Incidental Mutation 'R2122:Obsl1'
ID |
229533 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Obsl1
|
Ensembl Gene |
ENSMUSG00000026211 |
Gene Name |
obscurin-like 1 |
Synonyms |
|
MMRRC Submission |
040126-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.269)
|
Stock # |
R2122 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
75462469-75483134 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 75470527 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 1043
(R1043H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109197
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000113565]
[ENSMUST00000113567]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000113565
|
SMART Domains |
Protein: ENSMUSP00000109195 Gene: ENSMUSG00000026211
Domain | Start | End | E-Value | Type |
IGc2
|
24 |
91 |
1.23e-12 |
SMART |
IGc2
|
140 |
216 |
2.33e-13 |
SMART |
IGc2
|
258 |
326 |
1.48e-6 |
SMART |
IG
|
347 |
427 |
9.49e-5 |
SMART |
IG
|
435 |
511 |
1.04e-1 |
SMART |
FN3
|
518 |
601 |
6.6e-2 |
SMART |
PDB:2E6Q|A
|
608 |
714 |
5e-57 |
PDB |
Blast:IG_like
|
622 |
711 |
2e-50 |
BLAST |
IG
|
723 |
804 |
3.79e-4 |
SMART |
IG
|
814 |
893 |
2.58e-6 |
SMART |
IGc2
|
911 |
977 |
1.12e-6 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113567
AA Change: R1043H
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000109197 Gene: ENSMUSG00000026211 AA Change: R1043H
Domain | Start | End | E-Value | Type |
IGc2
|
24 |
91 |
1.23e-12 |
SMART |
IGc2
|
140 |
216 |
2.33e-13 |
SMART |
IGc2
|
258 |
326 |
1.48e-6 |
SMART |
IG
|
347 |
427 |
9.49e-5 |
SMART |
IG
|
435 |
511 |
1.04e-1 |
SMART |
FN3
|
518 |
601 |
6.6e-2 |
SMART |
PDB:2E6Q|A
|
608 |
714 |
8e-57 |
PDB |
Blast:IG_like
|
622 |
711 |
3e-50 |
BLAST |
IG
|
723 |
804 |
3.79e-4 |
SMART |
IG
|
814 |
893 |
2.58e-6 |
SMART |
IGc2
|
911 |
977 |
1.12e-6 |
SMART |
IG
|
996 |
1075 |
1.27e-5 |
SMART |
IGc2
|
1094 |
1160 |
4.07e-4 |
SMART |
IGc2
|
1186 |
1252 |
9.49e-5 |
SMART |
IG
|
1274 |
1353 |
7.41e-7 |
SMART |
IG
|
1363 |
1444 |
1.15e-3 |
SMART |
IG
|
1454 |
1533 |
8.33e-1 |
SMART |
IGc2
|
1549 |
1615 |
8.72e-4 |
SMART |
IG
|
1633 |
1712 |
1e-3 |
SMART |
IG
|
1723 |
1802 |
3.82e-9 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127507
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000132252
|
SMART Domains |
Protein: ENSMUSP00000117420 Gene: ENSMUSG00000026211
Domain | Start | End | E-Value | Type |
IG_like
|
1 |
59 |
2.8e-1 |
SMART |
IGc2
|
85 |
151 |
9.49e-5 |
SMART |
IG
|
175 |
254 |
2.64e-3 |
SMART |
IG
|
265 |
344 |
7.41e-7 |
SMART |
Blast:IG
|
354 |
417 |
4e-35 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000138352
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000145382
|
Predicted Effect |
unknown
Transcript: ENSMUST00000155084
AA Change: R848H
|
SMART Domains |
Protein: ENSMUSP00000114553 Gene: ENSMUSG00000026211 AA Change: R848H
Domain | Start | End | E-Value | Type |
SCOP:d1g1ca_
|
2 |
32 |
1e-3 |
SMART |
IGc2
|
64 |
132 |
1.48e-6 |
SMART |
IG
|
153 |
233 |
9.49e-5 |
SMART |
IG
|
241 |
317 |
1.04e-1 |
SMART |
FN3
|
324 |
407 |
6.6e-2 |
SMART |
PDB:2E6Q|A
|
414 |
520 |
4e-57 |
PDB |
Blast:IG_like
|
428 |
517 |
2e-50 |
BLAST |
IG
|
529 |
610 |
3.79e-4 |
SMART |
IG
|
620 |
699 |
2.58e-6 |
SMART |
IGc2
|
717 |
783 |
1.12e-6 |
SMART |
IG
|
802 |
881 |
1.27e-5 |
SMART |
IGc2
|
900 |
966 |
4.07e-4 |
SMART |
IGc2
|
992 |
1058 |
9.49e-5 |
SMART |
IG
|
1080 |
1159 |
7.41e-7 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150293
|
Meta Mutation Damage Score |
0.0706 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.2%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
G |
T |
7: 120,119,184 (GRCm39) |
G975V |
probably damaging |
Het |
Abcg5 |
T |
A |
17: 84,978,575 (GRCm39) |
E294D |
probably benign |
Het |
Actl10 |
G |
A |
2: 154,394,153 (GRCm39) |
R35H |
probably damaging |
Het |
Adamts12 |
C |
T |
15: 11,310,665 (GRCm39) |
T974I |
probably damaging |
Het |
Ahctf1 |
C |
A |
1: 179,597,017 (GRCm39) |
R43L |
probably damaging |
Het |
Arhgef10 |
A |
G |
8: 14,984,820 (GRCm39) |
D200G |
probably damaging |
Het |
Arhgef38 |
T |
C |
3: 132,866,514 (GRCm39) |
K208E |
probably benign |
Het |
Arhgef7 |
A |
T |
8: 11,778,256 (GRCm39) |
N2I |
possibly damaging |
Het |
Blvra |
T |
G |
2: 126,928,817 (GRCm39) |
S102A |
probably damaging |
Het |
Btn1a1 |
A |
G |
13: 23,645,691 (GRCm39) |
L226P |
probably damaging |
Het |
C2cd4d |
G |
T |
3: 94,270,925 (GRCm39) |
E64* |
probably null |
Het |
Ccna2 |
A |
G |
3: 36,622,875 (GRCm39) |
V209A |
probably damaging |
Het |
Cd55 |
T |
A |
1: 130,387,354 (GRCm39) |
D148V |
possibly damaging |
Het |
Cdh2 |
G |
A |
18: 16,907,600 (GRCm39) |
P46L |
probably benign |
Het |
Cldn11 |
A |
G |
3: 31,217,300 (GRCm39) |
Y156C |
probably damaging |
Het |
Cmtm2a |
T |
C |
8: 105,019,655 (GRCm39) |
R12G |
possibly damaging |
Het |
Cog2 |
T |
C |
8: 125,255,724 (GRCm39) |
S104P |
possibly damaging |
Het |
Col4a3 |
T |
G |
1: 82,632,678 (GRCm39) |
F184V |
unknown |
Het |
Col4a4 |
T |
A |
1: 82,434,592 (GRCm39) |
D1406V |
unknown |
Het |
Col6a1 |
T |
C |
10: 76,557,332 (GRCm39) |
T207A |
probably benign |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Dcdc2a |
T |
G |
13: 25,303,268 (GRCm39) |
S266R |
possibly damaging |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Ecel1 |
A |
G |
1: 87,075,997 (GRCm39) |
S727P |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,286,274 (GRCm39) |
V1063E |
probably damaging |
Het |
Enpp2 |
A |
T |
15: 54,761,188 (GRCm39) |
Y44* |
probably null |
Het |
Ep400 |
A |
T |
5: 110,856,716 (GRCm39) |
|
probably benign |
Het |
Exoc6b |
A |
G |
6: 84,598,464 (GRCm39) |
M779T |
probably benign |
Het |
F13a1 |
T |
A |
13: 37,209,653 (GRCm39) |
Y104F |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,906,278 (GRCm39) |
V146M |
probably damaging |
Het |
Fgf18 |
A |
C |
11: 33,068,003 (GRCm39) |
F129C |
probably damaging |
Het |
Fscn3 |
A |
G |
6: 28,430,388 (GRCm39) |
D186G |
probably benign |
Het |
Gm5773 |
G |
A |
3: 93,680,624 (GRCm39) |
G99R |
possibly damaging |
Het |
Grk1 |
A |
T |
8: 13,455,221 (GRCm39) |
Y35F |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,418,145 (GRCm39) |
V359A |
probably benign |
Het |
Hfm1 |
A |
G |
5: 107,044,121 (GRCm39) |
S567P |
probably damaging |
Het |
Il1rap |
A |
T |
16: 26,529,315 (GRCm39) |
H379L |
probably damaging |
Het |
Kctd5 |
T |
C |
17: 24,274,940 (GRCm39) |
T212A |
probably benign |
Het |
Krtap5-5 |
A |
T |
7: 141,783,240 (GRCm39) |
C137S |
unknown |
Het |
Lrp2 |
T |
C |
2: 69,314,051 (GRCm39) |
T2227A |
probably damaging |
Het |
Ltbp1 |
T |
A |
17: 75,617,154 (GRCm39) |
V1031E |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,286,440 (GRCm39) |
S249P |
probably benign |
Het |
Map1a |
T |
A |
2: 121,129,927 (GRCm39) |
Y248N |
probably damaging |
Het |
Mdc1 |
C |
T |
17: 36,158,835 (GRCm39) |
A405V |
probably benign |
Het |
Mfsd4b1 |
T |
C |
10: 39,878,647 (GRCm39) |
K417E |
possibly damaging |
Het |
Mroh2a |
T |
C |
1: 88,184,476 (GRCm39) |
V1453A |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,035,868 (GRCm39) |
E1027G |
probably damaging |
Het |
Nudt6 |
A |
C |
3: 37,466,554 (GRCm39) |
F80L |
probably benign |
Het |
Nxph1 |
A |
G |
6: 9,247,791 (GRCm39) |
K254R |
probably damaging |
Het |
Or10a4 |
A |
T |
7: 106,697,316 (GRCm39) |
I215F |
probably damaging |
Het |
Pde6d |
A |
G |
1: 86,473,524 (GRCm39) |
F91L |
probably benign |
Het |
Phldb2 |
T |
A |
16: 45,583,304 (GRCm39) |
I1065F |
probably damaging |
Het |
Ppp1r3a |
A |
T |
6: 14,721,874 (GRCm39) |
N317K |
possibly damaging |
Het |
Psmd1 |
T |
A |
1: 86,006,422 (GRCm39) |
S263T |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,396,581 (GRCm39) |
T112K |
possibly damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,454,425 (GRCm39) |
M156K |
probably benign |
Het |
Reg3a |
T |
C |
6: 78,358,119 (GRCm39) |
C17R |
possibly damaging |
Het |
Ripor2 |
A |
G |
13: 24,897,701 (GRCm39) |
S800G |
probably damaging |
Het |
Rnf168 |
T |
G |
16: 32,097,036 (GRCm39) |
L37R |
probably damaging |
Het |
Rnf31 |
A |
G |
14: 55,833,654 (GRCm39) |
D554G |
probably damaging |
Het |
Rpe |
T |
C |
1: 66,754,387 (GRCm39) |
M153T |
probably damaging |
Het |
Sacs |
A |
T |
14: 61,449,765 (GRCm39) |
Q3937L |
probably damaging |
Het |
Sap18 |
T |
A |
14: 58,036,011 (GRCm39) |
S66T |
probably damaging |
Het |
Slc20a1 |
T |
G |
2: 129,041,739 (GRCm39) |
I34S |
possibly damaging |
Het |
Slc25a30 |
A |
G |
14: 76,007,658 (GRCm39) |
S116P |
possibly damaging |
Het |
Speer4c1 |
T |
A |
5: 15,919,115 (GRCm39) |
D29V |
possibly damaging |
Het |
Stk40 |
C |
T |
4: 126,022,640 (GRCm39) |
T138I |
probably benign |
Het |
Susd3 |
A |
G |
13: 49,384,626 (GRCm39) |
Y254H |
probably damaging |
Het |
Tanc2 |
T |
C |
11: 105,786,775 (GRCm39) |
L858P |
probably damaging |
Het |
Tas2r106 |
A |
T |
6: 131,655,317 (GRCm39) |
L178H |
probably damaging |
Het |
Tfpt |
C |
T |
7: 3,631,930 (GRCm39) |
R60Q |
probably damaging |
Het |
Tmem44 |
T |
A |
16: 30,366,262 (GRCm39) |
K55* |
probably null |
Het |
Tnfsf9 |
A |
T |
17: 57,414,316 (GRCm39) |
|
probably null |
Het |
Ube3c |
T |
C |
5: 29,824,604 (GRCm39) |
I543T |
probably benign |
Het |
Ugt1a2 |
C |
A |
1: 88,128,735 (GRCm39) |
S126Y |
possibly damaging |
Het |
Vmn1r180 |
T |
A |
7: 23,652,566 (GRCm39) |
L243Q |
probably damaging |
Het |
Vmn2r15 |
A |
C |
5: 109,434,322 (GRCm39) |
V794G |
probably damaging |
Het |
Vmn2r24 |
A |
G |
6: 123,792,353 (GRCm39) |
D560G |
possibly damaging |
Het |
Wdr11 |
G |
A |
7: 129,233,490 (GRCm39) |
C1028Y |
probably damaging |
Het |
Zfp318 |
A |
G |
17: 46,724,297 (GRCm39) |
D2100G |
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,655,991 (GRCm39) |
Y789* |
probably null |
Het |
|
Other mutations in Obsl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Obsl1
|
APN |
1 |
75,467,518 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01111:Obsl1
|
APN |
1 |
75,473,789 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01140:Obsl1
|
APN |
1 |
75,466,400 (GRCm39) |
unclassified |
probably benign |
|
IGL02149:Obsl1
|
APN |
1 |
75,480,464 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02225:Obsl1
|
APN |
1 |
75,480,442 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02269:Obsl1
|
APN |
1 |
75,464,357 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02296:Obsl1
|
APN |
1 |
75,474,793 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02386:Obsl1
|
APN |
1 |
75,469,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Obsl1
|
APN |
1 |
75,481,890 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02601:Obsl1
|
APN |
1 |
75,466,264 (GRCm39) |
missense |
probably benign |
|
IGL03053:Obsl1
|
APN |
1 |
75,469,723 (GRCm39) |
missense |
probably benign |
|
IGL03181:Obsl1
|
APN |
1 |
75,469,228 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03402:Obsl1
|
APN |
1 |
75,463,443 (GRCm39) |
missense |
probably benign |
0.00 |
Jude
|
UTSW |
1 |
75,474,877 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Obsl1
|
UTSW |
1 |
75,482,811 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Obsl1
|
UTSW |
1 |
75,464,607 (GRCm39) |
missense |
probably benign |
0.06 |
R0281:Obsl1
|
UTSW |
1 |
75,469,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1343:Obsl1
|
UTSW |
1 |
75,469,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R1394:Obsl1
|
UTSW |
1 |
75,469,309 (GRCm39) |
missense |
probably damaging |
0.96 |
R1395:Obsl1
|
UTSW |
1 |
75,469,309 (GRCm39) |
missense |
probably damaging |
0.96 |
R1439:Obsl1
|
UTSW |
1 |
75,463,428 (GRCm39) |
nonsense |
probably null |
|
R1456:Obsl1
|
UTSW |
1 |
75,464,300 (GRCm39) |
nonsense |
probably null |
|
R1728:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1729:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1730:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1739:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1757:Obsl1
|
UTSW |
1 |
75,470,527 (GRCm39) |
missense |
probably benign |
|
R1762:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1783:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1784:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1785:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R1851:Obsl1
|
UTSW |
1 |
75,469,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R1864:Obsl1
|
UTSW |
1 |
75,469,753 (GRCm39) |
missense |
probably benign |
0.01 |
R1873:Obsl1
|
UTSW |
1 |
75,474,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Obsl1
|
UTSW |
1 |
75,474,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1980:Obsl1
|
UTSW |
1 |
75,482,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R1985:Obsl1
|
UTSW |
1 |
75,482,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R2069:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R2141:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R2142:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
R2184:Obsl1
|
UTSW |
1 |
75,478,861 (GRCm39) |
missense |
probably benign |
0.26 |
R2267:Obsl1
|
UTSW |
1 |
75,482,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2883:Obsl1
|
UTSW |
1 |
75,473,155 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3079:Obsl1
|
UTSW |
1 |
75,467,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R3749:Obsl1
|
UTSW |
1 |
75,474,890 (GRCm39) |
missense |
probably benign |
|
R4002:Obsl1
|
UTSW |
1 |
75,476,743 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4365:Obsl1
|
UTSW |
1 |
75,464,693 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4366:Obsl1
|
UTSW |
1 |
75,464,693 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4414:Obsl1
|
UTSW |
1 |
75,467,546 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Obsl1
|
UTSW |
1 |
75,480,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4799:Obsl1
|
UTSW |
1 |
75,466,145 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5081:Obsl1
|
UTSW |
1 |
75,464,607 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5389:Obsl1
|
UTSW |
1 |
75,479,905 (GRCm39) |
intron |
probably benign |
|
R5757:Obsl1
|
UTSW |
1 |
75,469,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R5890:Obsl1
|
UTSW |
1 |
75,470,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R5946:Obsl1
|
UTSW |
1 |
75,467,851 (GRCm39) |
missense |
probably damaging |
0.96 |
R6005:Obsl1
|
UTSW |
1 |
75,468,859 (GRCm39) |
splice site |
probably null |
|
R6118:Obsl1
|
UTSW |
1 |
75,468,722 (GRCm39) |
intron |
probably benign |
|
R6154:Obsl1
|
UTSW |
1 |
75,476,788 (GRCm39) |
missense |
probably benign |
0.19 |
R6317:Obsl1
|
UTSW |
1 |
75,466,273 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6379:Obsl1
|
UTSW |
1 |
75,479,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R6387:Obsl1
|
UTSW |
1 |
75,468,006 (GRCm39) |
missense |
probably benign |
0.03 |
R7084:Obsl1
|
UTSW |
1 |
75,464,394 (GRCm39) |
missense |
probably benign |
|
R7123:Obsl1
|
UTSW |
1 |
75,466,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Obsl1
|
UTSW |
1 |
75,466,360 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7291:Obsl1
|
UTSW |
1 |
75,466,161 (GRCm39) |
missense |
probably damaging |
0.98 |
R7305:Obsl1
|
UTSW |
1 |
75,470,590 (GRCm39) |
nonsense |
probably null |
|
R7366:Obsl1
|
UTSW |
1 |
75,479,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Obsl1
|
UTSW |
1 |
75,464,348 (GRCm39) |
missense |
probably benign |
|
R7474:Obsl1
|
UTSW |
1 |
75,474,828 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Obsl1
|
UTSW |
1 |
75,482,024 (GRCm39) |
missense |
probably damaging |
0.96 |
R7672:Obsl1
|
UTSW |
1 |
75,469,365 (GRCm39) |
missense |
probably benign |
0.18 |
R7715:Obsl1
|
UTSW |
1 |
75,478,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R7762:Obsl1
|
UTSW |
1 |
75,480,167 (GRCm39) |
missense |
probably benign |
|
R8005:Obsl1
|
UTSW |
1 |
75,482,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Obsl1
|
UTSW |
1 |
75,469,317 (GRCm39) |
missense |
probably benign |
0.12 |
R8379:Obsl1
|
UTSW |
1 |
75,480,501 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8381:Obsl1
|
UTSW |
1 |
75,480,501 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8383:Obsl1
|
UTSW |
1 |
75,480,501 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8396:Obsl1
|
UTSW |
1 |
75,480,350 (GRCm39) |
missense |
probably benign |
0.01 |
R8465:Obsl1
|
UTSW |
1 |
75,480,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8506:Obsl1
|
UTSW |
1 |
75,482,300 (GRCm39) |
missense |
probably benign |
0.00 |
R8710:Obsl1
|
UTSW |
1 |
75,469,326 (GRCm39) |
missense |
probably benign |
|
R8877:Obsl1
|
UTSW |
1 |
75,473,167 (GRCm39) |
nonsense |
probably null |
|
R8903:Obsl1
|
UTSW |
1 |
75,463,917 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8913:Obsl1
|
UTSW |
1 |
75,467,892 (GRCm39) |
missense |
probably benign |
0.00 |
R8924:Obsl1
|
UTSW |
1 |
75,482,841 (GRCm39) |
missense |
probably benign |
0.00 |
R8955:Obsl1
|
UTSW |
1 |
75,480,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Obsl1
|
UTSW |
1 |
75,482,027 (GRCm39) |
missense |
probably benign |
|
R9121:Obsl1
|
UTSW |
1 |
75,482,636 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9295:Obsl1
|
UTSW |
1 |
75,476,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Obsl1
|
UTSW |
1 |
75,482,391 (GRCm39) |
missense |
probably benign |
0.01 |
R9367:Obsl1
|
UTSW |
1 |
75,466,177 (GRCm39) |
missense |
probably benign |
0.18 |
R9459:Obsl1
|
UTSW |
1 |
75,474,884 (GRCm39) |
missense |
probably benign |
0.16 |
R9496:Obsl1
|
UTSW |
1 |
75,467,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R9497:Obsl1
|
UTSW |
1 |
75,467,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R9498:Obsl1
|
UTSW |
1 |
75,467,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R9502:Obsl1
|
UTSW |
1 |
75,466,267 (GRCm39) |
missense |
probably damaging |
0.98 |
R9546:Obsl1
|
UTSW |
1 |
75,482,030 (GRCm39) |
missense |
probably damaging |
0.98 |
R9550:Obsl1
|
UTSW |
1 |
75,474,910 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9561:Obsl1
|
UTSW |
1 |
75,480,157 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9687:Obsl1
|
UTSW |
1 |
75,479,670 (GRCm39) |
missense |
probably damaging |
1.00 |
V8831:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
X0061:Obsl1
|
UTSW |
1 |
75,463,412 (GRCm39) |
missense |
probably benign |
|
Z1088:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
Z1176:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
Z1177:Obsl1
|
UTSW |
1 |
75,467,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Obsl1
|
UTSW |
1 |
75,486,756 (GRCm38) |
missense |
probably benign |
|
Z1177:Obsl1
|
UTSW |
1 |
75,480,436 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TCTTTGATGGCTAAGACTGAGGAG -3'
(R):5'- CCTGTGCGGATCATATACCC -3'
Sequencing Primer
(F):5'- GACTGAGGAGTCTGGGAAAC -3'
(R):5'- TCATATACCCCCAGGACGAGGTG -3'
|
Posted On |
2014-09-17 |