Incidental Mutation 'R2044:Vmn2r6'
| ID |
221592 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r6
|
| Ensembl Gene |
ENSMUSG00000090581 |
| Gene Name |
vomeronasal 2, receptor 6 |
| Synonyms |
EG667069, EG620718 |
| MMRRC Submission |
040051-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.198)
|
| Stock # |
R2044 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
64444916-64472855 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 64445262 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 821
(V821A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000135148
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000165012]
[ENSMUST00000176481]
|
| AlphaFold |
H3BK29 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000165012
AA Change: V732A
PolyPhen 2
Score 0.956 (Sensitivity: 0.79; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000131831
Gene: ENSMUSG00000090581
AA Change: V732A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:ANF_receptor
|
1 |
416 |
1.4e-72 |
PFAM |
|
Pfam:Peripla_BP_6
|
58 |
244 |
1.2e-10 |
PFAM |
|
Pfam:NCD3G
|
458 |
511 |
1.8e-17 |
PFAM |
|
Pfam:7tm_3
|
542 |
779 |
3.9e-76 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000176481
AA Change: V821A
PolyPhen 2
Score 0.964 (Sensitivity: 0.78; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000135148
Gene: ENSMUSG00000090581
AA Change: V821A
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
88 |
505 |
9.8e-77 |
PFAM |
|
Pfam:Peripla_BP_6
|
142 |
331 |
3.4e-10 |
PFAM |
|
Pfam:NCD3G
|
547 |
600 |
5.4e-17 |
PFAM |
|
Pfam:7tm_3
|
633 |
867 |
3.9e-47 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.7%
|
| Validation Efficiency |
98% (92/94) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2410137M14Rik |
G |
A |
17: 37,288,986 (GRCm39) |
|
probably benign |
Het |
| Abhd15 |
A |
G |
11: 77,409,164 (GRCm39) |
T293A |
probably benign |
Het |
| Aldh1l1 |
C |
T |
6: 90,539,647 (GRCm39) |
P192L |
probably benign |
Het |
| Aldoart1 |
T |
G |
4: 72,770,779 (GRCm39) |
I10L |
probably benign |
Het |
| Ankhd1 |
G |
A |
18: 36,778,166 (GRCm39) |
G1653D |
probably benign |
Het |
| Ankk1 |
A |
C |
9: 49,330,664 (GRCm39) |
|
probably null |
Het |
| Astn1 |
A |
G |
1: 158,428,072 (GRCm39) |
T748A |
possibly damaging |
Het |
| Bmp7 |
C |
A |
2: 172,781,708 (GRCm39) |
R52L |
possibly damaging |
Het |
| Ccdc33 |
G |
A |
9: 57,938,395 (GRCm39) |
P859S |
possibly damaging |
Het |
| Ccny |
A |
G |
18: 9,449,644 (GRCm39) |
S10P |
probably damaging |
Het |
| Cdc6 |
C |
A |
11: 98,801,287 (GRCm39) |
F179L |
probably benign |
Het |
| Cdc7 |
T |
A |
5: 107,130,998 (GRCm39) |
V491E |
probably benign |
Het |
| Cdh23 |
G |
T |
10: 60,432,509 (GRCm39) |
S138R |
possibly damaging |
Het |
| Cenpc1 |
T |
C |
5: 86,185,614 (GRCm39) |
H299R |
probably benign |
Het |
| Ciart |
A |
T |
3: 95,786,013 (GRCm39) |
M354K |
probably benign |
Het |
| Clasrp |
G |
T |
7: 19,320,640 (GRCm39) |
|
probably benign |
Het |
| Col4a3 |
G |
A |
1: 82,674,040 (GRCm39) |
G1132E |
unknown |
Het |
| Crebbp |
G |
A |
16: 3,902,687 (GRCm39) |
T2184I |
probably benign |
Het |
| Cyp2r1 |
A |
C |
7: 114,149,640 (GRCm39) |
M458R |
probably damaging |
Het |
| Cyp7a1 |
C |
A |
4: 6,275,492 (GRCm39) |
R27M |
probably null |
Het |
| Ddhd2 |
A |
G |
8: 26,242,192 (GRCm39) |
F116L |
probably damaging |
Het |
| Dgkd |
G |
A |
1: 87,855,413 (GRCm39) |
R685K |
probably benign |
Het |
| Dnah2 |
A |
G |
11: 69,415,066 (GRCm39) |
S223P |
probably benign |
Het |
| Exph5 |
A |
T |
9: 53,283,979 (GRCm39) |
R353S |
possibly damaging |
Het |
| F11 |
C |
A |
8: 45,705,155 (GRCm39) |
V129F |
probably benign |
Het |
| F830045P16Rik |
A |
T |
2: 129,301,317 (GRCm39) |
S454T |
possibly damaging |
Het |
| Fam124a |
T |
C |
14: 62,824,656 (GRCm39) |
I50T |
probably damaging |
Het |
| Fam20c |
T |
C |
5: 138,741,982 (GRCm39) |
|
probably null |
Het |
| Fam234b |
A |
G |
6: 135,203,912 (GRCm39) |
T405A |
probably benign |
Het |
| Fbh1 |
C |
A |
2: 11,767,781 (GRCm39) |
V356L |
possibly damaging |
Het |
| Flywch1 |
G |
A |
17: 23,981,287 (GRCm39) |
Q132* |
probably null |
Het |
| Foxo6 |
T |
C |
4: 120,144,166 (GRCm39) |
D95G |
probably benign |
Het |
| Ggt5 |
T |
C |
10: 75,439,921 (GRCm39) |
F174S |
probably damaging |
Het |
| Gm7104 |
G |
A |
12: 88,252,551 (GRCm39) |
|
noncoding transcript |
Het |
| Gpr155 |
A |
G |
2: 73,203,977 (GRCm39) |
L279P |
probably damaging |
Het |
| H2-T23 |
A |
G |
17: 36,343,083 (GRCm39) |
L98P |
probably damaging |
Het |
| H4c16 |
G |
C |
6: 136,781,101 (GRCm39) |
R93G |
possibly damaging |
Het |
| Heatr5a |
A |
G |
12: 52,002,186 (GRCm39) |
V250A |
probably benign |
Het |
| Heyl |
A |
T |
4: 123,135,156 (GRCm39) |
I50F |
probably damaging |
Het |
| Ifitm10 |
A |
T |
7: 141,909,771 (GRCm39) |
S179R |
probably damaging |
Het |
| Isg15 |
A |
T |
4: 156,284,249 (GRCm39) |
I93N |
probably benign |
Het |
| Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
| Itga10 |
G |
A |
3: 96,565,006 (GRCm39) |
V985I |
probably benign |
Het |
| Kcnt2 |
T |
C |
1: 140,302,892 (GRCm39) |
I144T |
probably benign |
Het |
| Klk1 |
A |
C |
7: 43,878,458 (GRCm39) |
K104T |
possibly damaging |
Het |
| Lemd3 |
C |
A |
10: 120,769,347 (GRCm39) |
R654L |
probably damaging |
Het |
| Lmod1 |
A |
T |
1: 135,292,125 (GRCm39) |
M327L |
probably benign |
Het |
| Lonrf2 |
T |
C |
1: 38,846,131 (GRCm39) |
E347G |
probably benign |
Het |
| Ltbp1 |
A |
G |
17: 75,583,427 (GRCm39) |
Y409C |
probably damaging |
Het |
| Mecom |
A |
T |
3: 30,034,741 (GRCm39) |
Y312N |
probably damaging |
Het |
| Mmut |
A |
G |
17: 41,252,342 (GRCm39) |
T295A |
probably benign |
Het |
| Mrgprb3 |
C |
T |
7: 48,293,482 (GRCm39) |
C23Y |
possibly damaging |
Het |
| Nadk |
C |
A |
4: 155,669,898 (GRCm39) |
L194I |
probably damaging |
Het |
| Naxd |
A |
G |
8: 11,559,510 (GRCm39) |
I182V |
probably benign |
Het |
| Nbeal1 |
T |
A |
1: 60,358,846 (GRCm39) |
I1176K |
probably damaging |
Het |
| Nol4l |
C |
A |
2: 153,371,441 (GRCm39) |
R81L |
possibly damaging |
Het |
| Odad3 |
T |
G |
9: 21,903,154 (GRCm39) |
T419P |
possibly damaging |
Het |
| Or4k47 |
T |
A |
2: 111,452,159 (GRCm39) |
R87W |
probably benign |
Het |
| Or8g36 |
A |
T |
9: 39,422,674 (GRCm39) |
M114K |
probably damaging |
Het |
| Or9s15 |
G |
T |
1: 92,524,691 (GRCm39) |
R150L |
probably benign |
Het |
| Pcdh18 |
A |
G |
3: 49,709,389 (GRCm39) |
V642A |
probably benign |
Het |
| Pdzk1 |
G |
A |
3: 96,763,164 (GRCm39) |
|
probably benign |
Het |
| Per3 |
C |
T |
4: 151,118,395 (GRCm39) |
V233I |
probably benign |
Het |
| Pisd |
G |
A |
5: 32,922,140 (GRCm39) |
P267S |
possibly damaging |
Het |
| Prm1 |
T |
A |
16: 10,614,357 (GRCm39) |
|
probably benign |
Het |
| Ptprj |
A |
G |
2: 90,293,439 (GRCm39) |
V548A |
probably damaging |
Het |
| Ranbp3 |
G |
A |
17: 56,980,367 (GRCm39) |
|
probably benign |
Het |
| Raver2 |
T |
A |
4: 100,960,009 (GRCm39) |
V163D |
probably damaging |
Het |
| Rbm14 |
A |
T |
19: 4,853,905 (GRCm39) |
I159N |
possibly damaging |
Het |
| Rfx6 |
G |
A |
10: 51,594,222 (GRCm39) |
V381I |
probably benign |
Het |
| Rhobtb1 |
T |
C |
10: 69,108,693 (GRCm39) |
|
probably benign |
Het |
| Rpl28-ps4 |
T |
A |
6: 117,190,856 (GRCm39) |
|
noncoding transcript |
Het |
| Rsph10b |
A |
G |
5: 143,904,068 (GRCm39) |
|
probably null |
Het |
| Rspo4 |
A |
G |
2: 151,715,013 (GRCm39) |
K217E |
unknown |
Het |
| Scgb2b27 |
G |
A |
7: 33,712,710 (GRCm39) |
A44V |
possibly damaging |
Het |
| Sec14l2 |
G |
A |
11: 4,061,435 (GRCm39) |
|
probably benign |
Het |
| Sec31b |
T |
C |
19: 44,524,595 (GRCm39) |
N101D |
probably benign |
Het |
| Sema6a |
A |
T |
18: 47,439,496 (GRCm39) |
C9* |
probably null |
Het |
| Septin5 |
A |
C |
16: 18,441,762 (GRCm39) |
L331R |
probably benign |
Het |
| Slc16a11 |
C |
A |
11: 70,106,477 (GRCm39) |
Y238* |
probably null |
Het |
| Slc25a12 |
T |
C |
2: 71,142,892 (GRCm39) |
T210A |
probably benign |
Het |
| Slc35f1 |
A |
T |
10: 52,965,443 (GRCm39) |
Y286F |
probably damaging |
Het |
| Szt2 |
A |
T |
4: 118,233,645 (GRCm39) |
L2225* |
probably null |
Het |
| Thap12 |
T |
C |
7: 98,365,827 (GRCm39) |
L665P |
probably damaging |
Het |
| Tpsb2 |
T |
A |
17: 25,586,698 (GRCm39) |
W237R |
probably damaging |
Het |
| Tyk2 |
T |
C |
9: 21,031,637 (GRCm39) |
D451G |
probably damaging |
Het |
| Ube2j1 |
T |
A |
4: 33,049,696 (GRCm39) |
N231K |
probably benign |
Het |
| Vmn1r225 |
A |
T |
17: 20,722,852 (GRCm39) |
T98S |
possibly damaging |
Het |
| Vmn1r87 |
A |
T |
7: 12,865,748 (GRCm39) |
S180T |
probably benign |
Het |
| Zfp689 |
C |
A |
7: 127,043,998 (GRCm39) |
G211C |
probably damaging |
Het |
| Zfp827 |
A |
G |
8: 79,802,865 (GRCm39) |
D479G |
probably benign |
Het |
| Zfp995 |
A |
C |
17: 22,099,575 (GRCm39) |
F220V |
probably damaging |
Het |
|
| Other mutations in Vmn2r6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01547:Vmn2r6
|
APN |
3 |
64,445,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01968:Vmn2r6
|
APN |
3 |
64,463,766 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL02009:Vmn2r6
|
APN |
3 |
64,445,323 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
IGL02039:Vmn2r6
|
APN |
3 |
64,463,610 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02652:Vmn2r6
|
APN |
3 |
64,463,749 (GRCm39) |
missense |
probably benign |
0.24 |
|
IGL02737:Vmn2r6
|
APN |
3 |
64,463,911 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
IGL02808:Vmn2r6
|
APN |
3 |
64,463,917 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03066:Vmn2r6
|
APN |
3 |
64,472,574 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03331:Vmn2r6
|
APN |
3 |
64,445,428 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB010:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
|
BB020:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0010:Vmn2r6
|
UTSW |
3 |
64,466,966 (GRCm39) |
nonsense |
probably null |
|
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
|
R0206:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
|
R0208:Vmn2r6
|
UTSW |
3 |
64,447,333 (GRCm39) |
missense |
probably benign |
|
|
R0427:Vmn2r6
|
UTSW |
3 |
64,467,008 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0466:Vmn2r6
|
UTSW |
3 |
64,463,723 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1018:Vmn2r6
|
UTSW |
3 |
64,464,261 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1104:Vmn2r6
|
UTSW |
3 |
64,445,487 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1186:Vmn2r6
|
UTSW |
3 |
64,472,488 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1245:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R1295:Vmn2r6
|
UTSW |
3 |
64,445,694 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1473:Vmn2r6
|
UTSW |
3 |
64,445,579 (GRCm39) |
nonsense |
probably null |
|
|
R1498:Vmn2r6
|
UTSW |
3 |
64,463,890 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1925:Vmn2r6
|
UTSW |
3 |
64,463,698 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R2069:Vmn2r6
|
UTSW |
3 |
64,463,519 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R2253:Vmn2r6
|
UTSW |
3 |
64,467,139 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2261:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
|
R2262:Vmn2r6
|
UTSW |
3 |
64,464,090 (GRCm39) |
missense |
probably benign |
0.24 |
|
R2350:Vmn2r6
|
UTSW |
3 |
64,463,773 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2680:Vmn2r6
|
UTSW |
3 |
64,445,707 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2846:Vmn2r6
|
UTSW |
3 |
64,464,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R2860:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2861:Vmn2r6
|
UTSW |
3 |
64,454,760 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3766:Vmn2r6
|
UTSW |
3 |
64,463,929 (GRCm39) |
missense |
probably benign |
0.19 |
|
R3870:Vmn2r6
|
UTSW |
3 |
64,464,042 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4018:Vmn2r6
|
UTSW |
3 |
64,463,893 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4024:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4026:Vmn2r6
|
UTSW |
3 |
64,445,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R4227:Vmn2r6
|
UTSW |
3 |
64,445,369 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4526:Vmn2r6
|
UTSW |
3 |
64,445,145 (GRCm39) |
missense |
probably benign |
0.32 |
|
R4570:Vmn2r6
|
UTSW |
3 |
64,467,068 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4894:Vmn2r6
|
UTSW |
3 |
64,454,829 (GRCm39) |
missense |
probably benign |
|
|
R4934:Vmn2r6
|
UTSW |
3 |
64,463,766 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5057:Vmn2r6
|
UTSW |
3 |
64,445,207 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5059:Vmn2r6
|
UTSW |
3 |
64,445,044 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5148:Vmn2r6
|
UTSW |
3 |
64,464,015 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5155:Vmn2r6
|
UTSW |
3 |
64,445,935 (GRCm39) |
missense |
probably benign |
0.44 |
|
R5179:Vmn2r6
|
UTSW |
3 |
64,445,411 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5256:Vmn2r6
|
UTSW |
3 |
64,464,263 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5861:Vmn2r6
|
UTSW |
3 |
64,463,454 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5950:Vmn2r6
|
UTSW |
3 |
64,472,652 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6081:Vmn2r6
|
UTSW |
3 |
64,463,953 (GRCm39) |
missense |
probably benign |
0.25 |
|
R6173:Vmn2r6
|
UTSW |
3 |
64,467,176 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6190:Vmn2r6
|
UTSW |
3 |
64,445,424 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6240:Vmn2r6
|
UTSW |
3 |
64,464,226 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6433:Vmn2r6
|
UTSW |
3 |
64,454,801 (GRCm39) |
nonsense |
probably null |
|
|
R6645:Vmn2r6
|
UTSW |
3 |
64,464,297 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6791:Vmn2r6
|
UTSW |
3 |
64,445,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7265:Vmn2r6
|
UTSW |
3 |
64,464,195 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7503:Vmn2r6
|
UTSW |
3 |
64,447,372 (GRCm39) |
nonsense |
probably null |
|
|
R7562:Vmn2r6
|
UTSW |
3 |
64,463,941 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7584:Vmn2r6
|
UTSW |
3 |
64,472,683 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7611:Vmn2r6
|
UTSW |
3 |
64,472,563 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7759:Vmn2r6
|
UTSW |
3 |
64,463,991 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7834:Vmn2r6
|
UTSW |
3 |
64,445,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7933:Vmn2r6
|
UTSW |
3 |
64,467,224 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7982:Vmn2r6
|
UTSW |
3 |
64,467,241 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8024:Vmn2r6
|
UTSW |
3 |
64,467,245 (GRCm39) |
missense |
probably benign |
0.40 |
|
R8074:Vmn2r6
|
UTSW |
3 |
64,455,064 (GRCm39) |
intron |
probably benign |
|
|
R8169:Vmn2r6
|
UTSW |
3 |
64,447,310 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8337:Vmn2r6
|
UTSW |
3 |
64,463,526 (GRCm39) |
nonsense |
probably null |
|
|
R8736:Vmn2r6
|
UTSW |
3 |
64,467,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8962:Vmn2r6
|
UTSW |
3 |
64,463,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9139:Vmn2r6
|
UTSW |
3 |
64,464,277 (GRCm39) |
missense |
probably benign |
0.12 |
|
R9206:Vmn2r6
|
UTSW |
3 |
64,467,032 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9295:Vmn2r6
|
UTSW |
3 |
64,463,484 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9332:Vmn2r6
|
UTSW |
3 |
64,454,671 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9616:Vmn2r6
|
UTSW |
3 |
64,445,724 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9663:Vmn2r6
|
UTSW |
3 |
64,463,549 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9685:Vmn2r6
|
UTSW |
3 |
64,464,081 (GRCm39) |
missense |
probably benign |
0.19 |
|
X0020:Vmn2r6
|
UTSW |
3 |
64,445,871 (GRCm39) |
missense |
probably benign |
|
|
X0066:Vmn2r6
|
UTSW |
3 |
64,454,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Vmn2r6
|
UTSW |
3 |
64,463,746 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCCACCAACAGTTTCATCAGTG -3'
(R):5'- CTTACTTAGTGTTGGAGCCTCC -3'
Sequencing Primer
(F):5'- GTTCCTCTTTGGCCTCAGCAAG -3'
(R):5'- GAGCCTCCAAGCCTGTTCAAG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation