Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
A |
7: 41,275,837 (GRCm39) |
N513K |
possibly damaging |
Het |
Actl6a |
T |
A |
3: 32,779,469 (GRCm39) |
I399N |
probably damaging |
Het |
Adamts5 |
A |
G |
16: 85,666,971 (GRCm39) |
V507A |
probably damaging |
Het |
Ap3d1 |
A |
G |
10: 80,554,918 (GRCm39) |
V469A |
probably benign |
Het |
Arhgef4 |
G |
T |
1: 34,764,241 (GRCm39) |
|
probably null |
Het |
Arhgef4 |
A |
T |
1: 34,849,576 (GRCm39) |
Q389L |
probably benign |
Het |
Atad2 |
A |
G |
15: 57,980,194 (GRCm39) |
V106A |
possibly damaging |
Het |
Azin2 |
T |
C |
4: 128,841,341 (GRCm39) |
E275G |
probably damaging |
Het |
Bhlhe23 |
A |
G |
2: 180,418,143 (GRCm39) |
S132P |
probably damaging |
Het |
Capn12 |
A |
G |
7: 28,581,243 (GRCm39) |
Y32C |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,321,349 (GRCm39) |
S488T |
probably benign |
Het |
Cenpx |
A |
G |
11: 120,602,582 (GRCm39) |
V27A |
possibly damaging |
Het |
Clca3a2 |
G |
A |
3: 144,778,005 (GRCm39) |
P760L |
probably benign |
Het |
Clstn3 |
T |
C |
6: 124,408,571 (GRCm39) |
S951G |
probably benign |
Het |
Clybl |
C |
A |
14: 122,621,670 (GRCm39) |
P286Q |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,226,866 (GRCm39) |
M2741L |
probably benign |
Het |
Cntnap2 |
G |
A |
6: 47,026,183 (GRCm39) |
G944E |
probably damaging |
Het |
Col8a1 |
A |
C |
16: 57,447,283 (GRCm39) |
Y742* |
probably null |
Het |
Crb1 |
T |
C |
1: 139,171,051 (GRCm39) |
K780E |
probably damaging |
Het |
Crygc |
T |
A |
1: 65,112,376 (GRCm39) |
Y66F |
probably benign |
Het |
Cyp2b9 |
G |
A |
7: 25,873,004 (GRCm39) |
G49E |
possibly damaging |
Het |
D130043K22Rik |
T |
C |
13: 25,041,090 (GRCm39) |
S171P |
possibly damaging |
Het |
Dhx36 |
T |
C |
3: 62,378,895 (GRCm39) |
I890V |
probably benign |
Het |
Dpp9 |
C |
T |
17: 56,512,765 (GRCm39) |
G148S |
probably damaging |
Het |
Enpp4 |
A |
T |
17: 44,412,252 (GRCm39) |
L319* |
probably null |
Het |
Esyt1 |
T |
C |
10: 128,361,356 (GRCm39) |
S113G |
probably benign |
Het |
Fat1 |
A |
G |
8: 45,404,791 (GRCm39) |
D514G |
possibly damaging |
Het |
Fbxo16 |
G |
A |
14: 65,524,594 (GRCm39) |
R38Q |
probably damaging |
Het |
Fchsd1 |
A |
T |
18: 38,092,706 (GRCm39) |
M668K |
unknown |
Het |
Gpr149 |
C |
T |
3: 62,511,093 (GRCm39) |
S302N |
probably benign |
Het |
Gsap |
A |
G |
5: 21,433,064 (GRCm39) |
K258E |
probably benign |
Het |
Helq |
C |
A |
5: 100,939,218 (GRCm39) |
V443F |
probably benign |
Het |
Helq |
T |
A |
5: 100,939,219 (GRCm39) |
K442N |
probably damaging |
Het |
Ighv1-37 |
T |
C |
12: 114,860,123 (GRCm39) |
E29G |
possibly damaging |
Het |
Ighv1-9 |
C |
A |
12: 114,547,620 (GRCm39) |
M1I |
probably null |
Het |
Itga6 |
T |
G |
2: 71,671,477 (GRCm39) |
F743V |
probably benign |
Het |
Lpin1 |
C |
A |
12: 16,588,548 (GRCm39) |
D881Y |
|
Het |
Lypd8 |
T |
A |
11: 58,273,640 (GRCm39) |
C40S |
possibly damaging |
Het |
Macf1 |
C |
T |
4: 123,326,227 (GRCm39) |
R5092Q |
probably damaging |
Het |
Mcm7 |
A |
G |
5: 138,166,593 (GRCm39) |
|
probably null |
Het |
Micall2 |
G |
A |
5: 139,696,170 (GRCm39) |
T831I |
unknown |
Het |
Myo18b |
A |
T |
5: 113,022,927 (GRCm39) |
M155K |
unknown |
Het |
Nckap5 |
T |
A |
1: 125,867,928 (GRCm39) |
H201L |
unknown |
Het |
Ndst2 |
A |
T |
14: 20,779,240 (GRCm39) |
D333E |
possibly damaging |
Het |
Nlgn1 |
A |
G |
3: 25,966,804 (GRCm39) |
|
probably null |
Het |
Nup188 |
T |
G |
2: 30,232,397 (GRCm39) |
Y1483D |
probably benign |
Het |
Or4c109 |
A |
C |
2: 88,818,057 (GRCm39) |
L163* |
probably null |
Het |
Or52ae9 |
T |
A |
7: 103,390,319 (GRCm39) |
S43C |
probably benign |
Het |
Or52n4b |
A |
C |
7: 108,144,664 (GRCm39) |
I311L |
probably benign |
Het |
Or5p66 |
T |
A |
7: 107,885,526 (GRCm39) |
Y269F |
probably benign |
Het |
Or8g33 |
T |
A |
9: 39,337,635 (GRCm39) |
H244L |
probably damaging |
Het |
Peg3 |
A |
C |
7: 6,711,226 (GRCm39) |
I1332S |
possibly damaging |
Het |
Piezo2 |
T |
C |
18: 63,154,372 (GRCm39) |
K2469R |
probably damaging |
Het |
Pik3cg |
T |
C |
12: 32,247,312 (GRCm39) |
M804V |
probably damaging |
Het |
Polq |
A |
T |
16: 36,869,011 (GRCm39) |
I794F |
possibly damaging |
Het |
Rasgef1b |
A |
G |
5: 99,370,191 (GRCm39) |
V437A |
probably benign |
Het |
Rdm1 |
T |
A |
11: 101,518,857 (GRCm39) |
D21E |
probably benign |
Het |
Ripk4 |
G |
T |
16: 97,551,311 (GRCm39) |
Q219K |
possibly damaging |
Het |
Ropn1l |
T |
C |
15: 31,441,471 (GRCm39) |
I217V |
|
Het |
Sdf2 |
T |
C |
11: 78,136,858 (GRCm39) |
S13P |
unknown |
Het |
Selenbp1 |
A |
G |
3: 94,847,079 (GRCm39) |
T202A |
probably benign |
Het |
Slfn5 |
T |
C |
11: 82,850,933 (GRCm39) |
F410S |
possibly damaging |
Het |
Srrm2 |
A |
G |
17: 24,039,880 (GRCm39) |
T2175A |
probably benign |
Het |
St6galnac3 |
T |
C |
3: 153,117,360 (GRCm39) |
Y121C |
possibly damaging |
Het |
Stat1 |
A |
G |
1: 52,184,337 (GRCm39) |
N417S |
probably benign |
Het |
Tead1 |
T |
C |
7: 112,475,378 (GRCm39) |
F276L |
probably damaging |
Het |
Teddm3 |
A |
T |
16: 20,971,737 (GRCm39) |
S277R |
probably benign |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmem156 |
G |
A |
5: 65,231,127 (GRCm39) |
L248F |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,953,986 (GRCm39) |
S590G |
probably benign |
Het |
Trmt44 |
A |
G |
5: 35,731,422 (GRCm39) |
|
probably null |
Het |
Upp2 |
T |
A |
2: 58,668,022 (GRCm39) |
Y238* |
probably null |
Het |
Usp32 |
T |
C |
11: 84,930,838 (GRCm39) |
T531A |
probably damaging |
Het |
Vmn2r78 |
A |
T |
7: 86,569,431 (GRCm39) |
D108V |
probably benign |
Het |
Wdfy3 |
G |
T |
5: 102,078,830 (GRCm39) |
A824E |
probably benign |
Het |
Xylt1 |
T |
C |
7: 117,255,870 (GRCm39) |
V814A |
probably benign |
Het |
Zfy1 |
C |
T |
Y: 732,990 (GRCm39) |
R281H |
unknown |
Het |
|
Other mutations in Eml6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01071:Eml6
|
APN |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01407:Eml6
|
APN |
11 |
29,705,021 (GRCm39) |
nonsense |
probably null |
|
IGL01434:Eml6
|
APN |
11 |
29,769,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01578:Eml6
|
APN |
11 |
29,800,870 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01780:Eml6
|
APN |
11 |
29,755,175 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01821:Eml6
|
APN |
11 |
29,771,699 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01837:Eml6
|
APN |
11 |
29,727,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01904:Eml6
|
APN |
11 |
29,788,613 (GRCm39) |
nonsense |
probably null |
|
IGL01972:Eml6
|
APN |
11 |
29,788,451 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02134:Eml6
|
APN |
11 |
29,709,066 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02192:Eml6
|
APN |
11 |
29,755,743 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02377:Eml6
|
APN |
11 |
29,727,282 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02584:Eml6
|
APN |
11 |
29,699,387 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Eml6
|
APN |
11 |
29,734,236 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02810:Eml6
|
APN |
11 |
29,799,016 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02873:Eml6
|
APN |
11 |
29,830,700 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02880:Eml6
|
APN |
11 |
29,699,959 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03289:Eml6
|
APN |
11 |
29,745,328 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03301:Eml6
|
APN |
11 |
29,714,083 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03386:Eml6
|
APN |
11 |
29,699,934 (GRCm39) |
missense |
probably benign |
|
IGL03407:Eml6
|
APN |
11 |
29,856,330 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Eml6
|
UTSW |
11 |
29,752,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Eml6
|
UTSW |
11 |
29,832,088 (GRCm39) |
missense |
probably benign |
0.19 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0271:Eml6
|
UTSW |
11 |
29,798,949 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0304:Eml6
|
UTSW |
11 |
29,727,441 (GRCm39) |
missense |
probably benign |
0.00 |
R0415:Eml6
|
UTSW |
11 |
29,699,392 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0449:Eml6
|
UTSW |
11 |
29,843,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0538:Eml6
|
UTSW |
11 |
29,710,010 (GRCm39) |
splice site |
probably benign |
|
R0671:Eml6
|
UTSW |
11 |
29,755,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0766:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R0800:Eml6
|
UTSW |
11 |
29,699,877 (GRCm39) |
missense |
probably benign |
0.08 |
R0841:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R0879:Eml6
|
UTSW |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
R1061:Eml6
|
UTSW |
11 |
29,727,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1172:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1173:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1174:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1199:Eml6
|
UTSW |
11 |
29,705,044 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1311:Eml6
|
UTSW |
11 |
29,781,088 (GRCm39) |
splice site |
probably benign |
|
R1312:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R1355:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1370:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1457:Eml6
|
UTSW |
11 |
29,974,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1486:Eml6
|
UTSW |
11 |
29,755,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1511:Eml6
|
UTSW |
11 |
29,768,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Eml6
|
UTSW |
11 |
29,742,256 (GRCm39) |
splice site |
probably null |
|
R1642:Eml6
|
UTSW |
11 |
29,727,001 (GRCm39) |
critical splice donor site |
probably null |
|
R1682:Eml6
|
UTSW |
11 |
29,709,065 (GRCm39) |
missense |
probably benign |
0.13 |
R1687:Eml6
|
UTSW |
11 |
29,783,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Eml6
|
UTSW |
11 |
29,696,282 (GRCm39) |
nonsense |
probably null |
|
R1796:Eml6
|
UTSW |
11 |
29,831,975 (GRCm39) |
missense |
probably benign |
0.19 |
R1797:Eml6
|
UTSW |
11 |
29,832,041 (GRCm39) |
missense |
probably benign |
0.09 |
R1837:Eml6
|
UTSW |
11 |
29,699,802 (GRCm39) |
splice site |
probably null |
|
R1874:Eml6
|
UTSW |
11 |
29,781,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R1967:Eml6
|
UTSW |
11 |
29,974,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Eml6
|
UTSW |
11 |
29,783,075 (GRCm39) |
missense |
probably benign |
|
R2007:Eml6
|
UTSW |
11 |
29,798,814 (GRCm39) |
critical splice donor site |
probably null |
|
R2012:Eml6
|
UTSW |
11 |
29,781,128 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2198:Eml6
|
UTSW |
11 |
29,800,935 (GRCm39) |
missense |
probably benign |
0.01 |
R2217:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Eml6
|
UTSW |
11 |
29,752,434 (GRCm39) |
missense |
probably benign |
0.05 |
R2520:Eml6
|
UTSW |
11 |
29,741,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R2938:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R3085:Eml6
|
UTSW |
11 |
29,759,332 (GRCm39) |
missense |
probably damaging |
0.96 |
R3236:Eml6
|
UTSW |
11 |
29,781,097 (GRCm39) |
critical splice donor site |
probably null |
|
R3738:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3739:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3752:Eml6
|
UTSW |
11 |
29,759,360 (GRCm39) |
missense |
probably benign |
0.06 |
R3854:Eml6
|
UTSW |
11 |
29,699,905 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3941:Eml6
|
UTSW |
11 |
29,753,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R4034:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R4049:Eml6
|
UTSW |
11 |
29,788,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Eml6
|
UTSW |
11 |
29,755,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R4657:Eml6
|
UTSW |
11 |
29,755,108 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4662:Eml6
|
UTSW |
11 |
29,727,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Eml6
|
UTSW |
11 |
29,769,007 (GRCm39) |
nonsense |
probably null |
|
R4721:Eml6
|
UTSW |
11 |
29,788,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4729:Eml6
|
UTSW |
11 |
29,783,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Eml6
|
UTSW |
11 |
29,755,757 (GRCm39) |
missense |
probably benign |
0.22 |
R4810:Eml6
|
UTSW |
11 |
29,705,011 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4831:Eml6
|
UTSW |
11 |
29,727,052 (GRCm39) |
nonsense |
probably null |
|
R5035:Eml6
|
UTSW |
11 |
29,804,187 (GRCm39) |
missense |
probably benign |
0.00 |
R5064:Eml6
|
UTSW |
11 |
29,699,300 (GRCm39) |
missense |
probably benign |
0.12 |
R5103:Eml6
|
UTSW |
11 |
29,800,905 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5121:Eml6
|
UTSW |
11 |
29,694,606 (GRCm39) |
missense |
probably benign |
0.03 |
R5161:Eml6
|
UTSW |
11 |
29,974,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R5211:Eml6
|
UTSW |
11 |
29,804,145 (GRCm39) |
missense |
probably benign |
0.02 |
R5268:Eml6
|
UTSW |
11 |
29,753,108 (GRCm39) |
missense |
probably benign |
0.15 |
R5390:Eml6
|
UTSW |
11 |
29,710,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Eml6
|
UTSW |
11 |
29,714,126 (GRCm39) |
missense |
probably benign |
0.04 |
R6239:Eml6
|
UTSW |
11 |
29,699,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Eml6
|
UTSW |
11 |
29,769,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Eml6
|
UTSW |
11 |
29,759,321 (GRCm39) |
missense |
probably benign |
0.00 |
R6476:Eml6
|
UTSW |
11 |
29,741,971 (GRCm39) |
critical splice donor site |
probably null |
|
R6483:Eml6
|
UTSW |
11 |
29,699,875 (GRCm39) |
missense |
probably benign |
0.00 |
R6701:Eml6
|
UTSW |
11 |
29,735,748 (GRCm39) |
missense |
probably damaging |
0.98 |
R6753:Eml6
|
UTSW |
11 |
29,704,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Eml6
|
UTSW |
11 |
29,753,161 (GRCm39) |
missense |
probably benign |
0.23 |
R6847:Eml6
|
UTSW |
11 |
29,768,447 (GRCm39) |
missense |
probably benign |
0.00 |
R6855:Eml6
|
UTSW |
11 |
29,701,381 (GRCm39) |
splice site |
probably null |
|
R7168:Eml6
|
UTSW |
11 |
29,788,529 (GRCm39) |
missense |
probably benign |
0.01 |
R7175:Eml6
|
UTSW |
11 |
29,734,231 (GRCm39) |
missense |
probably benign |
0.00 |
R7305:Eml6
|
UTSW |
11 |
29,727,258 (GRCm39) |
missense |
probably benign |
0.01 |
R7615:Eml6
|
UTSW |
11 |
29,752,501 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7692:Eml6
|
UTSW |
11 |
29,703,085 (GRCm39) |
missense |
probably damaging |
0.98 |
R7980:Eml6
|
UTSW |
11 |
29,783,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Eml6
|
UTSW |
11 |
29,699,973 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8046:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R8049:Eml6
|
UTSW |
11 |
29,843,201 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8114:Eml6
|
UTSW |
11 |
29,704,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8425:Eml6
|
UTSW |
11 |
29,705,008 (GRCm39) |
missense |
probably benign |
0.00 |
R8799:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably benign |
0.11 |
R8945:Eml6
|
UTSW |
11 |
29,703,110 (GRCm39) |
missense |
probably damaging |
0.98 |
R8977:Eml6
|
UTSW |
11 |
29,734,182 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8986:Eml6
|
UTSW |
11 |
29,755,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9088:Eml6
|
UTSW |
11 |
29,768,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Eml6
|
UTSW |
11 |
29,755,791 (GRCm39) |
missense |
probably benign |
0.15 |
R9288:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9467:Eml6
|
UTSW |
11 |
29,769,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9534:Eml6
|
UTSW |
11 |
29,734,155 (GRCm39) |
missense |
possibly damaging |
0.45 |
RF037:Eml6
|
UTSW |
11 |
29,702,549 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF039:Eml6
|
UTSW |
11 |
29,702,551 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|