Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
A |
T |
5: 113,339,010 (GRCm39) |
M334K |
probably benign |
Het |
Abca1 |
A |
T |
4: 53,060,351 (GRCm39) |
I1525N |
probably benign |
Het |
Abca4 |
A |
T |
3: 121,879,275 (GRCm39) |
I398F |
|
Het |
Acbd3 |
A |
G |
1: 180,572,721 (GRCm39) |
D327G |
probably benign |
Het |
Acsm3 |
A |
G |
7: 119,383,166 (GRCm39) |
T544A |
probably damaging |
Het |
Atp11a |
C |
T |
8: 12,901,087 (GRCm39) |
T972M |
probably damaging |
Het |
Cbfb |
C |
T |
8: 105,929,123 (GRCm39) |
R147* |
probably null |
Het |
Ccdc17 |
G |
T |
4: 116,454,144 (GRCm39) |
R54L |
probably benign |
Het |
Cracdl |
T |
G |
1: 37,670,496 (GRCm39) |
E148A |
probably damaging |
Het |
Cuedc2 |
G |
T |
19: 46,319,399 (GRCm39) |
A223E |
probably benign |
Het |
Cul5 |
T |
C |
9: 53,532,474 (GRCm39) |
I787V |
probably benign |
Het |
D430041D05Rik |
T |
A |
2: 104,087,563 (GRCm39) |
H471L |
probably benign |
Het |
Ddx39a |
T |
C |
8: 84,448,916 (GRCm39) |
Y264H |
probably benign |
Het |
Dlgap3 |
C |
A |
4: 127,127,665 (GRCm39) |
R778S |
probably damaging |
Het |
Esrrg |
T |
C |
1: 187,930,848 (GRCm39) |
V313A |
probably damaging |
Het |
Fam124a |
T |
C |
14: 62,844,100 (GRCm39) |
I536T |
probably damaging |
Het |
Fbxo21 |
T |
C |
5: 118,127,272 (GRCm39) |
F275L |
possibly damaging |
Het |
Gabrg1 |
C |
A |
5: 70,999,558 (GRCm39) |
G2V |
possibly damaging |
Het |
Gcc1 |
G |
T |
6: 28,418,089 (GRCm39) |
A748D |
probably damaging |
Het |
Gjb6 |
T |
C |
14: 57,361,511 (GRCm39) |
D250G |
probably benign |
Het |
Gm44501 |
A |
T |
17: 40,889,872 (GRCm39) |
K129* |
probably null |
Het |
Hmcn2 |
T |
G |
2: 31,320,375 (GRCm39) |
L3952R |
|
Het |
Hpd |
A |
G |
5: 123,312,535 (GRCm39) |
I278T |
probably damaging |
Het |
Igsf3 |
T |
A |
3: 101,346,904 (GRCm39) |
F613Y |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,346,817 (GRCm39) |
F584S |
probably damaging |
Het |
Ik |
A |
G |
18: 36,886,635 (GRCm39) |
D369G |
probably benign |
Het |
Ikbke |
A |
G |
1: 131,198,719 (GRCm39) |
L365P |
probably damaging |
Het |
Il22ra2 |
A |
T |
10: 19,508,542 (GRCm39) |
Q190L |
possibly damaging |
Het |
Itga6 |
T |
C |
2: 71,679,834 (GRCm39) |
V1033A |
probably benign |
Het |
Kif18a |
T |
C |
2: 109,120,032 (GRCm39) |
Y112H |
probably damaging |
Het |
Krt75 |
T |
C |
15: 101,482,238 (GRCm39) |
H10R |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,790,734 (GRCm39) |
L93H |
probably benign |
Het |
Lrfn1 |
G |
A |
7: 28,158,183 (GRCm39) |
C34Y |
probably damaging |
Het |
Lrrc47 |
A |
T |
4: 154,101,920 (GRCm39) |
I396F |
probably damaging |
Het |
Mgat3 |
T |
A |
15: 80,095,641 (GRCm39) |
V156E |
probably benign |
Het |
Mtus2 |
A |
G |
5: 148,232,300 (GRCm39) |
D1120G |
possibly damaging |
Het |
Muc5ac |
G |
T |
7: 141,365,465 (GRCm39) |
E2700* |
probably null |
Het |
Nxpe5 |
A |
T |
5: 138,228,591 (GRCm39) |
|
probably benign |
Het |
Or51v15-ps1 |
T |
C |
7: 103,278,931 (GRCm39) |
T79A |
probably damaging |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Pcdhga4 |
T |
A |
18: 37,819,746 (GRCm39) |
S432T |
possibly damaging |
Het |
Pdk4 |
T |
A |
6: 5,486,716 (GRCm39) |
M353L |
probably benign |
Het |
Ppp1r13b |
T |
A |
12: 111,800,210 (GRCm39) |
K645N |
probably benign |
Het |
Ppt1 |
A |
T |
4: 122,751,367 (GRCm39) |
D288V |
possibly damaging |
Het |
Prkcb |
A |
G |
7: 122,181,663 (GRCm39) |
Y417C |
probably damaging |
Het |
Prss22 |
A |
G |
17: 24,215,721 (GRCm39) |
I67T |
probably damaging |
Het |
Rab29 |
T |
C |
1: 131,795,508 (GRCm39) |
V40A |
possibly damaging |
Het |
Rae1 |
T |
C |
2: 172,849,941 (GRCm39) |
|
probably null |
Het |
Rasa3 |
C |
T |
8: 13,630,033 (GRCm39) |
|
probably null |
Het |
Rasgrp3 |
A |
G |
17: 75,807,717 (GRCm39) |
D258G |
probably benign |
Het |
Rcc1 |
T |
A |
4: 132,062,808 (GRCm39) |
T208S |
probably benign |
Het |
Rgs3 |
C |
A |
4: 62,575,354 (GRCm39) |
Y580* |
probably null |
Het |
Rpe65 |
C |
T |
3: 159,328,318 (GRCm39) |
P405S |
probably damaging |
Het |
Rsf1 |
GGCGGC |
GGCGGCGGCAGCGGC |
7: 97,229,137 (GRCm39) |
|
probably benign |
Het |
Rsph4a |
A |
G |
10: 33,790,418 (GRCm39) |
E669G |
probably damaging |
Het |
Rusc1 |
A |
T |
3: 88,994,113 (GRCm39) |
V964E |
probably benign |
Het |
Rusc2 |
A |
G |
4: 43,415,897 (GRCm39) |
N401S |
probably damaging |
Het |
Slc10a1 |
G |
T |
12: 81,002,864 (GRCm39) |
T258K |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,747,418 (GRCm39) |
L323P |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,378,772 (GRCm39) |
I637F |
possibly damaging |
Het |
Slc8a2 |
A |
G |
7: 15,886,780 (GRCm39) |
E641G |
possibly damaging |
Het |
Sptbn2 |
G |
T |
19: 4,789,974 (GRCm39) |
A1321S |
probably damaging |
Het |
Ssh2 |
G |
T |
11: 77,283,976 (GRCm39) |
A77S |
possibly damaging |
Het |
St13 |
G |
T |
15: 81,250,587 (GRCm39) |
N316K |
probably damaging |
Het |
Taf10 |
A |
G |
7: 105,393,062 (GRCm39) |
M121T |
probably benign |
Het |
Tcta |
T |
C |
9: 108,182,942 (GRCm39) |
T68A |
probably damaging |
Het |
Timd2 |
A |
T |
11: 46,577,889 (GRCm39) |
Y81N |
probably damaging |
Het |
Tmed10 |
T |
C |
12: 85,397,621 (GRCm39) |
I123V |
probably benign |
Het |
Ttf1 |
T |
C |
2: 28,969,492 (GRCm39) |
|
probably null |
Het |
Tubg1 |
A |
G |
11: 101,016,886 (GRCm39) |
D396G |
probably damaging |
Het |
Uhmk1 |
A |
G |
1: 170,034,913 (GRCm39) |
|
probably null |
Het |
Unc13a |
C |
T |
8: 72,103,221 (GRCm39) |
A922T |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,219,379 (GRCm39) |
V525E |
probably damaging |
Het |
Usp28 |
C |
A |
9: 48,947,037 (GRCm39) |
Q823K |
probably damaging |
Het |
Vldlr |
A |
T |
19: 27,224,031 (GRCm39) |
I764F |
probably benign |
Het |
Vmn2r88 |
T |
C |
14: 51,648,641 (GRCm39) |
Y62H |
|
Het |
Zfp423 |
T |
A |
8: 88,507,725 (GRCm39) |
N873I |
possibly damaging |
Het |
|
Other mutations in Tln2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Tln2
|
APN |
9 |
67,251,469 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01110:Tln2
|
APN |
9 |
67,157,864 (GRCm39) |
nonsense |
probably null |
|
IGL01112:Tln2
|
APN |
9 |
67,219,093 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01307:Tln2
|
APN |
9 |
67,302,749 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01374:Tln2
|
APN |
9 |
67,169,205 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Tln2
|
APN |
9 |
67,277,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01865:Tln2
|
APN |
9 |
67,157,896 (GRCm39) |
nonsense |
probably null |
|
IGL01999:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02002:Tln2
|
APN |
9 |
67,263,980 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02005:Tln2
|
APN |
9 |
67,299,787 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02015:Tln2
|
APN |
9 |
67,268,721 (GRCm39) |
splice site |
probably benign |
|
IGL02368:Tln2
|
APN |
9 |
67,148,092 (GRCm39) |
splice site |
probably benign |
|
IGL02444:Tln2
|
APN |
9 |
67,165,874 (GRCm39) |
splice site |
probably benign |
|
IGL02646:Tln2
|
APN |
9 |
67,163,278 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02744:Tln2
|
APN |
9 |
67,136,658 (GRCm39) |
nonsense |
probably null |
|
IGL02869:Tln2
|
APN |
9 |
67,128,807 (GRCm39) |
splice site |
probably benign |
|
IGL02930:Tln2
|
APN |
9 |
67,300,944 (GRCm39) |
nonsense |
probably null |
|
IGL03100:Tln2
|
APN |
9 |
67,203,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03326:Tln2
|
APN |
9 |
67,241,539 (GRCm39) |
missense |
possibly damaging |
0.67 |
Harrier
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
Marsh
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
BB008:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
BB018:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0047:Tln2
|
UTSW |
9 |
67,147,954 (GRCm39) |
splice site |
probably benign |
|
R0107:Tln2
|
UTSW |
9 |
67,277,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Tln2
|
UTSW |
9 |
67,262,479 (GRCm39) |
missense |
probably benign |
0.22 |
R0884:Tln2
|
UTSW |
9 |
67,278,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R0947:Tln2
|
UTSW |
9 |
67,203,095 (GRCm39) |
missense |
probably benign |
0.08 |
R0989:Tln2
|
UTSW |
9 |
67,136,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1195:Tln2
|
UTSW |
9 |
67,165,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R1486:Tln2
|
UTSW |
9 |
67,219,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1527:Tln2
|
UTSW |
9 |
67,179,950 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1584:Tln2
|
UTSW |
9 |
67,203,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1636:Tln2
|
UTSW |
9 |
67,213,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1656:Tln2
|
UTSW |
9 |
67,134,389 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1707:Tln2
|
UTSW |
9 |
67,283,089 (GRCm39) |
missense |
probably benign |
0.00 |
R1749:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1751:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1761:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1767:Tln2
|
UTSW |
9 |
67,193,796 (GRCm39) |
missense |
probably benign |
0.01 |
R1815:Tln2
|
UTSW |
9 |
67,136,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Tln2
|
UTSW |
9 |
67,249,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Tln2
|
UTSW |
9 |
67,269,969 (GRCm39) |
nonsense |
probably null |
|
R1964:Tln2
|
UTSW |
9 |
67,249,417 (GRCm39) |
missense |
probably benign |
0.00 |
R1968:Tln2
|
UTSW |
9 |
67,163,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R2036:Tln2
|
UTSW |
9 |
67,179,986 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2038:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R2152:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Tln2
|
UTSW |
9 |
67,209,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Tln2
|
UTSW |
9 |
67,262,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Tln2
|
UTSW |
9 |
67,283,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3116:Tln2
|
UTSW |
9 |
67,262,421 (GRCm39) |
missense |
probably benign |
0.10 |
R3151:Tln2
|
UTSW |
9 |
67,237,829 (GRCm39) |
critical splice donor site |
probably null |
|
R3795:Tln2
|
UTSW |
9 |
67,163,197 (GRCm39) |
missense |
probably damaging |
0.97 |
R3953:Tln2
|
UTSW |
9 |
67,277,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R4450:Tln2
|
UTSW |
9 |
67,251,347 (GRCm39) |
critical splice donor site |
probably null |
|
R4685:Tln2
|
UTSW |
9 |
67,209,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Tln2
|
UTSW |
9 |
67,304,935 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R4696:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4697:Tln2
|
UTSW |
9 |
67,302,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4701:Tln2
|
UTSW |
9 |
67,253,809 (GRCm39) |
missense |
probably benign |
0.03 |
R4741:Tln2
|
UTSW |
9 |
67,293,837 (GRCm39) |
critical splice donor site |
probably null |
|
R4806:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4807:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4808:Tln2
|
UTSW |
9 |
67,239,015 (GRCm39) |
missense |
probably benign |
0.29 |
R4967:Tln2
|
UTSW |
9 |
67,262,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Tln2
|
UTSW |
9 |
67,261,750 (GRCm39) |
missense |
probably benign |
|
R5092:Tln2
|
UTSW |
9 |
67,163,310 (GRCm39) |
missense |
probably benign |
0.13 |
R5093:Tln2
|
UTSW |
9 |
67,241,596 (GRCm39) |
missense |
probably benign |
0.44 |
R5126:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5204:Tln2
|
UTSW |
9 |
67,261,764 (GRCm39) |
missense |
probably benign |
0.00 |
R5236:Tln2
|
UTSW |
9 |
67,273,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R5287:Tln2
|
UTSW |
9 |
67,149,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Tln2
|
UTSW |
9 |
67,219,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5571:Tln2
|
UTSW |
9 |
67,241,602 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5642:Tln2
|
UTSW |
9 |
67,203,640 (GRCm39) |
missense |
probably benign |
0.01 |
R5711:Tln2
|
UTSW |
9 |
67,299,829 (GRCm39) |
missense |
probably benign |
0.00 |
R5776:Tln2
|
UTSW |
9 |
67,165,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5791:Tln2
|
UTSW |
9 |
67,293,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R5866:Tln2
|
UTSW |
9 |
67,174,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Tln2
|
UTSW |
9 |
67,136,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Tln2
|
UTSW |
9 |
67,269,999 (GRCm39) |
missense |
probably benign |
0.02 |
R6106:Tln2
|
UTSW |
9 |
67,230,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R6175:Tln2
|
UTSW |
9 |
67,131,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R6385:Tln2
|
UTSW |
9 |
67,185,411 (GRCm39) |
missense |
probably benign |
0.45 |
R6430:Tln2
|
UTSW |
9 |
67,179,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R6441:Tln2
|
UTSW |
9 |
67,179,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R6738:Tln2
|
UTSW |
9 |
67,293,946 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6776:Tln2
|
UTSW |
9 |
67,170,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6794:Tln2
|
UTSW |
9 |
67,193,840 (GRCm39) |
missense |
probably benign |
0.07 |
R6850:Tln2
|
UTSW |
9 |
67,165,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6907:Tln2
|
UTSW |
9 |
67,304,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R6909:Tln2
|
UTSW |
9 |
67,299,814 (GRCm39) |
missense |
probably damaging |
0.97 |
R6951:Tln2
|
UTSW |
9 |
67,165,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R7015:Tln2
|
UTSW |
9 |
67,269,929 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7051:Tln2
|
UTSW |
9 |
67,253,699 (GRCm39) |
missense |
probably benign |
0.00 |
R7246:Tln2
|
UTSW |
9 |
67,170,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Tln2
|
UTSW |
9 |
67,253,743 (GRCm39) |
missense |
probably benign |
|
R7753:Tln2
|
UTSW |
9 |
67,302,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R7868:Tln2
|
UTSW |
9 |
67,255,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7931:Tln2
|
UTSW |
9 |
67,165,742 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Tln2
|
UTSW |
9 |
67,131,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8081:Tln2
|
UTSW |
9 |
67,264,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8164:Tln2
|
UTSW |
9 |
67,226,702 (GRCm39) |
missense |
probably benign |
0.31 |
R8192:Tln2
|
UTSW |
9 |
67,253,811 (GRCm39) |
nonsense |
probably null |
|
R8495:Tln2
|
UTSW |
9 |
67,261,749 (GRCm39) |
missense |
probably benign |
0.01 |
R8734:Tln2
|
UTSW |
9 |
67,179,936 (GRCm39) |
missense |
probably benign |
0.19 |
R8739:Tln2
|
UTSW |
9 |
67,165,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Tln2
|
UTSW |
9 |
67,274,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Tln2
|
UTSW |
9 |
67,230,304 (GRCm39) |
missense |
probably benign |
|
R8781:Tln2
|
UTSW |
9 |
67,163,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R8812:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8814:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8816:Tln2
|
UTSW |
9 |
67,128,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8816:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8833:Tln2
|
UTSW |
9 |
67,128,693 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8835:Tln2
|
UTSW |
9 |
67,304,975 (GRCm39) |
splice site |
probably benign |
|
R8837:Tln2
|
UTSW |
9 |
67,157,866 (GRCm39) |
missense |
probably damaging |
0.99 |
R8843:Tln2
|
UTSW |
9 |
67,302,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Tln2
|
UTSW |
9 |
67,237,834 (GRCm39) |
nonsense |
probably null |
|
R8867:Tln2
|
UTSW |
9 |
67,237,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R8921:Tln2
|
UTSW |
9 |
67,174,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R9080:Tln2
|
UTSW |
9 |
67,253,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9083:Tln2
|
UTSW |
9 |
67,269,927 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Tln2
|
UTSW |
9 |
67,128,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Tln2
|
UTSW |
9 |
67,277,980 (GRCm39) |
missense |
probably benign |
0.20 |
R9330:Tln2
|
UTSW |
9 |
67,229,213 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9343:Tln2
|
UTSW |
9 |
67,230,353 (GRCm39) |
missense |
probably benign |
0.10 |
R9355:Tln2
|
UTSW |
9 |
67,262,529 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9383:Tln2
|
UTSW |
9 |
67,278,043 (GRCm39) |
missense |
probably benign |
0.17 |
R9386:Tln2
|
UTSW |
9 |
67,273,249 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9407:Tln2
|
UTSW |
9 |
67,136,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Tln2
|
UTSW |
9 |
67,165,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R9642:Tln2
|
UTSW |
9 |
67,157,826 (GRCm39) |
missense |
probably benign |
0.02 |
R9703:Tln2
|
UTSW |
9 |
67,293,938 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Tln2
|
UTSW |
9 |
67,284,135 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Tln2
|
UTSW |
9 |
67,255,420 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Tln2
|
UTSW |
9 |
67,277,973 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tln2
|
UTSW |
9 |
67,253,767 (GRCm39) |
missense |
possibly damaging |
0.46 |
|