Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700062C07Rik |
A |
T |
18: 24,606,013 (GRCm39) |
N36I |
probably damaging |
Het |
A430033K04Rik |
T |
A |
5: 138,645,014 (GRCm39) |
Y300N |
possibly damaging |
Het |
Adipor2 |
T |
C |
6: 119,347,205 (GRCm39) |
Q26R |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,983,981 (GRCm39) |
M1755K |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,780,802 (GRCm38) |
V70E |
|
Het |
AI837181 |
C |
A |
19: 5,476,462 (GRCm39) |
S208R |
probably damaging |
Het |
Arhgap35 |
T |
G |
7: 16,295,652 (GRCm39) |
M1138L |
probably benign |
Het |
Card14 |
T |
G |
11: 119,228,573 (GRCm39) |
L633R |
probably damaging |
Het |
Carmil3 |
A |
G |
14: 55,731,352 (GRCm39) |
T144A |
probably benign |
Het |
Cbfa2t2 |
T |
A |
2: 154,357,895 (GRCm39) |
N223K |
probably benign |
Het |
Ccdc39 |
T |
C |
3: 33,884,254 (GRCm39) |
I363V |
probably benign |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Ccpg1 |
G |
T |
9: 72,920,609 (GRCm39) |
R741S |
probably benign |
Het |
Cenpc1 |
A |
G |
5: 86,161,366 (GRCm39) |
F855L |
probably damaging |
Het |
Cenpc1 |
A |
T |
5: 86,180,277 (GRCm39) |
M665K |
probably benign |
Het |
Cp |
A |
G |
3: 20,037,641 (GRCm39) |
H832R |
probably damaging |
Het |
Defa24 |
A |
G |
8: 22,224,565 (GRCm39) |
I5V |
probably benign |
Het |
Dlc1 |
A |
C |
8: 37,046,407 (GRCm39) |
L730R |
probably damaging |
Het |
Dmbt1 |
A |
T |
7: 130,668,351 (GRCm39) |
I536F |
unknown |
Het |
Eea1 |
A |
T |
10: 95,854,000 (GRCm39) |
I553F |
probably damaging |
Het |
Far1 |
T |
C |
7: 113,160,654 (GRCm39) |
V400A |
probably benign |
Het |
Fbrsl1 |
A |
T |
5: 110,580,880 (GRCm39) |
S126T |
probably benign |
Het |
Frmpd2 |
A |
T |
14: 33,244,838 (GRCm39) |
E552V |
possibly damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,237 (GRCm39) |
T562S |
probably benign |
Het |
Gm5475 |
T |
C |
15: 100,324,890 (GRCm39) |
F106S |
unknown |
Het |
Gpr12 |
T |
C |
5: 146,520,188 (GRCm39) |
T245A |
probably damaging |
Het |
Gsta2 |
A |
G |
9: 78,239,419 (GRCm39) |
Y166H |
probably benign |
Het |
H6pd |
A |
G |
4: 150,067,369 (GRCm39) |
V347A |
probably benign |
Het |
Ifih1 |
T |
C |
2: 62,475,977 (GRCm39) |
T100A |
probably benign |
Het |
Ift70b |
A |
G |
2: 75,767,838 (GRCm39) |
F305S |
probably damaging |
Het |
Itga2 |
C |
T |
13: 115,023,225 (GRCm39) |
W59* |
probably null |
Het |
Knstrn |
T |
A |
2: 118,661,869 (GRCm39) |
|
probably null |
Het |
Kprp |
A |
G |
3: 92,731,178 (GRCm39) |
V624A |
probably damaging |
Het |
Lmbrd2 |
A |
G |
15: 9,194,771 (GRCm39) |
Y591C |
probably damaging |
Het |
Map7d1 |
A |
G |
4: 126,126,666 (GRCm39) |
V842A |
unknown |
Het |
Mboat2 |
A |
T |
12: 24,881,708 (GRCm39) |
T4S |
probably benign |
Het |
Mcph1 |
T |
A |
8: 18,657,288 (GRCm39) |
|
probably null |
Het |
Mrtfb |
A |
T |
16: 13,218,898 (GRCm39) |
M515L |
possibly damaging |
Het |
Muc5b |
A |
G |
7: 141,411,272 (GRCm39) |
D1406G |
unknown |
Het |
Mylk |
G |
A |
16: 34,605,381 (GRCm39) |
G3D |
probably damaging |
Het |
Ndst4 |
A |
G |
3: 125,232,007 (GRCm39) |
D192G |
probably damaging |
Het |
Nemp1 |
G |
T |
10: 127,531,345 (GRCm39) |
R361L |
probably damaging |
Het |
Nol4 |
A |
C |
18: 23,172,846 (GRCm39) |
V85G |
probably benign |
Het |
Nrbf2 |
G |
A |
10: 67,103,605 (GRCm39) |
T166M |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,933,838 (GRCm39) |
E5342G |
probably damaging |
Het |
Or10al7 |
C |
A |
17: 38,366,442 (GRCm39) |
C5F |
probably damaging |
Het |
Or4f47 |
T |
A |
2: 111,972,905 (GRCm39) |
F205Y |
probably damaging |
Het |
Or4p19 |
C |
T |
2: 88,242,839 (GRCm39) |
M54I |
possibly damaging |
Het |
Or51d1 |
T |
G |
7: 102,348,252 (GRCm39) |
L269R |
probably damaging |
Het |
Or7d10 |
A |
G |
9: 19,831,631 (GRCm39) |
N42S |
possibly damaging |
Het |
Pakap |
G |
T |
4: 57,855,217 (GRCm39) |
R182L |
probably damaging |
Het |
Pde4dip |
A |
G |
3: 97,674,275 (GRCm39) |
S214P |
probably damaging |
Het |
Per3 |
A |
T |
4: 151,116,393 (GRCm39) |
C278* |
probably null |
Het |
Pi4k2a |
T |
C |
19: 42,079,125 (GRCm39) |
L62P |
probably damaging |
Het |
Plekha7 |
C |
A |
7: 115,780,447 (GRCm39) |
G126W |
probably damaging |
Het |
Ppp1r13b |
T |
C |
12: 111,801,353 (GRCm39) |
K567E |
probably damaging |
Het |
Pradc1 |
T |
A |
6: 85,424,548 (GRCm39) |
Q134L |
probably benign |
Het |
Pwp2 |
A |
G |
10: 78,012,170 (GRCm39) |
F628L |
probably benign |
Het |
Rab5c |
C |
T |
11: 100,606,928 (GRCm39) |
G217D |
probably benign |
Het |
Rad51ap2 |
G |
T |
12: 11,506,807 (GRCm39) |
S243I |
possibly damaging |
Het |
Rasgrp4 |
C |
A |
7: 28,847,855 (GRCm39) |
R432S |
probably damaging |
Het |
Rhot2 |
C |
T |
17: 26,061,402 (GRCm39) |
|
probably null |
Het |
Scn2a |
T |
A |
2: 65,594,113 (GRCm39) |
L1654Q |
probably damaging |
Het |
Skint6 |
A |
T |
4: 112,711,686 (GRCm39) |
|
probably null |
Het |
Slc22a28 |
T |
A |
19: 8,094,491 (GRCm39) |
T177S |
probably benign |
Het |
Slc25a24 |
G |
T |
3: 109,065,960 (GRCm39) |
Q272H |
probably null |
Het |
Slc3a1 |
A |
T |
17: 85,339,873 (GRCm39) |
I144F |
probably damaging |
Het |
Smg9 |
C |
T |
7: 24,105,495 (GRCm39) |
R176C |
possibly damaging |
Het |
Sorl1 |
A |
T |
9: 41,948,499 (GRCm39) |
L762Q |
probably damaging |
Het |
Srebf2 |
C |
A |
15: 82,088,270 (GRCm39) |
P1079T |
probably benign |
Het |
Sub1 |
A |
T |
15: 11,993,937 (GRCm39) |
S4T |
probably benign |
Het |
Tacr1 |
A |
T |
6: 82,469,692 (GRCm39) |
Y192F |
probably benign |
Het |
Tm4sf19 |
A |
T |
16: 32,224,814 (GRCm39) |
H54L |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,914,428 (GRCm39) |
L1838P |
probably damaging |
Het |
Trmt1l |
T |
C |
1: 151,333,539 (GRCm39) |
S681P |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,738,176 (GRCm39) |
V4167A |
unknown |
Het |
Unc13d |
T |
A |
11: 115,959,056 (GRCm39) |
M702L |
probably benign |
Het |
Vgll3 |
A |
G |
16: 65,636,404 (GRCm39) |
H240R |
probably benign |
Het |
Vmn1r189 |
C |
G |
13: 22,286,737 (GRCm39) |
W33C |
probably benign |
Het |
Vmn2r17 |
G |
A |
5: 109,576,337 (GRCm39) |
A403T |
possibly damaging |
Het |
Vmn2r2 |
G |
A |
3: 64,033,998 (GRCm39) |
T508I |
probably benign |
Het |
Vps54 |
T |
A |
11: 21,227,670 (GRCm39) |
|
probably null |
Het |
Wfs1 |
G |
A |
5: 37,125,134 (GRCm39) |
Q586* |
probably null |
Het |
Zbp1 |
A |
T |
2: 173,055,665 (GRCm39) |
H166Q |
unknown |
Het |
Zcchc3 |
G |
A |
2: 152,256,294 (GRCm39) |
A135V |
probably benign |
Het |
Zfp51 |
T |
C |
17: 21,683,960 (GRCm39) |
Y192H |
probably benign |
Het |
Zkscan2 |
T |
C |
7: 123,088,994 (GRCm39) |
T426A |
probably benign |
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 |
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 |
R9005:Dscam
|
UTSW |
16 |
96,602,580 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|