Incidental Mutation 'R9616:Vmn2r6'
| ID |
724566 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r6
|
| Ensembl Gene |
ENSMUSG00000090581 |
| Gene Name |
vomeronasal 2, receptor 6 |
| Synonyms |
EG620718, EG667069 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.184)
|
| Stock # |
R9616 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
64537561-64565298 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 64538303 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Proline
at position 667
(L667P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000135148
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000165012]
[ENSMUST00000176481]
|
| AlphaFold |
H3BK29 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000165012
AA Change: L578P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000131831
Gene: ENSMUSG00000090581
AA Change: L578P
| 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: L667P
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000135148
Gene: ENSMUSG00000090581
AA Change: L667P
| 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: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 99.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 91 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3110040M04Rik |
T |
A |
1: 151,204,729 (GRCm38) |
D189E |
probably benign |
Het |
| Abca13 |
A |
T |
11: 9,290,501 (GRCm38) |
H788L |
probably benign |
Het |
| Abcb1b |
A |
G |
5: 8,812,779 (GRCm38) |
I154V |
probably benign |
Het |
| Acsm4 |
A |
G |
7: 119,694,649 (GRCm38) |
N81S |
probably benign |
Het |
| Adamts5 |
G |
A |
16: 85,862,786 (GRCm38) |
H873Y |
probably benign |
Het |
| Aox4 |
C |
T |
1: 58,228,861 (GRCm38) |
T200I |
possibly damaging |
Het |
| Arhgap33 |
A |
G |
7: 30,529,942 (GRCm38) |
V336A |
probably damaging |
Het |
| Brca1 |
C |
T |
11: 101,525,857 (GRCm38) |
E484K |
probably damaging |
Het |
| Capn13 |
T |
A |
17: 73,365,969 (GRCm38) |
D113V |
probably benign |
Het |
| Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,397,572 (GRCm38) |
|
probably benign |
Het |
| Ceacam3 |
G |
A |
7: 17,158,153 (GRCm38) |
E274K |
|
Het |
| Cfh |
A |
T |
1: 140,102,516 (GRCm38) |
I891K |
probably damaging |
Het |
| Cgn |
A |
G |
3: 94,763,025 (GRCm38) |
S1041P |
probably damaging |
Het |
| Cldn18 |
T |
C |
9: 99,698,862 (GRCm38) |
D111G |
probably benign |
Het |
| Cnp |
G |
A |
11: 100,576,435 (GRCm38) |
R68Q |
probably benign |
Het |
| Cntn4 |
T |
A |
6: 106,697,564 (GRCm38) |
C1008* |
probably null |
Het |
| Cntnap5a |
T |
C |
1: 116,101,593 (GRCm38) |
I259T |
probably benign |
Het |
| Cubn |
A |
G |
2: 13,314,718 (GRCm38) |
I2897T |
probably benign |
Het |
| Cyp2c39 |
T |
A |
19: 39,513,204 (GRCm38) |
L67Q |
probably damaging |
Het |
| Dclk1 |
G |
A |
3: 55,480,433 (GRCm38) |
C100Y |
probably damaging |
Het |
| Ddc |
C |
T |
11: 11,822,288 (GRCm38) |
W349* |
probably null |
Het |
| Dennd3 |
A |
G |
15: 73,568,714 (GRCm38) |
E1198G |
probably benign |
Het |
| Dnah1 |
T |
C |
14: 31,304,443 (GRCm38) |
D826G |
probably null |
Het |
| Dpp4 |
T |
C |
2: 62,387,085 (GRCm38) |
Y56C |
probably damaging |
Het |
| Etv6 |
A |
G |
6: 134,266,332 (GRCm38) |
D350G |
possibly damaging |
Het |
| Fam129a |
T |
C |
1: 151,636,442 (GRCm38) |
Y32H |
probably damaging |
Het |
| Fat1 |
C |
A |
8: 44,953,038 (GRCm38) |
P942Q |
probably damaging |
Het |
| Fbxl5 |
A |
G |
5: 43,758,817 (GRCm38) |
F418L |
probably benign |
Het |
| Fbxo11 |
T |
A |
17: 88,008,670 (GRCm38) |
H368L |
|
Het |
| Fhl2 |
G |
T |
1: 43,128,386 (GRCm38) |
H182Q |
probably damaging |
Het |
| Gabpa |
T |
A |
16: 84,852,573 (GRCm38) |
C223S |
probably damaging |
Het |
| Gigyf2 |
T |
C |
1: 87,428,604 (GRCm38) |
I803T |
unknown |
Het |
| Greb1 |
A |
T |
12: 16,740,037 (GRCm38) |
N3K |
probably damaging |
Het |
| Hmcn1 |
T |
G |
1: 150,808,722 (GRCm38) |
S366R |
probably benign |
Het |
| Il17b |
A |
G |
18: 61,692,292 (GRCm38) |
Q133R |
probably benign |
Het |
| Inha |
T |
A |
1: 75,509,567 (GRCm38) |
S169T |
probably benign |
Het |
| Itsn1 |
G |
A |
16: 91,853,167 (GRCm38) |
R243H |
probably benign |
Het |
| Kcnu1 |
G |
GA |
8: 25,913,647 (GRCm38) |
|
probably null |
Het |
| Kdm1b |
A |
G |
13: 47,080,554 (GRCm38) |
E788G |
probably damaging |
Het |
| Kdm2a |
A |
T |
19: 4,320,280 (GRCm38) |
I1059N |
probably damaging |
Het |
| Klk1b9 |
G |
T |
7: 43,979,371 (GRCm38) |
G100C |
probably benign |
Het |
| Knl1 |
A |
T |
2: 119,076,944 (GRCm38) |
N1650Y |
probably damaging |
Het |
| Knl1 |
T |
C |
2: 119,069,513 (GRCm38) |
V565A |
probably benign |
Het |
| Lpp |
T |
C |
16: 24,761,969 (GRCm38) |
V270A |
probably benign |
Het |
| Lrrc15 |
A |
G |
16: 30,273,699 (GRCm38) |
L274P |
probably damaging |
Het |
| Mertk |
C |
T |
2: 128,801,335 (GRCm38) |
L885F |
probably benign |
Het |
| Mpst |
T |
A |
15: 78,410,161 (GRCm38) |
L31* |
probably null |
Het |
| Ms4a10 |
T |
C |
19: 10,967,076 (GRCm38) |
T115A |
possibly damaging |
Het |
| Myof |
A |
G |
19: 37,934,815 (GRCm38) |
I1330T |
possibly damaging |
Het |
| Ncam2 |
T |
C |
16: 81,443,254 (GRCm38) |
I201T |
probably damaging |
Het |
| Nefh |
T |
A |
11: 4,939,443 (GRCm38) |
K1059* |
probably null |
Het |
| Nek1 |
T |
C |
8: 61,020,073 (GRCm38) |
Y168H |
probably damaging |
Het |
| Nek11 |
T |
A |
9: 105,204,812 (GRCm38) |
T531S |
probably damaging |
Het |
| Nelfa |
G |
A |
5: 33,901,783 (GRCm38) |
P243S |
possibly damaging |
Het |
| Notum |
G |
T |
11: 120,660,148 (GRCm38) |
T64K |
|
Het |
| Olfr1504 |
A |
G |
19: 13,887,497 (GRCm38) |
S238P |
probably damaging |
Het |
| Olfr159 |
T |
A |
4: 43,770,193 (GRCm38) |
K273* |
probably null |
Het |
| Olfr691 |
A |
C |
7: 105,337,313 (GRCm38) |
Y134* |
probably null |
Het |
| Otof |
A |
G |
5: 30,382,364 (GRCm38) |
I1035T |
possibly damaging |
Het |
| Otud3 |
A |
G |
4: 138,897,614 (GRCm38) |
Y259H |
probably benign |
Het |
| Per1 |
G |
T |
11: 69,102,728 (GRCm38) |
C368F |
probably damaging |
Het |
| Pitrm1 |
G |
T |
13: 6,555,566 (GRCm38) |
R183L |
probably damaging |
Het |
| Prl3a1 |
C |
T |
13: 27,275,135 (GRCm38) |
A119V |
|
Het |
| Pycard |
C |
T |
7: 127,993,604 (GRCm38) |
G17E |
probably benign |
Het |
| Rnf13 |
A |
G |
3: 57,833,009 (GRCm38) |
D249G |
possibly damaging |
Het |
| Sdhaf2 |
T |
C |
19: 10,517,325 (GRCm38) |
Y33C |
probably damaging |
Het |
| Sdk2 |
A |
G |
11: 113,800,235 (GRCm38) |
V1838A |
probably benign |
Het |
| Sgo2b |
C |
T |
8: 63,927,240 (GRCm38) |
V853I |
probably benign |
Het |
| Slc1a4 |
T |
C |
11: 20,332,403 (GRCm38) |
T24A |
probably benign |
Het |
| Slc8a1 |
T |
C |
17: 81,647,978 (GRCm38) |
T544A |
probably benign |
Het |
| Sntg2 |
T |
C |
12: 30,276,733 (GRCm38) |
N143S |
probably benign |
Het |
| Sphkap |
T |
C |
1: 83,277,268 (GRCm38) |
E920G |
probably damaging |
Het |
| Srgap2 |
T |
A |
1: 131,325,090 (GRCm38) |
H132L |
|
Het |
| Srgap3 |
A |
T |
6: 112,771,563 (GRCm38) |
V376D |
probably damaging |
Het |
| Stxbp5l |
T |
C |
16: 37,215,952 (GRCm38) |
K434E |
probably damaging |
Het |
| Tab2 |
A |
T |
10: 7,919,241 (GRCm38) |
N492K |
possibly damaging |
Het |
| Tbc1d32 |
T |
C |
10: 56,161,150 (GRCm38) |
Q666R |
possibly damaging |
Het |
| Tekt4 |
T |
C |
17: 25,473,808 (GRCm38) |
|
probably null |
Het |
| Tnni3k |
G |
A |
3: 154,962,087 (GRCm38) |
Q230* |
probably null |
Het |
| Trp53bp1 |
A |
C |
2: 121,236,176 (GRCm38) |
S690A |
probably benign |
Het |
| Trpa1 |
C |
A |
1: 14,918,853 (GRCm38) |
|
probably benign |
Het |
| Trpm1 |
T |
G |
7: 64,208,384 (GRCm38) |
V324G |
probably damaging |
Het |
| Usp29 |
A |
G |
7: 6,963,180 (GRCm38) |
E674G |
possibly damaging |
Het |
| Vmn2r59 |
T |
C |
7: 42,011,875 (GRCm38) |
R839G |
probably damaging |
Het |
| Vmn2r91 |
T |
A |
17: 18,136,043 (GRCm38) |
F657L |
possibly damaging |
Het |
| Vps13d |
A |
G |
4: 145,098,131 (GRCm38) |
V2923A |
|
Het |
| Xylb |
T |
A |
9: 119,371,956 (GRCm38) |
L220Q |
probably damaging |
Het |
| Zbtb10 |
C |
T |
3: 9,251,413 (GRCm38) |
T95M |
probably benign |
Het |
| Zfp263 |
C |
T |
16: 3,749,618 (GRCm38) |
P599L |
probably damaging |
Het |
| Zfp532 |
A |
G |
18: 65,656,568 (GRCm38) |
E1026G |
probably benign |
Het |
| Zfp78 |
A |
G |
7: 6,379,079 (GRCm38) |
N376S |
probably benign |
Het |
|
| Other mutations in Vmn2r6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01547:Vmn2r6
|
APN |
3 |
64,538,104 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01968:Vmn2r6
|
APN |
3 |
64,556,345 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
IGL02009:Vmn2r6
|
APN |
3 |
64,537,902 (GRCm38) |
missense |
possibly damaging |
0.61 |
|
IGL02039:Vmn2r6
|
APN |
3 |
64,556,189 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02652:Vmn2r6
|
APN |
3 |
64,556,328 (GRCm38) |
missense |
probably benign |
0.24 |
|
IGL02737:Vmn2r6
|
APN |
3 |
64,556,490 (GRCm38) |
missense |
possibly damaging |
0.55 |
|
IGL02808:Vmn2r6
|
APN |
3 |
64,556,496 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03066:Vmn2r6
|
APN |
3 |
64,565,153 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL03331:Vmn2r6
|
APN |
3 |
64,538,007 (GRCm38) |
missense |
probably damaging |
1.00 |
|
BB010:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
|
BB020:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
|
R0010:Vmn2r6
|
UTSW |
3 |
64,559,545 (GRCm38) |
nonsense |
probably null |
|
|
R0206:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
|
R0206:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
|
R0208:Vmn2r6
|
UTSW |
3 |
64,539,912 (GRCm38) |
missense |
probably benign |
|
|
R0427:Vmn2r6
|
UTSW |
3 |
64,559,587 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0466:Vmn2r6
|
UTSW |
3 |
64,556,302 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1018:Vmn2r6
|
UTSW |
3 |
64,556,840 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1104:Vmn2r6
|
UTSW |
3 |
64,538,066 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R1186:Vmn2r6
|
UTSW |
3 |
64,565,067 (GRCm38) |
missense |
probably benign |
0.01 |
|
R1245:Vmn2r6
|
UTSW |
3 |
64,556,790 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R1295:Vmn2r6
|
UTSW |
3 |
64,538,273 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1473:Vmn2r6
|
UTSW |
3 |
64,538,158 (GRCm38) |
nonsense |
probably null |
|
|
R1498:Vmn2r6
|
UTSW |
3 |
64,556,469 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R1925:Vmn2r6
|
UTSW |
3 |
64,556,277 (GRCm38) |
missense |
possibly damaging |
0.87 |
|
R2044:Vmn2r6
|
UTSW |
3 |
64,537,841 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R2069:Vmn2r6
|
UTSW |
3 |
64,556,098 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R2253:Vmn2r6
|
UTSW |
3 |
64,559,718 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2261:Vmn2r6
|
UTSW |
3 |
64,556,669 (GRCm38) |
missense |
probably benign |
0.24 |
|
R2262:Vmn2r6
|
UTSW |
3 |
64,556,669 (GRCm38) |
missense |
probably benign |
0.24 |
|
R2350:Vmn2r6
|
UTSW |
3 |
64,556,352 (GRCm38) |
missense |
probably benign |
0.01 |
|
R2680:Vmn2r6
|
UTSW |
3 |
64,538,286 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R2846:Vmn2r6
|
UTSW |
3 |
64,556,790 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R2860:Vmn2r6
|
UTSW |
3 |
64,547,339 (GRCm38) |
missense |
probably benign |
0.00 |
|
R2861:Vmn2r6
|
UTSW |
3 |
64,547,339 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3766:Vmn2r6
|
UTSW |
3 |
64,556,508 (GRCm38) |
missense |
probably benign |
0.19 |
|
R3870:Vmn2r6
|
UTSW |
3 |
64,556,621 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R4018:Vmn2r6
|
UTSW |
3 |
64,556,472 (GRCm38) |
missense |
probably benign |
0.05 |
|
R4024:Vmn2r6
|
UTSW |
3 |
64,538,250 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R4026:Vmn2r6
|
UTSW |
3 |
64,538,250 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R4227:Vmn2r6
|
UTSW |
3 |
64,537,948 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R4526:Vmn2r6
|
UTSW |
3 |
64,537,724 (GRCm38) |
missense |
probably benign |
0.32 |
|
R4570:Vmn2r6
|
UTSW |
3 |
64,559,647 (GRCm38) |
missense |
probably benign |
0.31 |
|
R4894:Vmn2r6
|
UTSW |
3 |
64,547,408 (GRCm38) |
missense |
probably benign |
|
|
R4934:Vmn2r6
|
UTSW |
3 |
64,556,345 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5057:Vmn2r6
|
UTSW |
3 |
64,537,786 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5059:Vmn2r6
|
UTSW |
3 |
64,537,623 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R5148:Vmn2r6
|
UTSW |
3 |
64,556,594 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R5155:Vmn2r6
|
UTSW |
3 |
64,538,514 (GRCm38) |
missense |
probably benign |
0.44 |
|
R5179:Vmn2r6
|
UTSW |
3 |
64,537,990 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5256:Vmn2r6
|
UTSW |
3 |
64,556,842 (GRCm38) |
missense |
probably benign |
0.33 |
|
R5861:Vmn2r6
|
UTSW |
3 |
64,556,033 (GRCm38) |
missense |
probably benign |
0.00 |
|
R5950:Vmn2r6
|
UTSW |
3 |
64,565,231 (GRCm38) |
missense |
probably benign |
0.05 |
|
R6081:Vmn2r6
|
UTSW |
3 |
64,556,532 (GRCm38) |
missense |
probably benign |
0.25 |
|
R6173:Vmn2r6
|
UTSW |
3 |
64,559,755 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6190:Vmn2r6
|
UTSW |
3 |
64,538,003 (GRCm38) |
missense |
probably benign |
0.04 |
|
R6240:Vmn2r6
|
UTSW |
3 |
64,556,805 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6433:Vmn2r6
|
UTSW |
3 |
64,547,380 (GRCm38) |
nonsense |
probably null |
|
|
R6645:Vmn2r6
|
UTSW |
3 |
64,556,876 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6791:Vmn2r6
|
UTSW |
3 |
64,538,159 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7265:Vmn2r6
|
UTSW |
3 |
64,556,774 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7503:Vmn2r6
|
UTSW |
3 |
64,539,951 (GRCm38) |
nonsense |
probably null |
|
|
R7562:Vmn2r6
|
UTSW |
3 |
64,556,520 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7584:Vmn2r6
|
UTSW |
3 |
64,565,262 (GRCm38) |
missense |
probably benign |
0.07 |
|
R7611:Vmn2r6
|
UTSW |
3 |
64,565,142 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R7759:Vmn2r6
|
UTSW |
3 |
64,556,570 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7834:Vmn2r6
|
UTSW |
3 |
64,538,022 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7933:Vmn2r6
|
UTSW |
3 |
64,559,803 (GRCm38) |
missense |
probably benign |
0.02 |
|
R7982:Vmn2r6
|
UTSW |
3 |
64,559,820 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8024:Vmn2r6
|
UTSW |
3 |
64,559,824 (GRCm38) |
missense |
probably benign |
0.40 |
|
R8074:Vmn2r6
|
UTSW |
3 |
64,547,643 (GRCm38) |
intron |
probably benign |
|
|
R8169:Vmn2r6
|
UTSW |
3 |
64,539,889 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8337:Vmn2r6
|
UTSW |
3 |
64,556,105 (GRCm38) |
nonsense |
probably null |
|
|
R8736:Vmn2r6
|
UTSW |
3 |
64,559,800 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8962:Vmn2r6
|
UTSW |
3 |
64,556,155 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9139:Vmn2r6
|
UTSW |
3 |
64,556,856 (GRCm38) |
missense |
probably benign |
0.12 |
|
R9206:Vmn2r6
|
UTSW |
3 |
64,559,611 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R9295:Vmn2r6
|
UTSW |
3 |
64,556,063 (GRCm38) |
missense |
probably benign |
0.00 |
|
R9332:Vmn2r6
|
UTSW |
3 |
64,547,250 (GRCm38) |
missense |
probably benign |
0.01 |
|
R9663:Vmn2r6
|
UTSW |
3 |
64,556,128 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
R9685:Vmn2r6
|
UTSW |
3 |
64,556,660 (GRCm38) |
missense |
probably benign |
0.19 |
|
X0020:Vmn2r6
|
UTSW |
3 |
64,538,450 (GRCm38) |
missense |
probably benign |
|
|
X0066:Vmn2r6
|
UTSW |
3 |
64,547,378 (GRCm38) |
missense |
probably damaging |
1.00 |
|
Z1176:Vmn2r6
|
UTSW |
3 |
64,556,325 (GRCm38) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- AATGGGGTGCATGGATATTAGC -3'
(R):5'- AAATGACTGGTCCAATGCGG -3'
Sequencing Primer
(F):5'- GCCGAGTTTTAGATATGGAAATCCTG -3'
(R):5'- AACAAGTGTGTGCCAAAGC -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation