Incidental Mutation 'RF007:Naip1'
| ID |
602924 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Naip1
|
| Ensembl Gene |
ENSMUSG00000021640 |
| Gene Name |
NLR family, apoptosis inhibitory protein 1 |
| Synonyms |
Naip, Birc1a, D13Lsd1 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
RF007 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
100544272-100589372 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 100562642 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Lysine
at position 841
(M841K)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000022142
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022142]
[ENSMUST00000221727]
[ENSMUST00000221943]
[ENSMUST00000222155]
|
| AlphaFold |
Q9QWK5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000022142
AA Change: M841K
PolyPhen 2
Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)
|
| SMART Domains |
Protein: ENSMUSP00000022142
Gene: ENSMUSG00000021640
AA Change: M841K
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
36 |
51 |
N/A |
INTRINSIC |
|
BIR
|
58 |
129 |
1.18e-20 |
SMART |
|
BIR
|
157 |
229 |
1.06e-36 |
SMART |
|
BIR
|
276 |
347 |
7.82e-26 |
SMART |
|
AAA
|
462 |
603 |
1.14e-2 |
SMART |
|
low complexity region
|
908 |
919 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000221727
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000221943
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000222155
AA Change: M841K
PolyPhen 2
Score 0.029 (Sensitivity: 0.95; Specificity: 0.82)
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.7%
- 10x: 99.2%
- 20x: 98.2%
|
| Validation Efficiency |
97% (73/75) |
| MGI Phenotype |
PHENOTYPE: Mice homozygous for disruptions in this gene display a normal phenotype. [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 |
|---|
| Adgrl1 |
T |
A |
8: 84,661,401 (GRCm39) |
S933T |
probably benign |
Het |
| Adgrl2 |
G |
A |
3: 148,544,884 (GRCm39) |
T737I |
probably damaging |
Het |
| Adra2c |
T |
A |
5: 35,438,386 (GRCm39) |
V386E |
probably damaging |
Het |
| Agbl5 |
C |
A |
5: 31,060,589 (GRCm39) |
T761N |
unknown |
Het |
| Ahnak |
T |
A |
19: 8,990,965 (GRCm39) |
M4083K |
possibly damaging |
Het |
| Aldh1l1 |
A |
T |
6: 90,575,241 (GRCm39) |
I843F |
probably damaging |
Het |
| Ankhd1 |
GGCGGC |
GGCGGCTGCGGC |
18: 36,693,962 (GRCm39) |
|
probably benign |
Het |
| Arid1b |
GCG |
GCGCCG |
17: 5,045,869 (GRCm39) |
|
probably benign |
Het |
| B4galnt4 |
T |
C |
7: 140,650,609 (GRCm39) |
|
probably null |
Het |
| Blm |
C |
CTCCTCCTCCTAG |
7: 80,162,681 (GRCm39) |
|
probably null |
Het |
| Btg3 |
A |
G |
16: 78,129,836 (GRCm39) |
*52W |
probably null |
Het |
| Cc2d1a |
T |
C |
8: 84,861,298 (GRCm39) |
T796A |
probably damaging |
Het |
| Cd200r1 |
T |
C |
16: 44,610,374 (GRCm39) |
S161P |
possibly damaging |
Het |
| Cenpj |
A |
G |
14: 56,767,505 (GRCm39) |
|
probably null |
Het |
| Cfap251 |
G |
GGAT |
5: 123,392,317 (GRCm39) |
|
probably benign |
Het |
| Chd9 |
A |
G |
8: 91,760,578 (GRCm39) |
T2108A |
possibly damaging |
Het |
| Cherp |
TGGAGCG |
T |
8: 73,215,903 (GRCm39) |
|
probably benign |
Het |
| Cnot11 |
T |
C |
1: 39,581,575 (GRCm39) |
V372A |
probably damaging |
Het |
| Cntnap5b |
T |
C |
1: 100,091,795 (GRCm39) |
C179R |
probably damaging |
Het |
| Cntrl |
T |
A |
2: 35,060,512 (GRCm39) |
N1901K |
probably benign |
Het |
| Coil |
CTGG |
C |
11: 88,872,656 (GRCm39) |
|
probably benign |
Het |
| Col1a1 |
A |
G |
11: 94,833,866 (GRCm39) |
D488G |
probably damaging |
Het |
| Coro1a |
T |
C |
7: 126,301,024 (GRCm39) |
H130R |
probably damaging |
Het |
| Crybg3 |
A |
C |
16: 59,377,067 (GRCm39) |
S1396A |
possibly damaging |
Het |
| Csf2rb2 |
A |
G |
15: 78,176,126 (GRCm39) |
I259T |
probably benign |
Het |
| Cyp1a2 |
G |
T |
9: 57,589,253 (GRCm39) |
P187Q |
probably damaging |
Het |
| Cyp3a13 |
CATTATT |
CATT |
5: 137,892,525 (GRCm39) |
|
probably null |
Het |
| Dcun1d3 |
T |
C |
7: 119,458,726 (GRCm39) |
E103G |
possibly damaging |
Het |
| Dmkn |
T |
A |
7: 30,469,129 (GRCm39) |
|
probably null |
Het |
| Dna2 |
T |
C |
10: 62,802,474 (GRCm39) |
L864P |
probably damaging |
Het |
| Dnah14 |
T |
A |
1: 181,513,374 (GRCm39) |
M1909K |
probably benign |
Het |
| Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,326,227 (GRCm39) |
|
probably benign |
Het |
| Ecrg4 |
TTCTGTA |
T |
1: 43,776,352 (GRCm39) |
|
probably benign |
Het |
| Efna5 |
T |
C |
17: 62,920,389 (GRCm39) |
S163G |
probably benign |
Het |
| Entpd2 |
CTT |
CTTT |
2: 25,290,907 (GRCm39) |
|
probably null |
Het |
| Ercc4 |
C |
T |
16: 12,941,371 (GRCm39) |
S253L |
possibly damaging |
Het |
| Flywch1 |
ACCCA |
ACCCAATTCTGGTGTGGGGAGGCTACGTACTCTCCCA |
17: 23,981,138 (GRCm39) |
|
probably null |
Het |
| Flywch1 |
CCTGGTGT |
CCTGGTGTGGGGAGGCTACGTACTCACCCACTTCTGGTGT |
17: 23,981,145 (GRCm39) |
|
probably null |
Het |
| Folh1 |
T |
C |
7: 86,424,895 (GRCm39) |
T25A |
probably benign |
Het |
| Foxi3 |
C |
A |
6: 70,937,845 (GRCm39) |
T359K |
possibly damaging |
Het |
| Gab3 |
TTC |
TTCATC |
X: 74,043,631 (GRCm39) |
|
probably benign |
Het |
| Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
| Gab3 |
TCT |
TCTGCT |
X: 74,043,617 (GRCm39) |
|
probably benign |
Het |
| Gba2 |
G |
T |
4: 43,569,894 (GRCm39) |
L440M |
probably damaging |
Het |
| Gm14412 |
T |
A |
2: 177,007,494 (GRCm39) |
N134Y |
possibly damaging |
Het |
| Gpr88 |
A |
G |
3: 116,046,018 (GRCm39) |
S98P |
probably benign |
Het |
| Il1r1 |
A |
G |
1: 40,352,438 (GRCm39) |
Y539C |
probably damaging |
Het |
| Iqcf4 |
TTTCCTTTTCCTTTT |
TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTTCCTTTT |
9: 106,447,808 (GRCm39) |
|
probably benign |
Het |
| Lce1m |
CTGCT |
CTGCTTCCACTGTTGCT |
3: 92,925,451 (GRCm39) |
|
probably benign |
Het |
| Lkaaear1 |
T |
TATCTCCAGCTCC |
2: 181,339,352 (GRCm39) |
|
probably benign |
Het |
| Lkaaear1 |
CAGCTCCAGCTCCAGCTCCAGCTC |
CAGCTCCAGCTCTAGCTCCAGCTCCAGCTCCAGCTC |
2: 181,339,370 (GRCm39) |
|
probably benign |
Het |
| Ltb4r1 |
T |
A |
14: 56,005,426 (GRCm39) |
L243Q |
possibly damaging |
Het |
| Man2a1 |
T |
A |
17: 65,019,248 (GRCm39) |
V704D |
probably damaging |
Het |
| Map1a |
CTCCAGCTCCA |
CTCCAGCTCCAGCTCCAGCTCCAGCTCCAGTTCCAGCTCCA |
2: 121,136,789 (GRCm39) |
|
probably benign |
Het |
| Mcu |
G |
T |
10: 59,326,938 (GRCm39) |
A63E |
probably benign |
Het |
| Mrps31 |
A |
T |
8: 22,909,880 (GRCm39) |
D182V |
possibly damaging |
Het |
| Mslnl |
T |
A |
17: 25,962,202 (GRCm39) |
V200E |
possibly damaging |
Het |
| Ndufab1 |
T |
C |
7: 121,695,861 (GRCm39) |
K88E |
possibly damaging |
Het |
| Nlrp5 |
A |
C |
7: 23,117,586 (GRCm39) |
I437L |
probably benign |
Het |
| Nnt |
C |
T |
13: 119,533,393 (GRCm39) |
V91M |
probably damaging |
Het |
| Nusap1 |
TACACGTTAGCAGTGAGGAGCAAGCTGAGA |
TACACGTTAGCAGTGAGGAGCAAGCTGAGAGACACGTTAGCAGTGAGGAGCAAGCTGAGA |
2: 119,458,062 (GRCm39) |
|
probably benign |
Het |
| Nynrin |
T |
G |
14: 56,103,658 (GRCm39) |
|
probably null |
Het |
| Or12k5 |
T |
G |
2: 36,895,186 (GRCm39) |
T147P |
probably damaging |
Het |
| Or5ak22 |
C |
A |
2: 85,230,137 (GRCm39) |
A247S |
probably damaging |
Het |
| Or6c204 |
T |
A |
10: 129,022,562 (GRCm39) |
I243F |
probably damaging |
Het |
| Osbpl8 |
A |
G |
10: 111,112,328 (GRCm39) |
K481R |
possibly damaging |
Het |
| Padi6 |
T |
C |
4: 140,457,054 (GRCm39) |
D540G |
probably damaging |
Het |
| Pcmtd1 |
T |
C |
1: 7,225,329 (GRCm39) |
|
probably benign |
Het |
| Pdik1l |
TTTTTGTTTT |
TTTTTGTTTTGGTTTTGTTTT |
4: 134,006,679 (GRCm39) |
|
probably null |
Het |
| Phospho1 |
T |
C |
11: 95,721,881 (GRCm39) |
Y184H |
probably damaging |
Het |
| Pi4ka |
T |
A |
16: 17,115,097 (GRCm39) |
R1431W |
|
Het |
| Plxdc1 |
T |
A |
11: 97,869,504 (GRCm39) |
H28L |
probably benign |
Het |
| Pnma8a |
ACCTCATGATGCACCTGCTTCAACA |
ACCTCATGATGCACCTGCTTCAACACCTCATGATGCACCTGCTTCAACA |
7: 16,695,349 (GRCm39) |
|
probably benign |
Het |
| Ppp1r7 |
T |
C |
1: 93,274,011 (GRCm39) |
|
probably null |
Het |
| Ppp1r9a |
T |
A |
6: 4,906,657 (GRCm39) |
V404E |
probably damaging |
Het |
| Scfd1 |
T |
A |
12: 51,469,756 (GRCm39) |
S434T |
probably benign |
Het |
| Six5 |
A |
G |
7: 18,828,862 (GRCm39) |
S101G |
probably benign |
Het |
| Slc6a4 |
C |
A |
11: 76,910,008 (GRCm39) |
T421K |
probably damaging |
Het |
| Smarcd3 |
C |
A |
5: 24,801,068 (GRCm39) |
R113L |
probably damaging |
Het |
| Son |
T |
A |
16: 91,456,257 (GRCm39) |
M1668K |
possibly damaging |
Het |
| Spmap2l |
CTCCCCAGTCCCGCAAGGCCAG |
CTCCCCAGTCCCGCAAGGCCAGCGATCGTCCCCAGTCCCGCAAGGCCAG |
5: 77,164,255 (GRCm39) |
|
probably benign |
Het |
| Tcf25 |
A |
G |
8: 124,122,369 (GRCm39) |
D434G |
probably benign |
Het |
| Tcof1 |
CCAGAGATCCCC |
CCAGAGATCCCCGTGGCTGCCGAGATGGGCACTTTCACAGAGATCCCC |
18: 60,966,640 (GRCm39) |
|
probably benign |
Het |
| Tep1 |
A |
G |
14: 51,098,402 (GRCm39) |
V463A |
possibly damaging |
Het |
| Trav15-2-dv6-2 |
GGGAG |
GGGAGGAG |
14: 53,887,207 (GRCm39) |
|
probably benign |
Het |
| Trav15-2-dv6-2 |
AAG |
AAGCAG |
14: 53,887,212 (GRCm39) |
|
probably benign |
Het |
| Trav15-2-dv6-2 |
GGAG |
GGAGGAG |
14: 53,887,208 (GRCm39) |
|
probably benign |
Het |
| Trim24 |
A |
G |
6: 37,930,471 (GRCm39) |
K642E |
possibly damaging |
Het |
| Trim33 |
GGCCCCCGC |
GGC |
3: 103,187,533 (GRCm39) |
|
probably benign |
Het |
| Triobp |
CTCCCTGTGCCCAACGG |
CTCCCTGTGCCCAACGGAACAACCCCAGGATTCCCTGTGCCCAACGG |
15: 78,851,244 (GRCm39) |
|
probably benign |
Het |
| Trmu |
G |
T |
15: 85,776,770 (GRCm39) |
V161L |
possibly damaging |
Het |
| Try4 |
T |
A |
6: 41,282,297 (GRCm39) |
C206S |
probably damaging |
Het |
| Usp2 |
TTCACTTAC |
TTCACTTACTCATGTGACCTGTTCGTCACTTAC |
9: 44,000,418 (GRCm39) |
|
probably benign |
Het |
| Vmn1r62 |
A |
T |
7: 5,678,669 (GRCm39) |
M117L |
probably benign |
Het |
| Vmn2r104 |
A |
T |
17: 20,268,302 (GRCm39) |
Y56N |
probably benign |
Het |
| Xxylt1 |
C |
T |
16: 30,869,498 (GRCm39) |
D201N |
possibly damaging |
Het |
| Zfp563 |
T |
A |
17: 33,323,999 (GRCm39) |
I198K |
probably benign |
Het |
| Zfp612 |
T |
A |
8: 110,816,174 (GRCm39) |
C460* |
probably null |
Het |
| Zfp691 |
G |
A |
4: 119,027,932 (GRCm39) |
T100M |
probably benign |
Het |
| Zfp773 |
A |
T |
7: 7,135,689 (GRCm39) |
C302* |
probably null |
Het |
| Zmat2 |
A |
G |
18: 36,930,936 (GRCm39) |
E154G |
probably damaging |
Het |
| Zw10 |
T |
A |
9: 48,972,220 (GRCm39) |
I132N |
possibly damaging |
Het |
|
| Other mutations in Naip1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01115:Naip1
|
APN |
13 |
100,580,228 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01145:Naip1
|
APN |
13 |
100,545,629 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01356:Naip1
|
APN |
13 |
100,559,722 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01414:Naip1
|
APN |
13 |
100,545,681 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL01505:Naip1
|
APN |
13 |
100,562,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01573:Naip1
|
APN |
13 |
100,563,890 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01931:Naip1
|
APN |
13 |
100,545,540 (GRCm39) |
nonsense |
probably null |
|
|
IGL02043:Naip1
|
APN |
13 |
100,563,304 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02097:Naip1
|
APN |
13 |
100,562,096 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02331:Naip1
|
APN |
13 |
100,563,304 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02627:Naip1
|
APN |
13 |
100,562,156 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
IGL02675:Naip1
|
APN |
13 |
100,545,626 (GRCm39) |
missense |
probably benign |
|
|
IGL02801:Naip1
|
APN |
13 |
100,580,876 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02851:Naip1
|
APN |
13 |
100,569,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03038:Naip1
|
APN |
13 |
100,573,841 (GRCm39) |
nonsense |
probably null |
|
|
IGL03399:Naip1
|
APN |
13 |
100,545,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4340:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
|
FR4342:Naip1
|
UTSW |
13 |
100,561,979 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0051:Naip1
|
UTSW |
13 |
100,547,509 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0095:Naip1
|
UTSW |
13 |
100,559,591 (GRCm39) |
missense |
probably benign |
0.24 |
|
R0147:Naip1
|
UTSW |
13 |
100,563,418 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R0375:Naip1
|
UTSW |
13 |
100,545,656 (GRCm39) |
missense |
probably benign |
0.21 |
|
R0442:Naip1
|
UTSW |
13 |
100,581,024 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0455:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0491:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0614:Naip1
|
UTSW |
13 |
100,580,708 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0785:Naip1
|
UTSW |
13 |
100,559,593 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0785:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
|
R0787:Naip1
|
UTSW |
13 |
100,562,604 (GRCm39) |
missense |
probably benign |
0.22 |
|
R1081:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
|
R1177:Naip1
|
UTSW |
13 |
100,563,572 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1476:Naip1
|
UTSW |
13 |
100,563,378 (GRCm39) |
missense |
probably benign |
0.35 |
|
R1672:Naip1
|
UTSW |
13 |
100,559,657 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1809:Naip1
|
UTSW |
13 |
100,562,747 (GRCm39) |
missense |
probably benign |
|
|
R2057:Naip1
|
UTSW |
13 |
100,562,081 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R2182:Naip1
|
UTSW |
13 |
100,550,188 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2395:Naip1
|
UTSW |
13 |
100,559,614 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R2518:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3033:Naip1
|
UTSW |
13 |
100,568,966 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3122:Naip1
|
UTSW |
13 |
100,545,503 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3439:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4167:Naip1
|
UTSW |
13 |
100,580,794 (GRCm39) |
missense |
probably benign |
0.04 |
|
R4179:Naip1
|
UTSW |
13 |
100,562,684 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4212:Naip1
|
UTSW |
13 |
100,563,383 (GRCm39) |
splice site |
probably null |
|
|
R4639:Naip1
|
UTSW |
13 |
100,580,791 (GRCm39) |
missense |
probably benign |
0.31 |
|
R4674:Naip1
|
UTSW |
13 |
100,580,682 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4736:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4740:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R4778:Naip1
|
UTSW |
13 |
100,563,156 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4806:Naip1
|
UTSW |
13 |
100,562,129 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4855:Naip1
|
UTSW |
13 |
100,559,728 (GRCm39) |
splice site |
probably null |
|
|
R5740:Naip1
|
UTSW |
13 |
100,569,009 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R5797:Naip1
|
UTSW |
13 |
100,581,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R5806:Naip1
|
UTSW |
13 |
100,581,243 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R5895:Naip1
|
UTSW |
13 |
100,559,636 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5896:Naip1
|
UTSW |
13 |
100,559,636 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6023:Naip1
|
UTSW |
13 |
100,562,694 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6109:Naip1
|
UTSW |
13 |
100,563,690 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6117:Naip1
|
UTSW |
13 |
100,581,245 (GRCm39) |
start codon destroyed |
probably damaging |
0.99 |
|
R6133:Naip1
|
UTSW |
13 |
100,581,151 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6241:Naip1
|
UTSW |
13 |
100,562,169 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6335:Naip1
|
UTSW |
13 |
100,563,060 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6404:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6475:Naip1
|
UTSW |
13 |
100,545,596 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6508:Naip1
|
UTSW |
13 |
100,572,973 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6580:Naip1
|
UTSW |
13 |
100,581,157 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6600:Naip1
|
UTSW |
13 |
100,559,666 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6600:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6603:Naip1
|
UTSW |
13 |
100,559,666 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6603:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6633:Naip1
|
UTSW |
13 |
100,559,593 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6633:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
|
R6720:Naip1
|
UTSW |
13 |
100,559,585 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6805:Naip1
|
UTSW |
13 |
100,563,849 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7043:Naip1
|
UTSW |
13 |
100,563,422 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7615:Naip1
|
UTSW |
13 |
100,562,284 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7797:Naip1
|
UTSW |
13 |
100,580,986 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7820:Naip1
|
UTSW |
13 |
100,559,578 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7842:Naip1
|
UTSW |
13 |
100,563,506 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8117:Naip1
|
UTSW |
13 |
100,563,509 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R8132:Naip1
|
UTSW |
13 |
100,573,883 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R8177:Naip1
|
UTSW |
13 |
100,563,911 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8203:Naip1
|
UTSW |
13 |
100,562,328 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8283:Naip1
|
UTSW |
13 |
100,563,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8319:Naip1
|
UTSW |
13 |
100,565,721 (GRCm39) |
missense |
probably benign |
0.13 |
|
R8377:Naip1
|
UTSW |
13 |
100,562,374 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R8864:Naip1
|
UTSW |
13 |
100,562,828 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R8871:Naip1
|
UTSW |
13 |
100,580,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8987:Naip1
|
UTSW |
13 |
100,563,434 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9079:Naip1
|
UTSW |
13 |
100,559,727 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9275:Naip1
|
UTSW |
13 |
100,562,684 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9354:Naip1
|
UTSW |
13 |
100,563,994 (GRCm39) |
missense |
probably benign |
0.31 |
|
R9524:Naip1
|
UTSW |
13 |
100,563,101 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9617:Naip1
|
UTSW |
13 |
100,569,821 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9776:Naip1
|
UTSW |
13 |
100,559,584 (GRCm39) |
missense |
probably benign |
|
|
R9802:Naip1
|
UTSW |
13 |
100,562,713 (GRCm39) |
missense |
probably benign |
|
|
X0066:Naip1
|
UTSW |
13 |
100,573,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Y4335:Naip1
|
UTSW |
13 |
100,562,030 (GRCm39) |
missense |
probably benign |
0.00 |
|
Y4336:Naip1
|
UTSW |
13 |
100,562,030 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACTCTTCACCAGTAACAGGC -3'
(R):5'- CTTGAAGGCTTTGACCACCTAC -3'
Sequencing Primer
(F):5'- GGTGGTCCCTAAAGTATTGTAAATTC -3'
(R):5'- GATGAGACAGAGTTGCTG -3'
|
| Posted On |
2019-12-04 |
Incidental Mutation