Incidental Mutation 'R9015:Vmn2r72'
| ID |
685914 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r72
|
| Ensembl Gene |
ENSMUSG00000051877 |
| Gene Name |
vomeronasal 2, receptor 72 |
| Synonyms |
EG244114, Vmn2r72-ps |
| MMRRC Submission |
068845-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.089)
|
| Stock # |
R9015 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
7 |
| Chromosomal Location |
85386992-85404189 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 85398388 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Leucine
at position 531
(M531L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133014
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000063425]
|
| AlphaFold |
D3Z4N8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000063425
AA Change: M531L
PolyPhen 2
Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
|
| SMART Domains |
Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877
AA Change: M531L
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
18 |
N/A |
INTRINSIC |
|
Pfam:ANF_receptor
|
82 |
469 |
2.3e-28 |
PFAM |
|
Pfam:NCD3G
|
512 |
564 |
1.2e-18 |
PFAM |
|
Pfam:7tm_3
|
594 |
832 |
4e-53 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
100% (93/93) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 93 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam22 |
T |
C |
5: 8,136,688 (GRCm39) |
|
probably benign |
Het |
| Adamtsl1 |
A |
G |
4: 86,150,847 (GRCm39) |
D335G |
probably damaging |
Het |
| Adcy8 |
T |
C |
15: 64,597,206 (GRCm39) |
|
probably benign |
Het |
| Alas1 |
A |
T |
9: 106,113,670 (GRCm39) |
I525N |
probably benign |
Het |
| Aoah |
A |
T |
13: 21,184,197 (GRCm39) |
|
silent |
Het |
| Aox1 |
G |
A |
1: 58,382,851 (GRCm39) |
V1044M |
probably damaging |
Het |
| Apcdd1 |
A |
T |
18: 63,083,157 (GRCm39) |
Y329F |
possibly damaging |
Het |
| Arhgap10 |
A |
C |
8: 77,985,687 (GRCm39) |
C727G |
probably benign |
Het |
| Arid4a |
G |
A |
12: 71,122,168 (GRCm39) |
D528N |
possibly damaging |
Het |
| Atp8a1 |
A |
G |
5: 67,887,250 (GRCm39) |
V611A |
|
Het |
| BC004004 |
T |
C |
17: 29,517,637 (GRCm39) |
F284L |
probably damaging |
Het |
| Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
| Cep295 |
T |
C |
9: 15,244,264 (GRCm39) |
I1397M |
probably benign |
Het |
| Cep63 |
A |
G |
9: 102,496,111 (GRCm39) |
S99P |
probably damaging |
Het |
| Coq3 |
T |
A |
4: 21,899,107 (GRCm39) |
S147T |
probably benign |
Het |
| Crym |
A |
T |
7: 119,801,090 (GRCm39) |
S20T |
probably benign |
Het |
| Ctr9 |
T |
A |
7: 110,643,108 (GRCm39) |
N493K |
probably benign |
Het |
| Dchs2 |
A |
G |
3: 83,188,751 (GRCm39) |
I1372V |
possibly damaging |
Het |
| Ddi2 |
G |
A |
4: 141,412,747 (GRCm39) |
T55M |
probably benign |
Het |
| Dnah1 |
T |
C |
14: 30,986,316 (GRCm39) |
M3724V |
probably damaging |
Het |
| Dst |
A |
G |
1: 34,326,337 (GRCm39) |
I4690V |
probably benign |
Het |
| Ect2l |
T |
C |
10: 18,039,148 (GRCm39) |
T429A |
probably benign |
Het |
| Eif3c |
G |
T |
7: 126,155,538 (GRCm39) |
H577N |
probably damaging |
Het |
| Erg |
A |
G |
16: 95,162,126 (GRCm39) |
S334P |
possibly damaging |
Het |
| Faf2 |
A |
G |
13: 54,796,139 (GRCm39) |
S127G |
probably benign |
Het |
| Fbxl3 |
T |
A |
14: 103,329,790 (GRCm39) |
T141S |
possibly damaging |
Het |
| Fbxw4 |
T |
A |
19: 45,624,874 (GRCm39) |
M122L |
probably benign |
Het |
| Fgd4 |
T |
C |
16: 16,271,941 (GRCm39) |
M476V |
probably damaging |
Het |
| Flvcr2 |
A |
T |
12: 85,829,779 (GRCm39) |
I263F |
probably benign |
Het |
| Gadl1 |
A |
T |
9: 115,794,705 (GRCm39) |
R293S |
probably benign |
Het |
| Gm11983 |
G |
T |
11: 6,787,033 (GRCm39) |
F31L |
unknown |
Het |
| Gmnn |
A |
T |
13: 24,940,638 (GRCm39) |
N70K |
probably benign |
Het |
| Gpr3 |
A |
G |
4: 132,938,390 (GRCm39) |
V94A |
possibly damaging |
Het |
| Greb1l |
A |
G |
18: 10,541,675 (GRCm39) |
S1141G |
probably benign |
Het |
| Helz2 |
A |
T |
2: 180,870,792 (GRCm39) |
V2892E |
probably damaging |
Het |
| Hivep1 |
T |
A |
13: 42,311,849 (GRCm39) |
M1363K |
probably benign |
Het |
| Hk1 |
T |
A |
10: 62,128,118 (GRCm39) |
T336S |
possibly damaging |
Het |
| Hpgds |
A |
T |
6: 65,115,229 (GRCm39) |
I18N |
possibly damaging |
Het |
| Insrr |
T |
A |
3: 87,720,910 (GRCm39) |
L1056Q |
probably damaging |
Het |
| Ints10 |
A |
G |
8: 69,260,139 (GRCm39) |
M288V |
probably benign |
Het |
| Itgb6 |
T |
C |
2: 60,485,032 (GRCm39) |
D237G |
probably damaging |
Het |
| Kcnf1 |
A |
G |
12: 17,225,303 (GRCm39) |
I306T |
probably damaging |
Het |
| Kdm3b |
G |
A |
18: 34,963,212 (GRCm39) |
G1556D |
probably damaging |
Het |
| Kif5b |
A |
G |
18: 6,216,892 (GRCm39) |
L477P |
probably damaging |
Het |
| Klf5 |
T |
G |
14: 99,540,919 (GRCm39) |
*310G |
probably null |
Het |
| Lnx1 |
A |
G |
5: 74,780,783 (GRCm39) |
V246A |
probably benign |
Het |
| Ly75 |
C |
T |
2: 60,146,442 (GRCm39) |
E1279K |
probably benign |
Het |
| Lztr1 |
T |
A |
16: 17,337,305 (GRCm39) |
C233S |
probably benign |
Het |
| Mfsd6l |
T |
G |
11: 68,447,536 (GRCm39) |
I129S |
probably benign |
Het |
| Mrgprx2 |
T |
A |
7: 48,148,938 (GRCm39) |
|
probably benign |
Het |
| Ncapd2 |
A |
T |
6: 125,145,285 (GRCm39) |
|
probably benign |
Het |
| Or10ag53 |
T |
A |
2: 87,082,546 (GRCm39) |
Y88* |
probably null |
Het |
| Or12e9 |
T |
A |
2: 87,202,485 (GRCm39) |
M203K |
possibly damaging |
Het |
| Or2a25 |
G |
T |
6: 42,888,825 (GRCm39) |
V123L |
possibly damaging |
Het |
| Or8g30 |
A |
C |
9: 39,230,019 (GRCm39) |
V297G |
probably damaging |
Het |
| Pde6a |
A |
G |
18: 61,397,047 (GRCm39) |
H631R |
probably damaging |
Het |
| Pfkl |
C |
T |
10: 77,824,794 (GRCm39) |
G665D |
probably damaging |
Het |
| Pik3ap1 |
T |
A |
19: 41,270,430 (GRCm39) |
E753V |
probably damaging |
Het |
| Pik3cd |
G |
T |
4: 149,740,055 (GRCm39) |
R502S |
probably benign |
Het |
| Piwil2 |
T |
A |
14: 70,627,984 (GRCm39) |
I762L |
probably benign |
Het |
| Pkd1 |
T |
A |
17: 24,784,636 (GRCm39) |
L394* |
probably null |
Het |
| Plekhb2 |
A |
G |
1: 34,916,046 (GRCm39) |
D195G |
probably benign |
Het |
| Plppr5 |
T |
C |
3: 117,456,103 (GRCm39) |
M208T |
probably damaging |
Het |
| Polr2i |
G |
A |
7: 29,932,513 (GRCm39) |
V115I |
unknown |
Het |
| Prkacb |
T |
C |
3: 146,456,239 (GRCm39) |
S187G |
probably null |
Het |
| Prkag3 |
G |
T |
1: 74,780,353 (GRCm39) |
H437Q |
probably benign |
Het |
| Prlr |
T |
A |
15: 10,319,352 (GRCm39) |
Y94N |
probably damaging |
Het |
| Prmt6 |
T |
C |
3: 110,157,214 (GRCm39) |
I358M |
probably benign |
Het |
| Psd4 |
A |
G |
2: 24,287,492 (GRCm39) |
R475G |
|
Het |
| Rad51b |
G |
A |
12: 79,347,417 (GRCm39) |
C27Y |
probably damaging |
Het |
| Scfd2 |
A |
G |
5: 74,691,625 (GRCm39) |
L219P |
probably damaging |
Het |
| Scn5a |
G |
A |
9: 119,381,142 (GRCm39) |
|
probably benign |
Het |
| Sec24d |
T |
C |
3: 123,121,287 (GRCm39) |
V391A |
probably benign |
Het |
| Selenbp2 |
T |
A |
3: 94,607,332 (GRCm39) |
L251Q |
probably damaging |
Het |
| Sh3rf1 |
T |
C |
8: 61,827,202 (GRCm39) |
V652A |
probably benign |
Het |
| Slc11a2 |
A |
G |
15: 100,301,186 (GRCm39) |
V289A |
probably benign |
Het |
| Smim29 |
T |
C |
17: 27,783,223 (GRCm39) |
D48G |
probably benign |
Het |
| Sox8 |
T |
A |
17: 25,789,135 (GRCm39) |
Y121F |
probably damaging |
Het |
| Taar7a |
A |
T |
10: 23,868,733 (GRCm39) |
I216N |
probably damaging |
Het |
| Tanc1 |
T |
A |
2: 59,622,224 (GRCm39) |
S448T |
probably benign |
Het |
| Tas2r119 |
G |
A |
15: 32,178,226 (GRCm39) |
G264D |
probably damaging |
Het |
| Trav7-6 |
A |
G |
14: 53,954,604 (GRCm39) |
K65E |
probably benign |
Het |
| Trim17 |
A |
G |
11: 58,856,057 (GRCm39) |
E38G |
probably damaging |
Het |
| Trub2 |
A |
T |
2: 29,668,276 (GRCm39) |
|
probably benign |
Het |
| Ttn |
T |
A |
2: 76,571,964 (GRCm39) |
M26310L |
probably damaging |
Het |
| Unc13c |
T |
G |
9: 73,453,322 (GRCm39) |
I1823L |
probably benign |
Het |
| Vav2 |
C |
A |
2: 27,160,151 (GRCm39) |
E728* |
probably null |
Het |
| Virma |
A |
G |
4: 11,540,494 (GRCm39) |
D1465G |
probably benign |
Het |
| Vwa3b |
G |
A |
1: 37,203,597 (GRCm39) |
V59I |
possibly damaging |
Het |
| Xrcc1 |
G |
A |
7: 24,271,642 (GRCm39) |
E542K |
probably benign |
Het |
| Zdhhc6 |
T |
G |
19: 55,287,318 (GRCm39) |
T381P |
probably benign |
Het |
| Zdhhc8 |
T |
C |
16: 18,041,141 (GRCm39) |
S740G |
probably damaging |
Het |
| Zfp106 |
T |
C |
2: 120,364,019 (GRCm39) |
K819R |
probably damaging |
Het |
|
| Other mutations in Vmn2r72 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00931:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01019:Vmn2r72
|
APN |
7 |
85,387,542 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL01445:Vmn2r72
|
APN |
7 |
85,398,854 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02076:Vmn2r72
|
APN |
7 |
85,387,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02082:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02086:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02089:Vmn2r72
|
APN |
7 |
85,387,374 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02125:Vmn2r72
|
APN |
7 |
85,399,919 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02146:Vmn2r72
|
APN |
7 |
85,387,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02272:Vmn2r72
|
APN |
7 |
85,399,901 (GRCm39) |
missense |
probably benign |
|
|
IGL02514:Vmn2r72
|
APN |
7 |
85,387,907 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02662:Vmn2r72
|
APN |
7 |
85,387,391 (GRCm39) |
missense |
probably benign |
0.26 |
|
IGL02697:Vmn2r72
|
APN |
7 |
85,387,879 (GRCm39) |
missense |
probably benign |
0.36 |
|
IGL02733:Vmn2r72
|
APN |
7 |
85,401,021 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03070:Vmn2r72
|
APN |
7 |
85,401,249 (GRCm39) |
splice site |
probably benign |
|
|
IGL03150:Vmn2r72
|
APN |
7 |
85,400,384 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03159:Vmn2r72
|
APN |
7 |
85,404,162 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL03333:Vmn2r72
|
APN |
7 |
85,400,075 (GRCm39) |
missense |
probably benign |
0.10 |
|
R0081:Vmn2r72
|
UTSW |
7 |
85,401,044 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0090:Vmn2r72
|
UTSW |
7 |
85,404,084 (GRCm39) |
missense |
probably benign |
|
|
R0655:Vmn2r72
|
UTSW |
7 |
85,387,319 (GRCm39) |
nonsense |
probably null |
|
|
R0778:Vmn2r72
|
UTSW |
7 |
85,398,947 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1169:Vmn2r72
|
UTSW |
7 |
85,400,517 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1172:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1173:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1175:Vmn2r72
|
UTSW |
7 |
85,401,152 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1248:Vmn2r72
|
UTSW |
7 |
85,398,396 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1302:Vmn2r72
|
UTSW |
7 |
85,387,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1506:Vmn2r72
|
UTSW |
7 |
85,398,419 (GRCm39) |
missense |
probably benign |
|
|
R1632:Vmn2r72
|
UTSW |
7 |
85,401,000 (GRCm39) |
missense |
probably benign |
0.13 |
|
R1775:Vmn2r72
|
UTSW |
7 |
85,387,378 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1962:Vmn2r72
|
UTSW |
7 |
85,398,369 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2201:Vmn2r72
|
UTSW |
7 |
85,387,444 (GRCm39) |
missense |
probably benign |
0.12 |
|
R2290:Vmn2r72
|
UTSW |
7 |
85,387,549 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2327:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2424:Vmn2r72
|
UTSW |
7 |
85,400,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2655:Vmn2r72
|
UTSW |
7 |
85,400,477 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R2860:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2861:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2862:Vmn2r72
|
UTSW |
7 |
85,400,044 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3009:Vmn2r72
|
UTSW |
7 |
85,398,850 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3797:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3798:Vmn2r72
|
UTSW |
7 |
85,387,285 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3902:Vmn2r72
|
UTSW |
7 |
85,398,943 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R3959:Vmn2r72
|
UTSW |
7 |
85,400,339 (GRCm39) |
missense |
probably benign |
0.36 |
|
R3974:Vmn2r72
|
UTSW |
7 |
85,399,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4399:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4421:Vmn2r72
|
UTSW |
7 |
85,387,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4426:Vmn2r72
|
UTSW |
7 |
85,387,036 (GRCm39) |
nonsense |
probably null |
|
|
R4522:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4523:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4533:Vmn2r72
|
UTSW |
7 |
85,401,134 (GRCm39) |
missense |
probably benign |
0.44 |
|
R4691:Vmn2r72
|
UTSW |
7 |
85,387,119 (GRCm39) |
nonsense |
probably null |
|
|
R4781:Vmn2r72
|
UTSW |
7 |
85,387,069 (GRCm39) |
missense |
probably benign |
0.14 |
|
R4863:Vmn2r72
|
UTSW |
7 |
85,399,806 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R4952:Vmn2r72
|
UTSW |
7 |
85,400,317 (GRCm39) |
missense |
probably benign |
|
|
R4991:Vmn2r72
|
UTSW |
7 |
85,400,338 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4995:Vmn2r72
|
UTSW |
7 |
85,387,693 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5095:Vmn2r72
|
UTSW |
7 |
85,387,061 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5174:Vmn2r72
|
UTSW |
7 |
85,387,048 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5276:Vmn2r72
|
UTSW |
7 |
85,387,462 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5395:Vmn2r72
|
UTSW |
7 |
85,400,105 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5560:Vmn2r72
|
UTSW |
7 |
85,401,150 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5933:Vmn2r72
|
UTSW |
7 |
85,387,058 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6033:Vmn2r72
|
UTSW |
7 |
85,387,137 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6354:Vmn2r72
|
UTSW |
7 |
85,399,747 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6362:Vmn2r72
|
UTSW |
7 |
85,400,382 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6594:Vmn2r72
|
UTSW |
7 |
85,398,892 (GRCm39) |
missense |
probably benign |
0.32 |
|
R6794:Vmn2r72
|
UTSW |
7 |
85,387,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7113:Vmn2r72
|
UTSW |
7 |
85,399,011 (GRCm39) |
splice site |
probably null |
|
|
R7189:Vmn2r72
|
UTSW |
7 |
85,404,125 (GRCm39) |
missense |
probably benign |
0.36 |
|
R7266:Vmn2r72
|
UTSW |
7 |
85,387,482 (GRCm39) |
nonsense |
probably null |
|
|
R7323:Vmn2r72
|
UTSW |
7 |
85,399,771 (GRCm39) |
missense |
probably benign |
|
|
R7426:Vmn2r72
|
UTSW |
7 |
85,400,348 (GRCm39) |
missense |
probably benign |
|
|
R7606:Vmn2r72
|
UTSW |
7 |
85,400,362 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7651:Vmn2r72
|
UTSW |
7 |
85,401,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7688:Vmn2r72
|
UTSW |
7 |
85,404,098 (GRCm39) |
missense |
probably benign |
0.32 |
|
R7753:Vmn2r72
|
UTSW |
7 |
85,399,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7843:Vmn2r72
|
UTSW |
7 |
85,398,838 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8157:Vmn2r72
|
UTSW |
7 |
85,400,441 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8254:Vmn2r72
|
UTSW |
7 |
85,400,227 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8389:Vmn2r72
|
UTSW |
7 |
85,401,168 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8444:Vmn2r72
|
UTSW |
7 |
85,387,383 (GRCm39) |
missense |
probably benign |
|
|
R8989:Vmn2r72
|
UTSW |
7 |
85,404,134 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9080:Vmn2r72
|
UTSW |
7 |
85,387,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9269:Vmn2r72
|
UTSW |
7 |
85,400,411 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9317:Vmn2r72
|
UTSW |
7 |
85,404,022 (GRCm39) |
missense |
probably benign |
0.04 |
|
R9509:Vmn2r72
|
UTSW |
7 |
85,404,075 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Vmn2r72
|
UTSW |
7 |
85,398,399 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- CACAGTCAGTAATCTTTAGTATTCTGC -3'
(R):5'- TATGTGTGTTAAACCAGGTCTTTC -3'
Sequencing Primer
(F):5'- TGAGACAAAAATACAGTTCAAGAGAG -3'
(R):5'- AAACCAGGTCTTTCATTGTATCTCTG -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation