Incidental Mutation 'R1467:Vmn2r111'
| ID |
164626 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r111
|
| Ensembl Gene |
ENSMUSG00000095093 |
| Gene Name |
vomeronasal 2, receptor 111 |
| Synonyms |
EG210876 |
| MMRRC Submission |
039520-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.092)
|
| Stock # |
R1467 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
17 |
| Chromosomal Location |
22766922-22792254 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 22790028 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Leucine
at position 326
(H326L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000090148
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000092491]
|
| AlphaFold |
K7N674 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000092491
AA Change: H326L
PolyPhen 2
Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000090148
Gene: ENSMUSG00000095093
AA Change: H326L
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
73 |
469 |
2.5e-29 |
PFAM |
|
Pfam:NCD3G
|
512 |
565 |
1.1e-20 |
PFAM |
|
Pfam:7tm_3
|
595 |
833 |
5.6e-54 |
PFAM |
|
| Meta Mutation Damage Score |
0.6467 |
| Coding Region Coverage |
- 1x: 99.6%
- 3x: 98.1%
- 10x: 88.5%
- 20x: 62.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 98 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2010315B03Rik |
C |
A |
9: 124,058,093 (GRCm39) |
V9L |
possibly damaging |
Het |
| A630010A05Rik |
C |
A |
16: 14,436,447 (GRCm39) |
L167I |
possibly damaging |
Het |
| Abca14 |
A |
T |
7: 119,815,405 (GRCm39) |
M218L |
possibly damaging |
Het |
| Abca15 |
C |
A |
7: 119,939,761 (GRCm39) |
|
probably null |
Het |
| Acod1 |
T |
C |
14: 103,292,003 (GRCm39) |
F176L |
probably benign |
Het |
| Actr5 |
A |
G |
2: 158,480,617 (GRCm39) |
H545R |
probably benign |
Het |
| Adcy1 |
A |
G |
11: 7,088,396 (GRCm39) |
T472A |
probably damaging |
Het |
| Aldh1l1 |
A |
G |
6: 90,548,910 (GRCm39) |
K469R |
possibly damaging |
Het |
| Ambra1 |
A |
T |
2: 91,716,048 (GRCm39) |
Q853L |
probably damaging |
Het |
| Apol7e |
G |
T |
15: 77,601,966 (GRCm39) |
G188V |
probably damaging |
Het |
| AU018091 |
A |
T |
7: 3,214,089 (GRCm39) |
W43R |
probably benign |
Het |
| Baat |
A |
G |
4: 49,503,101 (GRCm39) |
V7A |
probably benign |
Het |
| Bcas1 |
C |
A |
2: 170,229,852 (GRCm39) |
Q249H |
possibly damaging |
Het |
| Bltp1 |
T |
A |
3: 37,090,094 (GRCm39) |
V676D |
probably damaging |
Het |
| Bptf |
G |
T |
11: 106,945,881 (GRCm39) |
Q2453K |
possibly damaging |
Het |
| Btg3 |
A |
G |
16: 78,161,688 (GRCm39) |
|
probably null |
Het |
| Cacna2d3 |
T |
C |
14: 29,055,736 (GRCm39) |
N298S |
possibly damaging |
Het |
| Carf |
G |
A |
1: 60,167,152 (GRCm39) |
V127I |
possibly damaging |
Het |
| Catsperg1 |
T |
C |
7: 28,884,433 (GRCm39) |
S916G |
probably damaging |
Het |
| Cers1 |
T |
C |
8: 70,775,819 (GRCm39) |
S274P |
possibly damaging |
Het |
| Ces4a |
T |
A |
8: 105,864,667 (GRCm39) |
V48E |
possibly damaging |
Het |
| Cfap54 |
T |
A |
10: 92,805,625 (GRCm39) |
H1495L |
probably benign |
Het |
| Cntnap5a |
T |
A |
1: 115,612,898 (GRCm39) |
L11* |
probably null |
Het |
| Cr2 |
C |
T |
1: 194,839,817 (GRCm39) |
G913R |
probably damaging |
Het |
| Cul9 |
A |
G |
17: 46,836,299 (GRCm39) |
L1155P |
probably damaging |
Het |
| Dlec1 |
A |
T |
9: 118,971,646 (GRCm39) |
D1278V |
probably damaging |
Het |
| Dmrt2 |
A |
G |
19: 25,650,970 (GRCm39) |
E52G |
possibly damaging |
Het |
| Dsp |
A |
G |
13: 38,376,688 (GRCm39) |
K1491R |
probably benign |
Het |
| Ecpas |
A |
G |
4: 58,832,753 (GRCm39) |
V869A |
probably benign |
Het |
| Eef1d |
A |
T |
15: 75,767,770 (GRCm39) |
D206E |
probably damaging |
Het |
| Erbb2 |
C |
T |
11: 98,327,001 (GRCm39) |
Q1137* |
probably null |
Het |
| Ercc2 |
T |
A |
7: 19,119,811 (GRCm39) |
D157E |
probably benign |
Het |
| Eri1 |
A |
G |
8: 35,936,284 (GRCm39) |
*346Q |
probably null |
Het |
| Espl1 |
A |
G |
15: 102,228,293 (GRCm39) |
E1689G |
probably benign |
Het |
| Fap |
C |
T |
2: 62,347,964 (GRCm39) |
V539I |
probably benign |
Het |
| Fasn |
A |
G |
11: 120,701,866 (GRCm39) |
F1871S |
probably benign |
Het |
| Gabpb1 |
T |
G |
2: 126,494,247 (GRCm39) |
Y126S |
probably damaging |
Het |
| Grm1 |
T |
C |
10: 10,595,702 (GRCm39) |
Y642C |
probably damaging |
Het |
| Heatr4 |
T |
C |
12: 84,024,841 (GRCm39) |
T327A |
possibly damaging |
Het |
| Hmbox1 |
T |
C |
14: 65,099,027 (GRCm39) |
D212G |
possibly damaging |
Het |
| Hmcn1 |
T |
A |
1: 150,565,341 (GRCm39) |
D2262V |
probably damaging |
Het |
| Hoxb9 |
A |
G |
11: 96,162,764 (GRCm39) |
T133A |
probably benign |
Het |
| Insr |
A |
T |
8: 3,219,720 (GRCm39) |
V934E |
probably damaging |
Het |
| Ipo9 |
T |
C |
1: 135,334,281 (GRCm39) |
E315G |
possibly damaging |
Het |
| Itga10 |
C |
T |
3: 96,559,545 (GRCm39) |
Q481* |
probably null |
Het |
| Kntc1 |
T |
A |
5: 123,925,047 (GRCm39) |
M1120K |
probably benign |
Het |
| Krt78 |
A |
G |
15: 101,854,728 (GRCm39) |
Y1028H |
possibly damaging |
Het |
| Lrrc38 |
A |
T |
4: 143,096,450 (GRCm39) |
I254F |
probably damaging |
Het |
| Lyrm7 |
A |
G |
11: 54,741,215 (GRCm39) |
F40L |
probably damaging |
Het |
| Mfsd4b1 |
C |
T |
10: 39,878,631 (GRCm39) |
S422N |
possibly damaging |
Het |
| Mlh3 |
A |
T |
12: 85,284,374 (GRCm39) |
L1380* |
probably null |
Het |
| Mrpl24 |
C |
A |
3: 87,829,744 (GRCm39) |
A110D |
probably benign |
Het |
| Mrps14 |
T |
C |
1: 160,024,520 (GRCm39) |
V17A |
probably benign |
Het |
| Mtcl1 |
T |
C |
17: 66,755,322 (GRCm39) |
D340G |
probably damaging |
Het |
| Neb |
T |
C |
2: 52,120,059 (GRCm39) |
Y3900C |
probably damaging |
Het |
| Neurod4 |
T |
C |
10: 130,106,473 (GRCm39) |
D267G |
probably benign |
Het |
| Nf1 |
A |
T |
11: 79,319,452 (GRCm39) |
I536F |
possibly damaging |
Het |
| Nkg7 |
C |
T |
7: 43,086,857 (GRCm39) |
P44S |
probably damaging |
Het |
| Or14c40 |
T |
C |
7: 86,313,185 (GRCm39) |
V105A |
possibly damaging |
Het |
| Or4a67 |
T |
C |
2: 88,597,832 (GRCm39) |
I276V |
probably benign |
Het |
| Pcif1 |
T |
C |
2: 164,731,058 (GRCm39) |
Y404H |
probably benign |
Het |
| Pcnx2 |
A |
T |
8: 126,480,289 (GRCm39) |
L2006Q |
possibly damaging |
Het |
| Pcnx3 |
A |
T |
19: 5,724,922 (GRCm39) |
S821T |
possibly damaging |
Het |
| Pde8b |
T |
A |
13: 95,170,680 (GRCm39) |
D662V |
probably damaging |
Het |
| Pkd1l3 |
C |
T |
8: 110,343,000 (GRCm39) |
P113S |
unknown |
Het |
| Pkd2l1 |
G |
T |
19: 44,142,648 (GRCm39) |
Q465K |
possibly damaging |
Het |
| Plch2 |
G |
T |
4: 155,068,189 (GRCm39) |
P1479Q |
probably benign |
Het |
| Plekhm3 |
A |
T |
1: 64,932,041 (GRCm39) |
I521N |
probably damaging |
Het |
| Pola2 |
A |
T |
19: 5,992,093 (GRCm39) |
Y526* |
probably null |
Het |
| Prss23 |
T |
C |
7: 89,159,217 (GRCm39) |
D284G |
probably damaging |
Het |
| Psme2b |
A |
G |
11: 48,836,467 (GRCm39) |
F160S |
probably damaging |
Het |
| Rap1gap2 |
A |
G |
11: 74,327,853 (GRCm39) |
V139A |
possibly damaging |
Het |
| Rbbp9 |
G |
T |
2: 144,385,777 (GRCm39) |
R163S |
possibly damaging |
Het |
| Rdh12 |
T |
C |
12: 79,260,522 (GRCm39) |
L206P |
probably damaging |
Het |
| Rhou |
T |
C |
8: 124,388,029 (GRCm39) |
W254R |
possibly damaging |
Het |
| Scfd1 |
A |
G |
12: 51,478,281 (GRCm39) |
K498E |
possibly damaging |
Het |
| Scn7a |
A |
G |
2: 66,519,902 (GRCm39) |
Y1001H |
probably benign |
Het |
| Setx |
T |
A |
2: 29,048,917 (GRCm39) |
V1981E |
probably damaging |
Het |
| Sfxn1 |
T |
C |
13: 54,247,890 (GRCm39) |
I205T |
possibly damaging |
Het |
| Shld2 |
G |
T |
14: 33,990,619 (GRCm39) |
H96N |
possibly damaging |
Het |
| Speer1g |
C |
T |
5: 11,180,337 (GRCm39) |
H82Y |
probably damaging |
Het |
| Spock1 |
G |
A |
13: 57,577,182 (GRCm39) |
R416C |
possibly damaging |
Het |
| Spred2 |
A |
G |
11: 19,968,109 (GRCm39) |
I222V |
probably benign |
Het |
| Stkld1 |
A |
T |
2: 26,839,407 (GRCm39) |
T358S |
probably benign |
Het |
| Strip1 |
T |
C |
3: 107,534,724 (GRCm39) |
E102G |
possibly damaging |
Het |
| Tars3 |
T |
C |
7: 65,305,444 (GRCm39) |
S223P |
probably damaging |
Het |
| Tdpoz1 |
T |
A |
3: 93,578,637 (GRCm39) |
E49V |
probably benign |
Het |
| Tert |
A |
G |
13: 73,776,328 (GRCm39) |
T360A |
probably benign |
Het |
| Tspear |
A |
G |
10: 77,717,026 (GRCm39) |
Y567C |
probably damaging |
Het |
| Ttc28 |
A |
G |
5: 111,433,254 (GRCm39) |
Q2096R |
probably benign |
Het |
| Ugt2b38 |
T |
G |
5: 87,560,232 (GRCm39) |
N361H |
probably damaging |
Het |
| Unc80 |
C |
T |
1: 66,560,740 (GRCm39) |
H823Y |
possibly damaging |
Het |
| Vmn2r18 |
A |
G |
5: 151,510,301 (GRCm39) |
F24S |
possibly damaging |
Het |
| Vmn2r82 |
A |
T |
10: 79,232,133 (GRCm39) |
I711F |
probably benign |
Het |
| Vwa8 |
C |
T |
14: 79,341,134 (GRCm39) |
Q1537* |
probably null |
Het |
| Wdr64 |
G |
A |
1: 175,603,288 (GRCm39) |
V630I |
probably benign |
Het |
| Wnt6 |
G |
T |
1: 74,821,434 (GRCm39) |
W84L |
probably damaging |
Het |
| Zfp11 |
C |
A |
5: 129,735,254 (GRCm39) |
R69L |
probably benign |
Het |
|
| Other mutations in Vmn2r111 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00932:Vmn2r111
|
APN |
17 |
22,767,734 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01306:Vmn2r111
|
APN |
17 |
22,787,965 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01309:Vmn2r111
|
APN |
17 |
22,787,997 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
IGL01457:Vmn2r111
|
APN |
17 |
22,790,966 (GRCm39) |
nonsense |
probably null |
|
|
IGL01465:Vmn2r111
|
APN |
17 |
22,767,718 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01505:Vmn2r111
|
APN |
17 |
22,767,553 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01571:Vmn2r111
|
APN |
17 |
22,790,373 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01715:Vmn2r111
|
APN |
17 |
22,788,054 (GRCm39) |
splice site |
probably benign |
|
|
IGL01962:Vmn2r111
|
APN |
17 |
22,767,265 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02190:Vmn2r111
|
APN |
17 |
22,789,754 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02496:Vmn2r111
|
APN |
17 |
22,787,837 (GRCm39) |
missense |
probably benign |
|
|
IGL02519:Vmn2r111
|
APN |
17 |
22,767,320 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02616:Vmn2r111
|
APN |
17 |
22,790,031 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
IGL02641:Vmn2r111
|
APN |
17 |
22,792,205 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
IGL02690:Vmn2r111
|
APN |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02698:Vmn2r111
|
APN |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03017:Vmn2r111
|
APN |
17 |
22,789,839 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0046:Vmn2r111
|
UTSW |
17 |
22,766,990 (GRCm39) |
missense |
probably benign |
|
|
R0064:Vmn2r111
|
UTSW |
17 |
22,791,053 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0519:Vmn2r111
|
UTSW |
17 |
22,792,102 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1439:Vmn2r111
|
UTSW |
17 |
22,790,097 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1467:Vmn2r111
|
UTSW |
17 |
22,790,028 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1636:Vmn2r111
|
UTSW |
17 |
22,790,380 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1647:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1648:Vmn2r111
|
UTSW |
17 |
22,788,042 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1697:Vmn2r111
|
UTSW |
17 |
22,767,041 (GRCm39) |
missense |
probably benign |
0.26 |
|
R1996:Vmn2r111
|
UTSW |
17 |
22,767,062 (GRCm39) |
missense |
probably benign |
0.21 |
|
R2040:Vmn2r111
|
UTSW |
17 |
22,767,395 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2075:Vmn2r111
|
UTSW |
17 |
22,778,043 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2134:Vmn2r111
|
UTSW |
17 |
22,792,085 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R2357:Vmn2r111
|
UTSW |
17 |
22,778,151 (GRCm39) |
splice site |
probably benign |
|
|
R3700:Vmn2r111
|
UTSW |
17 |
22,790,142 (GRCm39) |
nonsense |
probably null |
|
|
R3782:Vmn2r111
|
UTSW |
17 |
22,790,301 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4085:Vmn2r111
|
UTSW |
17 |
22,778,096 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4323:Vmn2r111
|
UTSW |
17 |
22,792,159 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4900:Vmn2r111
|
UTSW |
17 |
22,767,637 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5072:Vmn2r111
|
UTSW |
17 |
22,767,022 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5123:Vmn2r111
|
UTSW |
17 |
22,790,124 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5181:Vmn2r111
|
UTSW |
17 |
22,790,001 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R5357:Vmn2r111
|
UTSW |
17 |
22,767,083 (GRCm39) |
nonsense |
probably null |
|
|
R5398:Vmn2r111
|
UTSW |
17 |
22,792,252 (GRCm39) |
start codon destroyed |
probably null |
0.88 |
|
R5434:Vmn2r111
|
UTSW |
17 |
22,767,470 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5462:Vmn2r111
|
UTSW |
17 |
22,767,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6149:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6149:Vmn2r111
|
UTSW |
17 |
22,767,796 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6207:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6281:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6282:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6283:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6307:Vmn2r111
|
UTSW |
17 |
22,792,070 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6323:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6325:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6367:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6368:Vmn2r111
|
UTSW |
17 |
22,790,889 (GRCm39) |
missense |
probably benign |
0.38 |
|
R6369:Vmn2r111
|
UTSW |
17 |
22,767,583 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6489:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6490:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6546:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6547:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6557:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6654:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6655:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6657:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6659:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6660:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6664:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6798:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6799:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6801:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6893:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6895:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6897:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6922:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6923:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6944:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6945:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7017:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7018:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7024:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7031:Vmn2r111
|
UTSW |
17 |
22,790,226 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7039:Vmn2r111
|
UTSW |
17 |
22,767,165 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7053:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7054:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7055:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7056:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7145:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7146:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7246:Vmn2r111
|
UTSW |
17 |
22,767,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7259:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7260:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7327:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7401:Vmn2r111
|
UTSW |
17 |
22,790,067 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7514:Vmn2r111
|
UTSW |
17 |
22,767,380 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7651:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7781:Vmn2r111
|
UTSW |
17 |
22,789,714 (GRCm39) |
missense |
probably benign |
0.17 |
|
R7816:Vmn2r111
|
UTSW |
17 |
22,792,083 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7821:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R7838:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8078:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8080:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8117:Vmn2r111
|
UTSW |
17 |
22,790,469 (GRCm39) |
missense |
probably benign |
0.12 |
|
R8171:Vmn2r111
|
UTSW |
17 |
22,792,073 (GRCm39) |
missense |
probably benign |
0.10 |
|
R8195:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8197:Vmn2r111
|
UTSW |
17 |
22,778,032 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R8411:Vmn2r111
|
UTSW |
17 |
22,767,562 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8539:Vmn2r111
|
UTSW |
17 |
22,790,274 (GRCm39) |
missense |
probably benign |
0.23 |
|
R8540:Vmn2r111
|
UTSW |
17 |
22,778,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8540:Vmn2r111
|
UTSW |
17 |
22,778,023 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8557:Vmn2r111
|
UTSW |
17 |
22,790,910 (GRCm39) |
nonsense |
probably null |
|
|
R8720:Vmn2r111
|
UTSW |
17 |
22,792,194 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8729:Vmn2r111
|
UTSW |
17 |
22,767,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8843:Vmn2r111
|
UTSW |
17 |
22,767,011 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9184:Vmn2r111
|
UTSW |
17 |
22,790,822 (GRCm39) |
missense |
probably benign |
|
|
R9374:Vmn2r111
|
UTSW |
17 |
22,787,859 (GRCm39) |
missense |
probably benign |
0.17 |
|
R9452:Vmn2r111
|
UTSW |
17 |
22,778,132 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0026:Vmn2r111
|
UTSW |
17 |
22,767,676 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCACTTGCTTTGGGCATTTACAGTC -3'
(R):5'- ACAGTGTGCTTTGCCTTTGTCAAC -3'
Sequencing Primer
(F):5'- GTCCTTGGGCAGATTATCAAAC -3'
(R):5'- GTCAAGAGCTGAAGTGTATTACAACC -3'
|
| Posted On |
2014-03-28 |
Incidental Mutation