Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059E24Rik |
C |
T |
19: 21,630,075 (GRCm39) |
|
probably benign |
Het |
Abcd4 |
C |
T |
12: 84,655,356 (GRCm39) |
W369* |
probably null |
Het |
Abcf3 |
A |
G |
16: 20,368,056 (GRCm39) |
E98G |
probably benign |
Het |
Acaca |
A |
T |
11: 84,262,410 (GRCm39) |
D2004V |
probably damaging |
Het |
Acot5 |
G |
C |
12: 84,116,630 (GRCm39) |
M130I |
|
Het |
Adamts3 |
C |
T |
5: 89,825,693 (GRCm39) |
E1049K |
probably benign |
Het |
Agfg2 |
A |
T |
5: 137,650,744 (GRCm39) |
L456Q |
probably damaging |
Het |
Agtr1b |
T |
A |
3: 20,370,343 (GRCm39) |
T88S |
possibly damaging |
Het |
Amer2 |
G |
C |
14: 60,617,376 (GRCm39) |
D524H |
probably damaging |
Het |
Ankrd61 |
T |
A |
5: 143,831,676 (GRCm39) |
T43S |
probably benign |
Het |
Apcs |
A |
G |
1: 172,721,776 (GRCm39) |
L190P |
probably benign |
Het |
Arsg |
A |
G |
11: 109,381,346 (GRCm39) |
K30E |
probably benign |
Het |
Banp |
A |
T |
8: 122,705,441 (GRCm39) |
M104L |
possibly damaging |
Het |
Caskin1 |
A |
G |
17: 24,718,111 (GRCm39) |
Q268R |
probably benign |
Het |
Ccdc112 |
A |
G |
18: 46,429,455 (GRCm39) |
V81A |
probably damaging |
Het |
Cfap44 |
T |
C |
16: 44,280,517 (GRCm39) |
I1432T |
probably damaging |
Het |
Chd2 |
A |
T |
7: 73,134,294 (GRCm39) |
N684K |
probably damaging |
Het |
Creb1 |
T |
C |
1: 64,605,478 (GRCm39) |
|
probably null |
Het |
Ctsc |
C |
T |
7: 87,927,502 (GRCm39) |
T31I |
probably damaging |
Het |
Cttnbp2 |
C |
A |
6: 18,434,430 (GRCm39) |
R476L |
probably damaging |
Het |
Cwf19l1 |
T |
C |
19: 44,111,653 (GRCm39) |
D260G |
possibly damaging |
Het |
Cyp24a1 |
A |
T |
2: 170,336,005 (GRCm39) |
S211T |
probably damaging |
Het |
Ddx3y |
T |
C |
Y: 1,282,919 (GRCm39) |
N46D |
probably damaging |
Het |
Dgkz |
G |
T |
2: 91,769,090 (GRCm39) |
H653Q |
probably benign |
Het |
Dnajc16 |
A |
T |
4: 141,491,945 (GRCm39) |
I626N |
possibly damaging |
Het |
Dsc2 |
T |
C |
18: 20,171,151 (GRCm39) |
D616G |
probably benign |
Het |
Dst |
T |
A |
1: 34,267,774 (GRCm39) |
V3058E |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,858,959 (GRCm39) |
C1125S |
unknown |
Het |
Glyatl3 |
G |
A |
17: 41,223,619 (GRCm39) |
Q41* |
probably null |
Het |
Gm7694 |
T |
G |
1: 170,128,927 (GRCm39) |
I201L |
probably damaging |
Het |
Gnal |
C |
T |
18: 67,221,830 (GRCm39) |
R78* |
probably null |
Het |
Gtf3c1 |
T |
C |
7: 125,303,069 (GRCm39) |
D122G |
probably benign |
Het |
Htt |
G |
T |
5: 34,975,095 (GRCm39) |
D622Y |
possibly damaging |
Het |
Igkv4-92 |
A |
G |
6: 68,732,081 (GRCm39) |
C98R |
probably benign |
Het |
Incenp |
G |
A |
19: 9,855,088 (GRCm39) |
R608* |
probably null |
Het |
Kics2 |
A |
G |
10: 121,586,501 (GRCm39) |
Y272C |
probably damaging |
Het |
Kif3c |
G |
A |
12: 3,451,706 (GRCm39) |
R679H |
probably damaging |
Het |
Kng1 |
T |
A |
16: 22,898,146 (GRCm39) |
H515Q |
probably damaging |
Het |
Lamb2 |
T |
C |
9: 108,361,370 (GRCm39) |
|
probably null |
Het |
Malrd1 |
A |
T |
2: 15,850,140 (GRCm39) |
N1253I |
unknown |
Het |
Map3k21 |
A |
T |
8: 126,637,471 (GRCm39) |
D19V |
|
Het |
Marchf2 |
G |
T |
17: 33,915,207 (GRCm39) |
P129Q |
probably damaging |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Ms4a4d |
T |
A |
19: 11,533,564 (GRCm39) |
D148E |
possibly damaging |
Het |
Myl4 |
A |
G |
11: 104,468,384 (GRCm39) |
D36G |
probably damaging |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or2a25 |
T |
C |
6: 42,889,170 (GRCm39) |
S238P |
probably damaging |
Het |
Or5ac24 |
A |
T |
16: 59,165,929 (GRCm39) |
I45N |
probably damaging |
Het |
Or5an11 |
A |
G |
19: 12,245,704 (GRCm39) |
T37A |
probably benign |
Het |
Pard3 |
G |
A |
8: 128,003,647 (GRCm39) |
S123N |
probably damaging |
Het |
Parp8 |
T |
C |
13: 117,013,126 (GRCm39) |
N638D |
probably benign |
Het |
Pgpep1l |
A |
T |
7: 67,887,406 (GRCm39) |
S65T |
probably damaging |
Het |
Ppp1r13b |
A |
G |
12: 111,796,708 (GRCm39) |
V1068A |
probably benign |
Het |
Pramel20 |
G |
A |
4: 143,298,425 (GRCm39) |
D123N |
probably benign |
Het |
Prkd1 |
G |
A |
12: 50,430,185 (GRCm39) |
Q641* |
probably null |
Het |
Ptgr2 |
T |
C |
12: 84,344,873 (GRCm39) |
V82A |
possibly damaging |
Het |
Rbm34 |
G |
A |
8: 127,686,332 (GRCm39) |
P225S |
possibly damaging |
Het |
Rnps1 |
A |
T |
17: 24,637,496 (GRCm39) |
K46I |
unknown |
Het |
Shank1 |
T |
C |
7: 44,002,409 (GRCm39) |
V1376A |
probably benign |
Het |
Ski |
A |
T |
4: 155,306,317 (GRCm39) |
Y221N |
probably damaging |
Het |
Skint6 |
C |
A |
4: 113,095,347 (GRCm39) |
G104V |
probably damaging |
Het |
Slit2 |
G |
A |
5: 48,459,860 (GRCm39) |
C1380Y |
possibly damaging |
Het |
Smpd3 |
C |
T |
8: 106,984,058 (GRCm39) |
G554S |
probably benign |
Het |
Sorbs2 |
T |
G |
8: 46,248,774 (GRCm39) |
V675G |
probably benign |
Het |
Spdl1 |
C |
A |
11: 34,700,535 (GRCm39) |
C605F |
possibly damaging |
Het |
Syne1 |
C |
A |
10: 5,155,406 (GRCm39) |
D5568Y |
probably benign |
Het |
Tac1 |
C |
A |
6: 7,559,141 (GRCm39) |
A111D |
possibly damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tnfrsf1a |
T |
C |
6: 125,333,878 (GRCm39) |
C44R |
probably damaging |
Het |
Traf3ip3 |
T |
C |
1: 192,864,285 (GRCm39) |
Q366R |
probably benign |
Het |
Trip10 |
A |
G |
17: 57,569,416 (GRCm39) |
D479G |
probably damaging |
Het |
Trip11 |
T |
C |
12: 101,845,131 (GRCm39) |
T1536A |
probably benign |
Het |
Tstd3 |
G |
T |
4: 21,767,082 (GRCm39) |
A13E |
possibly damaging |
Het |
Urb1 |
T |
C |
16: 90,550,678 (GRCm39) |
K2058R |
probably benign |
Het |
Usp15 |
A |
T |
10: 122,982,703 (GRCm39) |
I304N |
possibly damaging |
Het |
Usp18 |
T |
G |
6: 121,229,529 (GRCm39) |
H49Q |
probably benign |
Het |
Vmn1r56 |
T |
A |
7: 5,199,389 (GRCm39) |
D76V |
probably damaging |
Het |
Wnk1 |
A |
G |
6: 119,939,393 (GRCm39) |
S167P |
probably damaging |
Het |
Zfp229 |
G |
A |
17: 21,965,731 (GRCm39) |
A654T |
possibly damaging |
Het |
Zfp977 |
C |
T |
7: 42,230,082 (GRCm39) |
V148I |
probably benign |
Het |
Znfx1 |
A |
T |
2: 166,880,656 (GRCm39) |
I1240N |
|
Het |
|
Other mutations in Dscam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Dscam
|
APN |
16 |
96,409,265 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00841:Dscam
|
APN |
16 |
96,621,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Dscam
|
APN |
16 |
96,445,082 (GRCm39) |
nonsense |
probably null |
|
IGL01358:Dscam
|
APN |
16 |
96,411,543 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01431:Dscam
|
APN |
16 |
96,453,278 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01444:Dscam
|
APN |
16 |
96,474,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01767:Dscam
|
APN |
16 |
96,456,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Dscam
|
APN |
16 |
96,486,550 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02020:Dscam
|
APN |
16 |
96,517,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02023:Dscam
|
APN |
16 |
96,602,397 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02057:Dscam
|
APN |
16 |
96,517,273 (GRCm39) |
nonsense |
probably null |
|
IGL02389:Dscam
|
APN |
16 |
96,442,097 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02409:Dscam
|
APN |
16 |
96,621,088 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02694:Dscam
|
APN |
16 |
96,394,476 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02899:Dscam
|
APN |
16 |
96,510,447 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02956:Dscam
|
APN |
16 |
96,602,472 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03035:Dscam
|
APN |
16 |
96,621,170 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03191:Dscam
|
APN |
16 |
96,621,969 (GRCm39) |
missense |
probably benign |
0.36 |
growler
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
Twostep
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
F6893:Dscam
|
UTSW |
16 |
96,857,660 (GRCm39) |
missense |
possibly damaging |
0.78 |
K3955:Dscam
|
UTSW |
16 |
96,474,887 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Dscam
|
UTSW |
16 |
96,394,585 (GRCm39) |
nonsense |
probably null |
|
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Dscam
|
UTSW |
16 |
96,474,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R0211:Dscam
|
UTSW |
16 |
96,517,279 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0280:Dscam
|
UTSW |
16 |
96,840,206 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0355:Dscam
|
UTSW |
16 |
96,456,105 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Dscam
|
UTSW |
16 |
96,857,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Dscam
|
UTSW |
16 |
96,573,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0492:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0534:Dscam
|
UTSW |
16 |
96,453,372 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0593:Dscam
|
UTSW |
16 |
96,573,608 (GRCm39) |
missense |
probably benign |
0.19 |
R0707:Dscam
|
UTSW |
16 |
96,626,982 (GRCm39) |
splice site |
probably null |
|
R0738:Dscam
|
UTSW |
16 |
96,620,981 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1017:Dscam
|
UTSW |
16 |
96,634,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Dscam
|
UTSW |
16 |
96,573,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Dscam
|
UTSW |
16 |
96,621,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Dscam
|
UTSW |
16 |
96,409,274 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1464:Dscam
|
UTSW |
16 |
96,602,453 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1464:Dscam
|
UTSW |
16 |
96,602,453 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1478:Dscam
|
UTSW |
16 |
96,592,110 (GRCm39) |
missense |
probably benign |
0.15 |
R1530:Dscam
|
UTSW |
16 |
96,621,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Dscam
|
UTSW |
16 |
96,621,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Dscam
|
UTSW |
16 |
96,486,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1824:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
0.00 |
R1933:Dscam
|
UTSW |
16 |
96,394,414 (GRCm39) |
missense |
probably benign |
0.00 |
R2005:Dscam
|
UTSW |
16 |
96,840,120 (GRCm39) |
missense |
probably benign |
0.02 |
R2006:Dscam
|
UTSW |
16 |
96,621,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Dscam
|
UTSW |
16 |
96,411,549 (GRCm39) |
missense |
probably benign |
0.00 |
R2177:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R2342:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Dscam
|
UTSW |
16 |
96,423,915 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2929:Dscam
|
UTSW |
16 |
96,486,612 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3055:Dscam
|
UTSW |
16 |
96,602,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R3157:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3159:Dscam
|
UTSW |
16 |
96,479,710 (GRCm39) |
missense |
probably benign |
0.16 |
R3944:Dscam
|
UTSW |
16 |
96,622,197 (GRCm39) |
missense |
probably damaging |
0.99 |
R4080:Dscam
|
UTSW |
16 |
96,484,972 (GRCm39) |
missense |
probably benign |
0.01 |
R4285:Dscam
|
UTSW |
16 |
96,510,309 (GRCm39) |
critical splice donor site |
probably null |
|
R4384:Dscam
|
UTSW |
16 |
96,510,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R4460:Dscam
|
UTSW |
16 |
96,411,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4575:Dscam
|
UTSW |
16 |
96,626,823 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4594:Dscam
|
UTSW |
16 |
96,519,196 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4643:Dscam
|
UTSW |
16 |
96,486,501 (GRCm39) |
missense |
probably damaging |
0.96 |
R4698:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Dscam
|
UTSW |
16 |
96,420,771 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4743:Dscam
|
UTSW |
16 |
96,631,256 (GRCm39) |
missense |
probably benign |
0.00 |
R4766:Dscam
|
UTSW |
16 |
96,445,188 (GRCm39) |
missense |
probably benign |
0.02 |
R4899:Dscam
|
UTSW |
16 |
96,485,018 (GRCm39) |
missense |
probably benign |
0.01 |
R4987:Dscam
|
UTSW |
16 |
96,498,721 (GRCm39) |
missense |
probably benign |
0.00 |
R4990:Dscam
|
UTSW |
16 |
96,626,715 (GRCm39) |
missense |
probably benign |
0.12 |
R5123:Dscam
|
UTSW |
16 |
96,573,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:Dscam
|
UTSW |
16 |
96,620,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5328:Dscam
|
UTSW |
16 |
96,474,878 (GRCm39) |
missense |
probably benign |
0.33 |
R5666:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5670:Dscam
|
UTSW |
16 |
96,519,364 (GRCm39) |
missense |
probably benign |
0.23 |
R5678:Dscam
|
UTSW |
16 |
96,592,100 (GRCm39) |
missense |
probably benign |
0.16 |
R5827:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R5907:Dscam
|
UTSW |
16 |
96,622,120 (GRCm39) |
missense |
probably damaging |
0.97 |
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6032:Dscam
|
UTSW |
16 |
96,451,191 (GRCm39) |
critical splice donor site |
probably null |
|
R6103:Dscam
|
UTSW |
16 |
96,626,781 (GRCm39) |
missense |
probably benign |
|
R6240:Dscam
|
UTSW |
16 |
96,420,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Dscam
|
UTSW |
16 |
96,474,914 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6361:Dscam
|
UTSW |
16 |
96,424,011 (GRCm39) |
missense |
probably benign |
0.08 |
R6405:Dscam
|
UTSW |
16 |
96,479,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R6444:Dscam
|
UTSW |
16 |
96,420,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Dscam
|
UTSW |
16 |
96,626,935 (GRCm39) |
missense |
probably benign |
0.00 |
R6598:Dscam
|
UTSW |
16 |
96,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Dscam
|
UTSW |
16 |
96,446,273 (GRCm39) |
missense |
probably benign |
0.06 |
R6792:Dscam
|
UTSW |
16 |
96,449,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R6792:Dscam
|
UTSW |
16 |
96,394,455 (GRCm39) |
missense |
probably damaging |
0.96 |
R6827:Dscam
|
UTSW |
16 |
96,840,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Dscam
|
UTSW |
16 |
96,631,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Dscam
|
UTSW |
16 |
96,631,100 (GRCm39) |
missense |
probably benign |
0.02 |
R6903:Dscam
|
UTSW |
16 |
96,621,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Dscam
|
UTSW |
16 |
96,620,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7146:Dscam
|
UTSW |
16 |
96,631,117 (GRCm39) |
nonsense |
probably null |
|
R7180:Dscam
|
UTSW |
16 |
96,626,764 (GRCm39) |
missense |
probably damaging |
0.97 |
R7209:Dscam
|
UTSW |
16 |
96,451,544 (GRCm39) |
splice site |
probably null |
|
R7247:Dscam
|
UTSW |
16 |
96,622,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R7269:Dscam
|
UTSW |
16 |
96,479,601 (GRCm39) |
missense |
probably benign |
0.00 |
R7301:Dscam
|
UTSW |
16 |
96,857,732 (GRCm39) |
missense |
probably benign |
0.01 |
R7328:Dscam
|
UTSW |
16 |
96,446,235 (GRCm39) |
nonsense |
probably null |
|
R7368:Dscam
|
UTSW |
16 |
96,445,131 (GRCm39) |
missense |
probably benign |
0.00 |
R7425:Dscam
|
UTSW |
16 |
96,430,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R7474:Dscam
|
UTSW |
16 |
96,621,089 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7536:Dscam
|
UTSW |
16 |
96,442,226 (GRCm39) |
splice site |
probably null |
|
R7624:Dscam
|
UTSW |
16 |
96,411,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7766:Dscam
|
UTSW |
16 |
96,592,101 (GRCm39) |
missense |
probably benign |
0.31 |
R7817:Dscam
|
UTSW |
16 |
96,442,064 (GRCm39) |
missense |
probably benign |
|
R7843:Dscam
|
UTSW |
16 |
96,626,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7911:Dscam
|
UTSW |
16 |
96,445,122 (GRCm39) |
missense |
probably benign |
0.01 |
R8108:Dscam
|
UTSW |
16 |
96,445,079 (GRCm39) |
missense |
probably benign |
0.01 |
R8128:Dscam
|
UTSW |
16 |
96,602,374 (GRCm39) |
splice site |
probably null |
|
R8770:Dscam
|
UTSW |
16 |
96,456,106 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8876:Dscam
|
UTSW |
16 |
96,420,828 (GRCm39) |
missense |
probably damaging |
0.96 |
R9009:Dscam
|
UTSW |
16 |
96,840,116 (GRCm39) |
missense |
probably benign |
0.10 |
R9168:Dscam
|
UTSW |
16 |
96,420,768 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9176:Dscam
|
UTSW |
16 |
96,486,553 (GRCm39) |
missense |
probably benign |
0.37 |
R9244:Dscam
|
UTSW |
16 |
96,486,429 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9339:Dscam
|
UTSW |
16 |
96,517,263 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9374:Dscam
|
UTSW |
16 |
96,857,857 (GRCm39) |
missense |
probably benign |
0.19 |
R9385:Dscam
|
UTSW |
16 |
96,840,203 (GRCm39) |
missense |
probably benign |
|
R9674:Dscam
|
UTSW |
16 |
96,442,036 (GRCm39) |
missense |
probably benign |
0.03 |
X0025:Dscam
|
UTSW |
16 |
96,510,361 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dscam
|
UTSW |
16 |
96,573,761 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Dscam
|
UTSW |
16 |
96,409,389 (GRCm39) |
missense |
probably damaging |
0.98 |
|