Incidental Mutation 'R4654:Vmn2r68'
| ID |
351546 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r68
|
| Ensembl Gene |
ENSMUSG00000096861 |
| Gene Name |
vomeronasal 2, receptor 68 |
| Synonyms |
Vmn2r68-ps, EG620697 |
| MMRRC Submission |
041914-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.084)
|
| Stock # |
R4654 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
85221518-85237704 bp(-) (GRCm38) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 85233561 bp (GRCm38)
|
| 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 |
|---|
| 9230113P08Rik |
T |
A |
9: 35,908,991 (GRCm38) |
C4S |
probably damaging |
Het |
| Adam3 |
A |
T |
8: 24,703,803 (GRCm38) |
C398S |
probably damaging |
Het |
| Adamts10 |
A |
G |
17: 33,537,330 (GRCm38) |
K316E |
possibly damaging |
Het |
| AI314180 |
A |
T |
4: 58,834,523 (GRCm38) |
I785N |
possibly damaging |
Het |
| Ap1m1 |
T |
C |
8: 72,252,873 (GRCm38) |
F238L |
possibly damaging |
Het |
| Aph1a |
T |
A |
3: 95,895,776 (GRCm38) |
D180E |
probably benign |
Het |
| Atp9b |
A |
G |
18: 80,891,878 (GRCm38) |
F201L |
probably benign |
Het |
| Btbd9 |
A |
C |
17: 30,485,587 (GRCm38) |
|
probably benign |
Het |
| C2cd5 |
T |
C |
6: 143,030,184 (GRCm38) |
T768A |
probably benign |
Het |
| Casq1 |
C |
T |
1: 172,210,398 (GRCm38) |
|
probably benign |
Het |
| Cltc |
A |
T |
11: 86,726,370 (GRCm38) |
M351K |
probably benign |
Het |
| Cnp |
A |
G |
11: 100,579,051 (GRCm38) |
E271G |
possibly damaging |
Het |
| Col22a1 |
T |
C |
15: 71,973,695 (GRCm38) |
D406G |
possibly damaging |
Het |
| Cylc2 |
T |
C |
4: 51,228,279 (GRCm38) |
S117P |
probably benign |
Het |
| Cyp2b13 |
T |
C |
7: 26,061,647 (GRCm38) |
L43P |
probably damaging |
Het |
| Cyp3a16 |
A |
G |
5: 145,436,457 (GRCm38) |
V500A |
probably benign |
Het |
| Dclk2 |
T |
C |
3: 86,836,376 (GRCm38) |
D262G |
probably damaging |
Het |
| Dcun1d3 |
A |
C |
7: 119,859,519 (GRCm38) |
Y98D |
probably damaging |
Het |
| Ddx39b |
A |
G |
17: 35,253,488 (GRCm38) |
*429W |
probably null |
Het |
| Dennd5b |
T |
C |
6: 149,006,837 (GRCm38) |
N986S |
probably damaging |
Het |
| Dusp9 |
G |
A |
X: 73,640,772 (GRCm38) |
R182Q |
probably benign |
Het |
| Edil3 |
A |
G |
13: 89,289,470 (GRCm38) |
K397E |
probably damaging |
Het |
| Ehd1 |
T |
C |
19: 6,276,964 (GRCm38) |
|
probably benign |
Het |
| Fam13a |
A |
T |
6: 58,987,167 (GRCm38) |
H93Q |
probably benign |
Het |
| Fam207a |
T |
C |
10: 77,490,026 (GRCm38) |
M170V |
possibly damaging |
Het |
| Fam69a |
T |
C |
5: 107,910,116 (GRCm38) |
|
probably null |
Het |
| Farp1 |
T |
C |
14: 121,276,304 (GRCm38) |
I837T |
possibly damaging |
Het |
| Fbxl5 |
T |
A |
5: 43,765,429 (GRCm38) |
I216F |
probably damaging |
Het |
| Gadl1 |
G |
A |
9: 115,941,340 (GRCm38) |
E74K |
probably damaging |
Het |
| Gnpnat1 |
A |
G |
14: 45,380,979 (GRCm38) |
V122A |
probably damaging |
Het |
| Hdac10 |
C |
T |
15: 89,126,833 (GRCm38) |
|
probably benign |
Het |
| Heatr5b |
T |
C |
17: 78,820,701 (GRCm38) |
S502G |
possibly damaging |
Het |
| Hr |
C |
A |
14: 70,563,573 (GRCm38) |
A695E |
probably damaging |
Het |
| Ift80 |
A |
T |
3: 68,918,537 (GRCm38) |
I490N |
possibly damaging |
Het |
| Ipo11 |
A |
G |
13: 106,834,184 (GRCm38) |
|
probably benign |
Het |
| Iqch |
T |
G |
9: 63,524,913 (GRCm38) |
Y400S |
probably damaging |
Het |
| Jag2 |
C |
T |
12: 112,913,646 (GRCm38) |
D702N |
probably benign |
Het |
| Kiss1r |
T |
A |
10: 79,921,790 (GRCm38) |
L326Q |
probably damaging |
Het |
| Lexm |
C |
A |
4: 106,610,415 (GRCm38) |
M341I |
probably benign |
Het |
| Lrrc42 |
A |
T |
4: 107,247,549 (GRCm38) |
I73N |
probably damaging |
Het |
| Lrrc55 |
C |
T |
2: 85,196,536 (GRCm38) |
G48D |
possibly damaging |
Het |
| Lrrk2 |
T |
C |
15: 91,765,681 (GRCm38) |
S1674P |
probably damaging |
Het |
| Mctp2 |
A |
G |
7: 72,090,194 (GRCm38) |
L816P |
probably damaging |
Het |
| Mipol1 |
A |
T |
12: 57,306,132 (GRCm38) |
T86S |
probably benign |
Het |
| Mkrn3 |
C |
T |
7: 62,419,704 (GRCm38) |
R113H |
probably damaging |
Het |
| Mmp1b |
A |
G |
9: 7,370,849 (GRCm38) |
V302A |
probably benign |
Het |
| Msc |
A |
T |
1: 14,755,829 (GRCm38) |
|
probably null |
Het |
| Msmo1 |
C |
A |
8: 64,727,854 (GRCm38) |
V9L |
probably benign |
Het |
| Nbeal2 |
G |
A |
9: 110,632,004 (GRCm38) |
R1630C |
probably damaging |
Het |
| Nlgn1 |
C |
T |
3: 26,133,701 (GRCm38) |
V12I |
possibly damaging |
Het |
| Npas3 |
T |
C |
12: 54,062,132 (GRCm38) |
|
probably null |
Het |
| Nr2e3 |
A |
G |
9: 59,949,072 (GRCm38) |
|
probably benign |
Het |
| Oca2 |
C |
T |
7: 56,328,812 (GRCm38) |
A576V |
probably benign |
Het |
| Olfr1444 |
T |
A |
19: 12,862,232 (GRCm38) |
C152* |
probably null |
Het |
| Olfr212 |
T |
C |
6: 116,516,448 (GRCm38) |
Y224H |
probably damaging |
Het |
| Olfr5 |
T |
C |
7: 6,481,046 (GRCm38) |
T37A |
probably benign |
Het |
| Parp6 |
A |
G |
9: 59,641,100 (GRCm38) |
|
probably null |
Het |
| Phlpp1 |
A |
T |
1: 106,339,501 (GRCm38) |
M715L |
probably benign |
Het |
| Pi4k2a |
G |
A |
19: 42,113,105 (GRCm38) |
|
probably null |
Het |
| Pik3ap1 |
A |
G |
19: 41,327,909 (GRCm38) |
S305P |
probably damaging |
Het |
| Plcg2 |
G |
A |
8: 117,504,315 (GRCm38) |
M45I |
probably benign |
Het |
| Ppm1m |
A |
T |
9: 106,196,402 (GRCm38) |
L317H |
probably damaging |
Het |
| Ppp1r21 |
T |
G |
17: 88,558,799 (GRCm38) |
M341R |
probably benign |
Het |
| Prdx3 |
A |
G |
19: 60,865,236 (GRCm38) |
V217A |
possibly damaging |
Het |
| Ptk2b |
A |
G |
14: 66,163,047 (GRCm38) |
V773A |
possibly damaging |
Het |
| Raly |
T |
C |
2: 154,857,456 (GRCm38) |
V60A |
probably damaging |
Het |
| Reps1 |
A |
G |
10: 18,114,400 (GRCm38) |
D420G |
probably damaging |
Het |
| Rev1 |
A |
T |
1: 38,079,256 (GRCm38) |
|
probably benign |
Het |
| Rgs2 |
T |
G |
1: 144,002,912 (GRCm38) |
|
probably benign |
Het |
| Rlf |
G |
T |
4: 121,150,601 (GRCm38) |
T394K |
probably benign |
Het |
| Rptn |
A |
T |
3: 93,397,485 (GRCm38) |
R708S |
possibly damaging |
Het |
| Sec23b |
T |
A |
2: 144,572,574 (GRCm38) |
M402K |
probably benign |
Het |
| Skiv2l |
A |
G |
17: 34,849,946 (GRCm38) |
C26R |
probably damaging |
Het |
| Smpd4 |
A |
G |
16: 17,642,128 (GRCm38) |
|
probably benign |
Het |
| Synj2 |
A |
G |
17: 6,013,538 (GRCm38) |
E434G |
probably damaging |
Het |
| Tatdn2 |
T |
A |
6: 113,707,365 (GRCm38) |
F64I |
probably benign |
Het |
| Tex21 |
A |
C |
12: 76,217,086 (GRCm38) |
H177Q |
probably benign |
Het |
| Tln1 |
T |
A |
4: 43,535,954 (GRCm38) |
Q2077L |
probably null |
Het |
| Tnrc6c |
T |
C |
11: 117,720,971 (GRCm38) |
V145A |
probably benign |
Het |
| Ttn |
C |
T |
2: 76,786,592 (GRCm38) |
|
probably benign |
Het |
| Uggt2 |
A |
G |
14: 119,032,258 (GRCm38) |
F954S |
possibly damaging |
Het |
| Ugt2a1 |
A |
G |
5: 87,486,224 (GRCm38) |
S175P |
probably damaging |
Het |
| Vcl |
A |
G |
14: 20,985,752 (GRCm38) |
|
probably null |
Het |
| Vegfa |
A |
T |
17: 46,025,250 (GRCm38) |
|
probably benign |
Het |
| Vmn2r7 |
A |
G |
3: 64,719,443 (GRCm38) |
Y142H |
probably benign |
Het |
| Wdr17 |
C |
T |
8: 54,681,399 (GRCm38) |
G349R |
probably damaging |
Het |
| Ybx3 |
G |
T |
6: 131,370,327 (GRCm38) |
R282S |
probably damaging |
Het |
| Zfp566 |
T |
C |
7: 30,077,769 (GRCm38) |
H329R |
probably damaging |
Het |
| Zfp786 |
T |
C |
6: 47,820,934 (GRCm38) |
I357V |
probably benign |
Het |
| Zfr2 |
C |
A |
10: 81,251,249 (GRCm38) |
|
probably null |
Het |
|
| Other mutations in Vmn2r68 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01391:Vmn2r68
|
APN |
7 |
85,237,611 (GRCm38) |
missense |
probably benign |
|
|
IGL01477:Vmn2r68
|
APN |
7 |
85,233,483 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01600:Vmn2r68
|
APN |
7 |
85,222,260 (GRCm38) |
missense |
probably benign |
0.39 |
|
IGL01979:Vmn2r68
|
APN |
7 |
85,222,117 (GRCm38) |
missense |
probably benign |
|
|
IGL01999:Vmn2r68
|
APN |
7 |
85,222,231 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02269:Vmn2r68
|
APN |
7 |
85,221,739 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
IGL02517:Vmn2r68
|
APN |
7 |
85,221,945 (GRCm38) |
nonsense |
probably null |
|
|
IGL02827:Vmn2r68
|
APN |
7 |
85,237,592 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02852:Vmn2r68
|
APN |
7 |
85,233,387 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02982:Vmn2r68
|
APN |
7 |
85,234,441 (GRCm38) |
missense |
probably benign |
0.12 |
|
IGL03099:Vmn2r68
|
APN |
7 |
85,222,240 (GRCm38) |
nonsense |
probably null |
|
|
IGL03166:Vmn2r68
|
APN |
7 |
85,222,123 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL03168:Vmn2r68
|
APN |
7 |
85,221,764 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03243:Vmn2r68
|
APN |
7 |
85,233,755 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
F5770:Vmn2r68
|
UTSW |
7 |
85,221,880 (GRCm38) |
missense |
probably benign |
0.01 |
|
R0280:Vmn2r68
|
UTSW |
7 |
85,233,258 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0280:Vmn2r68
|
UTSW |
7 |
85,233,249 (GRCm38) |
splice site |
probably benign |
|
|
R0281:Vmn2r68
|
UTSW |
7 |
85,233,258 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0281:Vmn2r68
|
UTSW |
7 |
85,233,249 (GRCm38) |
splice site |
probably benign |
|
|
R0348:Vmn2r68
|
UTSW |
7 |
85,221,676 (GRCm38) |
missense |
possibly damaging |
0.50 |
|
R0390:Vmn2r68
|
UTSW |
7 |
85,233,258 (GRCm38) |
critical splice donor site |
probably null |
|
|
R0390:Vmn2r68
|
UTSW |
7 |
85,233,249 (GRCm38) |
splice site |
probably benign |
|
|
R0722:Vmn2r68
|
UTSW |
7 |
85,221,586 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R1129:Vmn2r68
|
UTSW |
7 |
85,237,504 (GRCm38) |
splice site |
probably null |
|
|
R1136:Vmn2r68
|
UTSW |
7 |
85,222,341 (GRCm38) |
missense |
possibly damaging |
0.81 |
|
R1319:Vmn2r68
|
UTSW |
7 |
85,232,492 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R1614:Vmn2r68
|
UTSW |
7 |
85,221,738 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R1682:Vmn2r68
|
UTSW |
7 |
85,233,366 (GRCm38) |
missense |
possibly damaging |
0.68 |
|
R1837:Vmn2r68
|
UTSW |
7 |
85,233,678 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R1893:Vmn2r68
|
UTSW |
7 |
85,234,659 (GRCm38) |
nonsense |
probably null |
|
|
R1908:Vmn2r68
|
UTSW |
7 |
85,234,052 (GRCm38) |
missense |
probably benign |
0.09 |
|
R1909:Vmn2r68
|
UTSW |
7 |
85,234,052 (GRCm38) |
missense |
probably benign |
0.09 |
|
R1951:Vmn2r68
|
UTSW |
7 |
85,233,894 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2177:Vmn2r68
|
UTSW |
7 |
85,221,915 (GRCm38) |
missense |
probably benign |
0.01 |
|
R2178:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R2185:Vmn2r68
|
UTSW |
7 |
85,233,693 (GRCm38) |
nonsense |
probably null |
|
|
R2188:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R2282:Vmn2r68
|
UTSW |
7 |
85,221,651 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R2567:Vmn2r68
|
UTSW |
7 |
85,234,595 (GRCm38) |
missense |
probably benign |
|
|
R2869:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2869:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2870:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2870:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2871:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2871:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2873:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R2874:Vmn2r68
|
UTSW |
7 |
85,233,626 (GRCm38) |
missense |
probably benign |
0.25 |
|
R3149:Vmn2r68
|
UTSW |
7 |
85,237,667 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3401:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R3978:Vmn2r68
|
UTSW |
7 |
85,232,462 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4399:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4401:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4421:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4478:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4479:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4495:Vmn2r68
|
UTSW |
7 |
85,221,550 (GRCm38) |
frame shift |
probably null |
|
|
R4628:Vmn2r68
|
UTSW |
7 |
85,234,465 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4649:Vmn2r68
|
UTSW |
7 |
85,221,535 (GRCm38) |
missense |
probably benign |
|
|
R4793:Vmn2r68
|
UTSW |
7 |
85,234,440 (GRCm38) |
missense |
probably benign |
0.01 |
|
R5007:Vmn2r68
|
UTSW |
7 |
85,232,414 (GRCm38) |
missense |
probably benign |
|
|
R5021:Vmn2r68
|
UTSW |
7 |
85,233,734 (GRCm38) |
missense |
possibly damaging |
0.62 |
|
R5082:Vmn2r68
|
UTSW |
7 |
85,233,868 (GRCm38) |
missense |
probably benign |
0.12 |
|
R5177:Vmn2r68
|
UTSW |
7 |
85,221,991 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5221:Vmn2r68
|
UTSW |
7 |
85,221,877 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5514:Vmn2r68
|
UTSW |
7 |
85,237,559 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R5521:Vmn2r68
|
UTSW |
7 |
85,233,718 (GRCm38) |
missense |
probably benign |
0.03 |
|
R5563:Vmn2r68
|
UTSW |
7 |
85,222,075 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5664:Vmn2r68
|
UTSW |
7 |
85,233,770 (GRCm38) |
missense |
probably benign |
0.02 |
|
R5829:Vmn2r68
|
UTSW |
7 |
85,237,604 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6016:Vmn2r68
|
UTSW |
7 |
85,222,245 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6356:Vmn2r68
|
UTSW |
7 |
85,233,840 (GRCm38) |
missense |
possibly damaging |
0.85 |
|
R6413:Vmn2r68
|
UTSW |
7 |
85,221,765 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6418:Vmn2r68
|
UTSW |
7 |
85,233,707 (GRCm38) |
missense |
probably benign |
|
|
R6699:Vmn2r68
|
UTSW |
7 |
85,232,375 (GRCm38) |
missense |
possibly damaging |
0.58 |
|
R7287:Vmn2r68
|
UTSW |
7 |
85,222,252 (GRCm38) |
missense |
probably benign |
0.33 |
|
R7319:Vmn2r68
|
UTSW |
7 |
85,233,834 (GRCm38) |
missense |
probably benign |
|
|
R7374:Vmn2r68
|
UTSW |
7 |
85,232,399 (GRCm38) |
missense |
possibly damaging |
0.66 |
|
R7585:Vmn2r68
|
UTSW |
7 |
85,232,379 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7605:Vmn2r68
|
UTSW |
7 |
85,233,908 (GRCm38) |
missense |
probably benign |
0.01 |
|
R7892:Vmn2r68
|
UTSW |
7 |
85,234,514 (GRCm38) |
missense |
probably benign |
|
|
R7979:Vmn2r68
|
UTSW |
7 |
85,234,417 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8177:Vmn2r68
|
UTSW |
7 |
85,222,214 (GRCm38) |
nonsense |
probably null |
|
|
R8349:Vmn2r68
|
UTSW |
7 |
85,233,577 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8378:Vmn2r68
|
UTSW |
7 |
85,221,900 (GRCm38) |
missense |
probably benign |
0.00 |
|
R8397:Vmn2r68
|
UTSW |
7 |
85,237,514 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R8449:Vmn2r68
|
UTSW |
7 |
85,233,577 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8543:Vmn2r68
|
UTSW |
7 |
85,234,440 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8680:Vmn2r68
|
UTSW |
7 |
85,222,113 (GRCm38) |
missense |
possibly damaging |
0.68 |
|
R9056:Vmn2r68
|
UTSW |
7 |
85,222,212 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R9342:Vmn2r68
|
UTSW |
7 |
85,233,785 (GRCm38) |
missense |
probably benign |
0.39 |
|
R9734:Vmn2r68
|
UTSW |
7 |
85,233,549 (GRCm38) |
missense |
possibly damaging |
0.54 |
|
V7581:Vmn2r68
|
UTSW |
7 |
85,221,880 (GRCm38) |
missense |
probably benign |
0.01 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
85,222,081 (GRCm38) |
missense |
probably benign |
0.27 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
85,221,733 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1176:Vmn2r68
|
UTSW |
7 |
85,222,099 (GRCm38) |
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