Incidental Mutation 'R4654:Vmn2r68'
| ID |
351546 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r68
|
| Ensembl Gene |
ENSMUSG00000096861 |
| Gene Name |
vomeronasal 2, receptor 68 |
| Synonyms |
EG620697, Vmn2r68-ps |
| MMRRC Submission |
041914-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.085)
|
| Stock # |
R4654 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
84870726-84886912 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 84882769 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 328
(Q328*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000129411
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061074]
|
| AlphaFold |
L7N2B3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000061074
AA Change: Q328*
|
| SMART Domains |
Protein: ENSMUSP00000129411
Gene: ENSMUSG00000096861
AA Change: Q328*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
77 |
463 |
4.5e-28 |
PFAM |
|
Pfam:NCD3G
|
507 |
559 |
1.1e-18 |
PFAM |
|
Pfam:7tm_3
|
589 |
827 |
3.7e-53 |
PFAM |
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.2%
- 20x: 95.2%
|
| Validation Efficiency |
97% (98/101) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam3 |
A |
T |
8: 25,193,819 (GRCm39) |
C398S |
probably damaging |
Het |
| Adamts10 |
A |
G |
17: 33,756,304 (GRCm39) |
K316E |
possibly damaging |
Het |
| Ap1m1 |
T |
C |
8: 73,006,717 (GRCm39) |
F238L |
possibly damaging |
Het |
| Aph1a |
T |
A |
3: 95,803,088 (GRCm39) |
D180E |
probably benign |
Het |
| Atp9b |
A |
G |
18: 80,935,093 (GRCm39) |
F201L |
probably benign |
Het |
| Btbd9 |
A |
C |
17: 30,704,561 (GRCm39) |
|
probably benign |
Het |
| C2cd5 |
T |
C |
6: 142,975,910 (GRCm39) |
T768A |
probably benign |
Het |
| Casq1 |
C |
T |
1: 172,037,965 (GRCm39) |
|
probably benign |
Het |
| Cimap2 |
C |
A |
4: 106,467,612 (GRCm39) |
M341I |
probably benign |
Het |
| Cltc |
A |
T |
11: 86,617,196 (GRCm39) |
M351K |
probably benign |
Het |
| Cnp |
A |
G |
11: 100,469,877 (GRCm39) |
E271G |
possibly damaging |
Het |
| Col22a1 |
T |
C |
15: 71,845,544 (GRCm39) |
D406G |
possibly damaging |
Het |
| Cylc2 |
T |
C |
4: 51,228,279 (GRCm39) |
S117P |
probably benign |
Het |
| Cyp2b13 |
T |
C |
7: 25,761,072 (GRCm39) |
L43P |
probably damaging |
Het |
| Cyp3a16 |
A |
G |
5: 145,373,267 (GRCm39) |
V500A |
probably benign |
Het |
| Dclk2 |
T |
C |
3: 86,743,683 (GRCm39) |
D262G |
probably damaging |
Het |
| Dcun1d3 |
A |
C |
7: 119,458,742 (GRCm39) |
Y98D |
probably damaging |
Het |
| Ddx39b |
A |
G |
17: 35,472,464 (GRCm39) |
*429W |
probably null |
Het |
| Dennd5b |
T |
C |
6: 148,908,335 (GRCm39) |
N986S |
probably damaging |
Het |
| Dipk1a |
T |
C |
5: 108,057,982 (GRCm39) |
|
probably null |
Het |
| Dusp9 |
G |
A |
X: 72,684,378 (GRCm39) |
R182Q |
probably benign |
Het |
| Ecpas |
A |
T |
4: 58,834,523 (GRCm39) |
I785N |
possibly damaging |
Het |
| Edil3 |
A |
G |
13: 89,437,589 (GRCm39) |
K397E |
probably damaging |
Het |
| Ehd1 |
T |
C |
19: 6,326,994 (GRCm39) |
|
probably benign |
Het |
| Fam13a |
A |
T |
6: 58,964,152 (GRCm39) |
H93Q |
probably benign |
Het |
| Farp1 |
T |
C |
14: 121,513,716 (GRCm39) |
I837T |
possibly damaging |
Het |
| Fbxl5 |
T |
A |
5: 43,922,771 (GRCm39) |
I216F |
probably damaging |
Het |
| Gadl1 |
G |
A |
9: 115,770,408 (GRCm39) |
E74K |
probably damaging |
Het |
| Gnpnat1 |
A |
G |
14: 45,618,436 (GRCm39) |
V122A |
probably damaging |
Het |
| Hdac10 |
C |
T |
15: 89,011,036 (GRCm39) |
|
probably benign |
Het |
| Heatr5b |
T |
C |
17: 79,128,130 (GRCm39) |
S502G |
possibly damaging |
Het |
| Hr |
C |
A |
14: 70,801,013 (GRCm39) |
A695E |
probably damaging |
Het |
| Ift80 |
A |
T |
3: 68,825,870 (GRCm39) |
I490N |
possibly damaging |
Het |
| Ipo11 |
A |
G |
13: 106,970,692 (GRCm39) |
|
probably benign |
Het |
| Iqch |
T |
G |
9: 63,432,195 (GRCm39) |
Y400S |
probably damaging |
Het |
| Jag2 |
C |
T |
12: 112,877,266 (GRCm39) |
D702N |
probably benign |
Het |
| Kiss1r |
T |
A |
10: 79,757,624 (GRCm39) |
L326Q |
probably damaging |
Het |
| Lrrc42 |
A |
T |
4: 107,104,746 (GRCm39) |
I73N |
probably damaging |
Het |
| Lrrc55 |
C |
T |
2: 85,026,880 (GRCm39) |
G48D |
possibly damaging |
Het |
| Lrrk2 |
T |
C |
15: 91,649,884 (GRCm39) |
S1674P |
probably damaging |
Het |
| Mctp2 |
A |
G |
7: 71,739,942 (GRCm39) |
L816P |
probably damaging |
Het |
| Mipol1 |
A |
T |
12: 57,352,918 (GRCm39) |
T86S |
probably benign |
Het |
| Mkrn3 |
C |
T |
7: 62,069,452 (GRCm39) |
R113H |
probably damaging |
Het |
| Mmp1b |
A |
G |
9: 7,370,849 (GRCm39) |
V302A |
probably benign |
Het |
| Msc |
A |
T |
1: 14,826,053 (GRCm39) |
|
probably null |
Het |
| Msmo1 |
C |
A |
8: 65,180,888 (GRCm39) |
V9L |
probably benign |
Het |
| Nbeal2 |
G |
A |
9: 110,461,072 (GRCm39) |
R1630C |
probably damaging |
Het |
| Nlgn1 |
C |
T |
3: 26,187,850 (GRCm39) |
V12I |
possibly damaging |
Het |
| Npas3 |
T |
C |
12: 54,108,915 (GRCm39) |
|
probably null |
Het |
| Nr2e3 |
A |
G |
9: 59,856,355 (GRCm39) |
|
probably benign |
Het |
| Oca2 |
C |
T |
7: 55,978,560 (GRCm39) |
A576V |
probably benign |
Het |
| Or5b21 |
T |
A |
19: 12,839,596 (GRCm39) |
C152* |
probably null |
Het |
| Or6d12 |
T |
C |
6: 116,493,409 (GRCm39) |
Y224H |
probably damaging |
Het |
| Or6z7 |
T |
C |
7: 6,484,045 (GRCm39) |
T37A |
probably benign |
Het |
| Parp6 |
A |
G |
9: 59,548,383 (GRCm39) |
|
probably null |
Het |
| Pate13 |
T |
A |
9: 35,820,287 (GRCm39) |
C4S |
probably damaging |
Het |
| Phlpp1 |
A |
T |
1: 106,267,231 (GRCm39) |
M715L |
probably benign |
Het |
| Pi4k2a |
G |
A |
19: 42,101,544 (GRCm39) |
|
probably null |
Het |
| Pik3ap1 |
A |
G |
19: 41,316,348 (GRCm39) |
S305P |
probably damaging |
Het |
| Plcg2 |
G |
A |
8: 118,231,054 (GRCm39) |
M45I |
probably benign |
Het |
| Ppm1m |
A |
T |
9: 106,073,601 (GRCm39) |
L317H |
probably damaging |
Het |
| Ppp1r21 |
T |
G |
17: 88,866,227 (GRCm39) |
M341R |
probably benign |
Het |
| Prdx3 |
A |
G |
19: 60,853,674 (GRCm39) |
V217A |
possibly damaging |
Het |
| Ptk2b |
A |
G |
14: 66,400,496 (GRCm39) |
V773A |
possibly damaging |
Het |
| Raly |
T |
C |
2: 154,699,376 (GRCm39) |
V60A |
probably damaging |
Het |
| Reps1 |
A |
G |
10: 17,990,148 (GRCm39) |
D420G |
probably damaging |
Het |
| Rev1 |
A |
T |
1: 38,118,337 (GRCm39) |
|
probably benign |
Het |
| Rgs2 |
T |
G |
1: 143,878,650 (GRCm39) |
|
probably benign |
Het |
| Rlf |
G |
T |
4: 121,007,798 (GRCm39) |
T394K |
probably benign |
Het |
| Rptn |
A |
T |
3: 93,304,792 (GRCm39) |
R708S |
possibly damaging |
Het |
| Sec23b |
T |
A |
2: 144,414,494 (GRCm39) |
M402K |
probably benign |
Het |
| Skic2 |
A |
G |
17: 35,068,922 (GRCm39) |
C26R |
probably damaging |
Het |
| Slx9 |
T |
C |
10: 77,325,860 (GRCm39) |
M170V |
possibly damaging |
Het |
| Smpd4 |
A |
G |
16: 17,459,992 (GRCm39) |
|
probably benign |
Het |
| Synj2 |
A |
G |
17: 6,063,813 (GRCm39) |
E434G |
probably damaging |
Het |
| Tatdn2 |
T |
A |
6: 113,684,326 (GRCm39) |
F64I |
probably benign |
Het |
| Tex21 |
A |
C |
12: 76,263,860 (GRCm39) |
H177Q |
probably benign |
Het |
| Tln1 |
T |
A |
4: 43,535,954 (GRCm39) |
Q2077L |
probably null |
Het |
| Tnrc6c |
T |
C |
11: 117,611,797 (GRCm39) |
V145A |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,616,936 (GRCm39) |
|
probably benign |
Het |
| Uggt2 |
A |
G |
14: 119,269,670 (GRCm39) |
F954S |
possibly damaging |
Het |
| Ugt2a1 |
A |
G |
5: 87,634,083 (GRCm39) |
S175P |
probably damaging |
Het |
| Vcl |
A |
G |
14: 21,035,820 (GRCm39) |
|
probably null |
Het |
| Vegfa |
A |
T |
17: 46,336,176 (GRCm39) |
|
probably benign |
Het |
| Vmn2r7 |
A |
G |
3: 64,626,864 (GRCm39) |
Y142H |
probably benign |
Het |
| Wdr17 |
C |
T |
8: 55,134,434 (GRCm39) |
G349R |
probably damaging |
Het |
| Ybx3 |
G |
T |
6: 131,347,290 (GRCm39) |
R282S |
probably damaging |
Het |
| Zfp566 |
T |
C |
7: 29,777,194 (GRCm39) |
H329R |
probably damaging |
Het |
| Zfp786 |
T |
C |
6: 47,797,868 (GRCm39) |
I357V |
probably benign |
Het |
| Zfr2 |
C |
A |
10: 81,087,083 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Vmn2r68 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01391:Vmn2r68
|
APN |
7 |
84,886,819 (GRCm39) |
missense |
probably benign |
|
|
IGL01477:Vmn2r68
|
APN |
7 |
84,882,691 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01600:Vmn2r68
|
APN |
7 |
84,871,468 (GRCm39) |
missense |
probably benign |
0.39 |
|
IGL01979:Vmn2r68
|
APN |
7 |
84,871,325 (GRCm39) |
missense |
probably benign |
|
|
IGL01999:Vmn2r68
|
APN |
7 |
84,871,439 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02269:Vmn2r68
|
APN |
7 |
84,870,947 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
IGL02517:Vmn2r68
|
APN |
7 |
84,871,153 (GRCm39) |
nonsense |
probably null |
|
|
IGL02827:Vmn2r68
|
APN |
7 |
84,886,800 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02852:Vmn2r68
|
APN |
7 |
84,882,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02982:Vmn2r68
|
APN |
7 |
84,883,649 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL03099:Vmn2r68
|
APN |
7 |
84,871,448 (GRCm39) |
nonsense |
probably null |
|
|
IGL03166:Vmn2r68
|
APN |
7 |
84,871,331 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03168:Vmn2r68
|
APN |
7 |
84,870,972 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03243:Vmn2r68
|
APN |
7 |
84,882,963 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
F5770:Vmn2r68
|
UTSW |
7 |
84,871,088 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0280:Vmn2r68
|
UTSW |
7 |
84,882,466 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0280:Vmn2r68
|
UTSW |
7 |
84,882,457 (GRCm39) |
splice site |
probably benign |
|
|
R0281:Vmn2r68
|
UTSW |
7 |
84,882,466 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0281:Vmn2r68
|
UTSW |
7 |
84,882,457 (GRCm39) |
splice site |
probably benign |
|
|
R0348:Vmn2r68
|
UTSW |
7 |
84,870,884 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R0390:Vmn2r68
|
UTSW |
7 |
84,882,466 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0390:Vmn2r68
|
UTSW |
7 |
84,882,457 (GRCm39) |
splice site |
probably benign |
|
|
R0722:Vmn2r68
|
UTSW |
7 |
84,870,794 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1129:Vmn2r68
|
UTSW |
7 |
84,886,712 (GRCm39) |
splice site |
probably null |
|
|
R1136:Vmn2r68
|
UTSW |
7 |
84,871,549 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1319:Vmn2r68
|
UTSW |
7 |
84,881,700 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1614:Vmn2r68
|
UTSW |
7 |
84,870,946 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1682:Vmn2r68
|
UTSW |
7 |
84,882,574 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1837:Vmn2r68
|
UTSW |
7 |
84,882,886 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1893:Vmn2r68
|
UTSW |
7 |
84,883,867 (GRCm39) |
nonsense |
probably null |
|
|
R1908:Vmn2r68
|
UTSW |
7 |
84,883,260 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1909:Vmn2r68
|
UTSW |
7 |
84,883,260 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1951:Vmn2r68
|
UTSW |
7 |
84,883,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2177:Vmn2r68
|
UTSW |
7 |
84,871,123 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2178:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R2185:Vmn2r68
|
UTSW |
7 |
84,882,901 (GRCm39) |
nonsense |
probably null |
|
|
R2188:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R2282:Vmn2r68
|
UTSW |
7 |
84,870,859 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R2567:Vmn2r68
|
UTSW |
7 |
84,883,803 (GRCm39) |
missense |
probably benign |
|
|
R2869:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2869:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2870:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2870:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2871:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2871:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2873:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2874:Vmn2r68
|
UTSW |
7 |
84,882,834 (GRCm39) |
missense |
probably benign |
0.25 |
|
R3149:Vmn2r68
|
UTSW |
7 |
84,886,875 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3401:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R3978:Vmn2r68
|
UTSW |
7 |
84,881,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4399:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4401:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4421:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4478:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4479:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4495:Vmn2r68
|
UTSW |
7 |
84,870,758 (GRCm39) |
frame shift |
probably null |
|
|
R4628:Vmn2r68
|
UTSW |
7 |
84,883,673 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4649:Vmn2r68
|
UTSW |
7 |
84,870,743 (GRCm39) |
missense |
probably benign |
|
|
R4793:Vmn2r68
|
UTSW |
7 |
84,883,648 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5007:Vmn2r68
|
UTSW |
7 |
84,881,622 (GRCm39) |
missense |
probably benign |
|
|
R5021:Vmn2r68
|
UTSW |
7 |
84,882,942 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R5082:Vmn2r68
|
UTSW |
7 |
84,883,076 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5177:Vmn2r68
|
UTSW |
7 |
84,871,199 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5221:Vmn2r68
|
UTSW |
7 |
84,871,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5514:Vmn2r68
|
UTSW |
7 |
84,886,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5521:Vmn2r68
|
UTSW |
7 |
84,882,926 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5563:Vmn2r68
|
UTSW |
7 |
84,871,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5664:Vmn2r68
|
UTSW |
7 |
84,882,978 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5829:Vmn2r68
|
UTSW |
7 |
84,886,812 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6016:Vmn2r68
|
UTSW |
7 |
84,871,453 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6356:Vmn2r68
|
UTSW |
7 |
84,883,048 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6413:Vmn2r68
|
UTSW |
7 |
84,870,973 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6418:Vmn2r68
|
UTSW |
7 |
84,882,915 (GRCm39) |
missense |
probably benign |
|
|
R6699:Vmn2r68
|
UTSW |
7 |
84,881,583 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R7287:Vmn2r68
|
UTSW |
7 |
84,871,460 (GRCm39) |
missense |
probably benign |
0.33 |
|
R7319:Vmn2r68
|
UTSW |
7 |
84,883,042 (GRCm39) |
missense |
probably benign |
|
|
R7374:Vmn2r68
|
UTSW |
7 |
84,881,607 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R7585:Vmn2r68
|
UTSW |
7 |
84,881,587 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7605:Vmn2r68
|
UTSW |
7 |
84,883,116 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7892:Vmn2r68
|
UTSW |
7 |
84,883,722 (GRCm39) |
missense |
probably benign |
|
|
R7979:Vmn2r68
|
UTSW |
7 |
84,883,625 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8177:Vmn2r68
|
UTSW |
7 |
84,871,422 (GRCm39) |
nonsense |
probably null |
|
|
R8349:Vmn2r68
|
UTSW |
7 |
84,882,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8378:Vmn2r68
|
UTSW |
7 |
84,871,108 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8397:Vmn2r68
|
UTSW |
7 |
84,886,722 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8449:Vmn2r68
|
UTSW |
7 |
84,882,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8543:Vmn2r68
|
UTSW |
7 |
84,883,648 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8680:Vmn2r68
|
UTSW |
7 |
84,871,321 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R9056:Vmn2r68
|
UTSW |
7 |
84,871,420 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R9342:Vmn2r68
|
UTSW |
7 |
84,882,993 (GRCm39) |
missense |
probably benign |
0.39 |
|
R9734:Vmn2r68
|
UTSW |
7 |
84,882,757 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
V7581:Vmn2r68
|
UTSW |
7 |
84,871,088 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
84,871,289 (GRCm39) |
missense |
probably benign |
0.27 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
84,870,941 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
84,871,307 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATGGGCCACAGCATGTATAG -3'
(R):5'- GGAGACTACACCTCTCCCATAG -3'
Sequencing Primer
(F):5'- GCCACAGCATGTATAGCATTG -3'
(R):5'- AGACTACACCTCTCCCATAGATCTTG -3'
|
| Posted On |
2015-10-08 |
Incidental Mutation