Incidental Mutation 'R4855:Naip1'
| ID |
430183 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Naip1
|
| Ensembl Gene |
ENSMUSG00000021640 |
| Gene Name |
NLR family, apoptosis inhibitory protein 1 |
| Synonyms |
Naip, Birc1a, D13Lsd1 |
| MMRRC Submission |
042466-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4855 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
13 |
| Chromosomal Location |
100544272-100589372 bp(-) (GRCm39) |
| Type of Mutation |
splice site (3581 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 100559728 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000152253
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022142]
[ENSMUST00000221727]
[ENSMUST00000221943]
[ENSMUST00000222155]
|
| AlphaFold |
Q9QWK5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000022142
AA Change: D1092G
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000022142
Gene: ENSMUSG00000021640
AA Change: D1092G
| 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 null
Transcript: ENSMUST00000221727
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000221943
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000222155
AA Change: D1092G
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| Meta Mutation Damage Score |
0.2989 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.7%
- 20x: 93.5%
|
| Validation Efficiency |
98% (93/95) |
| 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 |
|---|
| 2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
| 2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
| Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
| Adad1 |
G |
T |
3: 37,139,260 (GRCm39) |
L443F |
probably damaging |
Het |
| Amph |
T |
A |
13: 19,268,378 (GRCm39) |
M70K |
probably damaging |
Het |
| Ankra2 |
T |
A |
13: 98,409,919 (GRCm39) |
L306H |
probably damaging |
Het |
| Arc |
A |
C |
15: 74,543,592 (GRCm39) |
D210E |
probably benign |
Het |
| Arhgap10 |
A |
G |
8: 78,159,367 (GRCm39) |
|
probably null |
Het |
| Atp8b5 |
T |
A |
4: 43,344,449 (GRCm39) |
N445K |
probably benign |
Het |
| C1qc |
G |
T |
4: 136,617,746 (GRCm39) |
Q117K |
probably benign |
Het |
| Cadps |
T |
A |
14: 12,822,449 (GRCm38) |
E97V |
unknown |
Het |
| Capn13 |
GCA |
G |
17: 73,658,501 (GRCm39) |
|
probably null |
Het |
| Cdk13 |
A |
T |
13: 17,895,868 (GRCm39) |
W1014R |
probably damaging |
Het |
| Cltb |
C |
T |
13: 54,746,908 (GRCm39) |
E23K |
probably damaging |
Het |
| Clvs2 |
A |
T |
10: 33,498,642 (GRCm39) |
I96N |
probably damaging |
Het |
| Cwf19l1 |
A |
G |
19: 44,103,006 (GRCm39) |
V403A |
probably damaging |
Het |
| Ddr2 |
A |
T |
1: 169,816,066 (GRCm39) |
L547Q |
possibly damaging |
Het |
| Ebf1 |
A |
T |
11: 44,863,735 (GRCm39) |
K354* |
probably null |
Het |
| Fat4 |
A |
G |
3: 38,942,466 (GRCm39) |
Q453R |
probably benign |
Het |
| Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
| Gata6 |
A |
G |
18: 11,054,497 (GRCm39) |
E142G |
possibly damaging |
Het |
| Gm14221 |
T |
C |
2: 160,416,600 (GRCm39) |
|
noncoding transcript |
Het |
| Gm42791 |
C |
A |
5: 148,896,247 (GRCm39) |
|
probably benign |
Het |
| Gm6370 |
G |
T |
5: 146,430,621 (GRCm39) |
V269L |
probably benign |
Het |
| Gphn |
G |
A |
12: 78,673,984 (GRCm39) |
V526M |
probably damaging |
Het |
| Gpt |
A |
T |
15: 76,583,485 (GRCm39) |
E206V |
probably damaging |
Het |
| Grm3 |
G |
A |
5: 9,620,047 (GRCm39) |
A399V |
probably damaging |
Het |
| Helq |
A |
T |
5: 100,931,025 (GRCm39) |
V575E |
possibly damaging |
Het |
| Herc4 |
A |
G |
10: 63,151,437 (GRCm39) |
|
probably null |
Het |
| Ifi207 |
A |
T |
1: 173,557,381 (GRCm39) |
N452K |
probably damaging |
Het |
| Ikbke |
A |
G |
1: 131,184,848 (GRCm39) |
|
probably null |
Het |
| Kbtbd2 |
A |
G |
6: 56,756,687 (GRCm39) |
F350L |
probably benign |
Het |
| Kmt2c |
A |
G |
5: 25,519,555 (GRCm39) |
V2185A |
probably benign |
Het |
| Lgi2 |
T |
C |
5: 52,695,849 (GRCm39) |
Q362R |
probably damaging |
Het |
| Lrit1 |
G |
A |
14: 36,783,773 (GRCm39) |
G367E |
possibly damaging |
Het |
| Lrp1 |
G |
A |
10: 127,446,311 (GRCm39) |
H78Y |
probably benign |
Het |
| Matk |
A |
G |
10: 81,098,720 (GRCm39) |
|
probably benign |
Het |
| Med21 |
G |
A |
6: 146,549,690 (GRCm39) |
G24S |
probably damaging |
Het |
| Met |
G |
T |
6: 17,558,796 (GRCm39) |
L1141F |
probably damaging |
Het |
| Mroh3 |
A |
T |
1: 136,128,677 (GRCm39) |
|
probably null |
Het |
| Mrpl15 |
T |
C |
1: 4,844,683 (GRCm39) |
I203V |
probably benign |
Het |
| Ndufa9 |
A |
C |
6: 126,804,505 (GRCm39) |
Y298* |
probably null |
Het |
| Neb |
T |
C |
2: 52,188,906 (GRCm39) |
E808G |
probably damaging |
Het |
| Nol4l |
C |
T |
2: 153,253,726 (GRCm39) |
G616S |
probably benign |
Het |
| Oprm1 |
T |
A |
10: 6,788,468 (GRCm39) |
C408S |
probably benign |
Het |
| Or2ag18 |
T |
C |
7: 106,405,463 (GRCm39) |
M69V |
probably benign |
Het |
| Or4f14 |
A |
G |
2: 111,742,444 (GRCm39) |
V277A |
probably benign |
Het |
| Or4k42 |
T |
G |
2: 111,320,293 (GRCm39) |
D70A |
probably damaging |
Het |
| Or52e7 |
T |
A |
7: 104,684,858 (GRCm39) |
I151N |
probably damaging |
Het |
| Or5ak20 |
T |
C |
2: 85,183,793 (GRCm39) |
N159S |
possibly damaging |
Het |
| Paqr3 |
A |
G |
5: 97,256,053 (GRCm39) |
I107T |
possibly damaging |
Het |
| Pex5l |
G |
A |
3: 33,196,989 (GRCm39) |
|
probably benign |
Het |
| Phf8-ps |
C |
T |
17: 33,285,713 (GRCm39) |
S363N |
probably benign |
Het |
| Pik3ap1 |
T |
C |
19: 41,316,284 (GRCm39) |
D326G |
probably benign |
Het |
| Plaa |
G |
T |
4: 94,474,645 (GRCm39) |
D252E |
probably damaging |
Het |
| Plxna2 |
G |
A |
1: 194,480,040 (GRCm39) |
V1404I |
probably benign |
Het |
| Ppargc1a |
G |
A |
5: 51,631,564 (GRCm39) |
A355V |
possibly damaging |
Het |
| Primpol |
A |
G |
8: 47,039,726 (GRCm39) |
S350P |
probably benign |
Het |
| Prlr |
T |
C |
15: 10,328,883 (GRCm39) |
S453P |
probably benign |
Het |
| Psmd5 |
T |
C |
2: 34,742,564 (GRCm39) |
|
probably benign |
Het |
| Robo2 |
A |
T |
16: 73,768,079 (GRCm39) |
V571E |
probably damaging |
Het |
| Sbspon |
A |
T |
1: 15,929,264 (GRCm39) |
S176T |
possibly damaging |
Het |
| Scyl2 |
G |
A |
10: 89,476,325 (GRCm39) |
|
probably benign |
Het |
| Sema3e |
T |
A |
5: 14,280,144 (GRCm39) |
V341E |
probably damaging |
Het |
| Serpinb3b |
A |
T |
1: 107,082,270 (GRCm39) |
F331L |
possibly damaging |
Het |
| Setd2 |
A |
G |
9: 110,401,022 (GRCm39) |
H1736R |
probably benign |
Het |
| Sidt2 |
A |
T |
9: 45,863,327 (GRCm39) |
D180E |
probably benign |
Het |
| Skint9 |
A |
T |
4: 112,248,208 (GRCm39) |
Y179N |
probably benign |
Het |
| Slc27a5 |
T |
C |
7: 12,722,560 (GRCm39) |
N638S |
probably benign |
Het |
| Slc6a4 |
T |
A |
11: 76,904,135 (GRCm39) |
W197R |
probably damaging |
Het |
| Spag17 |
A |
T |
3: 99,970,649 (GRCm39) |
M1278L |
probably benign |
Het |
| Sptbn1 |
T |
A |
11: 30,092,353 (GRCm39) |
I471F |
probably damaging |
Het |
| Tasor2 |
A |
T |
13: 3,616,680 (GRCm39) |
|
probably null |
Het |
| Teddm1a |
A |
G |
1: 153,768,382 (GRCm39) |
Q282R |
probably benign |
Het |
| Tex35 |
A |
G |
1: 156,927,295 (GRCm39) |
L160P |
probably damaging |
Het |
| Tfap2c |
T |
C |
2: 172,393,438 (GRCm39) |
Y118H |
probably damaging |
Het |
| Tpp1 |
T |
C |
7: 105,395,930 (GRCm39) |
Q533R |
probably benign |
Het |
| Ttc13 |
C |
T |
8: 125,401,174 (GRCm39) |
D730N |
probably damaging |
Het |
| Ufc1 |
A |
G |
1: 171,122,375 (GRCm39) |
|
probably benign |
Het |
| Vcpip1 |
A |
G |
1: 9,817,589 (GRCm39) |
W265R |
probably damaging |
Het |
| Wdr11 |
C |
G |
7: 129,202,158 (GRCm39) |
|
probably null |
Het |
| Xirp2 |
A |
G |
2: 67,341,408 (GRCm39) |
I1216M |
possibly damaging |
Het |
| Zswim2 |
A |
G |
2: 83,747,187 (GRCm39) |
|
probably null |
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 |
|
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 |
|
|
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 |
PCR Primer
(F):5'- TGGAGATCAAGCACCATCCTTAC -3'
(R):5'- TGTGAGTCTAGAGACCAGCAC -3'
Sequencing Primer
(F):5'- ACCATCCTTACCTAGTTTGGAGAGG -3'
(R):5'- GCCCTAGAGTCTGCCCATGATC -3'
|
| Posted On |
2016-09-14 |
Incidental Mutation