Incidental Mutation 'R7535:Sbno1'
ID |
583503 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Sbno1
|
Ensembl Gene |
ENSMUSG00000038095 |
Gene Name |
strawberry notch 1 |
Synonyms |
9330180L10Rik, sno |
MMRRC Submission |
045607-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7535 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
124506765-124564059 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 124551342 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Leucine to Proline
at position 47
(L47P)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000142481
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000065263]
[ENSMUST00000168651]
[ENSMUST00000196329]
[ENSMUST00000196644]
[ENSMUST00000196711]
[ENSMUST00000197777]
[ENSMUST00000198420]
[ENSMUST00000199808]
[ENSMUST00000199004]
[ENSMUST00000200474]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000065263
AA Change: L47P
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000066808 Gene: ENSMUSG00000038095 AA Change: L47P
Domain | Start | End | E-Value | Type |
low complexity region
|
217 |
234 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
254 |
559 |
3.6e-144 |
PFAM |
Pfam:ResIII
|
287 |
478 |
2.7e-8 |
PFAM |
low complexity region
|
633 |
649 |
N/A |
INTRINSIC |
low complexity region
|
727 |
748 |
N/A |
INTRINSIC |
low complexity region
|
779 |
797 |
N/A |
INTRINSIC |
low complexity region
|
815 |
838 |
N/A |
INTRINSIC |
coiled coil region
|
839 |
868 |
N/A |
INTRINSIC |
Pfam:Helicase_C_4
|
870 |
1146 |
3.6e-126 |
PFAM |
low complexity region
|
1365 |
1384 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000168651
AA Change: L47P
PolyPhen 2
Score 0.864 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000130860 Gene: ENSMUSG00000038095 AA Change: L47P
Domain | Start | End | E-Value | Type |
low complexity region
|
217 |
234 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
254 |
559 |
3.6e-144 |
PFAM |
Pfam:ResIII
|
287 |
478 |
2.7e-8 |
PFAM |
low complexity region
|
633 |
649 |
N/A |
INTRINSIC |
low complexity region
|
727 |
748 |
N/A |
INTRINSIC |
low complexity region
|
779 |
797 |
N/A |
INTRINSIC |
low complexity region
|
815 |
838 |
N/A |
INTRINSIC |
coiled coil region
|
839 |
868 |
N/A |
INTRINSIC |
Pfam:Helicase_C_4
|
870 |
1146 |
3.6e-126 |
PFAM |
low complexity region
|
1365 |
1384 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196329
|
SMART Domains |
Protein: ENSMUSP00000143084 Gene: ENSMUSG00000038095
Domain | Start | End | E-Value | Type |
low complexity region
|
35 |
51 |
N/A |
INTRINSIC |
low complexity region
|
182 |
199 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
217 |
525 |
1.4e-139 |
PFAM |
Pfam:ResIII
|
254 |
441 |
2.4e-8 |
PFAM |
low complexity region
|
598 |
614 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000196644
AA Change: L47P
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000142827 Gene: ENSMUSG00000038095 AA Change: L47P
Domain | Start | End | E-Value | Type |
low complexity region
|
217 |
234 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
252 |
560 |
4.3e-136 |
PFAM |
Pfam:ResIII
|
289 |
476 |
1.8e-6 |
PFAM |
low complexity region
|
633 |
649 |
N/A |
INTRINSIC |
low complexity region
|
727 |
748 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196711
|
SMART Domains |
Protein: ENSMUSP00000142980 Gene: ENSMUSG00000038095
Domain | Start | End | E-Value | Type |
low complexity region
|
35 |
51 |
N/A |
INTRINSIC |
low complexity region
|
182 |
199 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000197777
AA Change: L47P
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000198420
|
SMART Domains |
Protein: ENSMUSP00000142416 Gene: ENSMUSG00000038095
Domain | Start | End | E-Value | Type |
low complexity region
|
35 |
50 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000199808
AA Change: L47P
PolyPhen 2
Score 0.482 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000142481 Gene: ENSMUSG00000038095 AA Change: L47P
Domain | Start | End | E-Value | Type |
low complexity region
|
217 |
234 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
252 |
560 |
6e-139 |
PFAM |
Pfam:ResIII
|
289 |
476 |
1.3e-7 |
PFAM |
low complexity region
|
633 |
649 |
N/A |
INTRINSIC |
low complexity region
|
727 |
748 |
N/A |
INTRINSIC |
low complexity region
|
779 |
797 |
N/A |
INTRINSIC |
low complexity region
|
815 |
838 |
N/A |
INTRINSIC |
coiled coil region
|
839 |
868 |
N/A |
INTRINSIC |
Pfam:Helicase_C_4
|
870 |
1146 |
4.6e-120 |
PFAM |
low complexity region
|
1365 |
1384 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000199004
AA Change: L47P
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000143314 Gene: ENSMUSG00000038095 AA Change: L47P
Domain | Start | End | E-Value | Type |
low complexity region
|
217 |
234 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000200474
|
SMART Domains |
Protein: ENSMUSP00000143516 Gene: ENSMUSG00000038095
Domain | Start | End | E-Value | Type |
low complexity region
|
35 |
50 |
N/A |
INTRINSIC |
low complexity region
|
181 |
198 |
N/A |
INTRINSIC |
Pfam:AAA_34
|
218 |
523 |
2.3e-141 |
PFAM |
Pfam:ResIII
|
251 |
442 |
3.3e-7 |
PFAM |
low complexity region
|
597 |
613 |
N/A |
INTRINSIC |
low complexity region
|
691 |
712 |
N/A |
INTRINSIC |
low complexity region
|
743 |
755 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
100% (82/82) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
A |
10: 79,837,463 (GRCm39) |
L449Q |
probably benign |
Het |
Agtpbp1 |
T |
C |
13: 59,652,067 (GRCm39) |
T415A |
probably benign |
Het |
Akt3 |
A |
T |
1: 176,924,600 (GRCm39) |
V165D |
probably damaging |
Het |
Cbr2 |
T |
A |
11: 120,620,628 (GRCm39) |
I219F |
probably damaging |
Het |
Cdh20 |
T |
A |
1: 104,902,768 (GRCm39) |
D486E |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,949,523 (GRCm39) |
S103G |
possibly damaging |
Het |
Chd4 |
T |
A |
6: 125,105,836 (GRCm39) |
S1818T |
probably benign |
Het |
Chst5 |
T |
C |
8: 112,616,795 (GRCm39) |
D275G |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,724,328 (GRCm39) |
I244T |
probably damaging |
Het |
Cyp2c54 |
A |
G |
19: 40,058,716 (GRCm39) |
Y239H |
probably benign |
Het |
Czib |
T |
G |
4: 107,752,097 (GRCm39) |
S159A |
probably benign |
Het |
Ddx25 |
A |
G |
9: 35,454,951 (GRCm39) |
F446L |
possibly damaging |
Het |
Dgkb |
T |
C |
12: 38,186,646 (GRCm39) |
L265P |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,327,415 (GRCm39) |
S363P |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,327,323 (GRCm39) |
E1187G |
probably damaging |
Het |
Dop1b |
G |
A |
16: 93,603,249 (GRCm39) |
G2061R |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,376,765 (GRCm39) |
S1517P |
probably benign |
Het |
Epg5 |
T |
A |
18: 78,076,141 (GRCm39) |
V2513E |
probably benign |
Het |
Fryl |
T |
A |
5: 73,255,539 (GRCm39) |
T831S |
probably benign |
Het |
Gm6309 |
A |
T |
5: 146,105,100 (GRCm39) |
V271D |
probably damaging |
Het |
H2-M2 |
G |
T |
17: 37,793,528 (GRCm39) |
S159R |
probably benign |
Het |
Helq |
A |
G |
5: 100,937,999 (GRCm39) |
|
probably null |
Het |
Herc1 |
G |
C |
9: 66,382,135 (GRCm39) |
D3621H |
probably damaging |
Het |
Hsd11b2 |
A |
T |
8: 106,245,755 (GRCm39) |
I87F |
probably damaging |
Het |
Ice2 |
A |
G |
9: 69,339,360 (GRCm39) |
N959S |
probably damaging |
Het |
Ifi47 |
T |
A |
11: 48,987,452 (GRCm39) |
D406E |
probably damaging |
Het |
Ifit3 |
T |
G |
19: 34,565,280 (GRCm39) |
S275R |
probably damaging |
Het |
Insl5 |
C |
A |
4: 102,875,395 (GRCm39) |
K118N |
probably damaging |
Het |
Irf7 |
A |
T |
7: 140,844,550 (GRCm39) |
F158I |
probably benign |
Het |
Kat2b |
T |
C |
17: 53,931,431 (GRCm39) |
L143P |
probably damaging |
Het |
Klk1b1 |
A |
T |
7: 43,619,746 (GRCm39) |
N102Y |
probably damaging |
Het |
Krt13 |
C |
T |
11: 100,008,824 (GRCm39) |
G410S |
unknown |
Het |
Larp6 |
A |
T |
9: 60,631,437 (GRCm39) |
T70S |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,392,683 (GRCm39) |
E914G |
possibly damaging |
Het |
Mindy4 |
T |
C |
6: 55,274,738 (GRCm39) |
|
probably null |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Myom2 |
A |
G |
8: 15,167,679 (GRCm39) |
Y1088C |
probably damaging |
Het |
Mysm1 |
T |
C |
4: 94,840,452 (GRCm39) |
N655D |
probably benign |
Het |
Nbas |
T |
A |
12: 13,329,390 (GRCm39) |
S112T |
probably damaging |
Het |
Neb |
A |
G |
2: 52,055,115 (GRCm39) |
|
probably null |
Het |
Noxred1 |
G |
A |
12: 87,280,206 (GRCm39) |
A42V |
probably benign |
Het |
Olfm5 |
G |
A |
7: 103,803,444 (GRCm39) |
P340S |
possibly damaging |
Het |
Or11h4 |
G |
A |
14: 50,974,122 (GRCm39) |
P166S |
probably benign |
Het |
Or2l5 |
T |
C |
16: 19,333,544 (GRCm39) |
T281A |
probably damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,608 (GRCm39) |
V133A |
probably benign |
Het |
Or5m8 |
T |
A |
2: 85,822,245 (GRCm39) |
V28E |
probably benign |
Het |
Or9i1b |
A |
G |
19: 13,896,449 (GRCm39) |
K22E |
probably benign |
Het |
Pccb |
A |
T |
9: 100,876,615 (GRCm39) |
|
probably null |
Het |
Pnn |
T |
A |
12: 59,118,923 (GRCm39) |
V502E |
probably benign |
Het |
Pole2 |
A |
T |
12: 69,269,203 (GRCm39) |
I98K |
probably benign |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,484 (GRCm39) |
K111E |
probably benign |
Het |
Rbbp6 |
G |
A |
7: 122,589,366 (GRCm39) |
M351I |
probably benign |
Het |
Rgs19 |
T |
G |
2: 181,333,101 (GRCm39) |
H53P |
probably damaging |
Het |
Rin1 |
A |
T |
19: 5,102,564 (GRCm39) |
T369S |
probably benign |
Het |
Rnaset2b |
G |
A |
17: 7,259,138 (GRCm39) |
E135K |
possibly damaging |
Het |
Rprd2 |
G |
A |
3: 95,683,899 (GRCm39) |
P379S |
probably damaging |
Het |
Slamf6 |
T |
A |
1: 171,747,325 (GRCm39) |
L29Q |
unknown |
Het |
Slc16a14 |
T |
C |
1: 84,890,843 (GRCm39) |
Y154C |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,147,342 (GRCm39) |
F340S |
probably damaging |
Het |
Slc6a4 |
T |
G |
11: 76,905,976 (GRCm39) |
I259S |
possibly damaging |
Het |
Smarca4 |
G |
A |
9: 21,558,921 (GRCm39) |
V651I |
possibly damaging |
Het |
Susd5 |
C |
T |
9: 113,893,108 (GRCm39) |
A62V |
possibly damaging |
Het |
Syt1 |
T |
A |
10: 108,463,283 (GRCm39) |
|
probably null |
Het |
Taf10 |
T |
C |
7: 105,390,117 (GRCm39) |
I218T |
probably benign |
Het |
Tas1r1 |
C |
A |
4: 152,112,819 (GRCm39) |
V745F |
probably benign |
Het |
Tas2r125 |
C |
A |
6: 132,887,287 (GRCm39) |
T225K |
probably damaging |
Het |
Tcp11l2 |
G |
T |
10: 84,430,523 (GRCm39) |
R216L |
possibly damaging |
Het |
Tnks1bp1 |
C |
T |
2: 84,893,624 (GRCm39) |
Q1184* |
probably null |
Het |
Treml2 |
T |
A |
17: 48,609,847 (GRCm39) |
V93D |
probably damaging |
Het |
Trim11 |
G |
A |
11: 58,872,891 (GRCm39) |
E192K |
probably damaging |
Het |
Trim43a |
A |
G |
9: 88,470,201 (GRCm39) |
K336E |
probably damaging |
Het |
Tspan33 |
T |
A |
6: 29,717,588 (GRCm39) |
I268N |
possibly damaging |
Het |
Tstd2 |
C |
T |
4: 46,116,960 (GRCm39) |
C458Y |
probably damaging |
Het |
Ttc6 |
A |
G |
12: 57,623,305 (GRCm39) |
S235G |
probably benign |
Het |
Usp29 |
A |
C |
7: 6,964,219 (GRCm39) |
T21P |
possibly damaging |
Het |
Usp36 |
A |
T |
11: 118,152,872 (GRCm39) |
S1084T |
possibly damaging |
Het |
Vps39 |
T |
A |
2: 120,155,176 (GRCm39) |
N550I |
probably damaging |
Het |
Wdr47 |
A |
G |
3: 108,537,027 (GRCm39) |
I572V |
probably benign |
Het |
Zfp112 |
A |
T |
7: 23,826,135 (GRCm39) |
Y705F |
probably damaging |
Het |
Zfp282 |
A |
G |
6: 47,881,878 (GRCm39) |
T522A |
probably benign |
Het |
Zfp292 |
T |
C |
4: 34,811,487 (GRCm39) |
D524G |
probably benign |
Het |
Zfp90 |
A |
T |
8: 107,150,900 (GRCm39) |
K204N |
possibly damaging |
Het |
Zmym2 |
T |
C |
14: 57,194,536 (GRCm39) |
S1265P |
probably damaging |
Het |
|
Other mutations in Sbno1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00563:Sbno1
|
APN |
5 |
124,540,268 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:Sbno1
|
APN |
5 |
124,548,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01309:Sbno1
|
APN |
5 |
124,519,769 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01330:Sbno1
|
APN |
5 |
124,530,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01541:Sbno1
|
APN |
5 |
124,516,618 (GRCm39) |
splice site |
probably benign |
|
IGL01800:Sbno1
|
APN |
5 |
124,519,568 (GRCm39) |
splice site |
probably benign |
|
IGL01987:Sbno1
|
APN |
5 |
124,542,282 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02178:Sbno1
|
APN |
5 |
124,538,258 (GRCm39) |
splice site |
probably null |
|
IGL02544:Sbno1
|
APN |
5 |
124,542,046 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02572:Sbno1
|
APN |
5 |
124,519,740 (GRCm39) |
splice site |
probably benign |
|
IGL02592:Sbno1
|
APN |
5 |
124,538,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03033:Sbno1
|
APN |
5 |
124,514,213 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03089:Sbno1
|
APN |
5 |
124,525,374 (GRCm39) |
splice site |
probably benign |
|
IGL03131:Sbno1
|
APN |
5 |
124,526,668 (GRCm39) |
missense |
probably damaging |
1.00 |
Decrement
|
UTSW |
5 |
124,538,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R0200:Sbno1
|
UTSW |
5 |
124,522,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R0217:Sbno1
|
UTSW |
5 |
124,542,387 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0233:Sbno1
|
UTSW |
5 |
124,514,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Sbno1
|
UTSW |
5 |
124,514,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Sbno1
|
UTSW |
5 |
124,524,931 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0401:Sbno1
|
UTSW |
5 |
124,548,348 (GRCm39) |
missense |
probably damaging |
0.96 |
R0608:Sbno1
|
UTSW |
5 |
124,522,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R0615:Sbno1
|
UTSW |
5 |
124,548,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R0653:Sbno1
|
UTSW |
5 |
124,524,955 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0655:Sbno1
|
UTSW |
5 |
124,514,212 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1037:Sbno1
|
UTSW |
5 |
124,531,975 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1439:Sbno1
|
UTSW |
5 |
124,522,523 (GRCm39) |
splice site |
probably benign |
|
R1522:Sbno1
|
UTSW |
5 |
124,530,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R1590:Sbno1
|
UTSW |
5 |
124,522,567 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1618:Sbno1
|
UTSW |
5 |
124,542,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Sbno1
|
UTSW |
5 |
124,530,130 (GRCm39) |
splice site |
probably null |
|
R1779:Sbno1
|
UTSW |
5 |
124,526,580 (GRCm39) |
unclassified |
probably benign |
|
R2103:Sbno1
|
UTSW |
5 |
124,532,000 (GRCm39) |
missense |
probably damaging |
0.98 |
R2136:Sbno1
|
UTSW |
5 |
124,525,597 (GRCm39) |
splice site |
probably null |
|
R2149:Sbno1
|
UTSW |
5 |
124,540,182 (GRCm39) |
splice site |
probably null |
|
R2153:Sbno1
|
UTSW |
5 |
124,516,606 (GRCm39) |
missense |
probably benign |
|
R2154:Sbno1
|
UTSW |
5 |
124,516,574 (GRCm39) |
missense |
probably benign |
|
R2231:Sbno1
|
UTSW |
5 |
124,543,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R2879:Sbno1
|
UTSW |
5 |
124,526,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R3004:Sbno1
|
UTSW |
5 |
124,519,771 (GRCm39) |
missense |
probably damaging |
0.96 |
R3922:Sbno1
|
UTSW |
5 |
124,519,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R4061:Sbno1
|
UTSW |
5 |
124,526,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4096:Sbno1
|
UTSW |
5 |
124,529,983 (GRCm39) |
critical splice donor site |
probably null |
|
R4612:Sbno1
|
UTSW |
5 |
124,542,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Sbno1
|
UTSW |
5 |
124,542,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Sbno1
|
UTSW |
5 |
124,512,672 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4990:Sbno1
|
UTSW |
5 |
124,538,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Sbno1
|
UTSW |
5 |
124,546,538 (GRCm39) |
critical splice donor site |
probably null |
|
R5365:Sbno1
|
UTSW |
5 |
124,519,929 (GRCm39) |
frame shift |
probably null |
|
R5399:Sbno1
|
UTSW |
5 |
124,530,804 (GRCm39) |
missense |
probably benign |
0.09 |
R5704:Sbno1
|
UTSW |
5 |
124,533,956 (GRCm39) |
critical splice donor site |
probably null |
|
R5898:Sbno1
|
UTSW |
5 |
124,524,854 (GRCm39) |
intron |
probably benign |
|
R6136:Sbno1
|
UTSW |
5 |
124,516,554 (GRCm39) |
missense |
probably benign |
0.41 |
R6154:Sbno1
|
UTSW |
5 |
124,516,542 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6412:Sbno1
|
UTSW |
5 |
124,530,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R6414:Sbno1
|
UTSW |
5 |
124,533,994 (GRCm39) |
missense |
probably benign |
0.28 |
R6454:Sbno1
|
UTSW |
5 |
124,538,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R7085:Sbno1
|
UTSW |
5 |
124,519,783 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7176:Sbno1
|
UTSW |
5 |
124,530,944 (GRCm39) |
missense |
probably benign |
0.21 |
R7219:Sbno1
|
UTSW |
5 |
124,543,722 (GRCm39) |
missense |
probably benign |
0.00 |
R7673:Sbno1
|
UTSW |
5 |
124,551,279 (GRCm39) |
missense |
probably benign |
|
R7692:Sbno1
|
UTSW |
5 |
124,543,709 (GRCm39) |
missense |
probably benign |
0.35 |
R7745:Sbno1
|
UTSW |
5 |
124,530,962 (GRCm39) |
missense |
probably benign |
0.00 |
R7762:Sbno1
|
UTSW |
5 |
124,512,729 (GRCm39) |
missense |
probably benign |
0.19 |
R8012:Sbno1
|
UTSW |
5 |
124,522,565 (GRCm39) |
missense |
probably benign |
0.43 |
R8142:Sbno1
|
UTSW |
5 |
124,546,608 (GRCm39) |
missense |
probably benign |
|
R8164:Sbno1
|
UTSW |
5 |
124,512,684 (GRCm39) |
missense |
probably benign |
0.13 |
R8259:Sbno1
|
UTSW |
5 |
124,519,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R8289:Sbno1
|
UTSW |
5 |
124,542,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8717:Sbno1
|
UTSW |
5 |
124,512,618 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9045:Sbno1
|
UTSW |
5 |
124,543,720 (GRCm39) |
missense |
probably benign |
0.14 |
R9149:Sbno1
|
UTSW |
5 |
124,519,762 (GRCm39) |
missense |
probably benign |
0.01 |
R9529:Sbno1
|
UTSW |
5 |
124,517,413 (GRCm39) |
nonsense |
probably null |
|
Z1088:Sbno1
|
UTSW |
5 |
124,542,367 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1088:Sbno1
|
UTSW |
5 |
124,532,021 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
Predicted Primers |
PCR Primer
(F):5'- AGGCTAGCTAGGGATAAAGATCTTAC -3'
(R):5'- ATGCTGATCAAGTTTAGTCTGTTAC -3'
Sequencing Primer
(F):5'- AACGATCTCTGCAGCTCT -3'
(R):5'- TCAAGGATTCTGCAGGCTAC -3'
|
Posted On |
2019-10-17 |