Incidental Mutation 'R1498:Vmn2r6'
| ID |
169014 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Vmn2r6
|
| Ensembl Gene |
ENSMUSG00000090581 |
| Gene Name |
vomeronasal 2, receptor 6 |
| Synonyms |
EG620718, EG667069 |
| MMRRC Submission |
039549-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.184)
|
| Stock # |
R1498 (G1)
|
| Quality Score |
203 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
64537561-64565298 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 64556469 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Serine
at position 315
(T315S)
|
| 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: T226S
PolyPhen 2
Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000131831
Gene: ENSMUSG00000090581
AA Change: T226S
| 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: T315S
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000135148
Gene: ENSMUSG00000090581
AA Change: T315S
| 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: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 92.6%
|
| Validation Efficiency |
97% (83/86) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1600015I10Rik |
A |
G |
6: 48,931,371 (GRCm38) |
H435R |
probably benign |
Het |
| Acly |
A |
G |
11: 100,483,801 (GRCm38) |
S799P |
probably benign |
Het |
| Acvr1b |
T |
C |
15: 101,194,010 (GRCm38) |
F57S |
probably benign |
Het |
| Adamts5 |
T |
A |
16: 85,900,102 (GRCm38) |
T56S |
possibly damaging |
Het |
| Adrb2 |
T |
C |
18: 62,178,933 (GRCm38) |
T274A |
probably damaging |
Het |
| Agr3 |
A |
T |
12: 35,934,380 (GRCm38) |
|
probably null |
Het |
| Ankrd6 |
A |
G |
4: 32,810,289 (GRCm38) |
M405T |
probably benign |
Het |
| Aqp5 |
T |
C |
15: 99,593,247 (GRCm38) |
I60T |
probably damaging |
Het |
| Arf5 |
G |
T |
6: 28,426,154 (GRCm38) |
R180L |
probably benign |
Het |
| Asap3 |
A |
G |
4: 136,239,194 (GRCm38) |
N528D |
probably benign |
Het |
| Atmin |
G |
A |
8: 116,954,801 (GRCm38) |
E180K |
probably benign |
Het |
| Bcl11a |
A |
T |
11: 24,164,005 (GRCm38) |
E449D |
probably damaging |
Het |
| Cep128 |
A |
T |
12: 91,366,417 (GRCm38) |
F25I |
probably benign |
Het |
| Cfp |
GCAC |
GC |
X: 20,929,666 (GRCm38) |
|
probably null |
Het |
| Chpt1 |
T |
A |
10: 88,477,104 (GRCm38) |
Y282F |
possibly damaging |
Het |
| Cul7 |
A |
G |
17: 46,655,710 (GRCm38) |
D355G |
probably benign |
Het |
| Daxx |
T |
C |
17: 33,912,253 (GRCm38) |
Y385H |
probably damaging |
Het |
| Dnah2 |
A |
C |
11: 69,520,667 (GRCm38) |
|
probably null |
Het |
| Dscc1 |
CTGAATGAAT |
CTGAAT |
15: 55,080,176 (GRCm38) |
|
probably benign |
Het |
| Erc2 |
T |
A |
14: 28,302,898 (GRCm38) |
M578K |
probably benign |
Het |
| Evc |
T |
A |
5: 37,323,700 (GRCm38) |
H267L |
possibly damaging |
Het |
| Exosc10 |
A |
C |
4: 148,581,786 (GRCm38) |
Q837P |
possibly damaging |
Het |
| Fasn |
G |
A |
11: 120,815,419 (GRCm38) |
T1033I |
probably damaging |
Het |
| Fat1 |
C |
A |
8: 45,025,484 (GRCm38) |
Y2522* |
probably null |
Het |
| Fbxw8 |
G |
A |
5: 118,065,785 (GRCm38) |
|
probably benign |
Het |
| Fyn |
A |
G |
10: 39,532,124 (GRCm38) |
D321G |
possibly damaging |
Het |
| Gm14685 |
G |
T |
X: 73,127,655 (GRCm38) |
G218C |
probably damaging |
Het |
| Gm156 |
A |
G |
6: 129,771,740 (GRCm38) |
S105P |
probably damaging |
Het |
| Grm6 |
G |
A |
11: 50,857,256 (GRCm38) |
V398M |
probably damaging |
Het |
| Gtpbp1 |
T |
A |
15: 79,719,021 (GRCm38) |
|
probably null |
Het |
| Hnf1a |
A |
G |
5: 114,970,537 (GRCm38) |
V103A |
probably damaging |
Het |
| Hsp90aa1 |
A |
T |
12: 110,695,688 (GRCm38) |
|
probably null |
Het |
| Iqgap2 |
C |
T |
13: 95,646,805 (GRCm38) |
V1288I |
probably benign |
Het |
| Irx5 |
A |
G |
8: 92,359,886 (GRCm38) |
D199G |
probably damaging |
Het |
| Krt9 |
G |
T |
11: 100,188,369 (GRCm38) |
C732* |
probably null |
Het |
| Lifr |
T |
C |
15: 7,190,618 (GRCm38) |
S910P |
probably damaging |
Het |
| Lrig1 |
G |
A |
6: 94,627,987 (GRCm38) |
A209V |
possibly damaging |
Het |
| Lrrk1 |
T |
A |
7: 66,302,671 (GRCm38) |
R506* |
probably null |
Het |
| Lyst |
T |
A |
13: 13,650,375 (GRCm38) |
I1525K |
possibly damaging |
Het |
| Mad2l1 |
C |
T |
6: 66,539,842 (GRCm38) |
Q173* |
probably null |
Het |
| Mcoln1 |
T |
A |
8: 3,512,861 (GRCm38) |
I524N |
probably damaging |
Het |
| Mmp3 |
A |
T |
9: 7,446,967 (GRCm38) |
D49V |
possibly damaging |
Het |
| Morc3 |
A |
T |
16: 93,853,855 (GRCm38) |
N321I |
probably damaging |
Het |
| Mrpl48 |
T |
C |
7: 100,546,488 (GRCm38) |
|
probably benign |
Het |
| Myo6 |
T |
A |
9: 80,307,679 (GRCm38) |
D1231E |
probably damaging |
Het |
| Nlrc4 |
A |
G |
17: 74,446,413 (GRCm38) |
I325T |
probably benign |
Het |
| Olfr1079 |
A |
G |
2: 86,538,558 (GRCm38) |
V117A |
probably benign |
Het |
| Olfr1314 |
A |
T |
2: 112,092,593 (GRCm38) |
M36K |
probably benign |
Het |
| Olfr348 |
A |
T |
2: 36,787,346 (GRCm38) |
I274F |
probably damaging |
Het |
| Olfr699 |
T |
C |
7: 106,790,416 (GRCm38) |
Y195C |
possibly damaging |
Het |
| Olfr894 |
C |
G |
9: 38,219,380 (GRCm38) |
P183A |
probably damaging |
Het |
| Parvg |
T |
A |
15: 84,334,631 (GRCm38) |
S230T |
possibly damaging |
Het |
| Pcca |
T |
C |
14: 122,616,818 (GRCm38) |
I118T |
probably damaging |
Het |
| Pde6a |
A |
G |
18: 61,232,860 (GRCm38) |
N219S |
possibly damaging |
Het |
| Phldb1 |
G |
T |
9: 44,701,618 (GRCm38) |
P935Q |
possibly damaging |
Het |
| Plppr5 |
T |
C |
3: 117,662,612 (GRCm38) |
S261P |
probably damaging |
Het |
| Ppl |
T |
C |
16: 5,104,765 (GRCm38) |
N260S |
probably benign |
Het |
| Ppp1r3e |
A |
T |
14: 54,876,425 (GRCm38) |
H263Q |
probably benign |
Het |
| Ppp3cb |
T |
C |
14: 20,509,499 (GRCm38) |
|
probably null |
Het |
| Ppt2 |
A |
T |
17: 34,623,101 (GRCm38) |
D185E |
probably benign |
Het |
| Prr27 |
A |
T |
5: 87,850,741 (GRCm38) |
|
probably benign |
Het |
| Ptcd3 |
A |
T |
6: 71,893,495 (GRCm38) |
V327E |
probably damaging |
Het |
| Rsf1 |
GCG |
GCGACG |
7: 97,579,907 (GRCm38) |
|
probably benign |
Het |
| Rtp1 |
A |
T |
16: 23,431,220 (GRCm38) |
M112L |
probably benign |
Het |
| Slc22a5 |
A |
T |
11: 53,869,314 (GRCm38) |
L392Q |
probably damaging |
Het |
| Slc6a7 |
A |
G |
18: 60,996,692 (GRCm38) |
I614T |
probably benign |
Het |
| Slu7 |
C |
A |
11: 43,438,217 (GRCm38) |
P89T |
possibly damaging |
Het |
| Smarcc2 |
T |
C |
10: 128,482,192 (GRCm38) |
V618A |
probably benign |
Het |
| Sorl1 |
C |
T |
9: 42,041,073 (GRCm38) |
R729Q |
probably damaging |
Het |
| Sptbn2 |
T |
C |
19: 4,744,246 (GRCm38) |
F1493L |
possibly damaging |
Het |
| Sulf1 |
C |
T |
1: 12,848,350 (GRCm38) |
T66I |
probably damaging |
Het |
| Tgtp2 |
A |
G |
11: 49,059,338 (GRCm38) |
Y136H |
probably damaging |
Het |
| Tmem117 |
T |
C |
15: 94,638,361 (GRCm38) |
F92S |
probably damaging |
Het |
| Tmprss9 |
T |
A |
10: 80,895,100 (GRCm38) |
V820E |
probably benign |
Het |
| Tpcn2 |
A |
G |
7: 145,268,911 (GRCm38) |
Y266H |
probably damaging |
Het |
| Trat1 |
A |
G |
16: 48,734,941 (GRCm38) |
S143P |
probably benign |
Het |
| Vmn1r49 |
T |
A |
6: 90,072,316 (GRCm38) |
R235W |
probably damaging |
Het |
| Vmn1r71 |
A |
T |
7: 10,748,648 (GRCm38) |
C38S |
probably benign |
Het |
| Wdr36 |
A |
G |
18: 32,852,968 (GRCm38) |
D575G |
possibly damaging |
Het |
| Zfp292 |
G |
T |
4: 34,805,397 (GRCm38) |
A2549E |
possibly damaging |
Het |
| Zfp354a |
A |
T |
11: 51,070,246 (GRCm38) |
H426L |
probably damaging |
Het |
| Zfp407 |
C |
T |
18: 84,559,773 (GRCm38) |
A1072T |
probably benign |
Het |
| Zfp648 |
T |
A |
1: 154,205,373 (GRCm38) |
I426N |
probably damaging |
Het |
| Zfp72 |
T |
C |
13: 74,372,617 (GRCm38) |
N114S |
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 |
|
|
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 |
|
R9616:Vmn2r6
|
UTSW |
3 |
64,538,303 (GRCm38) |
missense |
probably damaging |
1.00 |
|
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'- GGTGGTCCACATTGTATGGCACAG -3'
(R):5'- AGGTGGGATATGCTTCTTCCTCCTC -3'
Sequencing Primer
(F):5'- TTGGGCCAGGTACAGTTAAAAG -3'
(R):5'- CCCAGTGATAAATTCCAGTCTGAGG -3'
|
| Posted On |
2014-04-13 |
Incidental Mutation