Incidental Mutation 'R7250:Samd9l'
ID |
563822 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Samd9l
|
Ensembl Gene |
ENSMUSG00000047735 |
Gene Name |
sterile alpha motif domain containing 9-like |
Synonyms |
ESTM25 |
MMRRC Submission |
045350-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7250 (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 3374201 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 1020
(D1020G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112688
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000120087]
[ENSMUST00000201638]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000120087
AA Change: D1020G
PolyPhen 2
Score 0.782 (Sensitivity: 0.85; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000112688 Gene: ENSMUSG00000047735 AA Change: D1020G
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: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
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: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
Actl7b |
T |
A |
4: 56,741,035 (GRCm39) |
M108L |
probably benign |
Het |
Adgrf3 |
T |
A |
5: 30,400,680 (GRCm39) |
I934L |
probably damaging |
Het |
Adprm |
A |
G |
11: 66,932,450 (GRCm39) |
V153A |
probably benign |
Het |
Aif1l |
G |
A |
2: 31,859,764 (GRCm39) |
V109M |
probably damaging |
Het |
Asphd1 |
T |
A |
7: 126,545,942 (GRCm39) |
E307V |
probably damaging |
Het |
Ate1 |
T |
A |
7: 130,121,701 (GRCm39) |
|
probably benign |
Het |
Borcs7 |
A |
G |
19: 46,688,047 (GRCm39) |
H64R |
probably damaging |
Het |
C1qtnf1 |
A |
G |
11: 118,339,176 (GRCm39) |
*282W |
probably null |
Het |
Cacna1c |
A |
G |
6: 118,574,966 (GRCm39) |
C1985R |
|
Het |
Cacna1c |
A |
T |
6: 118,673,412 (GRCm39) |
V647E |
|
Het |
Cacna1d |
A |
G |
14: 29,797,108 (GRCm39) |
S1497P |
probably damaging |
Het |
Cacna1e |
T |
A |
1: 154,576,235 (GRCm39) |
I133F |
possibly damaging |
Het |
Ccdc63 |
A |
T |
5: 122,260,906 (GRCm39) |
L206H |
probably damaging |
Het |
Cenatac |
A |
G |
9: 44,323,748 (GRCm39) |
|
probably null |
Het |
Cspg4b |
T |
G |
13: 113,455,349 (GRCm39) |
I465R |
|
Het |
D430041D05Rik |
T |
C |
2: 104,086,961 (GRCm39) |
T672A |
possibly damaging |
Het |
D630045J12Rik |
G |
T |
6: 38,119,546 (GRCm39) |
T1732K |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,507,736 (GRCm39) |
I158T |
probably damaging |
Het |
Ddx52 |
G |
A |
11: 83,835,392 (GRCm39) |
G106D |
probably benign |
Het |
Dock2 |
A |
G |
11: 34,586,032 (GRCm39) |
V550A |
probably benign |
Het |
Dock2 |
C |
T |
11: 34,586,120 (GRCm39) |
D521N |
probably damaging |
Het |
F13b |
T |
C |
1: 139,444,227 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
A |
G |
7: 100,908,892 (GRCm39) |
K431R |
possibly damaging |
Het |
Fez1 |
C |
T |
9: 36,779,090 (GRCm39) |
R256C |
probably damaging |
Het |
Gjd4 |
T |
A |
18: 9,280,391 (GRCm39) |
Q229L |
probably benign |
Het |
Gpr45 |
T |
A |
1: 43,071,531 (GRCm39) |
I58N |
probably damaging |
Het |
Gstm1 |
T |
A |
3: 107,923,709 (GRCm39) |
I99F |
probably damaging |
Het |
Gtpbp8 |
T |
A |
16: 44,564,225 (GRCm39) |
T149S |
probably damaging |
Het |
H2-Ab1 |
A |
G |
17: 34,486,481 (GRCm39) |
D180G |
probably damaging |
Het |
Hdhd5 |
A |
G |
6: 120,494,016 (GRCm39) |
I188T |
possibly damaging |
Het |
Hfm1 |
T |
C |
5: 107,052,197 (GRCm39) |
I300V |
probably benign |
Het |
Hnrnpr |
T |
G |
4: 136,059,746 (GRCm39) |
D283E |
probably benign |
Het |
Hsp90b1 |
T |
C |
10: 86,527,572 (GRCm39) |
E768G |
unknown |
Het |
Kcna4 |
C |
A |
2: 107,126,663 (GRCm39) |
Q466K |
possibly damaging |
Het |
Kcnk6 |
A |
G |
7: 28,931,619 (GRCm39) |
L97P |
probably benign |
Het |
Kics2 |
T |
C |
10: 121,581,376 (GRCm39) |
S126P |
possibly damaging |
Het |
Klf5 |
A |
G |
14: 99,536,455 (GRCm39) |
S9G |
probably benign |
Het |
Kmt2c |
C |
A |
5: 25,504,489 (GRCm39) |
K3606N |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,514,805 (GRCm39) |
T3013A |
probably benign |
Het |
Lancl1 |
A |
G |
1: 67,048,458 (GRCm39) |
Y207H |
possibly damaging |
Het |
Lipe |
G |
C |
7: 25,088,085 (GRCm39) |
|
probably benign |
Het |
Lrrc66 |
T |
A |
5: 73,768,224 (GRCm39) |
H239L |
probably benign |
Het |
Ltbp2 |
C |
T |
12: 84,834,166 (GRCm39) |
W1441* |
probably null |
Het |
Man2a1 |
T |
C |
17: 64,943,583 (GRCm39) |
S213P |
probably benign |
Het |
Mapre2 |
C |
T |
18: 23,991,119 (GRCm39) |
A171V |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,695,427 (GRCm39) |
D1155E |
probably damaging |
Het |
Mki67 |
T |
C |
7: 135,301,053 (GRCm39) |
D1327G |
possibly damaging |
Het |
Mx2 |
T |
C |
16: 97,348,664 (GRCm39) |
I279T |
probably damaging |
Het |
Myo5c |
A |
G |
9: 75,169,497 (GRCm39) |
T441A |
probably damaging |
Het |
Nlrp9a |
T |
G |
7: 26,258,143 (GRCm39) |
V587G |
possibly damaging |
Het |
Npas2 |
A |
T |
1: 39,377,188 (GRCm39) |
T517S |
probably damaging |
Het |
Npy1r |
T |
C |
8: 67,157,712 (GRCm39) |
S341P |
probably benign |
Het |
Ntm |
A |
G |
9: 29,322,988 (GRCm39) |
W11R |
probably benign |
Het |
Nxpe2 |
A |
T |
9: 48,238,096 (GRCm39) |
I53N |
possibly damaging |
Het |
Onecut2 |
T |
C |
18: 64,519,511 (GRCm39) |
F443L |
probably benign |
Het |
Or10g6 |
T |
A |
9: 39,934,050 (GRCm39) |
Y120* |
probably null |
Het |
Or2r2 |
A |
G |
6: 42,463,689 (GRCm39) |
V146A |
probably benign |
Het |
Or52ac1 |
A |
T |
7: 104,245,738 (GRCm39) |
Y217N |
probably damaging |
Het |
Parp2 |
T |
A |
14: 51,054,801 (GRCm39) |
V248E |
probably benign |
Het |
Pcdh12 |
C |
A |
18: 38,415,029 (GRCm39) |
V699L |
probably benign |
Het |
Pja2 |
G |
A |
17: 64,616,451 (GRCm39) |
P148L |
probably benign |
Het |
Poglut3 |
C |
T |
9: 53,301,821 (GRCm39) |
Q158* |
probably null |
Het |
Ppip5k2 |
T |
G |
1: 97,673,187 (GRCm39) |
D415A |
probably benign |
Het |
Prss47 |
A |
G |
13: 65,200,355 (GRCm39) |
S74P |
probably benign |
Het |
Ptprg |
G |
T |
14: 12,166,767 (GRCm38) |
M723I |
probably benign |
Het |
Qsox2 |
A |
T |
2: 26,118,444 (GRCm39) |
I109N |
probably damaging |
Het |
Ranbp3l |
A |
G |
15: 9,041,853 (GRCm39) |
E217G |
probably benign |
Het |
Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
Rgs12 |
T |
A |
5: 35,122,841 (GRCm39) |
F208Y |
probably damaging |
Het |
Rin3 |
C |
T |
12: 102,334,893 (GRCm39) |
T268I |
unknown |
Het |
Rttn |
T |
A |
18: 89,007,647 (GRCm39) |
D427E |
probably benign |
Het |
Samd13 |
G |
A |
3: 146,352,079 (GRCm39) |
P91S |
probably benign |
Het |
Sec62 |
T |
G |
3: 30,866,496 (GRCm39) |
L201V |
possibly damaging |
Het |
Setdb1 |
C |
T |
3: 95,261,852 (GRCm39) |
|
probably null |
Het |
Sf3a3 |
A |
T |
4: 124,616,708 (GRCm39) |
T197S |
probably benign |
Het |
Slc20a1 |
A |
T |
2: 129,051,844 (GRCm39) |
I618F |
possibly damaging |
Het |
Slc38a3 |
A |
T |
9: 107,533,865 (GRCm39) |
M186K |
probably benign |
Het |
Slc39a13 |
T |
C |
2: 90,893,503 (GRCm39) |
T319A |
probably benign |
Het |
Slc44a4 |
T |
C |
17: 35,137,520 (GRCm39) |
|
probably null |
Het |
St3gal1 |
A |
C |
15: 66,978,578 (GRCm39) |
D314E |
possibly damaging |
Het |
Suclg1 |
A |
G |
6: 73,248,074 (GRCm39) |
N265S |
probably benign |
Het |
Sult2b1 |
A |
T |
7: 45,433,361 (GRCm39) |
V2D |
unknown |
Het |
Supv3l1 |
T |
A |
10: 62,280,846 (GRCm39) |
I182F |
probably damaging |
Het |
Tcp11l2 |
T |
C |
10: 84,423,105 (GRCm39) |
|
probably null |
Het |
Tenm2 |
C |
A |
11: 35,963,625 (GRCm39) |
L935F |
probably damaging |
Het |
Tnks |
T |
A |
8: 35,318,912 (GRCm39) |
I790F |
probably damaging |
Het |
Top2b |
C |
T |
14: 16,420,411 (GRCm38) |
T1274I |
probably benign |
Het |
Tpi1 |
A |
T |
6: 124,789,441 (GRCm39) |
I178N |
probably damaging |
Het |
Trav9d-1 |
A |
T |
14: 53,030,153 (GRCm39) |
S86C |
probably damaging |
Het |
Treml2 |
A |
G |
17: 48,616,155 (GRCm39) |
E265G |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,668,685 (GRCm39) |
S744T |
possibly damaging |
Het |
Usp33 |
T |
A |
3: 152,097,999 (GRCm39) |
L909* |
probably null |
Het |
Vcan |
A |
G |
13: 89,869,805 (GRCm39) |
I210T |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,879,576 (GRCm39) |
|
probably null |
Het |
Vsig10l |
A |
T |
7: 43,113,099 (GRCm39) |
D17V |
probably benign |
Het |
Zbtb7b |
T |
A |
3: 89,286,976 (GRCm39) |
T498S |
probably benign |
Het |
Zfp366 |
T |
A |
13: 99,366,076 (GRCm39) |
H412Q |
probably damaging |
Het |
Zfp53 |
C |
A |
17: 21,729,840 (GRCm39) |
D624E |
probably damaging |
Het |
Zfp827 |
A |
T |
8: 79,916,721 (GRCm39) |
D432V |
|
Het |
Zic1 |
T |
C |
9: 91,247,028 (GRCm39) |
T15A |
probably damaging |
Het |
Zswim8 |
T |
C |
14: 20,770,036 (GRCm39) |
C1368R |
probably 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 |
|
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 |
R8098:Samd9l
|
UTSW |
6 |
3,375,549 (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'- TTTGCCCAGACTAAAGCAGTG -3'
(R):5'- CTTACACCAAGAAATATGGGAAACCTG -3'
Sequencing Primer
(F):5'- GAAGTGTCTTGCTAAAGCTTGAC -3'
(R):5'- TTCCACACTTCTAATAAGAACTGAAG -3'
|
Posted On |
2019-06-26 |