Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl1 |
T |
A |
8: 84,661,401 (GRCm39) |
S933T |
probably benign |
Het |
Adgrl2 |
G |
A |
3: 148,544,884 (GRCm39) |
T737I |
probably damaging |
Het |
Adra2c |
T |
A |
5: 35,438,386 (GRCm39) |
V386E |
probably damaging |
Het |
Agbl5 |
C |
A |
5: 31,060,589 (GRCm39) |
T761N |
unknown |
Het |
Ahnak |
T |
A |
19: 8,990,965 (GRCm39) |
M4083K |
possibly damaging |
Het |
Aldh1l1 |
A |
T |
6: 90,575,241 (GRCm39) |
I843F |
probably damaging |
Het |
Ankhd1 |
GGCGGC |
GGCGGCTGCGGC |
18: 36,693,962 (GRCm39) |
|
probably benign |
Het |
Arid1b |
GCG |
GCGCCG |
17: 5,045,869 (GRCm39) |
|
probably benign |
Het |
B4galnt4 |
T |
C |
7: 140,650,609 (GRCm39) |
|
probably null |
Het |
Blm |
C |
CTCCTCCTCCTAG |
7: 80,162,681 (GRCm39) |
|
probably null |
Het |
Btg3 |
A |
G |
16: 78,129,836 (GRCm39) |
*52W |
probably null |
Het |
Cc2d1a |
T |
C |
8: 84,861,298 (GRCm39) |
T796A |
probably damaging |
Het |
Cd200r1 |
T |
C |
16: 44,610,374 (GRCm39) |
S161P |
possibly damaging |
Het |
Cenpj |
A |
G |
14: 56,767,505 (GRCm39) |
|
probably null |
Het |
Cfap251 |
G |
GGAT |
5: 123,392,317 (GRCm39) |
|
probably benign |
Het |
Chd9 |
A |
G |
8: 91,760,578 (GRCm39) |
T2108A |
possibly damaging |
Het |
Cherp |
TGGAGCG |
T |
8: 73,215,903 (GRCm39) |
|
probably benign |
Het |
Cnot11 |
T |
C |
1: 39,581,575 (GRCm39) |
V372A |
probably damaging |
Het |
Cntnap5b |
T |
C |
1: 100,091,795 (GRCm39) |
C179R |
probably damaging |
Het |
Cntrl |
T |
A |
2: 35,060,512 (GRCm39) |
N1901K |
probably benign |
Het |
Coil |
CTGG |
C |
11: 88,872,656 (GRCm39) |
|
probably benign |
Het |
Col1a1 |
A |
G |
11: 94,833,866 (GRCm39) |
D488G |
probably damaging |
Het |
Coro1a |
T |
C |
7: 126,301,024 (GRCm39) |
H130R |
probably damaging |
Het |
Crybg3 |
A |
C |
16: 59,377,067 (GRCm39) |
S1396A |
possibly damaging |
Het |
Csf2rb2 |
A |
G |
15: 78,176,126 (GRCm39) |
I259T |
probably benign |
Het |
Cyp1a2 |
G |
T |
9: 57,589,253 (GRCm39) |
P187Q |
probably damaging |
Het |
Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
Dcun1d3 |
T |
C |
7: 119,458,726 (GRCm39) |
E103G |
possibly damaging |
Het |
Dmkn |
T |
A |
7: 30,469,129 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,802,474 (GRCm39) |
L864P |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,513,374 (GRCm39) |
M1909K |
probably benign |
Het |
Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,326,227 (GRCm39) |
|
probably benign |
Het |
Ecrg4 |
TTCTGTA |
T |
1: 43,776,352 (GRCm39) |
|
probably benign |
Het |
Efna5 |
T |
C |
17: 62,920,389 (GRCm39) |
S163G |
probably benign |
Het |
Entpd2 |
CTT |
CTTT |
2: 25,290,907 (GRCm39) |
|
probably null |
Het |
Ercc4 |
C |
T |
16: 12,941,371 (GRCm39) |
S253L |
possibly damaging |
Het |
Flywch1 |
ACCCA |
ACCCAATTCTGGTGTGGGGAGGCTACGTACTCTCCCA |
17: 23,981,138 (GRCm39) |
|
probably null |
Het |
Flywch1 |
CCTGGTGT |
CCTGGTGTGGGGAGGCTACGTACTCACCCACTTCTGGTGT |
17: 23,981,145 (GRCm39) |
|
probably null |
Het |
Folh1 |
T |
C |
7: 86,424,895 (GRCm39) |
T25A |
probably benign |
Het |
Foxi3 |
C |
A |
6: 70,937,845 (GRCm39) |
T359K |
possibly damaging |
Het |
Gab3 |
TTC |
TTCATC |
X: 74,043,631 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,617 (GRCm39) |
|
probably benign |
Het |
Gba2 |
G |
T |
4: 43,569,894 (GRCm39) |
L440M |
probably damaging |
Het |
Gm14412 |
T |
A |
2: 177,007,494 (GRCm39) |
N134Y |
possibly damaging |
Het |
Gpr88 |
A |
G |
3: 116,046,018 (GRCm39) |
S98P |
probably benign |
Het |
Il1r1 |
A |
G |
1: 40,352,438 (GRCm39) |
Y539C |
probably damaging |
Het |
Iqcf4 |
TTTCCTTTTCCTTTT |
TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTTCCTTTT |
9: 106,447,808 (GRCm39) |
|
probably benign |
Het |
Lce1m |
CTGCT |
CTGCTTCCACTGTTGCT |
3: 92,925,451 (GRCm39) |
|
probably benign |
Het |
Lkaaear1 |
T |
TATCTCCAGCTCC |
2: 181,339,352 (GRCm39) |
|
probably benign |
Het |
Lkaaear1 |
CAGCTCCAGCTCCAGCTCCAGCTC |
CAGCTCCAGCTCTAGCTCCAGCTCCAGCTCCAGCTC |
2: 181,339,370 (GRCm39) |
|
probably benign |
Het |
Ltb4r1 |
T |
A |
14: 56,005,426 (GRCm39) |
L243Q |
possibly damaging |
Het |
Man2a1 |
T |
A |
17: 65,019,248 (GRCm39) |
V704D |
probably damaging |
Het |
Map1a |
CTCCAGCTCCA |
CTCCAGCTCCAGCTCCAGCTCCAGCTCCAGTTCCAGCTCCA |
2: 121,136,789 (GRCm39) |
|
probably benign |
Het |
Mcu |
G |
T |
10: 59,326,938 (GRCm39) |
A63E |
probably benign |
Het |
Mrps31 |
A |
T |
8: 22,909,880 (GRCm39) |
D182V |
possibly damaging |
Het |
Mslnl |
T |
A |
17: 25,962,202 (GRCm39) |
V200E |
possibly damaging |
Het |
Naip1 |
A |
T |
13: 100,562,642 (GRCm39) |
M841K |
probably benign |
Het |
Ndufab1 |
T |
C |
7: 121,695,861 (GRCm39) |
K88E |
possibly damaging |
Het |
Nlrp5 |
A |
C |
7: 23,117,586 (GRCm39) |
I437L |
probably benign |
Het |
Nnt |
C |
T |
13: 119,533,393 (GRCm39) |
V91M |
probably damaging |
Het |
Nusap1 |
TACACGTTAGCAGTGAGGAGCAAGCTGAGA |
TACACGTTAGCAGTGAGGAGCAAGCTGAGAGACACGTTAGCAGTGAGGAGCAAGCTGAGA |
2: 119,458,062 (GRCm39) |
|
probably benign |
Het |
Nynrin |
T |
G |
14: 56,103,658 (GRCm39) |
|
probably null |
Het |
Or12k5 |
T |
G |
2: 36,895,186 (GRCm39) |
T147P |
probably damaging |
Het |
Or5ak22 |
C |
A |
2: 85,230,137 (GRCm39) |
A247S |
probably damaging |
Het |
Or6c204 |
T |
A |
10: 129,022,562 (GRCm39) |
I243F |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,112,328 (GRCm39) |
K481R |
possibly damaging |
Het |
Padi6 |
T |
C |
4: 140,457,054 (GRCm39) |
D540G |
probably damaging |
Het |
Pcmtd1 |
T |
C |
1: 7,225,329 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
TTTTTGTTTT |
TTTTTGTTTTGGTTTTGTTTT |
4: 134,006,679 (GRCm39) |
|
probably null |
Het |
Phospho1 |
T |
C |
11: 95,721,881 (GRCm39) |
Y184H |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,115,097 (GRCm39) |
R1431W |
|
Het |
Plxdc1 |
T |
A |
11: 97,869,504 (GRCm39) |
H28L |
probably benign |
Het |
Pnma8a |
ACCTCATGATGCACCTGCTTCAACA |
ACCTCATGATGCACCTGCTTCAACACCTCATGATGCACCTGCTTCAACA |
7: 16,695,349 (GRCm39) |
|
probably benign |
Het |
Ppp1r7 |
T |
C |
1: 93,274,011 (GRCm39) |
|
probably null |
Het |
Ppp1r9a |
T |
A |
6: 4,906,657 (GRCm39) |
V404E |
probably damaging |
Het |
Scfd1 |
T |
A |
12: 51,469,756 (GRCm39) |
S434T |
probably benign |
Het |
Six5 |
A |
G |
7: 18,828,862 (GRCm39) |
S101G |
probably benign |
Het |
Slc6a4 |
C |
A |
11: 76,910,008 (GRCm39) |
T421K |
probably damaging |
Het |
Smarcd3 |
C |
A |
5: 24,801,068 (GRCm39) |
R113L |
probably damaging |
Het |
Spmap2l |
CTCCCCAGTCCCGCAAGGCCAG |
CTCCCCAGTCCCGCAAGGCCAGCGATCGTCCCCAGTCCCGCAAGGCCAG |
5: 77,164,255 (GRCm39) |
|
probably benign |
Het |
Tcf25 |
A |
G |
8: 124,122,369 (GRCm39) |
D434G |
probably benign |
Het |
Tcof1 |
CCAGAGATCCCC |
CCAGAGATCCCCGTGGCTGCCGAGATGGGCACTTTCACAGAGATCCCC |
18: 60,966,640 (GRCm39) |
|
probably benign |
Het |
Tep1 |
A |
G |
14: 51,098,402 (GRCm39) |
V463A |
possibly damaging |
Het |
Trav15-2-dv6-2 |
GGGAG |
GGGAGGAG |
14: 53,887,207 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
AAG |
AAGCAG |
14: 53,887,212 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GGAG |
GGAGGAG |
14: 53,887,208 (GRCm39) |
|
probably benign |
Het |
Trim24 |
A |
G |
6: 37,930,471 (GRCm39) |
K642E |
possibly damaging |
Het |
Trim33 |
GGCCCCCGC |
GGC |
3: 103,187,533 (GRCm39) |
|
probably benign |
Het |
Triobp |
CTCCCTGTGCCCAACGG |
CTCCCTGTGCCCAACGGAACAACCCCAGGATTCCCTGTGCCCAACGG |
15: 78,851,244 (GRCm39) |
|
probably benign |
Het |
Trmu |
G |
T |
15: 85,776,770 (GRCm39) |
V161L |
possibly damaging |
Het |
Try4 |
T |
A |
6: 41,282,297 (GRCm39) |
C206S |
probably damaging |
Het |
Usp2 |
TTCACTTAC |
TTCACTTACTCATGTGACCTGTTCGTCACTTAC |
9: 44,000,418 (GRCm39) |
|
probably benign |
Het |
Vmn1r62 |
A |
T |
7: 5,678,669 (GRCm39) |
M117L |
probably benign |
Het |
Vmn2r104 |
A |
T |
17: 20,268,302 (GRCm39) |
Y56N |
probably benign |
Het |
Xxylt1 |
C |
T |
16: 30,869,498 (GRCm39) |
D201N |
possibly damaging |
Het |
Zfp563 |
T |
A |
17: 33,323,999 (GRCm39) |
I198K |
probably benign |
Het |
Zfp612 |
T |
A |
8: 110,816,174 (GRCm39) |
C460* |
probably null |
Het |
Zfp691 |
G |
A |
4: 119,027,932 (GRCm39) |
T100M |
probably benign |
Het |
Zfp773 |
A |
T |
7: 7,135,689 (GRCm39) |
C302* |
probably null |
Het |
Zmat2 |
A |
G |
18: 36,930,936 (GRCm39) |
E154G |
probably damaging |
Het |
Zw10 |
T |
A |
9: 48,972,220 (GRCm39) |
I132N |
possibly damaging |
Het |
|
Other mutations in Son |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Son
|
APN |
16 |
91,461,210 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01024:Son
|
APN |
16 |
91,452,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Son
|
APN |
16 |
91,457,024 (GRCm39) |
intron |
probably benign |
|
IGL01083:Son
|
APN |
16 |
91,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01115:Son
|
APN |
16 |
91,456,346 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01467:Son
|
APN |
16 |
91,454,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01506:Son
|
APN |
16 |
91,454,174 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:Son
|
APN |
16 |
91,454,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Son
|
APN |
16 |
91,452,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02473:Son
|
APN |
16 |
91,455,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02498:Son
|
APN |
16 |
91,453,713 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Son
|
APN |
16 |
91,452,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02530:Son
|
APN |
16 |
91,455,359 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02865:Son
|
APN |
16 |
91,448,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Son
|
APN |
16 |
91,453,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Son
|
UTSW |
16 |
91,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Son
|
UTSW |
16 |
91,457,054 (GRCm39) |
intron |
probably benign |
|
R0037:Son
|
UTSW |
16 |
91,461,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Son
|
UTSW |
16 |
91,456,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0056:Son
|
UTSW |
16 |
91,475,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0227:Son
|
UTSW |
16 |
91,453,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R0256:Son
|
UTSW |
16 |
91,453,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0302:Son
|
UTSW |
16 |
91,453,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Son
|
UTSW |
16 |
91,452,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Son
|
UTSW |
16 |
91,454,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Son
|
UTSW |
16 |
91,461,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Son
|
UTSW |
16 |
91,453,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Son
|
UTSW |
16 |
91,452,230 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1535:Son
|
UTSW |
16 |
91,456,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Son
|
UTSW |
16 |
91,456,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Son
|
UTSW |
16 |
91,454,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Son
|
UTSW |
16 |
91,457,114 (GRCm39) |
intron |
probably benign |
|
R2138:Son
|
UTSW |
16 |
91,456,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2245:Son
|
UTSW |
16 |
91,444,848 (GRCm39) |
splice site |
probably null |
|
R2351:Son
|
UTSW |
16 |
91,454,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2434:Son
|
UTSW |
16 |
91,451,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2871:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2872:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2889:Son
|
UTSW |
16 |
91,456,787 (GRCm39) |
unclassified |
probably benign |
|
R3712:Son
|
UTSW |
16 |
91,453,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R3913:Son
|
UTSW |
16 |
91,456,999 (GRCm39) |
intron |
probably benign |
|
R4172:Son
|
UTSW |
16 |
91,456,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4302:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4770:Son
|
UTSW |
16 |
91,455,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4881:Son
|
UTSW |
16 |
91,472,397 (GRCm39) |
missense |
probably benign |
0.31 |
R5020:Son
|
UTSW |
16 |
91,453,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Son
|
UTSW |
16 |
91,452,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Son
|
UTSW |
16 |
91,451,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5215:Son
|
UTSW |
16 |
91,453,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5243:Son
|
UTSW |
16 |
91,451,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Son
|
UTSW |
16 |
91,452,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5529:Son
|
UTSW |
16 |
91,452,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Son
|
UTSW |
16 |
91,468,301 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5763:Son
|
UTSW |
16 |
91,454,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Son
|
UTSW |
16 |
91,461,875 (GRCm39) |
intron |
probably benign |
|
R5788:Son
|
UTSW |
16 |
91,456,940 (GRCm39) |
intron |
probably benign |
|
R5992:Son
|
UTSW |
16 |
91,455,792 (GRCm39) |
missense |
probably benign |
0.04 |
R6314:Son
|
UTSW |
16 |
91,457,298 (GRCm39) |
intron |
probably benign |
|
R6371:Son
|
UTSW |
16 |
91,471,629 (GRCm39) |
|
|
|
R6429:Son
|
UTSW |
16 |
91,455,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6451:Son
|
UTSW |
16 |
91,454,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6489:Son
|
UTSW |
16 |
91,452,044 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6513:Son
|
UTSW |
16 |
91,456,835 (GRCm39) |
intron |
probably benign |
|
R6753:Son
|
UTSW |
16 |
91,454,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Son
|
UTSW |
16 |
91,451,673 (GRCm39) |
missense |
probably damaging |
0.97 |
R7070:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7079:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7110:Son
|
UTSW |
16 |
91,453,406 (GRCm39) |
missense |
probably benign |
0.01 |
R7120:Son
|
UTSW |
16 |
91,467,414 (GRCm39) |
missense |
unknown |
|
R7120:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7167:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7205:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7208:Son
|
UTSW |
16 |
91,458,990 (GRCm39) |
missense |
unknown |
|
R7219:Son
|
UTSW |
16 |
91,461,889 (GRCm39) |
missense |
unknown |
|
R7249:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7328:Son
|
UTSW |
16 |
91,455,278 (GRCm39) |
missense |
probably benign |
0.33 |
R7330:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7374:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7405:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7420:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7424:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7464:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7514:Son
|
UTSW |
16 |
91,451,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R7555:Son
|
UTSW |
16 |
91,455,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7716:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7718:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7778:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7824:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7856:Son
|
UTSW |
16 |
91,456,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7928:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7978:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8000:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8192:Son
|
UTSW |
16 |
91,452,437 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8221:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8233:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8255:Son
|
UTSW |
16 |
91,461,824 (GRCm39) |
missense |
unknown |
|
R8292:Son
|
UTSW |
16 |
91,453,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8407:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8468:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8495:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R8772:Son
|
UTSW |
16 |
91,454,826 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8796:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8862:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Son
|
UTSW |
16 |
91,455,057 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8991:Son
|
UTSW |
16 |
91,453,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Son
|
UTSW |
16 |
91,453,366 (GRCm39) |
missense |
probably benign |
0.04 |
R9086:Son
|
UTSW |
16 |
91,467,418 (GRCm39) |
missense |
unknown |
|
R9138:Son
|
UTSW |
16 |
91,452,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9232:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9241:Son
|
UTSW |
16 |
91,454,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R9258:Son
|
UTSW |
16 |
91,474,570 (GRCm39) |
missense |
unknown |
|
R9328:Son
|
UTSW |
16 |
91,452,645 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9420:Son
|
UTSW |
16 |
91,454,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Son
|
UTSW |
16 |
91,454,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9500:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9516:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9595:Son
|
UTSW |
16 |
91,454,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9679:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9719:Son
|
UTSW |
16 |
91,456,440 (GRCm39) |
missense |
probably damaging |
0.96 |
R9749:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9772:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9782:Son
|
UTSW |
16 |
91,444,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Son
|
UTSW |
16 |
91,453,699 (GRCm39) |
unclassified |
probably benign |
|
RF041:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Son
|
UTSW |
16 |
91,452,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
|