Incidental Mutation 'R4601:Vmn2r115'
| ID |
345668 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r115
|
| Ensembl Gene |
ENSMUSG00000091076 |
| Gene Name |
vomeronasal 2, receptor 115 |
| Synonyms |
V2Rp4, EG638102 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.094)
|
| Stock # |
R4601 (G1)
|
| Quality Score |
136 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
23562951-23579102 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 23565373 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Glutamine
at position 420
(L420Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000131447
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168175]
|
| AlphaFold |
E9Q0E7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000168175
AA Change: L420Q
PolyPhen 2
Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
|
| SMART Domains |
Protein: ENSMUSP00000131447
Gene: ENSMUSG00000091076
AA Change: L420Q
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
73 |
471 |
1.4e-28 |
PFAM |
|
Pfam:NCD3G
|
512 |
565 |
2.9e-20 |
PFAM |
|
Pfam:7tm_3
|
598 |
833 |
5e-55 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.1%
- 20x: 94.5%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aars2 |
T |
A |
17: 45,827,847 (GRCm39) |
D555E |
probably damaging |
Het |
| Abca16 |
T |
G |
7: 120,035,920 (GRCm39) |
F334L |
probably damaging |
Het |
| Abcc4 |
T |
A |
14: 118,869,575 (GRCm39) |
M186L |
probably benign |
Het |
| Agap3 |
T |
C |
5: 24,681,406 (GRCm39) |
L120P |
probably damaging |
Het |
| Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
| Aldh1a7 |
A |
T |
19: 20,693,343 (GRCm39) |
V192D |
probably damaging |
Het |
| Ankrd36 |
A |
G |
11: 5,520,102 (GRCm39) |
D59G |
probably benign |
Het |
| Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
| Cacna1e |
A |
G |
1: 154,347,359 (GRCm39) |
V936A |
probably benign |
Het |
| Camkv |
T |
C |
9: 107,823,295 (GRCm39) |
V107A |
probably damaging |
Het |
| Camp |
T |
C |
9: 109,677,730 (GRCm39) |
E80G |
probably damaging |
Het |
| Cblif |
A |
C |
19: 11,729,554 (GRCm39) |
D171A |
probably damaging |
Het |
| Ccdc66 |
T |
C |
14: 27,222,377 (GRCm39) |
N122S |
probably damaging |
Het |
| Cd101 |
G |
A |
3: 100,901,204 (GRCm39) |
T960M |
possibly damaging |
Het |
| Cdk18 |
A |
G |
1: 132,044,657 (GRCm39) |
V323A |
possibly damaging |
Het |
| Celf2 |
G |
T |
2: 6,590,831 (GRCm39) |
N279K |
possibly damaging |
Het |
| Cemip |
T |
C |
7: 83,600,826 (GRCm39) |
I932V |
probably damaging |
Het |
| Cep250 |
C |
A |
2: 155,803,973 (GRCm39) |
Q28K |
probably benign |
Het |
| Ces2f |
T |
C |
8: 105,676,596 (GRCm39) |
C97R |
probably damaging |
Het |
| Cfap126 |
G |
T |
1: 170,941,627 (GRCm39) |
G41C |
possibly damaging |
Het |
| Cfap96 |
A |
T |
8: 46,423,505 (GRCm39) |
I69N |
probably damaging |
Het |
| Chat |
T |
C |
14: 32,146,112 (GRCm39) |
M354V |
probably benign |
Het |
| Clca4b |
A |
T |
3: 144,632,945 (GRCm39) |
D168E |
possibly damaging |
Het |
| Cpxm1 |
T |
A |
2: 130,235,496 (GRCm39) |
M499L |
possibly damaging |
Het |
| Dennd3 |
T |
A |
15: 73,439,009 (GRCm39) |
W1126R |
probably damaging |
Het |
| Dgkb |
T |
C |
12: 38,652,819 (GRCm39) |
S735P |
probably damaging |
Het |
| Dlec1 |
T |
C |
9: 118,976,202 (GRCm39) |
|
probably null |
Het |
| Dnajc6 |
T |
C |
4: 101,468,461 (GRCm39) |
F166L |
probably damaging |
Het |
| Dph5 |
A |
G |
3: 115,693,426 (GRCm39) |
N115D |
possibly damaging |
Het |
| Ercc3 |
G |
A |
18: 32,378,624 (GRCm39) |
A202T |
probably benign |
Het |
| Erich3 |
A |
T |
3: 154,470,375 (GRCm39) |
D136V |
unknown |
Het |
| Exoc2 |
T |
C |
13: 31,066,251 (GRCm39) |
N475S |
probably benign |
Het |
| Fam217a |
T |
C |
13: 35,095,285 (GRCm39) |
D310G |
probably damaging |
Het |
| Fam53a |
C |
T |
5: 33,758,007 (GRCm39) |
S372N |
probably benign |
Het |
| Fbn2 |
C |
G |
18: 58,186,805 (GRCm39) |
G1699R |
probably damaging |
Het |
| Fbxo46 |
T |
C |
7: 18,869,489 (GRCm39) |
V36A |
probably benign |
Het |
| Fhip1a |
T |
C |
3: 85,648,487 (GRCm39) |
M26V |
probably damaging |
Het |
| G6pc1 |
A |
G |
11: 101,263,567 (GRCm39) |
Y127C |
probably damaging |
Het |
| Gba2 |
A |
G |
4: 43,573,810 (GRCm39) |
F161L |
probably damaging |
Het |
| Gja1 |
T |
C |
10: 56,264,325 (GRCm39) |
L228P |
probably damaging |
Het |
| Gm20834 |
A |
G |
Y: 10,323,178 (GRCm39) |
V86A |
probably benign |
Het |
| Hmcn1 |
A |
T |
1: 150,614,396 (GRCm39) |
C1337S |
probably damaging |
Het |
| Il1rl1 |
T |
A |
1: 40,480,460 (GRCm39) |
S30T |
possibly damaging |
Het |
| Itgb4 |
A |
G |
11: 115,896,548 (GRCm39) |
T1436A |
probably damaging |
Het |
| Itk |
T |
A |
11: 46,227,342 (GRCm39) |
Q427L |
probably benign |
Het |
| Klhdc4 |
T |
C |
8: 122,526,266 (GRCm39) |
E291G |
probably damaging |
Het |
| Map4 |
T |
A |
9: 109,881,887 (GRCm39) |
S250R |
possibly damaging |
Het |
| Mnt |
T |
A |
11: 74,727,285 (GRCm39) |
V57E |
possibly damaging |
Het |
| Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
| Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
| Mtcl2 |
T |
C |
2: 156,881,844 (GRCm39) |
K736R |
probably benign |
Het |
| Musk |
A |
T |
4: 58,301,625 (GRCm39) |
I128F |
probably damaging |
Het |
| Myh4 |
G |
A |
11: 67,141,136 (GRCm39) |
A733T |
possibly damaging |
Het |
| Myo5a |
T |
A |
9: 75,043,670 (GRCm39) |
F220I |
probably damaging |
Het |
| Npas3 |
A |
G |
12: 54,091,361 (GRCm39) |
H305R |
probably damaging |
Het |
| Nrcam |
A |
T |
12: 44,637,839 (GRCm39) |
Y1132F |
probably damaging |
Het |
| Nt5c3b |
A |
C |
11: 100,323,744 (GRCm39) |
D189E |
probably benign |
Het |
| Nuf2 |
A |
G |
1: 169,333,683 (GRCm39) |
L331P |
probably damaging |
Het |
| Nup214 |
C |
T |
2: 31,887,977 (GRCm39) |
T646I |
probably benign |
Het |
| Or14j9 |
T |
C |
17: 37,875,076 (GRCm39) |
N42S |
probably damaging |
Het |
| Pcdh18 |
T |
C |
3: 49,699,174 (GRCm39) |
E1096G |
probably damaging |
Het |
| Pgm2 |
T |
A |
5: 64,265,070 (GRCm39) |
F364I |
probably benign |
Het |
| Pikfyve |
A |
G |
1: 65,273,421 (GRCm39) |
N612S |
probably damaging |
Het |
| Pla2g4e |
T |
G |
2: 120,016,863 (GRCm39) |
H226P |
possibly damaging |
Het |
| Ppp3cb |
T |
C |
14: 20,570,714 (GRCm39) |
N339S |
possibly damaging |
Het |
| Prkd2 |
G |
T |
7: 16,577,573 (GRCm39) |
|
probably benign |
Het |
| Rnf133 |
T |
C |
6: 23,649,041 (GRCm39) |
E296G |
possibly damaging |
Het |
| Sav1 |
A |
T |
12: 70,031,095 (GRCm39) |
D142E |
probably benign |
Het |
| Scn3b |
C |
A |
9: 40,199,719 (GRCm39) |
P212T |
probably damaging |
Het |
| Sel1l |
A |
T |
12: 91,799,827 (GRCm39) |
|
probably null |
Het |
| Septin9 |
A |
G |
11: 117,251,310 (GRCm39) |
K543E |
probably damaging |
Het |
| Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
| Slc35e2 |
T |
C |
4: 155,702,106 (GRCm39) |
F290S |
probably benign |
Het |
| Snrpa |
A |
G |
7: 26,894,958 (GRCm39) |
M1T |
probably null |
Het |
| Sptlc3 |
G |
A |
2: 139,478,600 (GRCm39) |
V520I |
probably benign |
Het |
| Srpk3 |
A |
G |
X: 72,818,547 (GRCm39) |
H79R |
possibly damaging |
Het |
| Stox2 |
A |
G |
8: 47,645,970 (GRCm39) |
S497P |
probably damaging |
Het |
| Stradb |
G |
A |
1: 59,032,731 (GRCm39) |
S361N |
probably damaging |
Het |
| Sult3a2 |
T |
C |
10: 33,658,083 (GRCm39) |
K10R |
probably benign |
Het |
| Susd4 |
A |
G |
1: 182,686,025 (GRCm39) |
N192D |
probably damaging |
Het |
| Tcp10a |
T |
A |
17: 7,593,374 (GRCm39) |
D32E |
probably benign |
Het |
| Tdpoz4 |
T |
A |
3: 93,704,339 (GRCm39) |
V212D |
probably damaging |
Het |
| Tdrd5 |
T |
A |
1: 156,111,944 (GRCm39) |
T479S |
probably benign |
Het |
| Tex10 |
T |
C |
4: 48,452,946 (GRCm39) |
D671G |
probably benign |
Het |
| Tex55 |
A |
G |
16: 38,648,380 (GRCm39) |
V243A |
probably benign |
Het |
| Traj37 |
T |
C |
14: 54,418,996 (GRCm39) |
|
probably benign |
Het |
| Ttc7b |
G |
A |
12: 100,466,376 (GRCm39) |
R79C |
probably damaging |
Het |
| Wdr24 |
T |
A |
17: 26,047,181 (GRCm39) |
|
probably null |
Het |
| Wdr81 |
T |
A |
11: 75,336,484 (GRCm39) |
Q516L |
probably damaging |
Het |
| Zfp516 |
A |
G |
18: 82,974,164 (GRCm39) |
T121A |
probably benign |
Het |
| Zmat1 |
A |
T |
X: 133,873,694 (GRCm39) |
S566T |
probably damaging |
Homo |
|
| Other mutations in Vmn2r115 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00990:Vmn2r115
|
APN |
17 |
23,575,934 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,345 (GRCm39) |
nonsense |
probably null |
|
|
IGL00990:Vmn2r115
|
APN |
17 |
23,578,371 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,135 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,252 (GRCm39) |
missense |
probably benign |
0.14 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,578,323 (GRCm39) |
missense |
probably benign |
0.22 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,150 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,180 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,567,008 (GRCm39) |
nonsense |
probably null |
|
|
IGL00990:Vmn2r115
|
APN |
17 |
23,578,798 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,578,753 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,238 (GRCm39) |
missense |
probably benign |
0.19 |
|
IGL00990:Vmn2r115
|
APN |
17 |
23,565,346 (GRCm39) |
missense |
probably benign |
0.30 |
|
IGL01073:Vmn2r115
|
APN |
17 |
23,564,971 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL01101:Vmn2r115
|
APN |
17 |
23,564,971 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL01300:Vmn2r115
|
APN |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01415:Vmn2r115
|
APN |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02309:Vmn2r115
|
APN |
17 |
23,564,113 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02863:Vmn2r115
|
APN |
17 |
23,578,257 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0023:Vmn2r115
|
UTSW |
17 |
23,565,252 (GRCm39) |
missense |
probably benign |
0.14 |
|
R0197:Vmn2r115
|
UTSW |
17 |
23,578,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0361:Vmn2r115
|
UTSW |
17 |
23,564,196 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0601:Vmn2r115
|
UTSW |
17 |
23,579,074 (GRCm39) |
missense |
probably null |
0.51 |
|
R0676:Vmn2r115
|
UTSW |
17 |
23,565,238 (GRCm39) |
missense |
probably benign |
0.19 |
|
R0685:Vmn2r115
|
UTSW |
17 |
23,578,249 (GRCm39) |
missense |
probably benign |
|
|
R0865:Vmn2r115
|
UTSW |
17 |
23,565,382 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R1124:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1145:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1146:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1207:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1266:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1318:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1367:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1376:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1376:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1420:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1469:Vmn2r115
|
UTSW |
17 |
23,564,992 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1469:Vmn2r115
|
UTSW |
17 |
23,564,992 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1604:Vmn2r115
|
UTSW |
17 |
23,564,245 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1645:Vmn2r115
|
UTSW |
17 |
23,565,192 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R1646:Vmn2r115
|
UTSW |
17 |
23,578,513 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1650:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1678:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1716:Vmn2r115
|
UTSW |
17 |
23,566,795 (GRCm39) |
missense |
probably benign |
|
|
R1846:Vmn2r115
|
UTSW |
17 |
23,578,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1847:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1885:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R1887:Vmn2r115
|
UTSW |
17 |
23,565,007 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1937:Vmn2r115
|
UTSW |
17 |
23,578,388 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2007:Vmn2r115
|
UTSW |
17 |
23,566,927 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2120:Vmn2r115
|
UTSW |
17 |
23,578,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3161:Vmn2r115
|
UTSW |
17 |
23,575,998 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R3780:Vmn2r115
|
UTSW |
17 |
23,564,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3806:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R3982:Vmn2r115
|
UTSW |
17 |
23,578,948 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4019:Vmn2r115
|
UTSW |
17 |
23,579,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4039:Vmn2r115
|
UTSW |
17 |
23,564,077 (GRCm39) |
missense |
probably benign |
0.26 |
|
R4087:Vmn2r115
|
UTSW |
17 |
23,565,358 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4089:Vmn2r115
|
UTSW |
17 |
23,565,358 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4379:Vmn2r115
|
UTSW |
17 |
23,564,197 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4417:Vmn2r115
|
UTSW |
17 |
23,564,854 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4874:Vmn2r115
|
UTSW |
17 |
23,578,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5466:Vmn2r115
|
UTSW |
17 |
23,579,030 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5613:Vmn2r115
|
UTSW |
17 |
23,564,307 (GRCm39) |
missense |
probably benign |
|
|
R5821:Vmn2r115
|
UTSW |
17 |
23,566,937 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6120:Vmn2r115
|
UTSW |
17 |
23,565,003 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6193:Vmn2r115
|
UTSW |
17 |
23,575,983 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6213:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R6290:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
R6319:Vmn2r115
|
UTSW |
17 |
23,566,877 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6495:Vmn2r115
|
UTSW |
17 |
23,578,572 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6599:Vmn2r115
|
UTSW |
17 |
23,565,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6764:Vmn2r115
|
UTSW |
17 |
23,565,046 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6970:Vmn2r115
|
UTSW |
17 |
23,564,989 (GRCm39) |
missense |
probably benign |
0.23 |
|
R7023:Vmn2r115
|
UTSW |
17 |
23,578,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7236:Vmn2r115
|
UTSW |
17 |
23,578,576 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7353:Vmn2r115
|
UTSW |
17 |
23,564,887 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R7483:Vmn2r115
|
UTSW |
17 |
23,565,371 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7743:Vmn2r115
|
UTSW |
17 |
23,564,772 (GRCm39) |
nonsense |
probably null |
|
|
R8005:Vmn2r115
|
UTSW |
17 |
23,563,124 (GRCm39) |
nonsense |
probably null |
|
|
R8191:Vmn2r115
|
UTSW |
17 |
23,578,530 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8544:Vmn2r115
|
UTSW |
17 |
23,564,773 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8890:Vmn2r115
|
UTSW |
17 |
23,578,497 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9098:Vmn2r115
|
UTSW |
17 |
23,564,803 (GRCm39) |
missense |
probably benign |
|
|
R9114:Vmn2r115
|
UTSW |
17 |
23,564,307 (GRCm39) |
missense |
probably benign |
|
|
R9189:Vmn2r115
|
UTSW |
17 |
23,564,784 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9351:Vmn2r115
|
UTSW |
17 |
23,578,482 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9397:Vmn2r115
|
UTSW |
17 |
23,564,152 (GRCm39) |
nonsense |
probably null |
|
|
R9410:Vmn2r115
|
UTSW |
17 |
23,578,915 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9593:Vmn2r115
|
UTSW |
17 |
23,578,184 (GRCm39) |
missense |
probably damaging |
0.99 |
|
V5622:Vmn2r115
|
UTSW |
17 |
23,578,333 (GRCm39) |
missense |
probably benign |
|
|
V5622:Vmn2r115
|
UTSW |
17 |
23,565,201 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0023:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
X0033:Vmn2r115
|
UTSW |
17 |
23,578,962 (GRCm39) |
small deletion |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TCAGCCTCTAAATGTAAGACACTG -3'
(R):5'- TCTACATGGACAGATTCTGCCTC -3'
Sequencing Primer
(F):5'- TGTAAGACACTGAAGAACTGCTC -3'
(R):5'- AGATTCTGCCTCATAGTATATTCGC -3'
|
| Posted On |
2015-09-25 |
Incidental Mutation