Incidental Mutation 'R8098:Samd9l'
ID |
630303 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Samd9l
|
Ensembl Gene |
ENSMUSG00000047735 |
Gene Name |
sterile alpha motif domain containing 9-like |
Synonyms |
ESTM25 |
MMRRC Submission |
067530-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R8098 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
3372257-3399571 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 3375549 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Valine
at position 571
(I571V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112688
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000120087]
[ENSMUST00000201638]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000120087
AA Change: I571V
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000112688 Gene: ENSMUSG00000047735 AA Change: I571V
Domain | Start | End | E-Value | Type |
SCOP:d1kw4a_
|
8 |
75 |
4e-8 |
SMART |
Blast:SAM
|
11 |
75 |
1e-30 |
BLAST |
low complexity region
|
96 |
115 |
N/A |
INTRINSIC |
low complexity region
|
385 |
397 |
N/A |
INTRINSIC |
low complexity region
|
530 |
541 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201638
|
SMART Domains |
Protein: ENSMUSP00000144632 Gene: ENSMUSG00000047735
Domain | Start | End | E-Value | Type |
Pfam:Ste50p-SAM
|
10 |
80 |
1.2e-8 |
PFAM |
Pfam:SAM_2
|
11 |
68 |
8.7e-6 |
PFAM |
Pfam:SAM_1
|
12 |
71 |
2.5e-7 |
PFAM |
|
Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.3%
- 20x: 98.4%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice that are either heterozygous or homozygous for a reporter allele develop myeloid diseases and acute myelogenous leukemia. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,384,618 (GRCm39) |
L449P |
probably damaging |
Het |
Abca15 |
A |
G |
7: 119,960,619 (GRCm39) |
S694G |
probably benign |
Het |
Abcc6 |
A |
G |
7: 45,646,089 (GRCm39) |
L800P |
probably damaging |
Het |
Adam15 |
T |
A |
3: 89,251,193 (GRCm39) |
D504V |
probably damaging |
Het |
Adnp |
T |
C |
2: 168,024,452 (GRCm39) |
T948A |
probably benign |
Het |
Akap11 |
T |
C |
14: 78,750,362 (GRCm39) |
D675G |
|
Het |
Atp13a3 |
A |
C |
16: 30,173,115 (GRCm39) |
V254G |
possibly damaging |
Het |
Atp1a1 |
A |
G |
3: 101,489,365 (GRCm39) |
I749T |
probably damaging |
Het |
B3glct |
T |
A |
5: 149,673,965 (GRCm39) |
Y369* |
probably null |
Het |
Bms1 |
C |
T |
6: 118,361,219 (GRCm39) |
R1204H |
probably damaging |
Het |
Btla |
T |
A |
16: 45,064,612 (GRCm39) |
L188* |
probably null |
Het |
Btn2a2 |
A |
G |
13: 23,666,058 (GRCm39) |
V258A |
probably benign |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,307,338 (GRCm39) |
H1782R |
probably benign |
Het |
Calcoco1 |
T |
C |
15: 102,624,759 (GRCm39) |
D172G |
probably benign |
Het |
Ccdc192 |
A |
T |
18: 57,800,403 (GRCm39) |
I185L |
probably benign |
Het |
Ciart |
G |
A |
3: 95,788,656 (GRCm39) |
P61L |
probably damaging |
Het |
Ckap4 |
A |
G |
10: 84,369,499 (GRCm39) |
S78P |
probably damaging |
Het |
Col6a3 |
A |
T |
1: 90,731,383 (GRCm39) |
D1623E |
probably benign |
Het |
Col7a1 |
A |
G |
9: 108,785,763 (GRCm39) |
T411A |
unknown |
Het |
Cpt1a |
A |
C |
19: 3,420,849 (GRCm39) |
I436L |
probably benign |
Het |
Cyp2c23 |
T |
A |
19: 44,004,242 (GRCm39) |
I173F |
probably benign |
Het |
Dcun1d2 |
T |
C |
8: 13,311,396 (GRCm39) |
T198A |
probably benign |
Het |
Ddx50 |
A |
C |
10: 62,460,922 (GRCm39) |
|
probably null |
Het |
Depdc1b |
A |
G |
13: 108,460,593 (GRCm39) |
T68A |
probably damaging |
Het |
Dgkq |
G |
A |
5: 108,800,334 (GRCm39) |
R546W |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,710,188 (GRCm39) |
W1493* |
probably null |
Het |
Dnah17 |
A |
G |
11: 117,941,193 (GRCm39) |
S3219P |
probably damaging |
Het |
Egf |
T |
A |
3: 129,484,486 (GRCm39) |
Y986F |
probably benign |
Het |
Ell3 |
TCTCCTC |
TCTC |
2: 121,269,937 (GRCm39) |
|
probably benign |
Het |
Ep400 |
A |
T |
5: 110,841,117 (GRCm39) |
M1805K |
unknown |
Het |
Exoc3 |
A |
G |
13: 74,320,271 (GRCm39) |
M730T |
probably benign |
Het |
Fbxl13 |
T |
A |
5: 21,825,716 (GRCm39) |
M129L |
probably benign |
Het |
Fem1al |
A |
G |
11: 29,774,450 (GRCm39) |
S336P |
possibly damaging |
Het |
Gins4 |
T |
A |
8: 23,727,037 (GRCm39) |
M19L |
probably benign |
Het |
Gm3238 |
T |
C |
10: 77,606,474 (GRCm39) |
N229S |
unknown |
Het |
Gpd2 |
T |
A |
2: 57,180,020 (GRCm39) |
V89D |
possibly damaging |
Het |
Hectd4 |
G |
A |
5: 121,459,461 (GRCm39) |
V777I |
possibly damaging |
Het |
Hgf |
T |
A |
5: 16,766,059 (GRCm39) |
V65E |
probably benign |
Het |
Hnrnpdl |
A |
G |
5: 100,185,779 (GRCm39) |
S169P |
probably benign |
Het |
Igfbp3 |
T |
C |
11: 7,160,104 (GRCm39) |
D183G |
possibly damaging |
Het |
Il16 |
A |
G |
7: 83,295,767 (GRCm39) |
V1134A |
probably damaging |
Het |
Kcnn4 |
A |
G |
7: 24,083,504 (GRCm39) |
D395G |
probably damaging |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Kif13a |
T |
C |
13: 46,968,780 (GRCm39) |
N354S |
probably damaging |
Het |
Lrp1 |
C |
T |
10: 127,410,324 (GRCm39) |
R1474Q |
possibly damaging |
Het |
Map3k9 |
T |
C |
12: 81,780,888 (GRCm39) |
Q424R |
probably damaging |
Het |
Mkx |
A |
C |
18: 6,992,784 (GRCm39) |
S167A |
possibly damaging |
Het |
Ms4a14 |
A |
G |
19: 11,281,979 (GRCm39) |
F193S |
possibly damaging |
Het |
Myo18a |
A |
T |
11: 77,736,227 (GRCm39) |
D1508V |
probably damaging |
Het |
Nek4 |
T |
A |
14: 30,685,908 (GRCm39) |
N273K |
probably benign |
Het |
Nipal3 |
A |
T |
4: 135,179,709 (GRCm39) |
V403D |
possibly damaging |
Het |
Nlrp6 |
G |
A |
7: 140,503,168 (GRCm39) |
V425M |
probably damaging |
Het |
Or13p4 |
A |
T |
4: 118,547,406 (GRCm39) |
V81E |
possibly damaging |
Het |
Or14j6 |
A |
G |
17: 38,215,250 (GRCm39) |
D271G |
probably damaging |
Het |
Or4c122 |
T |
A |
2: 89,079,652 (GRCm39) |
M117L |
possibly damaging |
Het |
Or9k2 |
T |
C |
10: 129,998,916 (GRCm39) |
K93R |
probably benign |
Het |
Otub1 |
A |
T |
19: 7,181,794 (GRCm39) |
D27E |
probably damaging |
Het |
Pcnx2 |
T |
C |
8: 126,495,040 (GRCm39) |
D1607G |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,071,178 (GRCm39) |
Y16C |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Prph2 |
A |
T |
17: 47,230,892 (GRCm39) |
M262L |
probably benign |
Het |
Pxdn |
C |
T |
12: 30,056,601 (GRCm39) |
L1271F |
probably damaging |
Het |
Rnf10 |
A |
C |
5: 115,389,438 (GRCm39) |
I243S |
probably damaging |
Het |
Scube1 |
C |
T |
15: 83,543,289 (GRCm39) |
G183D |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,857,028 (GRCm39) |
V426A |
probably benign |
Het |
Slc20a1 |
T |
C |
2: 129,051,041 (GRCm39) |
L566P |
probably damaging |
Het |
Slc22a3 |
A |
G |
17: 12,642,619 (GRCm39) |
|
probably null |
Het |
Snx11 |
G |
T |
11: 96,661,500 (GRCm39) |
S168R |
probably benign |
Het |
Snx5 |
T |
C |
2: 144,097,482 (GRCm39) |
N218D |
probably benign |
Het |
Snx7 |
A |
T |
3: 117,632,583 (GRCm39) |
D169E |
probably benign |
Het |
Soat1 |
A |
G |
1: 156,274,180 (GRCm39) |
L77P |
probably damaging |
Het |
Sucnr1 |
T |
A |
3: 59,994,162 (GRCm39) |
V230E |
probably damaging |
Het |
Supv3l1 |
T |
C |
10: 62,265,282 (GRCm39) |
K753E |
probably benign |
Het |
Tango6 |
T |
G |
8: 107,468,990 (GRCm39) |
L829V |
possibly damaging |
Het |
Tek |
T |
C |
4: 94,715,907 (GRCm39) |
V443A |
probably benign |
Het |
Tet1 |
A |
T |
10: 62,714,859 (GRCm39) |
L312Q |
probably damaging |
Het |
Tgm1 |
A |
T |
14: 55,947,991 (GRCm39) |
N269K |
probably damaging |
Het |
Thrb |
A |
T |
14: 18,008,645 (GRCm38) |
D168V |
probably damaging |
Het |
Tk2 |
C |
T |
8: 104,957,804 (GRCm39) |
V181I |
probably benign |
Het |
Tm6sf2 |
T |
C |
8: 70,526,972 (GRCm39) |
L47P |
probably damaging |
Het |
Tmcc3 |
T |
A |
10: 94,415,078 (GRCm39) |
M291K |
probably benign |
Het |
Tnfrsf21 |
A |
G |
17: 43,350,790 (GRCm39) |
E318G |
probably benign |
Het |
Ttc7 |
T |
C |
17: 87,641,756 (GRCm39) |
V451A |
probably benign |
Het |
Ugt2b36 |
A |
T |
5: 87,240,252 (GRCm39) |
D44E |
probably benign |
Het |
Usp17la |
G |
T |
7: 104,510,138 (GRCm39) |
V248L |
probably damaging |
Het |
Utp20 |
A |
C |
10: 88,588,810 (GRCm39) |
I2453S |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,863,817 (GRCm39) |
I566N |
possibly damaging |
Het |
Zfp282 |
A |
G |
6: 47,867,652 (GRCm39) |
D276G |
probably benign |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
Zfp866 |
T |
C |
8: 70,218,628 (GRCm39) |
K331E |
probably benign |
Het |
Zkscan17 |
A |
T |
11: 59,394,410 (GRCm39) |
W64R |
possibly damaging |
Het |
|
Other mutations in Samd9l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00538:Samd9l
|
APN |
6 |
3,376,779 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00550:Samd9l
|
APN |
6 |
3,374,594 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01100:Samd9l
|
APN |
6 |
3,375,863 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01321:Samd9l
|
APN |
6 |
3,376,259 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01553:Samd9l
|
APN |
6 |
3,375,566 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01575:Samd9l
|
APN |
6 |
3,376,734 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01896:Samd9l
|
APN |
6 |
3,375,120 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01915:Samd9l
|
APN |
6 |
3,373,864 (GRCm39) |
nonsense |
probably null |
|
IGL02063:Samd9l
|
APN |
6 |
3,372,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:Samd9l
|
APN |
6 |
3,376,575 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02145:Samd9l
|
APN |
6 |
3,374,105 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02163:Samd9l
|
APN |
6 |
3,374,246 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02256:Samd9l
|
APN |
6 |
3,376,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02508:Samd9l
|
APN |
6 |
3,374,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Samd9l
|
APN |
6 |
3,375,760 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02968:Samd9l
|
APN |
6 |
3,376,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03058:Samd9l
|
APN |
6 |
3,374,980 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03068:Samd9l
|
APN |
6 |
3,375,348 (GRCm39) |
nonsense |
probably null |
|
IGL03160:Samd9l
|
APN |
6 |
3,374,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03372:Samd9l
|
APN |
6 |
3,375,314 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03385:Samd9l
|
APN |
6 |
3,376,208 (GRCm39) |
missense |
probably damaging |
0.99 |
boston_lager
|
UTSW |
6 |
3,375,761 (GRCm39) |
missense |
probably benign |
0.12 |
ipa
|
UTSW |
6 |
3,376,347 (GRCm39) |
missense |
probably damaging |
1.00 |
Paine
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
probably damaging |
0.99 |
samad
|
UTSW |
6 |
3,374,032 (GRCm39) |
nonsense |
probably null |
|
IGL03054:Samd9l
|
UTSW |
6 |
3,376,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Samd9l
|
UTSW |
6 |
3,374,946 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0112:Samd9l
|
UTSW |
6 |
3,376,031 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0356:Samd9l
|
UTSW |
6 |
3,375,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0370:Samd9l
|
UTSW |
6 |
3,377,264 (GRCm39) |
start gained |
probably benign |
|
R0398:Samd9l
|
UTSW |
6 |
3,374,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Samd9l
|
UTSW |
6 |
3,372,725 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0833:Samd9l
|
UTSW |
6 |
3,372,725 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0880:Samd9l
|
UTSW |
6 |
3,377,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R1110:Samd9l
|
UTSW |
6 |
3,374,267 (GRCm39) |
missense |
probably benign |
0.44 |
R1155:Samd9l
|
UTSW |
6 |
3,376,939 (GRCm39) |
missense |
probably benign |
0.01 |
R1268:Samd9l
|
UTSW |
6 |
3,376,113 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1293:Samd9l
|
UTSW |
6 |
3,373,947 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1478:Samd9l
|
UTSW |
6 |
3,376,369 (GRCm39) |
missense |
probably benign |
0.06 |
R1573:Samd9l
|
UTSW |
6 |
3,375,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1590:Samd9l
|
UTSW |
6 |
3,375,761 (GRCm39) |
missense |
probably benign |
0.12 |
R1611:Samd9l
|
UTSW |
6 |
3,373,771 (GRCm39) |
missense |
probably benign |
0.00 |
R1754:Samd9l
|
UTSW |
6 |
3,373,126 (GRCm39) |
missense |
probably damaging |
0.96 |
R1759:Samd9l
|
UTSW |
6 |
3,373,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Samd9l
|
UTSW |
6 |
3,375,264 (GRCm39) |
nonsense |
probably null |
|
R1829:Samd9l
|
UTSW |
6 |
3,375,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1935:Samd9l
|
UTSW |
6 |
3,376,269 (GRCm39) |
missense |
probably benign |
0.01 |
R2154:Samd9l
|
UTSW |
6 |
3,372,945 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2228:Samd9l
|
UTSW |
6 |
3,376,910 (GRCm39) |
missense |
probably benign |
0.08 |
R3622:Samd9l
|
UTSW |
6 |
3,374,032 (GRCm39) |
nonsense |
probably null |
|
R3903:Samd9l
|
UTSW |
6 |
3,376,830 (GRCm39) |
nonsense |
probably null |
|
R3904:Samd9l
|
UTSW |
6 |
3,376,830 (GRCm39) |
nonsense |
probably null |
|
R3945:Samd9l
|
UTSW |
6 |
3,377,029 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4091:Samd9l
|
UTSW |
6 |
3,376,887 (GRCm39) |
missense |
probably benign |
0.22 |
R4602:Samd9l
|
UTSW |
6 |
3,373,937 (GRCm39) |
frame shift |
probably null |
|
R4602:Samd9l
|
UTSW |
6 |
3,373,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Samd9l
|
UTSW |
6 |
3,376,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R4747:Samd9l
|
UTSW |
6 |
3,375,504 (GRCm39) |
nonsense |
probably null |
|
R4762:Samd9l
|
UTSW |
6 |
3,375,623 (GRCm39) |
missense |
probably benign |
0.01 |
R4814:Samd9l
|
UTSW |
6 |
3,372,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R4934:Samd9l
|
UTSW |
6 |
3,375,621 (GRCm39) |
nonsense |
probably null |
|
R5026:Samd9l
|
UTSW |
6 |
3,375,284 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5048:Samd9l
|
UTSW |
6 |
3,374,157 (GRCm39) |
missense |
probably benign |
0.35 |
R5130:Samd9l
|
UTSW |
6 |
3,374,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5271:Samd9l
|
UTSW |
6 |
3,376,156 (GRCm39) |
missense |
probably benign |
0.02 |
R5328:Samd9l
|
UTSW |
6 |
3,376,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R5507:Samd9l
|
UTSW |
6 |
3,373,898 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5587:Samd9l
|
UTSW |
6 |
3,373,291 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5846:Samd9l
|
UTSW |
6 |
3,376,754 (GRCm39) |
missense |
probably benign |
|
R5881:Samd9l
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5889:Samd9l
|
UTSW |
6 |
3,376,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Samd9l
|
UTSW |
6 |
3,377,252 (GRCm39) |
missense |
probably benign |
0.00 |
R6199:Samd9l
|
UTSW |
6 |
3,376,686 (GRCm39) |
missense |
probably benign |
0.13 |
R6298:Samd9l
|
UTSW |
6 |
3,375,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Samd9l
|
UTSW |
6 |
3,376,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Samd9l
|
UTSW |
6 |
3,376,896 (GRCm39) |
missense |
probably benign |
|
R6601:Samd9l
|
UTSW |
6 |
3,377,229 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6655:Samd9l
|
UTSW |
6 |
3,377,247 (GRCm39) |
missense |
probably benign |
0.22 |
R6803:Samd9l
|
UTSW |
6 |
3,375,446 (GRCm39) |
missense |
probably damaging |
0.97 |
R6864:Samd9l
|
UTSW |
6 |
3,374,750 (GRCm39) |
missense |
probably benign |
0.14 |
R6905:Samd9l
|
UTSW |
6 |
3,375,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R6919:Samd9l
|
UTSW |
6 |
3,376,313 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7060:Samd9l
|
UTSW |
6 |
3,372,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R7073:Samd9l
|
UTSW |
6 |
3,375,856 (GRCm39) |
nonsense |
probably null |
|
R7250:Samd9l
|
UTSW |
6 |
3,374,201 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7307:Samd9l
|
UTSW |
6 |
3,372,600 (GRCm39) |
nonsense |
probably null |
|
R7351:Samd9l
|
UTSW |
6 |
3,374,157 (GRCm39) |
missense |
probably benign |
0.35 |
R7423:Samd9l
|
UTSW |
6 |
3,374,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7610:Samd9l
|
UTSW |
6 |
3,376,754 (GRCm39) |
missense |
probably benign |
|
R7667:Samd9l
|
UTSW |
6 |
3,375,975 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7672:Samd9l
|
UTSW |
6 |
3,373,646 (GRCm39) |
missense |
probably benign |
0.16 |
R7680:Samd9l
|
UTSW |
6 |
3,376,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R7680:Samd9l
|
UTSW |
6 |
3,372,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7814:Samd9l
|
UTSW |
6 |
3,374,793 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7829:Samd9l
|
UTSW |
6 |
3,374,749 (GRCm39) |
missense |
probably benign |
0.00 |
R8000:Samd9l
|
UTSW |
6 |
3,373,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8698:Samd9l
|
UTSW |
6 |
3,373,843 (GRCm39) |
missense |
probably benign |
0.06 |
R8785:Samd9l
|
UTSW |
6 |
3,377,064 (GRCm39) |
missense |
probably damaging |
0.99 |
R8795:Samd9l
|
UTSW |
6 |
3,374,221 (GRCm39) |
nonsense |
probably null |
|
R8806:Samd9l
|
UTSW |
6 |
3,376,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R8832:Samd9l
|
UTSW |
6 |
3,374,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Samd9l
|
UTSW |
6 |
3,374,577 (GRCm39) |
missense |
probably damaging |
0.98 |
R9023:Samd9l
|
UTSW |
6 |
3,373,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Samd9l
|
UTSW |
6 |
3,373,493 (GRCm39) |
missense |
probably benign |
0.16 |
R9108:Samd9l
|
UTSW |
6 |
3,373,104 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9213:Samd9l
|
UTSW |
6 |
3,376,856 (GRCm39) |
missense |
probably benign |
0.23 |
R9494:Samd9l
|
UTSW |
6 |
3,375,830 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9504:Samd9l
|
UTSW |
6 |
3,372,621 (GRCm39) |
missense |
probably benign |
0.17 |
R9655:Samd9l
|
UTSW |
6 |
3,373,578 (GRCm39) |
missense |
probably benign |
0.00 |
R9688:Samd9l
|
UTSW |
6 |
3,377,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R9696:Samd9l
|
UTSW |
6 |
3,375,078 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9721:Samd9l
|
UTSW |
6 |
3,375,854 (GRCm39) |
missense |
possibly damaging |
0.69 |
X0026:Samd9l
|
UTSW |
6 |
3,375,560 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Samd9l
|
UTSW |
6 |
3,374,477 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Samd9l
|
UTSW |
6 |
3,376,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CACAGAGGATTTCCAATGCACTC -3'
(R):5'- TGGCAGAGAGATAGAGCTTCTG -3'
Sequencing Primer
(F):5'- CATTTTCTCCAGAATAACAGAGGAGG -3'
(R):5'- GGGGTTAGAAGACTTATTTCATTCC -3'
|
Posted On |
2020-06-30 |