Incidental Mutation 'R9776:Naip1'
| ID |
733731 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Naip1
|
| Ensembl Gene |
ENSMUSG00000021640 |
| Gene Name |
NLR family, apoptosis inhibitory protein 1 |
| Synonyms |
Naip, Birc1a, D13Lsd1 |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R9776 (G1)
|
| Quality Score |
156.008 |
|
Status
|
Not validated
|
| Chromosome |
13 |
| Chromosomal Location |
100544272-100589372 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 100559584 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Methionine to Threonine
at position 1140
(M1140T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000152583
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022142]
[ENSMUST00000221727]
[ENSMUST00000221943]
[ENSMUST00000222155]
|
| AlphaFold |
Q9QWK5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000022142
AA Change: M1140T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000022142
Gene: ENSMUSG00000021640
AA Change: M1140T
| 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: M1140T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| Meta Mutation Damage Score |
0.0898 |
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 99.4%
- 20x: 98.5%
|
| Validation Efficiency |
|
| 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: 83 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700069L16Rik |
T |
G |
5: 113,861,765 (GRCm39) |
Q35P |
unknown |
Het |
| 2010109A12Rik |
T |
A |
5: 93,361,305 (GRCm39) |
*120K |
probably null |
Het |
| 2700049A03Rik |
A |
G |
12: 71,235,448 (GRCm39) |
T1133A |
possibly damaging |
Het |
| A830005F24Rik |
G |
A |
13: 48,667,758 (GRCm39) |
R20Q |
unknown |
Het |
| Acta2 |
T |
C |
19: 34,223,481 (GRCm39) |
T205A |
probably benign |
Het |
| Adcy5 |
A |
G |
16: 35,100,725 (GRCm39) |
D759G |
probably damaging |
Het |
| Ankk1 |
T |
A |
9: 49,330,714 (GRCm39) |
M276L |
probably benign |
Het |
| Arfgef2 |
G |
A |
2: 166,713,447 (GRCm39) |
E1283K |
probably damaging |
Het |
| Arhgef26 |
G |
T |
3: 62,246,803 (GRCm39) |
|
probably benign |
Het |
| Arhgef28 |
A |
C |
13: 98,133,415 (GRCm39) |
S351A |
probably benign |
Het |
| Arih2 |
C |
T |
9: 108,484,504 (GRCm39) |
G436S |
probably damaging |
Het |
| Bptf |
T |
C |
11: 106,969,396 (GRCm39) |
T1013A |
probably damaging |
Het |
| Camsap1 |
A |
T |
2: 25,828,166 (GRCm39) |
V1186E |
probably benign |
Het |
| Capn10 |
G |
T |
1: 92,871,586 (GRCm39) |
A395S |
possibly damaging |
Het |
| Ccdc184 |
A |
T |
15: 98,066,737 (GRCm39) |
T181S |
probably damaging |
Het |
| Clasp1 |
T |
C |
1: 118,509,108 (GRCm39) |
I1345T |
possibly damaging |
Het |
| Cpsf1 |
A |
T |
15: 76,486,779 (GRCm39) |
H252Q |
probably damaging |
Het |
| Ctnna2 |
T |
A |
6: 77,582,172 (GRCm39) |
M363L |
probably benign |
Het |
| Cyp24a1 |
G |
A |
2: 170,338,625 (GRCm39) |
P24S |
probably benign |
Het |
| D130040H23Rik |
A |
G |
8: 69,755,566 (GRCm39) |
H341R |
probably damaging |
Het |
| Dclk3 |
A |
G |
9: 111,298,226 (GRCm39) |
E590G |
probably damaging |
Het |
| Ear2 |
A |
T |
14: 44,340,729 (GRCm39) |
Y129F |
probably benign |
Het |
| Egf |
A |
G |
3: 129,530,514 (GRCm39) |
L216P |
probably damaging |
Het |
| Fbxw9 |
T |
A |
8: 85,792,523 (GRCm39) |
H319Q |
probably damaging |
Het |
| Gipr |
A |
G |
7: 18,891,487 (GRCm39) |
S397P |
probably damaging |
Het |
| Gxylt2 |
G |
T |
6: 100,682,072 (GRCm39) |
E90* |
probably null |
Het |
| Hnf1b |
T |
C |
11: 83,784,283 (GRCm39) |
V473A |
probably benign |
Het |
| Iffo1 |
G |
A |
6: 125,130,436 (GRCm39) |
E475K |
probably damaging |
Het |
| Ifi206 |
T |
A |
1: 173,308,075 (GRCm39) |
R640S |
|
Het |
| Ipmk |
A |
G |
10: 71,217,439 (GRCm39) |
S328G |
probably damaging |
Het |
| Kcnq1 |
A |
T |
7: 142,737,368 (GRCm39) |
I229F |
probably damaging |
Het |
| Kif9 |
C |
A |
9: 110,350,398 (GRCm39) |
T763N |
probably benign |
Het |
| Klhl36 |
C |
T |
8: 120,601,129 (GRCm39) |
Q383* |
probably null |
Het |
| Lrp4 |
G |
T |
2: 91,316,179 (GRCm39) |
V766F |
probably damaging |
Het |
| Mettl26 |
T |
A |
17: 26,094,511 (GRCm39) |
M3K |
probably benign |
Het |
| Muc16 |
T |
A |
9: 18,570,675 (GRCm39) |
I615F |
unknown |
Het |
| Myo7b |
T |
A |
18: 32,133,068 (GRCm39) |
Q427L |
probably benign |
Het |
| Ncapg |
G |
A |
5: 45,829,834 (GRCm39) |
V179I |
probably damaging |
Het |
| Nme4 |
C |
T |
17: 26,314,410 (GRCm39) |
G6E |
possibly damaging |
Het |
| Nr1h4 |
T |
C |
10: 89,319,311 (GRCm39) |
Y185C |
probably damaging |
Het |
| Nt5c3b |
T |
C |
11: 100,327,012 (GRCm39) |
I95V |
probably benign |
Het |
| Ntaq1 |
A |
G |
15: 58,004,913 (GRCm39) |
T9A |
probably benign |
Het |
| Or2y3 |
C |
T |
17: 38,393,470 (GRCm39) |
R133H |
probably benign |
Het |
| Or5g9 |
A |
T |
2: 85,552,145 (GRCm39) |
Y132F |
probably damaging |
Het |
| Or5t16 |
A |
T |
2: 86,819,055 (GRCm39) |
I155N |
probably damaging |
Het |
| Pappa2 |
G |
T |
1: 158,611,481 (GRCm39) |
P1494Q |
probably damaging |
Het |
| Pdzd2 |
A |
G |
15: 12,457,909 (GRCm39) |
F144S |
probably benign |
Het |
| Phactr3 |
A |
G |
2: 177,975,896 (GRCm39) |
H547R |
probably damaging |
Het |
| Pik3c2b |
T |
A |
1: 133,018,588 (GRCm39) |
S1012T |
possibly damaging |
Het |
| Plppr2 |
G |
A |
9: 21,859,107 (GRCm39) |
G408D |
probably damaging |
Het |
| Pom121 |
T |
A |
5: 135,420,554 (GRCm39) |
N289I |
unknown |
Het |
| Ppa1 |
T |
A |
10: 61,487,362 (GRCm39) |
S30T |
probably damaging |
Het |
| Rgs5 |
A |
T |
1: 169,518,089 (GRCm39) |
K108* |
probably null |
Het |
| Rpap1 |
A |
G |
2: 119,607,278 (GRCm39) |
V287A |
probably benign |
Het |
| Ryr1 |
A |
G |
7: 28,774,664 (GRCm39) |
Y2326H |
probably damaging |
Het |
| Ryr2 |
A |
G |
13: 11,707,599 (GRCm39) |
S2813P |
probably damaging |
Het |
| Sap25 |
T |
C |
5: 137,640,702 (GRCm39) |
|
probably null |
Het |
| Senp5 |
T |
C |
16: 31,782,279 (GRCm39) |
Y739C |
probably damaging |
Het |
| Slc25a29 |
A |
T |
12: 108,793,017 (GRCm39) |
L187Q |
possibly damaging |
Het |
| Slc7a2 |
C |
T |
8: 41,358,641 (GRCm39) |
T328M |
probably damaging |
Het |
| Slc7a8 |
T |
C |
14: 55,018,759 (GRCm39) |
N9S |
probably benign |
Het |
| Snx18 |
A |
G |
13: 113,754,039 (GRCm39) |
V298A |
probably benign |
Het |
| Spo11 |
T |
A |
2: 172,833,904 (GRCm39) |
I342N |
possibly damaging |
Het |
| Ssc5d |
A |
G |
7: 4,932,367 (GRCm39) |
K344E |
probably benign |
Het |
| Sspo |
A |
T |
6: 48,439,269 (GRCm39) |
D1639V |
probably benign |
Het |
| Stk32b |
T |
C |
5: 37,617,001 (GRCm39) |
D285G |
probably benign |
Het |
| Sult1b1 |
T |
C |
5: 87,662,815 (GRCm39) |
D295G |
probably benign |
Het |
| Syt5 |
A |
G |
7: 4,544,831 (GRCm39) |
L274P |
probably damaging |
Het |
| Tas1r2 |
T |
C |
4: 139,396,208 (GRCm39) |
S545P |
possibly damaging |
Het |
| Tbc1d17 |
T |
G |
7: 44,490,696 (GRCm39) |
D632A |
probably damaging |
Het |
| Tbc1d2 |
A |
G |
4: 46,650,007 (GRCm39) |
S10P |
probably benign |
Het |
| Tlk1 |
A |
T |
2: 70,555,908 (GRCm39) |
I417N |
probably damaging |
Het |
| Tmem184a |
C |
T |
5: 139,791,984 (GRCm39) |
R348H |
possibly damaging |
Het |
| Togaram2 |
T |
A |
17: 72,023,508 (GRCm39) |
V808D |
possibly damaging |
Het |
| Tpr |
A |
G |
1: 150,324,939 (GRCm39) |
Q2397R |
probably benign |
Het |
| Trav7-4 |
A |
G |
14: 53,698,994 (GRCm39) |
D47G |
possibly damaging |
Het |
| Usp17le |
T |
A |
7: 104,419,814 (GRCm39) |
M35L |
probably benign |
Het |
| Vegfc |
C |
T |
8: 54,633,829 (GRCm39) |
S262L |
probably benign |
Het |
| Vmn2r74 |
T |
A |
7: 85,605,212 (GRCm39) |
I479L |
possibly damaging |
Het |
| Vps13a |
A |
T |
19: 16,736,958 (GRCm39) |
F126L |
probably benign |
Het |
| Zfp945 |
C |
A |
17: 23,070,582 (GRCm39) |
C460F |
possibly damaging |
Het |
| Zmym4 |
G |
T |
4: 126,804,942 (GRCm39) |
S439R |
possibly damaging |
Het |
| Zscan4-ps3 |
A |
G |
7: 11,344,093 (GRCm39) |
E17G |
probably 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 |
|
R9802:Naip1
|
UTSW |
13 |
100,562,713 (GRCm39) |
missense |
probably benign |
|
|
RF007:Naip1
|
UTSW |
13 |
100,562,642 (GRCm39) |
missense |
probably benign |
0.03 |
|
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 |
|
| Posted On |
2022-11-14 |
Incidental Mutation