Incidental Mutation 'R9211:Nebl'
| ID |
698831 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Nebl
|
| Ensembl Gene |
ENSMUSG00000053702 |
| Gene Name |
nebulette |
| Synonyms |
Lnebl, D830029A09Rik, A630080F05Rik, 1200007O21Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R9211 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
17348720-17736275 bp(-) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
A to G
at 17393501 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000137567
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028080]
[ENSMUST00000124270]
[ENSMUST00000131957]
[ENSMUST00000132418]
[ENSMUST00000177966]
|
| AlphaFold |
Q0II04 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028080
|
| SMART Domains |
Protein: ENSMUSP00000028080
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
LIM
|
4 |
56 |
6.95e-14 |
SMART |
|
NEBU
|
62 |
92 |
3.35e-8 |
SMART |
|
NEBU
|
98 |
128 |
4.88e-10 |
SMART |
|
NEBU
|
134 |
164 |
3.82e-3 |
SMART |
|
SH3
|
213 |
270 |
2.12e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124270
|
| SMART Domains |
Protein: ENSMUSP00000117805
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
|
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
|
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
|
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
|
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
|
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
|
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
|
NEBU
|
245 |
275 |
1.57e0 |
SMART |
|
NEBU
|
280 |
310 |
9.67e-1 |
SMART |
|
NEBU
|
315 |
345 |
6.25e-8 |
SMART |
|
NEBU
|
351 |
381 |
5.97e-5 |
SMART |
|
NEBU
|
387 |
418 |
2.56e-4 |
SMART |
|
NEBU
|
425 |
455 |
8.91e-4 |
SMART |
|
NEBU
|
462 |
492 |
4.92e-6 |
SMART |
|
NEBU
|
499 |
529 |
2.33e-7 |
SMART |
|
NEBU
|
536 |
566 |
1.84e-5 |
SMART |
|
NEBU
|
571 |
601 |
2.23e-4 |
SMART |
|
NEBU
|
602 |
632 |
1.24e-2 |
SMART |
|
NEBU
|
664 |
694 |
6.6e-7 |
SMART |
|
NEBU
|
695 |
725 |
6.86e-5 |
SMART |
|
NEBU
|
726 |
756 |
2.03e-7 |
SMART |
|
NEBU
|
761 |
791 |
1.74e-6 |
SMART |
|
NEBU
|
797 |
827 |
3.82e-3 |
SMART |
|
SH3
|
957 |
1014 |
2.12e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000124611
|
| SMART Domains |
Protein: ENSMUSP00000116065
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
NEBU
|
3 |
33 |
4.88e-10 |
SMART |
|
NEBU
|
39 |
69 |
3.82e-3 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131957
|
| SMART Domains |
Protein: ENSMUSP00000118525
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
|
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
|
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
|
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
|
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
|
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
|
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
|
NEBU
|
245 |
275 |
7.35e0 |
SMART |
|
NEBU
|
280 |
310 |
6.25e-8 |
SMART |
|
NEBU
|
316 |
346 |
5.97e-5 |
SMART |
|
NEBU
|
352 |
383 |
2.56e-4 |
SMART |
|
NEBU
|
390 |
420 |
8.91e-4 |
SMART |
|
NEBU
|
427 |
457 |
4.92e-6 |
SMART |
|
NEBU
|
464 |
494 |
2.33e-7 |
SMART |
|
NEBU
|
501 |
525 |
1.02e2 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000132418
|
| SMART Domains |
Protein: ENSMUSP00000122024
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
11 |
25 |
N/A |
INTRINSIC |
|
NEBU
|
30 |
60 |
1.21e-5 |
SMART |
|
NEBU
|
65 |
95 |
5.4e-3 |
SMART |
|
NEBU
|
102 |
132 |
4.46e-4 |
SMART |
|
NEBU
|
139 |
169 |
1.31e-1 |
SMART |
|
NEBU
|
173 |
203 |
5.4e-3 |
SMART |
|
NEBU
|
207 |
237 |
2.74e-4 |
SMART |
|
NEBU
|
245 |
275 |
7.35e0 |
SMART |
|
NEBU
|
280 |
310 |
6.25e-8 |
SMART |
|
NEBU
|
316 |
346 |
5.97e-5 |
SMART |
|
NEBU
|
352 |
383 |
2.56e-4 |
SMART |
|
NEBU
|
390 |
420 |
4.78e-4 |
SMART |
|
NEBU
|
427 |
450 |
6.81e1 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000177966
|
| SMART Domains |
Protein: ENSMUSP00000137567
Gene: ENSMUSG00000053702
| Domain | Start | End | E-Value | Type |
|---|
|
NEBU
|
5 |
35 |
2.23e-4 |
SMART |
|
NEBU
|
36 |
66 |
3.28e-2 |
SMART |
|
NEBU
|
67 |
97 |
6.6e-7 |
SMART |
|
NEBU
|
98 |
120 |
2e1 |
SMART |
|
| Meta Mutation Damage Score |
0.9491 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
99% (86/87) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3110009E18Rik |
G |
T |
1: 120,099,161 (GRCm39) |
D85Y |
possibly damaging |
Het |
| Accs |
T |
C |
2: 93,668,614 (GRCm39) |
R315G |
probably damaging |
Het |
| Adam3 |
A |
C |
8: 25,177,910 (GRCm39) |
W668G |
probably benign |
Het |
| Adgrb2 |
T |
A |
4: 129,886,199 (GRCm39) |
V113E |
probably benign |
Het |
| Anapc4 |
C |
T |
5: 53,007,994 (GRCm39) |
T391I |
possibly damaging |
Het |
| Angpt2 |
C |
T |
8: 18,748,078 (GRCm39) |
G394D |
probably benign |
Het |
| Ankrd31 |
C |
G |
13: 97,029,551 (GRCm39) |
L1662V |
possibly damaging |
Het |
| Ankrd36 |
A |
G |
11: 5,612,370 (GRCm39) |
D1234G |
possibly damaging |
Het |
| Ankrd6 |
C |
T |
4: 32,806,580 (GRCm39) |
V558M |
probably damaging |
Het |
| Ankrd61 |
T |
A |
5: 143,828,358 (GRCm39) |
M206L |
probably benign |
Het |
| Arhgap33 |
C |
T |
7: 30,223,023 (GRCm39) |
G970R |
possibly damaging |
Het |
| Atf7 |
A |
G |
15: 102,437,117 (GRCm39) |
V115A |
unknown |
Het |
| Atp2c2 |
A |
T |
8: 120,446,032 (GRCm39) |
R65S |
probably benign |
Het |
| Atp8b5 |
T |
A |
4: 43,367,960 (GRCm39) |
M861K |
probably damaging |
Het |
| Bmi1 |
T |
C |
2: 18,689,152 (GRCm39) |
S279P |
probably benign |
Het |
| Bptf |
T |
G |
11: 106,946,124 (GRCm39) |
S2372R |
probably damaging |
Het |
| Cacnb2 |
A |
T |
2: 14,879,308 (GRCm39) |
I15L |
unknown |
Het |
| Card11 |
A |
G |
5: 140,869,375 (GRCm39) |
M807T |
probably benign |
Het |
| Ccdc175 |
A |
T |
12: 72,153,458 (GRCm39) |
D704E |
probably damaging |
Het |
| Cd300ld |
T |
A |
11: 114,878,386 (GRCm39) |
Y42F |
probably damaging |
Het |
| Cdh1 |
A |
T |
8: 107,390,962 (GRCm39) |
T693S |
probably benign |
Het |
| Clca4b |
T |
C |
3: 144,638,214 (GRCm39) |
Y16C |
possibly damaging |
Het |
| Col4a4 |
A |
G |
1: 82,506,501 (GRCm39) |
I273T |
unknown |
Het |
| Coro2b |
C |
A |
9: 62,427,662 (GRCm39) |
V9L |
probably benign |
Het |
| Crnkl1 |
T |
C |
2: 145,774,773 (GRCm39) |
D55G |
probably damaging |
Het |
| Dcps |
T |
A |
9: 35,035,872 (GRCm39) |
N338I |
probably damaging |
Het |
| Dusp2 |
A |
T |
2: 127,179,311 (GRCm39) |
H222L |
probably benign |
Het |
| Dync1li1 |
C |
A |
9: 114,518,012 (GRCm39) |
Y21* |
probably null |
Het |
| Efhb |
T |
G |
17: 53,756,507 (GRCm39) |
Q381H |
probably damaging |
Het |
| Elac2 |
A |
T |
11: 64,869,864 (GRCm39) |
|
probably benign |
Het |
| Etaa1 |
A |
G |
11: 17,896,053 (GRCm39) |
V688A |
possibly damaging |
Het |
| Fam120c |
C |
T |
X: 150,127,495 (GRCm39) |
H84Y |
probably benign |
Het |
| Fbxl7 |
T |
A |
15: 26,789,616 (GRCm39) |
N37I |
probably damaging |
Het |
| Fndc3b |
A |
T |
3: 27,523,086 (GRCm39) |
W498R |
probably damaging |
Het |
| Galc |
G |
A |
12: 98,173,699 (GRCm39) |
A621V |
probably benign |
Het |
| Gch1 |
A |
T |
14: 47,426,519 (GRCm39) |
I69N |
probably damaging |
Het |
| Gdpd4 |
T |
C |
7: 97,615,466 (GRCm39) |
V97A |
possibly damaging |
Het |
| Hirip3 |
C |
T |
7: 126,463,567 (GRCm39) |
R485* |
probably null |
Het |
| Hmgcs2 |
C |
T |
3: 98,204,748 (GRCm39) |
T302I |
possibly damaging |
Het |
| Ing5 |
A |
T |
1: 93,740,409 (GRCm39) |
K137I |
possibly damaging |
Het |
| Kcnh8 |
T |
A |
17: 53,146,236 (GRCm39) |
Y375N |
probably damaging |
Het |
| Kdm3a |
C |
A |
6: 71,573,674 (GRCm39) |
W963L |
probably benign |
Het |
| Klra17 |
T |
G |
6: 129,842,651 (GRCm39) |
I216L |
possibly damaging |
Het |
| Kmt2e |
A |
G |
5: 23,669,770 (GRCm39) |
K86E |
possibly damaging |
Het |
| Krt42 |
T |
C |
11: 100,155,867 (GRCm39) |
N293S |
possibly damaging |
Het |
| Lrrc8d |
T |
A |
5: 105,960,216 (GRCm39) |
W209R |
probably damaging |
Het |
| Mettl23 |
C |
T |
11: 116,734,469 (GRCm39) |
P13S |
unknown |
Het |
| Ncln |
T |
C |
10: 81,323,527 (GRCm39) |
Y540C |
probably damaging |
Het |
| Neb |
C |
G |
2: 52,135,360 (GRCm39) |
G3250A |
probably damaging |
Het |
| Nqo2 |
A |
T |
13: 34,156,399 (GRCm39) |
T38S |
probably benign |
Het |
| Obscn |
A |
T |
11: 59,026,693 (GRCm39) |
I170N |
probably benign |
Het |
| Or2bd2 |
G |
T |
7: 6,443,417 (GRCm39) |
G173W |
probably damaging |
Het |
| Or4c100 |
A |
G |
2: 88,356,170 (GRCm39) |
D81G |
probably benign |
Het |
| Or5af2 |
A |
T |
11: 58,708,709 (GRCm39) |
N292Y |
probably damaging |
Het |
| Or5p6 |
C |
T |
7: 107,630,798 (GRCm39) |
V251I |
probably damaging |
Het |
| Or7g28 |
T |
A |
9: 19,271,824 (GRCm39) |
I276F |
possibly damaging |
Het |
| Or8k38 |
A |
T |
2: 86,488,024 (GRCm39) |
Y259* |
probably null |
Het |
| Pacs1 |
A |
T |
19: 5,189,057 (GRCm39) |
V775E |
probably damaging |
Het |
| Pheta2 |
A |
T |
15: 82,225,227 (GRCm39) |
|
probably benign |
Het |
| Pmfbp1 |
T |
C |
8: 110,262,445 (GRCm39) |
I713T |
probably benign |
Het |
| Pnma8b |
A |
G |
7: 16,679,589 (GRCm39) |
D191G |
unknown |
Het |
| Polr1a |
T |
C |
6: 71,943,521 (GRCm39) |
I1252T |
probably damaging |
Het |
| Prss16 |
A |
T |
13: 22,192,754 (GRCm39) |
M110K |
probably benign |
Het |
| Pygo2 |
T |
C |
3: 89,338,038 (GRCm39) |
|
probably null |
Het |
| Rab5b |
C |
A |
10: 128,519,063 (GRCm39) |
|
probably null |
Het |
| Reln |
G |
T |
5: 22,549,200 (GRCm39) |
Y69* |
probably null |
Het |
| Rgs12 |
T |
A |
5: 35,123,165 (GRCm39) |
M316K |
probably damaging |
Het |
| Rmi2 |
T |
C |
16: 10,657,743 (GRCm39) |
C118R |
possibly damaging |
Het |
| Rnf223 |
T |
A |
4: 156,216,834 (GRCm39) |
C70S |
probably damaging |
Het |
| Rxrb |
T |
A |
17: 34,255,626 (GRCm39) |
F371Y |
probably damaging |
Het |
| Smurf2 |
T |
A |
11: 106,759,463 (GRCm39) |
S78C |
probably damaging |
Het |
| Sorbs1 |
A |
T |
19: 40,332,798 (GRCm39) |
|
probably null |
Het |
| Spag17 |
C |
T |
3: 100,032,614 (GRCm39) |
|
probably benign |
Het |
| Spidr |
T |
C |
16: 15,871,319 (GRCm39) |
H217R |
probably benign |
Het |
| Tiam2 |
T |
G |
17: 3,498,729 (GRCm39) |
V835G |
possibly damaging |
Het |
| Tm2d2 |
C |
T |
8: 25,510,548 (GRCm39) |
R136* |
probably null |
Het |
| Tnks |
C |
T |
8: 35,316,489 (GRCm39) |
D877N |
probably damaging |
Het |
| Tns1 |
A |
G |
1: 73,956,948 (GRCm39) |
L491P |
possibly damaging |
Het |
| Trps1 |
A |
G |
15: 50,694,840 (GRCm39) |
I485T |
probably damaging |
Het |
| Tubgcp5 |
A |
G |
7: 55,456,331 (GRCm39) |
S308G |
probably benign |
Het |
| Ugt8a |
T |
C |
3: 125,661,130 (GRCm39) |
H454R |
probably damaging |
Het |
| Usp32 |
G |
T |
11: 84,913,559 (GRCm39) |
T924K |
probably damaging |
Het |
| Vmn2r91 |
A |
T |
17: 18,356,819 (GRCm39) |
K829* |
probably null |
Het |
| Zfc3h1 |
T |
C |
10: 115,248,328 (GRCm39) |
F1146L |
possibly damaging |
Het |
| Zfp729a |
G |
T |
13: 67,767,820 (GRCm39) |
A803E |
probably benign |
Het |
| Zfp990 |
A |
G |
4: 145,264,171 (GRCm39) |
T390A |
probably damaging |
Het |
|
| Other mutations in Nebl |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02146:Nebl
|
APN |
2 |
17,353,679 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02732:Nebl
|
APN |
2 |
17,457,295 (GRCm39) |
splice site |
probably benign |
|
|
IGL03241:Nebl
|
APN |
2 |
17,397,975 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL03334:Nebl
|
APN |
2 |
17,418,522 (GRCm39) |
missense |
probably damaging |
0.98 |
|
BB008:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
|
BB018:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0068:Nebl
|
UTSW |
2 |
17,439,782 (GRCm39) |
nonsense |
probably null |
|
|
R0127:Nebl
|
UTSW |
2 |
17,397,794 (GRCm39) |
missense |
probably benign |
0.31 |
|
R0128:Nebl
|
UTSW |
2 |
17,397,834 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R0130:Nebl
|
UTSW |
2 |
17,397,834 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R0130:Nebl
|
UTSW |
2 |
17,395,737 (GRCm39) |
start gained |
probably benign |
|
|
R0537:Nebl
|
UTSW |
2 |
17,409,026 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R0743:Nebl
|
UTSW |
2 |
17,415,929 (GRCm39) |
missense |
probably benign |
|
|
R0884:Nebl
|
UTSW |
2 |
17,415,929 (GRCm39) |
missense |
probably benign |
|
|
R1364:Nebl
|
UTSW |
2 |
17,397,848 (GRCm39) |
unclassified |
probably benign |
|
|
R1638:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1711:Nebl
|
UTSW |
2 |
17,393,565 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1933:Nebl
|
UTSW |
2 |
17,380,103 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R1990:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1991:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1992:Nebl
|
UTSW |
2 |
17,457,321 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2062:Nebl
|
UTSW |
2 |
17,401,932 (GRCm39) |
missense |
probably benign |
0.39 |
|
R2183:Nebl
|
UTSW |
2 |
17,409,027 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2325:Nebl
|
UTSW |
2 |
17,397,827 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R2679:Nebl
|
UTSW |
2 |
17,429,402 (GRCm39) |
missense |
probably benign |
0.03 |
|
R2877:Nebl
|
UTSW |
2 |
17,439,740 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2878:Nebl
|
UTSW |
2 |
17,439,740 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3079:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3080:Nebl
|
UTSW |
2 |
17,381,462 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3878:Nebl
|
UTSW |
2 |
17,398,063 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R3947:Nebl
|
UTSW |
2 |
17,382,917 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4983:Nebl
|
UTSW |
2 |
17,380,082 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5006:Nebl
|
UTSW |
2 |
17,393,582 (GRCm39) |
splice site |
probably null |
|
|
R5256:Nebl
|
UTSW |
2 |
17,438,786 (GRCm39) |
missense |
probably benign |
0.37 |
|
R5491:Nebl
|
UTSW |
2 |
17,439,783 (GRCm39) |
nonsense |
probably null |
|
|
R5533:Nebl
|
UTSW |
2 |
17,398,079 (GRCm39) |
nonsense |
probably null |
|
|
R5597:Nebl
|
UTSW |
2 |
17,382,978 (GRCm39) |
missense |
probably benign |
|
|
R5658:Nebl
|
UTSW |
2 |
17,353,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5933:Nebl
|
UTSW |
2 |
17,408,998 (GRCm39) |
missense |
probably benign |
|
|
R6056:Nebl
|
UTSW |
2 |
17,455,045 (GRCm39) |
missense |
probably benign |
0.13 |
|
R6161:Nebl
|
UTSW |
2 |
17,735,641 (GRCm39) |
missense |
probably benign |
0.26 |
|
R6646:Nebl
|
UTSW |
2 |
17,381,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6784:Nebl
|
UTSW |
2 |
17,439,725 (GRCm39) |
nonsense |
probably null |
|
|
R6935:Nebl
|
UTSW |
2 |
17,353,637 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7196:Nebl
|
UTSW |
2 |
17,457,329 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7671:Nebl
|
UTSW |
2 |
17,395,727 (GRCm39) |
nonsense |
probably null |
|
|
R7728:Nebl
|
UTSW |
2 |
17,375,325 (GRCm39) |
missense |
|
|
|
R7931:Nebl
|
UTSW |
2 |
17,381,433 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8007:Nebl
|
UTSW |
2 |
17,375,300 (GRCm39) |
missense |
|
|
|
R8048:Nebl
|
UTSW |
2 |
17,429,333 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8118:Nebl
|
UTSW |
2 |
17,384,631 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8317:Nebl
|
UTSW |
2 |
17,355,568 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8349:Nebl
|
UTSW |
2 |
17,418,593 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8360:Nebl
|
UTSW |
2 |
17,465,298 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8392:Nebl
|
UTSW |
2 |
17,457,363 (GRCm39) |
missense |
probably benign |
0.36 |
|
R8449:Nebl
|
UTSW |
2 |
17,418,593 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8537:Nebl
|
UTSW |
2 |
17,355,520 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8778:Nebl
|
UTSW |
2 |
17,409,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8893:Nebl
|
UTSW |
2 |
17,735,671 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R8894:Nebl
|
UTSW |
2 |
17,380,036 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8906:Nebl
|
UTSW |
2 |
17,382,928 (GRCm39) |
missense |
probably benign |
0.18 |
|
R8929:Nebl
|
UTSW |
2 |
17,397,991 (GRCm39) |
nonsense |
probably null |
|
|
R9054:Nebl
|
UTSW |
2 |
17,415,907 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9119:Nebl
|
UTSW |
2 |
17,405,370 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9225:Nebl
|
UTSW |
2 |
17,405,322 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R9296:Nebl
|
UTSW |
2 |
17,429,451 (GRCm39) |
splice site |
probably benign |
|
|
R9310:Nebl
|
UTSW |
2 |
17,353,678 (GRCm39) |
missense |
probably benign |
0.16 |
|
R9474:Nebl
|
UTSW |
2 |
17,374,421 (GRCm39) |
nonsense |
probably null |
|
|
X0012:Nebl
|
UTSW |
2 |
17,448,605 (GRCm39) |
missense |
probably benign |
0.16 |
|
X0025:Nebl
|
UTSW |
2 |
17,409,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GGAGACCTTTGATAGCTGATGAC -3'
(R):5'- GCGTTTGTAACAGGAAGATCTAGG -3'
Sequencing Primer
(F):5'- TCCACTAGCAGCCTTTGGATGAAG -3'
(R):5'- TTGTAACAGGAAGATCTAGGACTTG -3'
|
| Posted On |
2022-02-07 |
Incidental Mutation