Incidental Mutation 'R8968:2210408I21Rik'
| ID |
682884 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
2210408I21Rik
|
| Ensembl Gene |
ENSMUSG00000071252 |
| Gene Name |
RIKEN cDNA 2210408I21 gene |
| Synonyms |
|
| MMRRC Submission |
068802-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R8968 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
13 |
| Chromosomal Location |
77135540-77613784 bp(+) (GRCm38) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 77332310 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Stop codon
at position 1153
(L1153*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000127449
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000168779]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000168779
AA Change: L1153*
|
| SMART Domains |
Protein: ENSMUSP00000127449
Gene: ENSMUSG00000071252
AA Change: L1153*
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
121 |
133 |
N/A |
INTRINSIC |
|
low complexity region
|
151 |
164 |
N/A |
INTRINSIC |
|
Pfam:DUF4495
|
515 |
832 |
1.6e-140 |
PFAM |
|
low complexity region
|
1241 |
1255 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.9%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2410089E03Rik |
A |
T |
15: 8,201,281 (GRCm38) |
H1014L |
possibly damaging |
Het |
| 2810474O19Rik |
T |
A |
6: 149,327,166 (GRCm38) |
V570D |
probably damaging |
Het |
| Adamts2 |
T |
C |
11: 50,792,723 (GRCm38) |
I944T |
possibly damaging |
Het |
| Aqp9 |
A |
T |
9: 71,138,203 (GRCm38) |
C67* |
probably null |
Het |
| Armt1 |
G |
T |
10: 4,454,150 (GRCm38) |
G412W |
probably damaging |
Het |
| B4galt1 |
T |
C |
4: 40,807,243 (GRCm38) |
D381G |
probably benign |
Het |
| Bmp5 |
A |
T |
9: 75,873,297 (GRCm38) |
H292L |
probably benign |
Het |
| Brpf1 |
T |
C |
6: 113,322,549 (GRCm38) |
F1181S |
probably damaging |
Het |
| Btbd7 |
C |
A |
12: 102,812,766 (GRCm38) |
G414C |
probably damaging |
Het |
| Ccdc65 |
A |
T |
15: 98,718,842 (GRCm38) |
K204* |
probably null |
Het |
| Cdk5 |
T |
A |
5: 24,422,381 (GRCm38) |
K88M |
probably damaging |
Het |
| Cdrt4 |
T |
A |
11: 62,992,808 (GRCm38) |
L112Q |
probably damaging |
Het |
| Cenpb |
T |
C |
2: 131,178,627 (GRCm38) |
E417G |
unknown |
Het |
| Cep135 |
T |
C |
5: 76,606,729 (GRCm38) |
I351T |
possibly damaging |
Het |
| Ces1d |
A |
T |
8: 93,187,755 (GRCm38) |
S226R |
probably damaging |
Het |
| Cfap97 |
T |
A |
8: 46,170,077 (GRCm38) |
V168E |
possibly damaging |
Het |
| CN725425 |
T |
C |
15: 91,245,887 (GRCm38) |
C318R |
possibly damaging |
Het |
| Cnga3 |
T |
A |
1: 37,261,379 (GRCm38) |
D393E |
probably benign |
Het |
| Cpsf1 |
G |
A |
15: 76,601,969 (GRCm38) |
R358* |
probably null |
Het |
| Cyp2b23 |
G |
A |
7: 26,679,538 (GRCm38) |
P167L |
probably damaging |
Het |
| Cyp2c70 |
A |
T |
19: 40,153,615 (GRCm38) |
H477Q |
probably benign |
Het |
| D930020B18Rik |
A |
C |
10: 121,654,816 (GRCm38) |
Y107S |
probably damaging |
Het |
| Dhrs1 |
A |
T |
14: 55,740,735 (GRCm38) |
F216I |
probably benign |
Het |
| Dmgdh |
A |
T |
13: 93,709,259 (GRCm38) |
K474* |
probably null |
Het |
| Dsp |
T |
C |
13: 38,151,620 (GRCm38) |
I11T |
possibly damaging |
Het |
| Erh |
G |
T |
12: 80,637,508 (GRCm38) |
A65E |
probably benign |
Het |
| Fmnl1 |
AGGCTCTGG |
AGG |
11: 103,186,618 (GRCm38) |
|
probably benign |
Het |
| Grid2 |
A |
C |
6: 64,666,155 (GRCm38) |
H967P |
probably benign |
Het |
| Hc |
A |
G |
2: 35,032,305 (GRCm38) |
I503T |
possibly damaging |
Het |
| Herc3 |
T |
C |
6: 58,890,198 (GRCm38) |
L824S |
probably damaging |
Het |
| Hfm1 |
T |
C |
5: 106,917,573 (GRCm38) |
D80G |
probably benign |
Het |
| Hjurp |
CTCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCT |
C |
1: 88,266,277 (GRCm38) |
|
probably benign |
Het |
| Hspa1l |
A |
G |
17: 34,977,254 (GRCm38) |
K90E |
possibly damaging |
Het |
| Impa2 |
G |
A |
18: 67,318,427 (GRCm38) |
V264I |
probably benign |
Het |
| Ipmk |
C |
T |
10: 71,363,503 (GRCm38) |
R65W |
probably damaging |
Het |
| Klhl38 |
C |
T |
15: 58,322,104 (GRCm38) |
V410I |
probably benign |
Het |
| Lcn4 |
A |
G |
2: 26,668,348 (GRCm38) |
I175T |
possibly damaging |
Het |
| Lipo2 |
C |
A |
19: 33,749,517 (GRCm38) |
W40L |
probably damaging |
Het |
| Mgam |
A |
T |
6: 40,757,811 (GRCm38) |
|
probably null |
Het |
| Myo16 |
T |
A |
8: 10,569,700 (GRCm38) |
I1417N |
unknown |
Het |
| Olfr1052 |
G |
A |
2: 86,298,182 (GRCm38) |
R122H |
probably benign |
Het |
| Olfr1196 |
T |
A |
2: 88,700,793 (GRCm38) |
I179F |
probably benign |
Het |
| Olfr136 |
A |
T |
17: 38,335,429 (GRCm38) |
T91S |
possibly damaging |
Het |
| Olfr603 |
A |
T |
7: 103,383,460 (GRCm38) |
C181S |
probably damaging |
Het |
| Pcdha11 |
A |
G |
18: 37,012,254 (GRCm38) |
N466S |
probably damaging |
Het |
| Pif1 |
C |
T |
9: 65,591,794 (GRCm38) |
T432M |
probably damaging |
Het |
| Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,499,669 (GRCm38) |
|
probably null |
Het |
| Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 109,623,788 (GRCm38) |
|
probably benign |
Het |
| Pole |
T |
C |
5: 110,312,083 (GRCm38) |
S1118P |
possibly damaging |
Het |
| Ppp4r4 |
T |
C |
12: 103,600,447 (GRCm38) |
M652T |
probably benign |
Het |
| Prex2 |
A |
T |
1: 11,110,338 (GRCm38) |
K376* |
probably null |
Het |
| Prps1l1 |
A |
T |
12: 34,985,206 (GRCm38) |
I107F |
probably damaging |
Het |
| Rfc1 |
C |
T |
5: 65,275,435 (GRCm38) |
V761I |
probably benign |
Het |
| Ripk4 |
T |
C |
16: 97,746,003 (GRCm38) |
E353G |
probably benign |
Het |
| Robo2 |
C |
A |
16: 73,971,053 (GRCm38) |
|
probably null |
Het |
| Rrm1 |
C |
T |
7: 102,468,338 (GRCm38) |
A745V |
probably benign |
Het |
| Sash1 |
A |
T |
10: 8,730,415 (GRCm38) |
V737D |
probably benign |
Het |
| Sel1l2 |
T |
C |
2: 140,285,289 (GRCm38) |
K101E |
probably benign |
Het |
| Selenbp2 |
A |
T |
3: 94,700,030 (GRCm38) |
I253F |
probably benign |
Het |
| Setd1a |
C |
T |
7: 127,786,107 (GRCm38) |
P662L |
possibly damaging |
Het |
| Slc16a6 |
C |
T |
11: 109,454,950 (GRCm38) |
V496I |
possibly damaging |
Het |
| Slc4a4 |
A |
T |
5: 89,084,653 (GRCm38) |
M239L |
probably benign |
Het |
| Slc7a8 |
G |
C |
14: 54,781,293 (GRCm38) |
A12G |
probably benign |
Het |
| Snx30 |
T |
C |
4: 59,886,517 (GRCm38) |
S309P |
possibly damaging |
Het |
| Spen |
T |
C |
4: 141,470,390 (GRCm38) |
N3389S |
probably benign |
Het |
| Spg11 |
T |
C |
2: 122,092,206 (GRCm38) |
T921A |
probably damaging |
Het |
| Tanc2 |
T |
A |
11: 105,867,574 (GRCm38) |
D720E |
possibly damaging |
Het |
| Tmprss9 |
A |
T |
10: 80,894,329 (GRCm38) |
I688F |
possibly damaging |
Het |
| Trap1 |
A |
G |
16: 4,044,626 (GRCm38) |
V596A |
possibly damaging |
Het |
| Ttc32 |
G |
T |
12: 9,030,187 (GRCm38) |
R44L |
probably benign |
Het |
| Tusc3 |
T |
A |
8: 39,130,744 (GRCm38) |
N288K |
probably benign |
Het |
| Ush2a |
G |
A |
1: 188,395,759 (GRCm38) |
G656E |
probably damaging |
Het |
| Vill |
T |
C |
9: 119,063,603 (GRCm38) |
|
probably null |
Het |
| Vmn1r5 |
A |
T |
6: 56,986,197 (GRCm38) |
R286* |
probably null |
Het |
| Vmn2r14 |
T |
C |
5: 109,217,667 (GRCm38) |
T514A |
probably benign |
Het |
| Vmn2r32 |
G |
A |
7: 7,474,205 (GRCm38) |
H396Y |
probably benign |
Het |
| Vmn2r75 |
A |
T |
7: 86,171,557 (GRCm38) |
Y56* |
probably null |
Het |
| Wdfy3 |
C |
T |
5: 101,864,117 (GRCm38) |
S2668N |
probably benign |
Het |
| Wdr72 |
G |
A |
9: 74,152,447 (GRCm38) |
D392N |
probably benign |
Het |
| Zfp518a |
A |
C |
19: 40,913,426 (GRCm38) |
K600Q |
possibly damaging |
Het |
|
| Other mutations in 2210408I21Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00164:2210408I21Rik
|
APN |
13 |
77,323,358 (GRCm38) |
splice site |
probably benign |
|
|
IGL01154:2210408I21Rik
|
APN |
13 |
77,281,094 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL01461:2210408I21Rik
|
APN |
13 |
77,281,095 (GRCm38) |
missense |
probably benign |
0.25 |
|
IGL01624:2210408I21Rik
|
APN |
13 |
77,193,086 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL02033:2210408I21Rik
|
APN |
13 |
77,259,876 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
IGL02621:2210408I21Rik
|
APN |
13 |
77,260,031 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
IGL02718:2210408I21Rik
|
APN |
13 |
77,174,872 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02823:2210408I21Rik
|
APN |
13 |
77,261,955 (GRCm38) |
missense |
probably damaging |
0.96 |
|
IGL02859:2210408I21Rik
|
APN |
13 |
77,267,699 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
IGL03006:2210408I21Rik
|
APN |
13 |
77,323,772 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL03072:2210408I21Rik
|
APN |
13 |
77,259,997 (GRCm38) |
missense |
probably benign |
|
|
IGL03184:2210408I21Rik
|
APN |
13 |
77,323,451 (GRCm38) |
missense |
possibly damaging |
0.63 |
|
IGL03275:2210408I21Rik
|
APN |
13 |
77,298,555 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
PIT4651001:2210408I21Rik
|
UTSW |
13 |
77,259,895 (GRCm38) |
missense |
probably benign |
|
|
R0226:2210408I21Rik
|
UTSW |
13 |
77,303,425 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R0323:2210408I21Rik
|
UTSW |
13 |
77,298,555 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R0614:2210408I21Rik
|
UTSW |
13 |
77,192,663 (GRCm38) |
missense |
probably benign |
0.26 |
|
R0894:2210408I21Rik
|
UTSW |
13 |
77,323,607 (GRCm38) |
missense |
probably benign |
0.18 |
|
R1165:2210408I21Rik
|
UTSW |
13 |
77,334,287 (GRCm38) |
missense |
probably benign |
0.06 |
|
R1509:2210408I21Rik
|
UTSW |
13 |
77,192,647 (GRCm38) |
missense |
probably benign |
|
|
R1711:2210408I21Rik
|
UTSW |
13 |
77,269,920 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R1714:2210408I21Rik
|
UTSW |
13 |
77,316,360 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R1718:2210408I21Rik
|
UTSW |
13 |
77,245,370 (GRCm38) |
intron |
probably benign |
|
|
R1836:2210408I21Rik
|
UTSW |
13 |
77,323,374 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1893:2210408I21Rik
|
UTSW |
13 |
77,267,809 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R2035:2210408I21Rik
|
UTSW |
13 |
77,612,642 (GRCm38) |
makesense |
probably null |
|
|
R2329:2210408I21Rik
|
UTSW |
13 |
77,303,325 (GRCm38) |
missense |
probably benign |
0.04 |
|
R2897:2210408I21Rik
|
UTSW |
13 |
77,323,521 (GRCm38) |
missense |
probably benign |
0.33 |
|
R3688:2210408I21Rik
|
UTSW |
13 |
77,267,849 (GRCm38) |
missense |
possibly damaging |
0.52 |
|
R4153:2210408I21Rik
|
UTSW |
13 |
77,193,173 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4387:2210408I21Rik
|
UTSW |
13 |
77,316,574 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4388:2210408I21Rik
|
UTSW |
13 |
77,316,574 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4499:2210408I21Rik
|
UTSW |
13 |
77,316,527 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R4614:2210408I21Rik
|
UTSW |
13 |
77,254,256 (GRCm38) |
splice site |
probably null |
|
|
R4798:2210408I21Rik
|
UTSW |
13 |
77,323,724 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R4943:2210408I21Rik
|
UTSW |
13 |
77,245,327 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R5045:2210408I21Rik
|
UTSW |
13 |
77,267,808 (GRCm38) |
splice site |
probably null |
|
|
R5387:2210408I21Rik
|
UTSW |
13 |
77,259,973 (GRCm38) |
missense |
probably benign |
0.11 |
|
R5500:2210408I21Rik
|
UTSW |
13 |
77,303,389 (GRCm38) |
missense |
probably benign |
0.33 |
|
R5686:2210408I21Rik
|
UTSW |
13 |
77,303,314 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R6111:2210408I21Rik
|
UTSW |
13 |
77,327,902 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R6135:2210408I21Rik
|
UTSW |
13 |
77,254,216 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R6188:2210408I21Rik
|
UTSW |
13 |
77,183,731 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R6388:2210408I21Rik
|
UTSW |
13 |
77,262,111 (GRCm38) |
missense |
probably benign |
|
|
R6588:2210408I21Rik
|
UTSW |
13 |
77,192,647 (GRCm38) |
missense |
probably benign |
|
|
R6632:2210408I21Rik
|
UTSW |
13 |
77,281,067 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R6638:2210408I21Rik
|
UTSW |
13 |
77,303,402 (GRCm38) |
missense |
probably benign |
0.07 |
|
R6755:2210408I21Rik
|
UTSW |
13 |
77,327,875 (GRCm38) |
missense |
probably benign |
|
|
R6971:2210408I21Rik
|
UTSW |
13 |
77,193,187 (GRCm38) |
missense |
possibly damaging |
0.90 |
|
R7079:2210408I21Rik
|
UTSW |
13 |
77,254,204 (GRCm38) |
missense |
possibly damaging |
0.86 |
|
R7130:2210408I21Rik
|
UTSW |
13 |
77,269,902 (GRCm38) |
missense |
possibly damaging |
0.93 |
|
R7215:2210408I21Rik
|
UTSW |
13 |
77,323,571 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R7272:2210408I21Rik
|
UTSW |
13 |
77,323,536 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7331:2210408I21Rik
|
UTSW |
13 |
77,183,609 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R7561:2210408I21Rik
|
UTSW |
13 |
77,193,195 (GRCm38) |
missense |
probably benign |
|
|
R7684:2210408I21Rik
|
UTSW |
13 |
77,612,540 (GRCm38) |
nonsense |
probably null |
|
|
R7728:2210408I21Rik
|
UTSW |
13 |
77,316,477 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R7881:2210408I21Rik
|
UTSW |
13 |
77,323,566 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R7963:2210408I21Rik
|
UTSW |
13 |
77,192,554 (GRCm38) |
missense |
probably benign |
0.02 |
|
R8008:2210408I21Rik
|
UTSW |
13 |
77,281,115 (GRCm38) |
missense |
probably benign |
0.28 |
|
R8024:2210408I21Rik
|
UTSW |
13 |
77,612,594 (GRCm38) |
missense |
probably benign |
|
|
R8170:2210408I21Rik
|
UTSW |
13 |
77,263,594 (GRCm38) |
missense |
probably benign |
0.06 |
|
R8201:2210408I21Rik
|
UTSW |
13 |
77,193,159 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R8255:2210408I21Rik
|
UTSW |
13 |
77,267,731 (GRCm38) |
missense |
possibly damaging |
0.71 |
|
R8296:2210408I21Rik
|
UTSW |
13 |
77,267,777 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8476:2210408I21Rik
|
UTSW |
13 |
77,261,901 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R8526:2210408I21Rik
|
UTSW |
13 |
77,269,816 (GRCm38) |
nonsense |
probably null |
|
|
R8746:2210408I21Rik
|
UTSW |
13 |
77,303,410 (GRCm38) |
missense |
probably benign |
0.01 |
|
R8812:2210408I21Rik
|
UTSW |
13 |
77,332,352 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8870:2210408I21Rik
|
UTSW |
13 |
77,323,721 (GRCm38) |
missense |
possibly damaging |
0.96 |
|
R8885:2210408I21Rik
|
UTSW |
13 |
77,323,406 (GRCm38) |
missense |
possibly damaging |
0.91 |
|
R8910:2210408I21Rik
|
UTSW |
13 |
77,323,649 (GRCm38) |
missense |
probably benign |
0.03 |
|
R8911:2210408I21Rik
|
UTSW |
13 |
77,281,115 (GRCm38) |
missense |
probably benign |
0.28 |
|
R8965:2210408I21Rik
|
UTSW |
13 |
77,612,604 (GRCm38) |
missense |
probably benign |
0.02 |
|
R8989:2210408I21Rik
|
UTSW |
13 |
77,612,605 (GRCm38) |
missense |
probably benign |
0.01 |
|
R9163:2210408I21Rik
|
UTSW |
13 |
77,245,281 (GRCm38) |
missense |
possibly damaging |
0.73 |
|
R9378:2210408I21Rik
|
UTSW |
13 |
77,323,616 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R9478:2210408I21Rik
|
UTSW |
13 |
77,303,454 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R9523:2210408I21Rik
|
UTSW |
13 |
77,259,869 (GRCm38) |
missense |
possibly damaging |
0.53 |
|
R9595:2210408I21Rik
|
UTSW |
13 |
77,316,447 (GRCm38) |
missense |
probably benign |
|
|
X0066:2210408I21Rik
|
UTSW |
13 |
77,183,640 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
Z1088:2210408I21Rik
|
UTSW |
13 |
77,174,891 (GRCm38) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTCATTCATCATGTGAGGATTTG -3'
(R):5'- TTCTGACACACAGGAGCCATAG -3'
Sequencing Primer
(F):5'- ACGTTTAACTTGGTTTTGTTAGGTG -3'
(R):5'- CACAGGAGCCATAGATTTAAGTTAC -3'
|
| Posted On |
2021-10-11 |
Incidental Mutation