Incidental Mutation 'R4648:Nynrin'
| ID |
350520 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Nynrin
|
| Ensembl Gene |
ENSMUSG00000075592 |
| Gene Name |
NYN domain and retroviral integrase containing |
| Synonyms |
|
| MMRRC Submission |
041909-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4648 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
14 |
| Chromosomal Location |
56091572-56112193 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 56110351 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 1819
(Y1819*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000129557
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000100529]
[ENSMUST00000168479]
|
| AlphaFold |
Q5DTZ0 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000100529
AA Change: Y1819*
|
| SMART Domains |
Protein: ENSMUSP00000098098
Gene: ENSMUSG00000075592
AA Change: Y1819*
| 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 |
probably null
Transcript: ENSMUST00000168479
AA Change: Y1819*
|
| SMART Domains |
Protein: ENSMUSP00000129557
Gene: ENSMUSG00000075592
AA Change: Y1819*
| 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 |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000181218
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700031F05Rik |
G |
T |
X: 101,904,515 (GRCm39) |
N132K |
possibly damaging |
Het |
| 2010315B03Rik |
T |
A |
9: 124,056,228 (GRCm39) |
Y232F |
probably benign |
Het |
| 2310079G19Rik |
T |
C |
16: 88,424,255 (GRCm39) |
S79G |
probably benign |
Het |
| 4930568D16Rik |
T |
A |
2: 35,244,458 (GRCm39) |
Y298F |
probably damaging |
Het |
| Alpk2 |
A |
G |
18: 65,482,953 (GRCm39) |
F352L |
probably damaging |
Het |
| Angpt1 |
T |
A |
15: 42,539,580 (GRCm39) |
Y93F |
probably benign |
Het |
| Ankrd33b |
T |
C |
15: 31,325,170 (GRCm39) |
*129W |
probably null |
Het |
| Atp5pf |
T |
C |
16: 84,625,343 (GRCm39) |
M87V |
probably benign |
Het |
| Atp8b3 |
A |
G |
10: 80,361,457 (GRCm39) |
S822P |
possibly damaging |
Het |
| Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
| Bbs2 |
A |
T |
8: 94,807,507 (GRCm39) |
V429E |
probably damaging |
Het |
| Bccip |
C |
T |
7: 133,316,628 (GRCm39) |
L83F |
probably damaging |
Het |
| Brd9 |
G |
A |
13: 74,088,895 (GRCm39) |
V198I |
probably benign |
Het |
| C1galt1c1 |
A |
T |
X: 37,720,349 (GRCm39) |
S216T |
probably benign |
Het |
| Calhm1 |
A |
G |
19: 47,132,240 (GRCm39) |
L125P |
probably damaging |
Het |
| Ccdc110 |
A |
T |
8: 46,395,705 (GRCm39) |
Q532L |
possibly damaging |
Het |
| Cdh19 |
G |
A |
1: 110,852,907 (GRCm39) |
L343F |
probably benign |
Het |
| Cep350 |
A |
G |
1: 155,778,344 (GRCm39) |
S1653P |
possibly damaging |
Het |
| Cmtm4 |
A |
G |
8: 105,082,952 (GRCm39) |
I135T |
possibly damaging |
Het |
| Cmya5 |
A |
G |
13: 93,230,336 (GRCm39) |
L1584P |
possibly damaging |
Het |
| Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
| Crp |
A |
G |
1: 172,525,704 (GRCm39) |
M1V |
probably null |
Het |
| Csmd1 |
G |
A |
8: 16,048,788 (GRCm39) |
Q2305* |
probably null |
Het |
| Cyp2c38 |
T |
A |
19: 39,449,132 (GRCm39) |
I74F |
probably benign |
Het |
| Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
| Dcaf1 |
A |
T |
9: 106,742,876 (GRCm39) |
|
probably benign |
Het |
| Dhx16 |
C |
G |
17: 36,196,527 (GRCm39) |
A565G |
probably benign |
Het |
| Dock7 |
C |
A |
4: 98,857,881 (GRCm39) |
E1448* |
probably null |
Het |
| Dpf2 |
C |
T |
19: 5,957,109 (GRCm39) |
R38H |
probably damaging |
Het |
| E030030I06Rik |
T |
A |
10: 22,024,744 (GRCm39) |
R56S |
unknown |
Het |
| Etnk1 |
A |
G |
6: 143,141,000 (GRCm39) |
Y248C |
probably damaging |
Het |
| Ext1 |
A |
G |
15: 52,953,383 (GRCm39) |
S494P |
possibly damaging |
Het |
| Gk2 |
T |
C |
5: 97,603,579 (GRCm39) |
S420G |
probably benign |
Het |
| Gm26596 |
T |
C |
10: 112,765,064 (GRCm39) |
|
probably benign |
Het |
| Gm5414 |
G |
T |
15: 101,536,543 (GRCm39) |
N27K |
possibly damaging |
Het |
| Gskip |
A |
G |
12: 105,664,988 (GRCm39) |
D9G |
probably benign |
Het |
| H2-K2 |
T |
A |
17: 34,194,989 (GRCm39) |
|
noncoding transcript |
Het |
| Hk1 |
T |
G |
10: 62,140,558 (GRCm39) |
S105R |
probably benign |
Het |
| Hmg20b |
T |
A |
10: 81,184,416 (GRCm39) |
Q129L |
probably damaging |
Het |
| Idnk |
A |
G |
13: 58,310,683 (GRCm39) |
D67G |
probably benign |
Het |
| Igfbp5 |
G |
T |
1: 72,903,222 (GRCm39) |
H118N |
probably benign |
Het |
| Irf4 |
A |
T |
13: 30,947,580 (GRCm39) |
Y427F |
probably benign |
Het |
| Khdc3 |
A |
G |
9: 73,009,868 (GRCm39) |
E26G |
possibly damaging |
Het |
| Kif7 |
T |
C |
7: 79,358,939 (GRCm39) |
D512G |
probably damaging |
Het |
| Lamb3 |
T |
A |
1: 193,013,665 (GRCm39) |
I513N |
probably damaging |
Het |
| Lipo3 |
A |
G |
19: 33,760,860 (GRCm39) |
L174P |
probably damaging |
Het |
| Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
| Map3k21 |
A |
G |
8: 126,668,850 (GRCm39) |
D812G |
probably benign |
Het |
| Mast2 |
G |
T |
4: 116,172,036 (GRCm39) |
Y637* |
probably null |
Het |
| Matn2 |
T |
C |
15: 34,428,679 (GRCm39) |
I681T |
probably damaging |
Het |
| Med18 |
A |
T |
4: 132,190,274 (GRCm39) |
V37D |
possibly damaging |
Het |
| Mip |
T |
A |
10: 128,062,922 (GRCm39) |
H122Q |
probably benign |
Het |
| Mmp13 |
A |
T |
9: 7,274,233 (GRCm39) |
D180V |
probably damaging |
Het |
| Mpg |
C |
A |
11: 32,180,034 (GRCm39) |
C187* |
probably null |
Het |
| Mtmr14 |
A |
G |
6: 113,237,567 (GRCm39) |
E256G |
probably benign |
Het |
| Myo7b |
C |
T |
18: 32,100,178 (GRCm39) |
|
probably null |
Het |
| Nhsl3 |
G |
T |
4: 129,115,733 (GRCm39) |
T977K |
probably benign |
Het |
| Nmt1 |
T |
A |
11: 102,954,743 (GRCm39) |
V425D |
probably damaging |
Het |
| Or10ak16 |
A |
G |
4: 118,751,147 (GRCm39) |
N289S |
possibly damaging |
Het |
| Or4c107 |
T |
A |
2: 88,789,556 (GRCm39) |
F249I |
probably damaging |
Het |
| Or5i1 |
T |
C |
2: 87,613,565 (GRCm39) |
V227A |
possibly damaging |
Het |
| Otof |
T |
C |
5: 30,540,914 (GRCm39) |
E875G |
possibly damaging |
Het |
| Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
| Phc1 |
T |
C |
6: 122,298,872 (GRCm39) |
I699V |
possibly damaging |
Het |
| Prkdc |
T |
G |
16: 15,634,638 (GRCm39) |
D3594E |
probably benign |
Het |
| Pstpip1 |
A |
T |
9: 56,032,502 (GRCm39) |
D246V |
probably damaging |
Het |
| Rbm46 |
A |
T |
3: 82,771,765 (GRCm39) |
D283E |
probably benign |
Het |
| Ror2 |
A |
T |
13: 53,439,536 (GRCm39) |
C9* |
probably null |
Het |
| Setd1b |
C |
T |
5: 123,286,175 (GRCm39) |
A407V |
unknown |
Het |
| Slc26a4 |
T |
G |
12: 31,590,525 (GRCm39) |
D376A |
possibly damaging |
Het |
| Smarcad1 |
A |
G |
6: 65,044,073 (GRCm39) |
E215G |
probably benign |
Het |
| Spag16 |
G |
A |
1: 69,866,194 (GRCm39) |
R11Q |
probably null |
Het |
| Sult1d1 |
T |
A |
5: 87,713,954 (GRCm39) |
Q30L |
probably benign |
Het |
| Tbc1d5 |
A |
G |
17: 51,043,251 (GRCm39) |
C746R |
probably benign |
Het |
| Tdh |
A |
G |
14: 63,731,205 (GRCm39) |
L323P |
possibly damaging |
Het |
| Tet2 |
A |
T |
3: 133,193,843 (GRCm39) |
M197K |
probably benign |
Het |
| Tnn |
T |
C |
1: 159,973,612 (GRCm39) |
M252V |
probably benign |
Het |
| Trdn |
G |
T |
10: 33,071,977 (GRCm39) |
E215* |
probably null |
Het |
| Trem1 |
G |
A |
17: 48,551,590 (GRCm39) |
V84I |
probably benign |
Het |
| Tspan5 |
T |
C |
3: 138,604,076 (GRCm39) |
F154L |
probably damaging |
Het |
| Usp45 |
A |
G |
4: 21,825,044 (GRCm39) |
R647G |
probably benign |
Het |
| Usp50 |
T |
A |
2: 126,619,953 (GRCm39) |
I120F |
probably damaging |
Het |
| Vil1 |
T |
C |
1: 74,471,457 (GRCm39) |
M746T |
probably benign |
Het |
| Washc4 |
T |
A |
10: 83,410,407 (GRCm39) |
M665K |
possibly damaging |
Het |
| Zfp750 |
T |
C |
11: 121,402,706 (GRCm39) |
T681A |
probably benign |
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 |
|
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 |
|
|
R7361:Nynrin
|
UTSW |
14 |
56,107,857 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
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'- CCGAGAACAGGCGTTTCAAG -3'
(R):5'- TTCAGCAAAGCTTTACAAAGGG -3'
Sequencing Primer
(F):5'- CGTTTCAAGAGGGAGAGCC -3'
(R):5'- AGGGAACTTCTCCGCACAAGG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation