |
probably damaging |
Het |
Rflna |
A |
T |
5: 125,087,541 (GRCm39) |
I93F |
probably damaging |
Het |
Rnpc3 |
T |
A |
3: 113,414,805 (GRCm39) |
M193L |
probably benign |
Het |
Sema3e |
A |
T |
5: 14,214,169 (GRCm39) |
I145F |
possibly damaging |
Het |
Serpinb1b |
C |
A |
13: 33,271,500 (GRCm39) |
N90K |
probably damaging |
Het |
Sfswap |
A |
G |
5: 129,620,345 (GRCm39) |
D538G |
possibly damaging |
Het |
Snx14 |
A |
T |
9: 88,289,453 (GRCm39) |
D266E |
possibly damaging |
Het |
Stat4 |
C |
T |
1: 52,115,711 (GRCm39) |
T217M |
possibly damaging |
Het |
Taf13 |
T |
C |
3: 108,485,444 (GRCm39) |
M40T |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,523,047 (GRCm39) |
T1530A |
probably damaging |
Het |
Tenm4 |
C |
T |
7: 96,555,148 (GRCm39) |
P2618S |
probably benign |
Het |
Tnfrsf14 |
T |
C |
4: 155,007,710 (GRCm39) |
I220M |
possibly damaging |
Het |
Tnk2 |
T |
C |
16: 32,484,718 (GRCm39) |
W60R |
probably damaging |
Het |
Tph2 |
A |
T |
10: 115,015,614 (GRCm39) |
|
probably benign |
Het |
Unc13b |
A |
T |
4: 43,177,564 (GRCm39) |
K2797N |
unknown |
Het |
Upf1 |
C |
G |
8: 70,785,973 (GRCm39) |
M995I |
probably benign |
Het |
Upf1 |
G |
A |
8: 70,785,972 (GRCm39) |
P996S |
probably benign |
Het |
Vcan |
C |
T |
13: 89,840,439 (GRCm39) |
V1702M |
probably benign |
Het |
Vmn2r57 |
T |
C |
7: 41,077,020 (GRCm39) |
D382G |
probably benign |
Het |
Xxylt1 |
C |
T |
16: 30,899,964 (GRCm39) |
A64T |
probably benign |
Het |
Zcchc8 |
A |
G |
5: 123,841,070 (GRCm39) |
S407P |
probably damaging |
Het |
Zdhhc19 |
T |
A |
16: 32,317,187 (GRCm39) |
F109Y |
probably damaging |
Het |
Zfp638 |
T |
C |
6: 83,931,745 (GRCm39) |
|
probably null |
Het |
Zfp691 |
A |
G |
4: 119,027,861 (GRCm39) |
S124P |
probably damaging |
Het |
Zfp804a |
T |
A |
2: 82,089,450 (GRCm39) |
V1093D |
probably damaging |
Het |
Zfp986 |
A |
C |
4: 145,625,550 (GRCm39) |
Q70P |
probably benign |
Het |
|
Other mutations in Otof |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Otof
|
APN |
5 |
30,533,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00391:Otof
|
APN |
5 |
30,532,967 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00579:Otof
|
APN |
5 |
30,556,666 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00671:Otof
|
APN |
5 |
30,543,097 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01019:Otof
|
APN |
5 |
30,562,560 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01025:Otof
|
APN |
5 |
30,541,597 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01086:Otof
|
APN |
5 |
30,533,617 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01110:Otof
|
APN |
5 |
30,619,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01160:Otof
|
APN |
5 |
30,538,879 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01285:Otof
|
APN |
5 |
30,562,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01329:Otof
|
APN |
5 |
30,598,723 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01337:Otof
|
APN |
5 |
30,576,856 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01337:Otof
|
APN |
5 |
30,563,121 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01834:Otof
|
APN |
5 |
30,556,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Otof
|
APN |
5 |
30,536,598 (GRCm39) |
splice site |
probably benign |
|
IGL01969:Otof
|
APN |
5 |
30,539,827 (GRCm39) |
splice site |
probably benign |
|
IGL02075:Otof
|
APN |
5 |
30,528,070 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02077:Otof
|
APN |
5 |
30,556,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Otof
|
APN |
5 |
30,531,336 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02227:Otof
|
APN |
5 |
30,528,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Otof
|
APN |
5 |
30,534,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Otof
|
APN |
5 |
30,531,426 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02864:Otof
|
APN |
5 |
30,543,685 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03176:Otof
|
APN |
5 |
30,562,520 (GRCm39) |
splice site |
probably null |
|
R0285:Otof
|
UTSW |
5 |
30,536,877 (GRCm39) |
critical splice donor site |
probably null |
|
R0421:Otof
|
UTSW |
5 |
30,528,912 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0570:Otof
|
UTSW |
5 |
30,529,225 (GRCm39) |
splice site |
probably benign |
|
R0599:Otof
|
UTSW |
5 |
30,528,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Otof
|
UTSW |
5 |
30,539,705 (GRCm39) |
missense |
probably benign |
0.01 |
R0715:Otof
|
UTSW |
5 |
30,552,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1019:Otof
|
UTSW |
5 |
30,528,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R1183:Otof
|
UTSW |
5 |
30,529,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Otof
|
UTSW |
5 |
30,536,039 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Otof
|
UTSW |
5 |
30,537,571 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Otof
|
UTSW |
5 |
30,537,571 (GRCm39) |
missense |
probably benign |
0.00 |
R1474:Otof
|
UTSW |
5 |
30,536,876 (GRCm39) |
critical splice donor site |
probably null |
|
R1524:Otof
|
UTSW |
5 |
30,536,900 (GRCm39) |
missense |
probably benign |
0.03 |
R1563:Otof
|
UTSW |
5 |
30,528,349 (GRCm39) |
missense |
probably benign |
0.00 |
R1732:Otof
|
UTSW |
5 |
30,543,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Otof
|
UTSW |
5 |
30,536,054 (GRCm39) |
missense |
probably benign |
0.00 |
R1845:Otof
|
UTSW |
5 |
30,529,067 (GRCm39) |
nonsense |
probably null |
|
R1925:Otof
|
UTSW |
5 |
30,551,532 (GRCm39) |
missense |
probably benign |
0.37 |
R1938:Otof
|
UTSW |
5 |
30,533,713 (GRCm39) |
missense |
probably benign |
0.00 |
R1968:Otof
|
UTSW |
5 |
30,545,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Otof
|
UTSW |
5 |
30,578,381 (GRCm39) |
missense |
probably benign |
0.01 |
R1999:Otof
|
UTSW |
5 |
30,546,116 (GRCm39) |
missense |
probably benign |
0.19 |
R2027:Otof
|
UTSW |
5 |
30,578,358 (GRCm39) |
missense |
probably benign |
0.08 |
R2138:Otof
|
UTSW |
5 |
30,619,114 (GRCm39) |
missense |
probably benign |
0.01 |
R2173:Otof
|
UTSW |
5 |
30,543,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Otof
|
UTSW |
5 |
30,527,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Otof
|
UTSW |
5 |
30,540,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Otof
|
UTSW |
5 |
30,539,145 (GRCm39) |
missense |
probably benign |
0.03 |
R3442:Otof
|
UTSW |
5 |
30,529,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Otof
|
UTSW |
5 |
30,542,610 (GRCm39) |
missense |
probably benign |
|
R3715:Otof
|
UTSW |
5 |
30,534,215 (GRCm39) |
nonsense |
probably null |
|
R3806:Otof
|
UTSW |
5 |
30,543,843 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3975:Otof
|
UTSW |
5 |
30,528,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Otof
|
UTSW |
5 |
30,556,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Otof
|
UTSW |
5 |
30,576,850 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4166:Otof
|
UTSW |
5 |
30,539,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4451:Otof
|
UTSW |
5 |
30,542,508 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4485:Otof
|
UTSW |
5 |
30,532,344 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4600:Otof
|
UTSW |
5 |
30,529,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Otof
|
UTSW |
5 |
30,540,914 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4648:Otof
|
UTSW |
5 |
30,540,914 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4669:Otof
|
UTSW |
5 |
30,578,318 (GRCm39) |
critical splice donor site |
probably null |
|
R4773:Otof
|
UTSW |
5 |
30,552,026 (GRCm39) |
missense |
probably benign |
0.05 |
R4839:Otof
|
UTSW |
5 |
30,576,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R4907:Otof
|
UTSW |
5 |
30,536,005 (GRCm39) |
critical splice donor site |
probably null |
|
R4961:Otof
|
UTSW |
5 |
30,540,837 (GRCm39) |
intron |
probably benign |
|
R4991:Otof
|
UTSW |
5 |
30,551,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Otof
|
UTSW |
5 |
30,540,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R5036:Otof
|
UTSW |
5 |
30,541,783 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5038:Otof
|
UTSW |
5 |
30,541,783 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5253:Otof
|
UTSW |
5 |
30,527,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Otof
|
UTSW |
5 |
30,534,064 (GRCm39) |
missense |
probably benign |
0.01 |
R5365:Otof
|
UTSW |
5 |
30,539,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Otof
|
UTSW |
5 |
30,532,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Otof
|
UTSW |
5 |
30,529,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R6318:Otof
|
UTSW |
5 |
30,571,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Otof
|
UTSW |
5 |
30,529,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6671:Otof
|
UTSW |
5 |
30,576,877 (GRCm39) |
missense |
probably benign |
|
R6701:Otof
|
UTSW |
5 |
30,528,141 (GRCm39) |
nonsense |
probably null |
|
R6792:Otof
|
UTSW |
5 |
30,532,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:Otof
|
UTSW |
5 |
30,545,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Otof
|
UTSW |
5 |
30,528,987 (GRCm39) |
missense |
probably damaging |
0.96 |
R7037:Otof
|
UTSW |
5 |
30,538,882 (GRCm39) |
missense |
probably benign |
0.32 |
R7060:Otof
|
UTSW |
5 |
30,545,700 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7089:Otof
|
UTSW |
5 |
30,528,912 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7165:Otof
|
UTSW |
5 |
30,532,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R7178:Otof
|
UTSW |
5 |
30,540,878 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7298:Otof
|
UTSW |
5 |
30,545,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Otof
|
UTSW |
5 |
30,527,614 (GRCm39) |
missense |
probably benign |
0.45 |
R7397:Otof
|
UTSW |
5 |
30,533,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7400:Otof
|
UTSW |
5 |
30,542,532 (GRCm39) |
missense |
probably benign |
0.04 |
R7428:Otof
|
UTSW |
5 |
30,547,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Otof
|
UTSW |
5 |
30,552,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Otof
|
UTSW |
5 |
30,528,364 (GRCm39) |
missense |
probably benign |
0.00 |
R7714:Otof
|
UTSW |
5 |
30,527,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R8002:Otof
|
UTSW |
5 |
30,537,954 (GRCm39) |
missense |
probably benign |
0.10 |
R8032:Otof
|
UTSW |
5 |
30,619,142 (GRCm39) |
start codon destroyed |
probably benign |
0.07 |
R8153:Otof
|
UTSW |
5 |
30,546,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Otof
|
UTSW |
5 |
30,537,538 (GRCm39) |
missense |
probably benign |
0.37 |
R8159:Otof
|
UTSW |
5 |
30,537,538 (GRCm39) |
missense |
probably benign |
0.37 |
R8441:Otof
|
UTSW |
5 |
30,538,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R8813:Otof
|
UTSW |
5 |
30,540,242 (GRCm39) |
missense |
probably benign |
0.02 |
R8835:Otof
|
UTSW |
5 |
30,528,264 (GRCm39) |
missense |
probably benign |
0.44 |
R8852:Otof
|
UTSW |
5 |
30,529,044 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8869:Otof
|
UTSW |
5 |
30,578,325 (GRCm39) |
missense |
probably benign |
0.08 |
R9029:Otof
|
UTSW |
5 |
30,527,419 (GRCm39) |
critical splice donor site |
probably null |
|
R9031:Otof
|
UTSW |
5 |
30,537,532 (GRCm39) |
missense |
probably benign |
|
R9061:Otof
|
UTSW |
5 |
30,546,001 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9100:Otof
|
UTSW |
5 |
30,539,696 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9121:Otof
|
UTSW |
5 |
30,536,462 (GRCm39) |
missense |
probably benign |
0.04 |
R9188:Otof
|
UTSW |
5 |
30,534,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Otof
|
UTSW |
5 |
30,542,469 (GRCm39) |
missense |
probably benign |
|
R9280:Otof
|
UTSW |
5 |
30,528,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R9395:Otof
|
UTSW |
5 |
30,532,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Otof
|
UTSW |
5 |
30,540,863 (GRCm39) |
critical splice donor site |
probably null |
|
R9407:Otof
|
UTSW |
5 |
30,538,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Otof
|
UTSW |
5 |
30,539,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9665:Otof
|
UTSW |
5 |
30,584,895 (GRCm39) |
missense |
probably benign |
0.22 |
R9748:Otof
|
UTSW |
5 |
30,540,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R9783:Otof
|
UTSW |
5 |
30,536,576 (GRCm39) |
missense |
probably benign |
|
Z1176:Otof
|
UTSW |
5 |
30,528,930 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Otof
|
UTSW |
5 |
30,541,002 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Otof
|
UTSW |
5 |
30,533,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|