Incidental Mutation 'R4982:D430041D05Rik'
| ID |
384890 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
D430041D05Rik
|
| Ensembl Gene |
ENSMUSG00000068373 |
| Gene Name |
RIKEN cDNA D430041D05 gene |
| Synonyms |
G2 |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.236)
|
| Stock # |
R4982 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
103973418-104241358 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 104085732 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 83
(V83A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000124980
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000089726]
[ENSMUST00000136156]
[ENSMUST00000141159]
[ENSMUST00000149466]
[ENSMUST00000230671]
|
| AlphaFold |
A0A2R8VKG2 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000089726
AA Change: V255A
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000106756
Gene: ENSMUSG00000068373
AA Change: V255A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
|
low complexity region
|
206 |
215 |
N/A |
INTRINSIC |
|
low complexity region
|
218 |
230 |
N/A |
INTRINSIC |
|
low complexity region
|
234 |
253 |
N/A |
INTRINSIC |
|
Pfam:DUF3827
|
498 |
1134 |
2.4e-282 |
PFAM |
|
low complexity region
|
1196 |
1217 |
N/A |
INTRINSIC |
|
low complexity region
|
1331 |
1351 |
N/A |
INTRINSIC |
|
low complexity region
|
1360 |
1372 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000136156
AA Change: V255A
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000139015
|
| SMART Domains |
Protein: ENSMUSP00000124519
Gene: ENSMUSG00000068373
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
|
low complexity region
|
150 |
159 |
N/A |
INTRINSIC |
|
low complexity region
|
162 |
174 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000141159
AA Change: V140A
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
| SMART Domains |
Protein: ENSMUSP00000117041
Gene: ENSMUSG00000068373
AA Change: V140A
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
55 |
70 |
N/A |
INTRINSIC |
|
low complexity region
|
91 |
100 |
N/A |
INTRINSIC |
|
low complexity region
|
103 |
115 |
N/A |
INTRINSIC |
|
low complexity region
|
119 |
138 |
N/A |
INTRINSIC |
|
Pfam:DUF3827
|
383 |
1020 |
8.2e-280 |
PFAM |
|
low complexity region
|
1082 |
1103 |
N/A |
INTRINSIC |
|
low complexity region
|
1217 |
1237 |
N/A |
INTRINSIC |
|
low complexity region
|
1246 |
1258 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000149165
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000149466
AA Change: V83A
PolyPhen 2
Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000124980
Gene: ENSMUSG00000068373
AA Change: V83A
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
|
low complexity region
|
34 |
43 |
N/A |
INTRINSIC |
|
low complexity region
|
46 |
58 |
N/A |
INTRINSIC |
|
low complexity region
|
62 |
81 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150450
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151310
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000230671
AA Change: V939A
PolyPhen 2
Score 0.068 (Sensitivity: 0.94; Specificity: 0.84)
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 71 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
A |
T |
11: 9,242,348 (GRCm39) |
I1404L |
possibly damaging |
Het |
| Adra1b |
A |
G |
11: 43,726,057 (GRCm39) |
S287P |
probably damaging |
Het |
| Atxn2 |
G |
T |
5: 121,952,406 (GRCm39) |
A1280S |
possibly damaging |
Het |
| Bbip1 |
T |
C |
19: 53,920,639 (GRCm39) |
|
probably null |
Het |
| Bbs2 |
A |
G |
8: 94,808,982 (GRCm39) |
|
probably null |
Het |
| Bcl11b |
A |
T |
12: 107,932,031 (GRCm39) |
C180* |
probably null |
Het |
| Bltp3a |
T |
C |
17: 28,105,580 (GRCm39) |
F702S |
probably benign |
Het |
| Bod1l |
A |
G |
5: 41,977,816 (GRCm39) |
V1166A |
probably benign |
Het |
| Bora |
C |
T |
14: 99,284,788 (GRCm39) |
P13S |
probably damaging |
Het |
| C2cd4c |
T |
C |
10: 79,449,075 (GRCm39) |
E24G |
probably benign |
Het |
| Ccne1 |
A |
T |
7: 37,799,996 (GRCm39) |
I196N |
probably damaging |
Het |
| Chsy3 |
C |
T |
18: 59,542,647 (GRCm39) |
S595L |
probably benign |
Het |
| Chsy3 |
T |
A |
18: 59,542,839 (GRCm39) |
I659N |
possibly damaging |
Het |
| Cntrob |
T |
A |
11: 69,202,188 (GRCm39) |
|
probably null |
Het |
| Col5a2 |
G |
A |
1: 45,428,618 (GRCm39) |
P983S |
possibly damaging |
Het |
| Crat |
T |
A |
2: 30,297,148 (GRCm39) |
|
probably null |
Het |
| Ctnnbl1 |
C |
T |
2: 157,678,473 (GRCm39) |
H359Y |
probably benign |
Het |
| Dixdc1 |
A |
G |
9: 50,593,902 (GRCm39) |
S488P |
possibly damaging |
Het |
| Dmrta1 |
T |
C |
4: 89,576,801 (GRCm39) |
C86R |
probably damaging |
Het |
| Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
| Fam171a1 |
G |
A |
2: 3,179,505 (GRCm39) |
|
probably null |
Het |
| Fam222b |
T |
C |
11: 78,045,569 (GRCm39) |
C249R |
probably damaging |
Het |
| Fbxw18 |
T |
A |
9: 109,531,719 (GRCm39) |
|
probably benign |
Het |
| Fes |
T |
C |
7: 80,036,952 (GRCm39) |
Y44C |
probably damaging |
Het |
| Gimap6 |
A |
G |
6: 48,684,933 (GRCm39) |
V51A |
probably benign |
Het |
| Gpr75 |
C |
T |
11: 30,841,463 (GRCm39) |
L123F |
possibly damaging |
Het |
| Gpr75 |
C |
A |
11: 30,841,462 (GRCm39) |
H122Q |
probably damaging |
Het |
| Greb1 |
A |
G |
12: 16,774,762 (GRCm39) |
S212P |
probably damaging |
Het |
| Grin3a |
T |
C |
4: 49,665,512 (GRCm39) |
H1041R |
probably benign |
Het |
| Ifna5 |
A |
G |
4: 88,753,861 (GRCm39) |
N34D |
probably damaging |
Het |
| Ift140 |
A |
T |
17: 25,255,968 (GRCm39) |
H221L |
probably damaging |
Het |
| Igsf3 |
T |
C |
3: 101,342,983 (GRCm39) |
V540A |
probably benign |
Het |
| Il10ra |
A |
G |
9: 45,180,357 (GRCm39) |
L5S |
probably damaging |
Het |
| Klra2 |
A |
T |
6: 131,197,152 (GRCm39) |
D282E |
probably benign |
Het |
| Lyst |
T |
A |
13: 13,900,539 (GRCm39) |
H3138Q |
probably damaging |
Het |
| Malrd1 |
A |
G |
2: 16,046,940 (GRCm39) |
T1689A |
probably benign |
Het |
| Mon2 |
A |
T |
10: 122,831,694 (GRCm39) |
L1671M |
probably damaging |
Het |
| Mpped1 |
T |
C |
15: 83,720,528 (GRCm39) |
F71S |
probably damaging |
Het |
| Mtpap |
C |
A |
18: 4,396,332 (GRCm39) |
H541Q |
probably benign |
Het |
| Muc5ac |
T |
A |
7: 141,363,193 (GRCm39) |
|
probably benign |
Het |
| Mybbp1a |
T |
C |
11: 72,336,040 (GRCm39) |
I451T |
probably damaging |
Het |
| Myh7 |
T |
A |
14: 55,210,224 (GRCm39) |
E1827V |
probably damaging |
Het |
| Or1j14 |
A |
T |
2: 36,417,409 (GRCm39) |
|
probably null |
Het |
| Or2h15 |
A |
T |
17: 38,441,468 (GRCm39) |
I205N |
probably damaging |
Het |
| Or5p75-ps1 |
T |
A |
7: 108,107,855 (GRCm39) |
Y197* |
probably null |
Het |
| Or8b8 |
C |
A |
9: 37,808,811 (GRCm39) |
T37N |
probably damaging |
Het |
| Os9 |
C |
T |
10: 126,956,920 (GRCm39) |
R23H |
possibly damaging |
Het |
| Otud6b |
A |
G |
4: 14,815,607 (GRCm39) |
L261P |
probably damaging |
Het |
| Pcdhga2 |
A |
G |
18: 37,802,476 (GRCm39) |
N107D |
probably benign |
Het |
| Pclo |
C |
T |
5: 14,729,308 (GRCm39) |
|
probably benign |
Het |
| Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
| Phtf1 |
T |
A |
3: 103,906,024 (GRCm39) |
S524T |
probably damaging |
Het |
| Pkdrej |
A |
C |
15: 85,703,197 (GRCm39) |
L913R |
probably damaging |
Het |
| Pld1 |
C |
A |
3: 28,085,447 (GRCm39) |
A201D |
probably damaging |
Het |
| Rorb |
T |
A |
19: 18,955,052 (GRCm39) |
Q103L |
probably benign |
Het |
| Sec24d |
C |
T |
3: 123,093,255 (GRCm39) |
T284M |
probably benign |
Het |
| Serpinb3b |
T |
C |
1: 107,085,484 (GRCm39) |
I86V |
probably benign |
Het |
| Serpinb6a |
A |
T |
13: 34,102,857 (GRCm39) |
M201K |
probably damaging |
Het |
| Snx8 |
A |
G |
5: 140,337,989 (GRCm39) |
S219P |
probably benign |
Het |
| Sp8 |
C |
T |
12: 118,812,160 (GRCm39) |
T5I |
probably damaging |
Het |
| Tanc1 |
A |
G |
2: 59,630,287 (GRCm39) |
N749D |
probably damaging |
Het |
| Tarm1 |
G |
C |
7: 3,537,612 (GRCm39) |
P284A |
probably damaging |
Het |
| Tbx15 |
A |
T |
3: 99,161,390 (GRCm39) |
E65V |
probably benign |
Het |
| Ticam1 |
T |
A |
17: 56,579,020 (GRCm39) |
H25L |
probably benign |
Het |
| Tmprss11g |
T |
A |
5: 86,640,674 (GRCm39) |
L170F |
probably damaging |
Het |
| Tnfsf9 |
A |
G |
17: 57,414,504 (GRCm39) |
*310W |
probably null |
Het |
| Tsks |
C |
T |
7: 44,593,418 (GRCm39) |
T128I |
possibly damaging |
Het |
| Vmn1r175 |
A |
T |
7: 23,508,494 (GRCm39) |
N44K |
possibly damaging |
Het |
| Vmn1r45 |
A |
G |
6: 89,910,847 (GRCm39) |
I41T |
probably damaging |
Het |
| Ythdc2 |
A |
G |
18: 45,004,532 (GRCm39) |
N1102S |
probably benign |
Het |
| Zswim4 |
C |
T |
8: 84,953,296 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in D430041D05Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00838:D430041D05Rik
|
APN |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01114:D430041D05Rik
|
APN |
2 |
104,088,511 (GRCm39) |
nonsense |
probably null |
|
|
IGL01669:D430041D05Rik
|
APN |
2 |
104,085,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02015:D430041D05Rik
|
APN |
2 |
104,060,749 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02037:D430041D05Rik
|
APN |
2 |
104,038,559 (GRCm39) |
splice site |
probably benign |
|
|
IGL02268:D430041D05Rik
|
APN |
2 |
104,071,500 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02294:D430041D05Rik
|
APN |
2 |
104,085,351 (GRCm39) |
missense |
probably benign |
0.42 |
|
IGL02457:D430041D05Rik
|
APN |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02601:D430041D05Rik
|
APN |
2 |
104,060,631 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02647:D430041D05Rik
|
APN |
2 |
104,078,611 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02679:D430041D05Rik
|
APN |
2 |
104,060,650 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
IGL02926:D430041D05Rik
|
APN |
2 |
104,044,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03171:D430041D05Rik
|
APN |
2 |
104,071,508 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL03178:D430041D05Rik
|
APN |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03371:D430041D05Rik
|
APN |
2 |
104,078,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0027:D430041D05Rik
|
UTSW |
2 |
104,085,389 (GRCm39) |
missense |
probably benign |
|
|
R0064:D430041D05Rik
|
UTSW |
2 |
104,079,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0135:D430041D05Rik
|
UTSW |
2 |
104,085,379 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R0227:D430041D05Rik
|
UTSW |
2 |
104,035,545 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R0265:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0268:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0282:D430041D05Rik
|
UTSW |
2 |
104,031,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0366:D430041D05Rik
|
UTSW |
2 |
104,085,685 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0402:D430041D05Rik
|
UTSW |
2 |
103,998,509 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0436:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0441:D430041D05Rik
|
UTSW |
2 |
103,998,292 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0540:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0607:D430041D05Rik
|
UTSW |
2 |
104,063,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0613:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0626:D430041D05Rik
|
UTSW |
2 |
103,998,295 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0747:D430041D05Rik
|
UTSW |
2 |
104,060,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0864:D430041D05Rik
|
UTSW |
2 |
104,060,773 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R0980:D430041D05Rik
|
UTSW |
2 |
104,079,690 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1014:D430041D05Rik
|
UTSW |
2 |
104,088,674 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1254:D430041D05Rik
|
UTSW |
2 |
104,031,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1364:D430041D05Rik
|
UTSW |
2 |
103,985,363 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R1456:D430041D05Rik
|
UTSW |
2 |
104,038,428 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1574:D430041D05Rik
|
UTSW |
2 |
104,051,553 (GRCm39) |
small deletion |
probably benign |
|
|
R1604:D430041D05Rik
|
UTSW |
2 |
104,035,487 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1605:D430041D05Rik
|
UTSW |
2 |
104,085,915 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R1623:D430041D05Rik
|
UTSW |
2 |
103,983,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1634:D430041D05Rik
|
UTSW |
2 |
104,051,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1834:D430041D05Rik
|
UTSW |
2 |
103,998,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1885:D430041D05Rik
|
UTSW |
2 |
104,060,800 (GRCm39) |
missense |
probably benign |
0.39 |
|
R2080:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2101:D430041D05Rik
|
UTSW |
2 |
103,979,175 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2240:D430041D05Rik
|
UTSW |
2 |
103,987,161 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2923:D430041D05Rik
|
UTSW |
2 |
104,085,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3751:D430041D05Rik
|
UTSW |
2 |
104,085,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R3862:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R3863:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R3864:D430041D05Rik
|
UTSW |
2 |
104,044,522 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R3949:D430041D05Rik
|
UTSW |
2 |
104,087,713 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4493:D430041D05Rik
|
UTSW |
2 |
104,086,684 (GRCm39) |
missense |
probably benign |
0.02 |
|
R4526:D430041D05Rik
|
UTSW |
2 |
104,022,778 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4592:D430041D05Rik
|
UTSW |
2 |
104,063,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4598:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4599:D430041D05Rik
|
UTSW |
2 |
104,038,528 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4647:D430041D05Rik
|
UTSW |
2 |
104,088,788 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4765:D430041D05Rik
|
UTSW |
2 |
104,044,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4808:D430041D05Rik
|
UTSW |
2 |
104,031,455 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4868:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5144:D430041D05Rik
|
UTSW |
2 |
104,088,847 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5255:D430041D05Rik
|
UTSW |
2 |
104,086,945 (GRCm39) |
missense |
probably benign |
0.26 |
|
R5356:D430041D05Rik
|
UTSW |
2 |
104,085,754 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5368:D430041D05Rik
|
UTSW |
2 |
104,078,629 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5963:D430041D05Rik
|
UTSW |
2 |
104,078,630 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R5993:D430041D05Rik
|
UTSW |
2 |
103,998,412 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6122:D430041D05Rik
|
UTSW |
2 |
104,086,637 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6410:D430041D05Rik
|
UTSW |
2 |
103,998,548 (GRCm39) |
splice site |
probably null |
|
|
R6804:D430041D05Rik
|
UTSW |
2 |
103,979,371 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6850:D430041D05Rik
|
UTSW |
2 |
104,031,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6853:D430041D05Rik
|
UTSW |
2 |
104,071,500 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7034:D430041D05Rik
|
UTSW |
2 |
104,022,883 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7146:D430041D05Rik
|
UTSW |
2 |
104,088,698 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7250:D430041D05Rik
|
UTSW |
2 |
104,086,961 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7251:D430041D05Rik
|
UTSW |
2 |
104,051,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7313:D430041D05Rik
|
UTSW |
2 |
104,085,910 (GRCm39) |
missense |
probably benign |
|
|
R7359:D430041D05Rik
|
UTSW |
2 |
104,044,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7361:D430041D05Rik
|
UTSW |
2 |
104,085,363 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7436:D430041D05Rik
|
UTSW |
2 |
104,087,447 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7472:D430041D05Rik
|
UTSW |
2 |
104,240,484 (GRCm39) |
missense |
unknown |
|
|
R7492:D430041D05Rik
|
UTSW |
2 |
104,031,650 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7631:D430041D05Rik
|
UTSW |
2 |
103,979,363 (GRCm39) |
nonsense |
probably null |
|
|
R7672:D430041D05Rik
|
UTSW |
2 |
104,071,581 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7721:D430041D05Rik
|
UTSW |
2 |
104,088,874 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7754:D430041D05Rik
|
UTSW |
2 |
104,087,504 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7882:D430041D05Rik
|
UTSW |
2 |
104,087,974 (GRCm39) |
nonsense |
probably null |
|
|
R7896:D430041D05Rik
|
UTSW |
2 |
104,088,385 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7986:D430041D05Rik
|
UTSW |
2 |
104,087,096 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8005:D430041D05Rik
|
UTSW |
2 |
104,088,599 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R8016:D430041D05Rik
|
UTSW |
2 |
104,022,864 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8054:D430041D05Rik
|
UTSW |
2 |
103,985,390 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8058:D430041D05Rik
|
UTSW |
2 |
103,979,128 (GRCm39) |
makesense |
probably null |
|
|
R8100:D430041D05Rik
|
UTSW |
2 |
104,087,287 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8461:D430041D05Rik
|
UTSW |
2 |
103,998,280 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R8695:D430041D05Rik
|
UTSW |
2 |
104,085,299 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8885:D430041D05Rik
|
UTSW |
2 |
104,071,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9007:D430041D05Rik
|
UTSW |
2 |
104,087,930 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9009:D430041D05Rik
|
UTSW |
2 |
104,240,521 (GRCm39) |
start gained |
probably benign |
|
|
R9335:D430041D05Rik
|
UTSW |
2 |
104,078,674 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9348:D430041D05Rik
|
UTSW |
2 |
104,088,337 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9384:D430041D05Rik
|
UTSW |
2 |
104,087,920 (GRCm39) |
missense |
probably benign |
|
|
R9483:D430041D05Rik
|
UTSW |
2 |
104,087,563 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9489:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9605:D430041D05Rik
|
UTSW |
2 |
104,087,189 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9613:D430041D05Rik
|
UTSW |
2 |
104,060,737 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9698:D430041D05Rik
|
UTSW |
2 |
103,985,396 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0024:D430041D05Rik
|
UTSW |
2 |
104,022,911 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
Z1176:D430041D05Rik
|
UTSW |
2 |
104,087,201 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:D430041D05Rik
|
UTSW |
2 |
103,985,280 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:D430041D05Rik
|
UTSW |
2 |
104,071,536 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACCAGTGTGCATGGCTTGTG -3'
(R):5'- AGACTGTGGTGTGTGCATCC -3'
Sequencing Primer
(F):5'- TGCATGGCTTGTGGCTTC -3'
(R):5'- GCAGTGGAAACCTCTGTGTC -3'
|
| Posted On |
2016-05-10 |
Incidental Mutation