Incidental Mutation 'R7361:Nynrin'
ID |
571371 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nynrin
|
Ensembl Gene |
ENSMUSG00000075592 |
Gene Name |
NYN domain and retroviral integrase containing |
Synonyms |
|
MMRRC Submission |
045447-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7361 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
14 |
Chromosomal Location |
56091572-56112193 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 56107857 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Leucine
at position 988
(H988L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000098098
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100529]
[ENSMUST00000168479]
|
AlphaFold |
Q5DTZ0 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000100529
AA Change: H988L
PolyPhen 2
Score 0.712 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000098098 Gene: ENSMUSG00000075592 AA Change: H988L
Domain | Start | End | E-Value | Type |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
Pfam:RNase_Zc3h12a
|
739 |
890 |
1.6e-54 |
PFAM |
low complexity region
|
938 |
952 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1228 |
N/A |
INTRINSIC |
low complexity region
|
1390 |
1397 |
N/A |
INTRINSIC |
PDB:3S3O|B
|
1478 |
1706 |
6e-8 |
PDB |
SCOP:d1cxqa_
|
1552 |
1646 |
2e-12 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000168479
AA Change: H988L
PolyPhen 2
Score 0.712 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000129557 Gene: ENSMUSG00000075592 AA Change: H988L
Domain | Start | End | E-Value | Type |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
Pfam:RNase_Zc3h12a
|
739 |
890 |
5.5e-54 |
PFAM |
low complexity region
|
938 |
952 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1228 |
N/A |
INTRINSIC |
low complexity region
|
1390 |
1397 |
N/A |
INTRINSIC |
PDB:3S3O|B
|
1478 |
1706 |
6e-8 |
PDB |
SCOP:d1cxqa_
|
1552 |
1646 |
2e-12 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630073D07Rik |
C |
T |
6: 132,604,434 (GRCm39) |
V4I |
unknown |
Het |
Actn1 |
A |
T |
12: 80,240,489 (GRCm39) |
D199E |
probably benign |
Het |
Adam17 |
T |
C |
12: 21,375,602 (GRCm39) |
D739G |
probably damaging |
Het |
Agmat |
T |
C |
4: 141,474,163 (GRCm39) |
S15P |
probably benign |
Het |
Ahsa2 |
A |
G |
11: 23,441,099 (GRCm39) |
S229P |
probably damaging |
Het |
Arhgef3 |
A |
G |
14: 26,987,535 (GRCm39) |
D36G |
possibly damaging |
Het |
C6 |
C |
A |
15: 4,826,404 (GRCm39) |
Y662* |
probably null |
Het |
Ccs |
T |
C |
19: 4,883,378 (GRCm39) |
D140G |
probably benign |
Het |
Cdc42bpb |
A |
G |
12: 111,312,039 (GRCm39) |
L65P |
probably damaging |
Het |
Cdh24 |
A |
T |
14: 54,876,378 (GRCm39) |
V149E |
possibly damaging |
Het |
Cdk12 |
C |
A |
11: 98,101,294 (GRCm39) |
S384* |
probably null |
Het |
Cep350 |
G |
A |
1: 155,777,237 (GRCm39) |
A1701V |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,060,307 (GRCm39) |
Q104R |
not run |
Het |
Chd5 |
A |
G |
4: 152,447,745 (GRCm39) |
H537R |
probably damaging |
Het |
Cln5 |
T |
A |
14: 103,313,339 (GRCm39) |
V197D |
probably damaging |
Het |
Coq7 |
A |
G |
7: 118,128,798 (GRCm39) |
V79A |
probably benign |
Het |
Cp |
A |
T |
3: 20,018,470 (GRCm39) |
N58I |
probably benign |
Het |
Cplx2 |
A |
T |
13: 54,526,639 (GRCm39) |
M16L |
probably benign |
Het |
Crot |
A |
G |
5: 9,027,534 (GRCm39) |
L266S |
probably damaging |
Het |
Ctbs |
T |
A |
3: 146,164,509 (GRCm39) |
Y221N |
probably damaging |
Het |
Cul7 |
T |
A |
17: 46,967,933 (GRCm39) |
L707Q |
probably damaging |
Het |
D430041D05Rik |
G |
A |
2: 104,085,363 (GRCm39) |
T378I |
possibly damaging |
Het |
Dixdc1 |
T |
C |
9: 50,599,953 (GRCm39) |
I364V |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,982,477 (GRCm39) |
H2564L |
probably damaging |
Het |
Dnajc3 |
T |
C |
14: 119,175,576 (GRCm39) |
Y26H |
probably benign |
Het |
Dpysl2 |
G |
A |
14: 67,071,664 (GRCm39) |
H159Y |
possibly damaging |
Het |
Ehmt1 |
T |
A |
2: 24,746,713 (GRCm39) |
K423I |
possibly damaging |
Het |
Eif1ad4 |
A |
G |
12: 87,862,170 (GRCm39) |
N11D |
unknown |
Het |
Enpp7 |
A |
G |
11: 118,882,985 (GRCm39) |
N353S |
probably benign |
Het |
Ext1 |
G |
A |
15: 53,208,119 (GRCm39) |
A214V |
probably damaging |
Het |
Fbh1 |
A |
T |
2: 11,751,887 (GRCm39) |
I937N |
probably damaging |
Het |
Fbxo39 |
T |
C |
11: 72,207,800 (GRCm39) |
Y51H |
possibly damaging |
Het |
Firrm |
A |
T |
1: 163,813,602 (GRCm39) |
D207E |
possibly damaging |
Het |
Fry |
A |
G |
5: 150,360,312 (GRCm39) |
H1986R |
possibly damaging |
Het |
Grem2 |
T |
C |
1: 174,664,514 (GRCm39) |
K112E |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,005,027 (GRCm39) |
V586A |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,280,450 (GRCm39) |
L586I |
possibly damaging |
Het |
Il18 |
T |
C |
9: 50,490,614 (GRCm39) |
I83T |
probably damaging |
Het |
Irs1 |
A |
T |
1: 82,266,835 (GRCm39) |
Y460* |
probably null |
Het |
Jak1 |
G |
T |
4: 101,041,536 (GRCm39) |
Q161K |
possibly damaging |
Het |
Jakmip1 |
T |
A |
5: 37,276,148 (GRCm39) |
L486Q |
probably damaging |
Het |
Jmjd1c |
C |
A |
10: 67,054,143 (GRCm39) |
Q16K |
probably benign |
Het |
Kidins220 |
T |
C |
12: 25,106,999 (GRCm39) |
L1393P |
probably benign |
Het |
Klhl24 |
A |
C |
16: 19,936,750 (GRCm39) |
I453L |
probably benign |
Het |
Krtap2-4 |
C |
T |
11: 99,505,420 (GRCm39) |
D64N |
probably damaging |
Het |
Man1a |
T |
A |
10: 53,784,105 (GRCm39) |
D592V |
probably damaging |
Het |
Mepe |
T |
A |
5: 104,485,009 (GRCm39) |
Y50N |
probably benign |
Het |
Mier3 |
G |
A |
13: 111,841,783 (GRCm39) |
G115S |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,754,670 (GRCm38) |
S1515T |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,529,251 (GRCm39) |
D1408G |
probably benign |
Het |
Nav1 |
T |
C |
1: 135,380,591 (GRCm39) |
M1443V |
unknown |
Het |
Nckap1l |
A |
C |
15: 103,379,709 (GRCm39) |
N332T |
possibly damaging |
Het |
Neurl4 |
T |
A |
11: 69,802,905 (GRCm39) |
L1467Q |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,038,718 (GRCm39) |
N1287S |
probably benign |
Het |
Nr4a3 |
C |
T |
4: 48,083,203 (GRCm39) |
P579S |
probably benign |
Het |
Nrxn2 |
A |
T |
19: 6,567,112 (GRCm39) |
H1329L |
probably benign |
Het |
Or1e34 |
T |
A |
11: 73,778,827 (GRCm39) |
I124F |
probably damaging |
Het |
Or4c31 |
A |
G |
2: 88,291,836 (GRCm39) |
T70A |
probably benign |
Het |
Or4c3d |
A |
G |
2: 89,882,089 (GRCm39) |
I193T |
probably benign |
Het |
Or52e3 |
G |
T |
7: 102,869,830 (GRCm39) |
D302Y |
possibly damaging |
Het |
Or7g35 |
T |
A |
9: 19,495,856 (GRCm39) |
F8I |
probably benign |
Het |
Pclo |
G |
A |
5: 14,843,882 (GRCm39) |
S1534N |
probably damaging |
Het |
Pign |
A |
G |
1: 105,512,778 (GRCm39) |
V635A |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,664,177 (GRCm39) |
T134A |
probably damaging |
Het |
Plcb4 |
A |
T |
2: 135,818,068 (GRCm39) |
N790I |
possibly damaging |
Het |
Plxna2 |
G |
T |
1: 194,482,087 (GRCm39) |
C1453F |
probably damaging |
Het |
Plxna4 |
A |
G |
6: 32,173,057 (GRCm39) |
|
probably null |
Het |
Pnpla2 |
A |
G |
7: 141,037,344 (GRCm39) |
I116V |
possibly damaging |
Het |
Polq |
A |
G |
16: 36,880,790 (GRCm39) |
T985A |
probably benign |
Het |
Pramel11 |
T |
C |
4: 143,622,456 (GRCm39) |
T300A |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,555,490 (GRCm39) |
N50S |
probably benign |
Het |
Ptgfrn |
G |
A |
3: 100,984,760 (GRCm39) |
A144V |
probably benign |
Het |
Rad54b |
G |
A |
4: 11,599,782 (GRCm39) |
G329S |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,809,364 (GRCm39) |
L931S |
probably benign |
Het |
Saxo4 |
T |
G |
19: 10,456,943 (GRCm39) |
D134A |
probably damaging |
Het |
Sipa1l2 |
A |
G |
8: 126,180,071 (GRCm39) |
S1109P |
probably damaging |
Het |
Slc26a7 |
G |
T |
4: 14,546,305 (GRCm39) |
N341K |
probably damaging |
Het |
Smg1 |
A |
C |
7: 117,784,200 (GRCm39) |
D958E |
unknown |
Het |
Smg6 |
T |
A |
11: 74,820,979 (GRCm39) |
S417T |
probably benign |
Het |
Srgap3 |
A |
G |
6: 112,723,882 (GRCm39) |
V550A |
probably damaging |
Het |
Terb1 |
T |
A |
8: 105,195,431 (GRCm39) |
D570V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,076 (GRCm39) |
V1787A |
probably benign |
Het |
Tor1a |
A |
T |
2: 30,853,753 (GRCm39) |
D192E |
probably benign |
Het |
Tpr |
T |
C |
1: 150,323,372 (GRCm39) |
S2379P |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,728,163 (GRCm39) |
F1138L |
probably damaging |
Het |
Trpv1 |
T |
C |
11: 73,151,203 (GRCm39) |
L797P |
probably damaging |
Het |
Tut1 |
T |
C |
19: 8,942,698 (GRCm39) |
L595P |
probably damaging |
Het |
Ubl7 |
T |
C |
9: 57,821,905 (GRCm39) |
S85P |
probably damaging |
Het |
Urb1 |
C |
A |
16: 90,571,656 (GRCm39) |
S1051I |
probably damaging |
Het |
Usp17le |
A |
G |
7: 104,418,084 (GRCm39) |
W353R |
probably damaging |
Het |
Usp44 |
T |
C |
10: 93,682,330 (GRCm39) |
L260S |
probably benign |
Het |
Wsb1 |
T |
A |
11: 79,131,623 (GRCm39) |
|
probably null |
Het |
Xrcc2 |
A |
T |
5: 25,897,755 (GRCm39) |
C65S |
probably damaging |
Het |
Zfp316 |
T |
A |
5: 143,240,430 (GRCm39) |
M530L |
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,382,563 (GRCm39) |
H590R |
probably damaging |
Het |
Zfp983 |
T |
A |
17: 21,880,850 (GRCm39) |
H259Q |
probably damaging |
Het |
|
Other mutations in Nynrin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Nynrin
|
APN |
14 |
56,105,905 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01131:Nynrin
|
APN |
14 |
56,110,142 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01357:Nynrin
|
APN |
14 |
56,107,874 (GRCm39) |
missense |
probably benign |
|
IGL01537:Nynrin
|
APN |
14 |
56,109,502 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01583:Nynrin
|
APN |
14 |
56,107,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Nynrin
|
APN |
14 |
56,101,611 (GRCm39) |
missense |
probably benign |
|
IGL02161:Nynrin
|
APN |
14 |
56,101,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02167:Nynrin
|
APN |
14 |
56,100,792 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02247:Nynrin
|
APN |
14 |
56,109,167 (GRCm39) |
nonsense |
probably null |
|
IGL02302:Nynrin
|
APN |
14 |
56,105,962 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02524:Nynrin
|
APN |
14 |
56,108,931 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02600:Nynrin
|
APN |
14 |
56,101,449 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02639:Nynrin
|
APN |
14 |
56,108,112 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02654:Nynrin
|
APN |
14 |
56,100,716 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02659:Nynrin
|
APN |
14 |
56,103,554 (GRCm39) |
unclassified |
probably benign |
|
IGL02736:Nynrin
|
APN |
14 |
56,108,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02949:Nynrin
|
APN |
14 |
56,109,837 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4458001:Nynrin
|
UTSW |
14 |
56,101,425 (GRCm39) |
missense |
probably benign |
0.39 |
R0017:Nynrin
|
UTSW |
14 |
56,109,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R0078:Nynrin
|
UTSW |
14 |
56,100,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Nynrin
|
UTSW |
14 |
56,109,255 (GRCm39) |
missense |
probably benign |
0.08 |
R0211:Nynrin
|
UTSW |
14 |
56,109,255 (GRCm39) |
missense |
probably benign |
0.08 |
R0413:Nynrin
|
UTSW |
14 |
56,109,648 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0609:Nynrin
|
UTSW |
14 |
56,110,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Nynrin
|
UTSW |
14 |
56,105,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Nynrin
|
UTSW |
14 |
56,091,646 (GRCm39) |
intron |
probably benign |
|
R1222:Nynrin
|
UTSW |
14 |
56,100,998 (GRCm39) |
missense |
probably benign |
0.02 |
R1385:Nynrin
|
UTSW |
14 |
56,102,356 (GRCm39) |
missense |
probably benign |
0.00 |
R1820:Nynrin
|
UTSW |
14 |
56,107,835 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1829:Nynrin
|
UTSW |
14 |
56,110,404 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1874:Nynrin
|
UTSW |
14 |
56,100,950 (GRCm39) |
missense |
probably benign |
0.04 |
R1927:Nynrin
|
UTSW |
14 |
56,101,049 (GRCm39) |
missense |
probably benign |
0.00 |
R2233:Nynrin
|
UTSW |
14 |
56,109,524 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3018:Nynrin
|
UTSW |
14 |
56,100,867 (GRCm39) |
missense |
probably benign |
0.00 |
R3154:Nynrin
|
UTSW |
14 |
56,101,044 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3853:Nynrin
|
UTSW |
14 |
56,101,562 (GRCm39) |
missense |
probably benign |
0.24 |
R4648:Nynrin
|
UTSW |
14 |
56,110,351 (GRCm39) |
nonsense |
probably null |
|
R4722:Nynrin
|
UTSW |
14 |
56,091,852 (GRCm39) |
missense |
probably damaging |
0.97 |
R4735:Nynrin
|
UTSW |
14 |
56,107,625 (GRCm39) |
missense |
probably benign |
0.03 |
R4736:Nynrin
|
UTSW |
14 |
56,101,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Nynrin
|
UTSW |
14 |
56,100,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Nynrin
|
UTSW |
14 |
56,102,326 (GRCm39) |
missense |
probably benign |
|
R4816:Nynrin
|
UTSW |
14 |
56,109,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Nynrin
|
UTSW |
14 |
56,101,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5372:Nynrin
|
UTSW |
14 |
56,105,948 (GRCm39) |
missense |
probably benign |
0.01 |
R5432:Nynrin
|
UTSW |
14 |
56,101,923 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5800:Nynrin
|
UTSW |
14 |
56,108,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Nynrin
|
UTSW |
14 |
56,101,683 (GRCm39) |
missense |
probably benign |
0.00 |
R6149:Nynrin
|
UTSW |
14 |
56,091,780 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6244:Nynrin
|
UTSW |
14 |
56,105,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R6350:Nynrin
|
UTSW |
14 |
56,105,533 (GRCm39) |
missense |
probably benign |
0.19 |
R6379:Nynrin
|
UTSW |
14 |
56,107,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Nynrin
|
UTSW |
14 |
56,109,227 (GRCm39) |
missense |
probably benign |
0.00 |
R6501:Nynrin
|
UTSW |
14 |
56,100,989 (GRCm39) |
missense |
probably benign |
|
R6702:Nynrin
|
UTSW |
14 |
56,101,935 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6703:Nynrin
|
UTSW |
14 |
56,101,935 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6907:Nynrin
|
UTSW |
14 |
56,101,335 (GRCm39) |
missense |
probably benign |
0.20 |
R6908:Nynrin
|
UTSW |
14 |
56,101,335 (GRCm39) |
missense |
probably benign |
0.20 |
R6928:Nynrin
|
UTSW |
14 |
56,101,335 (GRCm39) |
missense |
probably benign |
0.20 |
R6934:Nynrin
|
UTSW |
14 |
56,101,335 (GRCm39) |
missense |
probably benign |
0.20 |
R6935:Nynrin
|
UTSW |
14 |
56,101,335 (GRCm39) |
missense |
probably benign |
0.20 |
R7197:Nynrin
|
UTSW |
14 |
56,109,380 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:Nynrin
|
UTSW |
14 |
56,110,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Nynrin
|
UTSW |
14 |
56,107,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R7335:Nynrin
|
UTSW |
14 |
56,101,371 (GRCm39) |
missense |
probably benign |
|
R7368:Nynrin
|
UTSW |
14 |
56,107,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R7443:Nynrin
|
UTSW |
14 |
56,108,873 (GRCm39) |
missense |
probably benign |
0.18 |
R7584:Nynrin
|
UTSW |
14 |
56,109,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R7677:Nynrin
|
UTSW |
14 |
56,107,693 (GRCm39) |
missense |
probably benign |
|
R7723:Nynrin
|
UTSW |
14 |
56,109,502 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7776:Nynrin
|
UTSW |
14 |
56,103,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Nynrin
|
UTSW |
14 |
56,107,980 (GRCm39) |
missense |
probably benign |
|
R7842:Nynrin
|
UTSW |
14 |
56,102,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Nynrin
|
UTSW |
14 |
56,108,886 (GRCm39) |
missense |
probably damaging |
0.96 |
R8040:Nynrin
|
UTSW |
14 |
56,108,982 (GRCm39) |
missense |
probably benign |
0.01 |
R8159:Nynrin
|
UTSW |
14 |
56,102,517 (GRCm39) |
missense |
probably benign |
|
R8159:Nynrin
|
UTSW |
14 |
56,100,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R8258:Nynrin
|
UTSW |
14 |
56,100,815 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8259:Nynrin
|
UTSW |
14 |
56,100,815 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8343:Nynrin
|
UTSW |
14 |
56,101,248 (GRCm39) |
missense |
probably benign |
|
R8504:Nynrin
|
UTSW |
14 |
56,107,703 (GRCm39) |
missense |
probably benign |
0.01 |
R8671:Nynrin
|
UTSW |
14 |
56,107,899 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8691:Nynrin
|
UTSW |
14 |
56,110,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Nynrin
|
UTSW |
14 |
56,109,120 (GRCm39) |
missense |
probably benign |
|
R8777-TAIL:Nynrin
|
UTSW |
14 |
56,109,120 (GRCm39) |
missense |
probably benign |
|
R9041:Nynrin
|
UTSW |
14 |
56,108,753 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9346:Nynrin
|
UTSW |
14 |
56,100,495 (GRCm39) |
missense |
probably benign |
0.01 |
R9366:Nynrin
|
UTSW |
14 |
56,100,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R9690:Nynrin
|
UTSW |
14 |
56,108,204 (GRCm39) |
missense |
probably benign |
0.00 |
RF007:Nynrin
|
UTSW |
14 |
56,103,658 (GRCm39) |
splice site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- TGAACTGAGTGATGACGCTG -3'
(R):5'- GTCAGAGATAACATCCCGGTG -3'
Sequencing Primer
(F):5'- ACGCCGAACCTTTGGAGGATC -3'
(R):5'- GTGGGAATCCATGAAGCCC -3'
|
Posted On |
2019-09-13 |