Incidental Mutation 'R0883:1110002E22Rik'
ID 80739
Institutional Source Beutler Lab
Gene Symbol 1110002E22Rik
Ensembl Gene ENSMUSG00000090066
Gene Name RIKEN cDNA 1110002E22 gene
Synonyms
MMRRC Submission 039050-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.544) question?
Stock # R0883 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 138065052-138081506 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 138069871 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 1607 (L1607P)
Ref Sequence ENSEMBL: ENSMUSP00000123851 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053318] [ENSMUST00000163080]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000053318
Predicted Effect probably damaging
Transcript: ENSMUST00000163080
AA Change: L1607P

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000123851
Gene: ENSMUSG00000090066
AA Change: L1607P

DomainStartEndE-ValueType
low complexity region 44 55 N/A INTRINSIC
low complexity region 87 102 N/A INTRINSIC
low complexity region 229 247 N/A INTRINSIC
low complexity region 422 438 N/A INTRINSIC
low complexity region 459 505 N/A INTRINSIC
low complexity region 667 680 N/A INTRINSIC
low complexity region 937 948 N/A INTRINSIC
low complexity region 995 1007 N/A INTRINSIC
low complexity region 1105 1115 N/A INTRINSIC
low complexity region 1224 1242 N/A INTRINSIC
low complexity region 1376 1385 N/A INTRINSIC
Pfam:DUF4585 1598 1667 6.9e-32 PFAM
low complexity region 1723 1738 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184925
Meta Mutation Damage Score 0.1768 question?
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 99.0%
  • 10x: 97.8%
  • 20x: 96.1%
Validation Efficiency 98% (148/151)
Allele List at MGI
Other mutations in this stock
Total: 150 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700016H13Rik T C 5: 103,648,821 (GRCm38) *118W probably null Het
1700061G19Rik A T 17: 56,883,835 (GRCm38) N468Y probably benign Het
4930595M18Rik G T X: 81,420,931 (GRCm38) T390N possibly damaging Het
Abca13 C T 11: 9,291,238 (GRCm38) Q1034* probably null Het
Adgra3 T C 5: 49,960,723 (GRCm38) H1161R probably damaging Het
AF529169 T C 9: 89,602,417 (GRCm38) H309R probably benign Het
Aff1 T C 5: 103,826,138 (GRCm38) probably benign Het
Agap2 A G 10: 127,091,702 (GRCm38) T1131A possibly damaging Het
Ankrd12 A G 17: 65,985,132 (GRCm38) V1102A probably benign Het
Ankrd54 A T 15: 79,062,731 (GRCm38) C23S probably damaging Het
Anxa10 C T 8: 62,077,967 (GRCm38) V70I probably benign Het
Asap3 T C 4: 136,234,325 (GRCm38) probably benign Het
Asb13 T C 13: 3,645,052 (GRCm38) probably null Het
Atp6v1a A T 16: 44,101,692 (GRCm38) probably benign Het
Atp8b1 T G 18: 64,564,541 (GRCm38) I411L probably benign Het
Baiap3 T A 17: 25,249,101 (GRCm38) N313I probably damaging Het
Bok T C 1: 93,686,487 (GRCm38) I14T probably benign Het
Bri3bp T A 5: 125,441,744 (GRCm38) probably null Het
C2cd2l A G 9: 44,316,202 (GRCm38) L186P probably damaging Het
Cadm2 A T 16: 66,882,814 (GRCm38) C44S probably damaging Het
Capn11 T C 17: 45,638,881 (GRCm38) probably benign Het
Carm1 T A 9: 21,569,591 (GRCm38) probably benign Het
Ccdc189 T C 7: 127,584,862 (GRCm38) E261G probably damaging Het
Ccdc27 T C 4: 154,036,484 (GRCm38) E285G unknown Het
Cct3 T A 3: 88,313,557 (GRCm38) D298E probably damaging Het
Cd59b T A 2: 104,080,986 (GRCm38) probably benign Het
Cdh2 T C 18: 16,629,576 (GRCm38) N437S probably benign Het
Celsr3 T A 9: 108,842,633 (GRCm38) I2470N probably damaging Het
Cfap100 G A 6: 90,415,906 (GRCm38) probably benign Het
Cfap45 A T 1: 172,532,189 (GRCm38) R98S possibly damaging Het
Cfap54 T A 10: 92,870,669 (GRCm38) H2757L unknown Het
Chd1 C A 17: 15,725,431 (GRCm38) N72K probably benign Het
Cntn4 A T 6: 106,667,540 (GRCm38) probably benign Het
Cstf2t A T 19: 31,084,626 (GRCm38) M521L probably benign Het
Daam2 A T 17: 49,498,883 (GRCm38) probably benign Het
Ddias A T 7: 92,859,337 (GRCm38) W457R probably benign Het
Ddr2 C T 1: 169,994,629 (GRCm38) V417I probably benign Het
Dhx57 T C 17: 80,270,371 (GRCm38) T570A probably damaging Het
Dmp1 A G 5: 104,207,630 (GRCm38) E32G possibly damaging Het
Dtymk C T 1: 93,801,788 (GRCm38) V14M possibly damaging Het
Dync2li1 G A 17: 84,649,271 (GRCm38) M286I probably benign Het
Eea1 G A 10: 96,021,667 (GRCm38) D664N possibly damaging Het
Esp6 G T 17: 40,565,396 (GRCm38) V112L probably benign Het
Fam83h G T 15: 76,006,169 (GRCm38) Q127K probably damaging Het
Gabbr2 G A 4: 46,677,474 (GRCm38) T802I probably benign Het
Gart C A 16: 91,623,403 (GRCm38) D851Y possibly damaging Het
Gemin6 T A 17: 80,228,095 (GRCm38) H161Q probably damaging Het
Gm10912 T C 2: 104,066,530 (GRCm38) S5P probably benign Het
Gm4907 A T X: 23,907,051 (GRCm38) I264F probably benign Het
Gm5941 G A X: 92,490,211 (GRCm38) A62T possibly damaging Het
Gng2 G T 14: 19,891,295 (GRCm38) D26E probably benign Het
Gpr33 A G 12: 52,023,635 (GRCm38) V207A probably benign Het
Gstm3 T A 3: 107,966,270 (GRCm38) probably benign Het
Havcr1 T C 11: 46,752,432 (GRCm38) C60R probably damaging Het
Hspg2 T C 4: 137,541,440 (GRCm38) S2157P probably benign Het
Ift140 A G 17: 25,090,933 (GRCm38) T1105A probably benign Het
Igsf8 C A 1: 172,316,259 (GRCm38) A56D possibly damaging Het
Kat6a G T 8: 22,862,214 (GRCm38) A5S probably damaging Het
Kctd16 A G 18: 40,530,775 (GRCm38) E319G probably damaging Het
Kmo T C 1: 175,647,140 (GRCm38) V157A possibly damaging Het
Lrp5 T A 19: 3,605,308 (GRCm38) I1071F probably damaging Het
Lrrc17 A G 5: 21,561,278 (GRCm38) T253A probably benign Het
Mast2 T A 4: 116,311,767 (GRCm38) H769L probably damaging Het
Mast4 T C 13: 102,853,900 (GRCm38) K50E probably damaging Het
Mbd5 A G 2: 49,256,689 (GRCm38) T304A possibly damaging Het
Mbp T C 18: 82,572,870 (GRCm38) S73P probably damaging Het
Mc5r T A 18: 68,339,092 (GRCm38) V174E probably damaging Het
Med13 T A 11: 86,307,038 (GRCm38) T736S probably benign Het
Med13l T C 5: 118,671,002 (GRCm38) probably benign Het
Mlh3 C G 12: 85,235,714 (GRCm38) A1382P possibly damaging Het
Mpdz T C 4: 81,359,991 (GRCm38) probably benign Het
Muc5ac A G 7: 141,796,265 (GRCm38) T582A possibly damaging Het
Mum1l1 T A X: 139,235,695 (GRCm38) D327E probably damaging Het
Nalcn A G 14: 123,464,740 (GRCm38) F453S probably damaging Het
Nrap T A 19: 56,345,474 (GRCm38) M902L probably damaging Het
Nup85 C T 11: 115,568,370 (GRCm38) R100* probably null Het
Nxf1 T G 19: 8,764,591 (GRCm38) N296K probably damaging Het
Ogg1 A G 6: 113,328,420 (GRCm38) T65A probably damaging Het
Ogt A G X: 101,644,199 (GRCm38) probably benign Het
Olfr1258 A G 2: 89,930,201 (GRCm38) T131A probably benign Het
Olfr1298 C T 2: 111,645,791 (GRCm38) V69I probably benign Het
Olfr504 T A 7: 108,565,276 (GRCm38) N173I probably benign Het
Olfr558 T A 7: 102,709,995 (GRCm38) H245Q probably damaging Het
Ovol2 T C 2: 144,331,790 (GRCm38) D24G probably damaging Het
Pabpc1 A G 15: 36,599,054 (GRCm38) probably benign Het
Pak6 T C 2: 118,693,687 (GRCm38) L441P probably damaging Het
Pappa T A 4: 65,189,315 (GRCm38) C654* probably null Het
Paqr6 T A 3: 88,365,991 (GRCm38) S97T probably damaging Het
Parp14 T C 16: 35,858,518 (GRCm38) N360S probably benign Het
Pclo G T 5: 14,677,859 (GRCm38) G2244* probably null Het
Pdzrn3 A T 6: 101,155,942 (GRCm38) probably null Het
Pes1 T C 11: 3,975,557 (GRCm38) M220T probably damaging Het
Phip A T 9: 82,876,221 (GRCm38) V1473E probably benign Het
Pkd2l2 T A 18: 34,430,268 (GRCm38) probably null Het
Plch1 T C 3: 63,753,256 (GRCm38) D302G probably damaging Het
Plekhh2 A G 17: 84,618,031 (GRCm38) T1419A probably benign Het
Ppara A T 15: 85,798,171 (GRCm38) E356V probably damaging Het
Ppp1r37 G A 7: 19,532,177 (GRCm38) P555S probably benign Het
Ppp6r1 T C 7: 4,639,710 (GRCm38) E545G possibly damaging Het
Proser3 G A 7: 30,540,699 (GRCm38) H327Y probably damaging Het
Prss43 T A 9: 110,829,508 (GRCm38) I292N probably damaging Het
Pygl G C 12: 70,206,404 (GRCm38) N271K probably damaging Het
Rassf7 T A 7: 141,216,990 (GRCm38) probably benign Het
Rfx2 T C 17: 56,803,722 (GRCm38) Y88C probably damaging Het
Rpl6 T C 5: 121,208,478 (GRCm38) V214A probably benign Het
Rspo1 T A 4: 124,991,432 (GRCm38) probably null Het
Sav1 A C 12: 69,966,205 (GRCm38) L366V probably benign Het
Sema3b T G 9: 107,604,156 (GRCm38) T52P possibly damaging Het
Senp6 A G 9: 80,116,559 (GRCm38) D40G probably damaging Het
Sh3pxd2a A G 19: 47,268,207 (GRCm38) S719P probably damaging Het
Shank1 C T 7: 44,352,294 (GRCm38) R1146W unknown Het
Slc34a3 G T 2: 25,231,233 (GRCm38) D307E probably benign Het
Slc35b3 T C 13: 38,937,275 (GRCm38) I330V probably benign Het
Slc4a10 G A 2: 62,243,398 (GRCm38) C268Y probably benign Het
Slco6d1 A G 1: 98,421,399 (GRCm38) E65G probably benign Het
Slit2 A G 5: 48,245,573 (GRCm38) probably benign Het
Smcr8 T C 11: 60,778,115 (GRCm38) Y30H probably damaging Het
Snap47 A G 11: 59,438,500 (GRCm38) probably benign Het
Snrnp25 G A 11: 32,206,960 (GRCm38) V15I probably damaging Het
Spns2 T C 11: 72,454,397 (GRCm38) Y449C probably damaging Het
Stab2 T A 10: 86,924,450 (GRCm38) probably benign Het
Strip1 C A 3: 107,614,613 (GRCm38) D750Y probably damaging Het
Taf1c A T 8: 119,599,983 (GRCm38) I438N probably damaging Het
Tbc1d2 T A 4: 46,609,003 (GRCm38) K745* probably null Het
Tctn1 T C 5: 122,264,144 (GRCm38) T76A probably damaging Het
Tfpi T C 2: 84,443,320 (GRCm38) probably benign Het
Timm44 A T 8: 4,266,592 (GRCm38) H317Q probably benign Het
Tnfaip1 A T 11: 78,530,014 (GRCm38) probably benign Het
Tnpo3 A T 6: 29,554,993 (GRCm38) probably benign Het
Top3b T C 16: 16,879,437 (GRCm38) probably benign Het
Trak1 T A 9: 121,453,285 (GRCm38) M410K possibly damaging Het
Trpm3 C A 19: 22,978,654 (GRCm38) P1160Q probably damaging Het
Tyk2 T A 9: 21,111,137 (GRCm38) T799S possibly damaging Het
Ubfd1 G A 7: 122,067,491 (GRCm38) probably benign Het
Unc13a G A 8: 71,642,173 (GRCm38) R1272* probably null Het
Unc45b T A 11: 82,940,205 (GRCm38) L797Q possibly damaging Het
Urb2 C T 8: 124,030,970 (GRCm38) Q1139* probably null Het
Vmn2r66 A T 7: 85,007,862 (GRCm38) S112T probably benign Het
Vmn2r71 A T 7: 85,623,634 (GRCm38) D552V probably benign Het
Vmn2r76 A G 7: 86,228,696 (GRCm38) Y498H probably benign Het
Vmn2r84 A C 10: 130,391,115 (GRCm38) W285G probably damaging Het
Vps72 G T 3: 95,122,583 (GRCm38) L304F probably damaging Het
Wiz A T 17: 32,356,441 (GRCm38) I907N probably damaging Het
Yaf2 T C 15: 93,285,536 (GRCm38) K131R probably damaging Het
Zfp141 A T 7: 42,476,056 (GRCm38) Y331N possibly damaging Het
Zfp324 G T 7: 12,971,024 (GRCm38) C380F probably damaging Het
Zfp521 T C 18: 13,845,062 (GRCm38) T765A probably benign Het
Zfp616 A T 11: 74,085,674 (GRCm38) H923L probably damaging Het
Zfpm1 C T 8: 122,335,846 (GRCm38) T548M probably damaging Het
Zp2 A T 7: 120,143,576 (GRCm38) probably benign Het
Other mutations in 1110002E22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0026:1110002E22Rik UTSW 3 138,066,805 (GRCm38) missense possibly damaging 0.95
R0047:1110002E22Rik UTSW 3 138,066,264 (GRCm38) missense probably damaging 0.97
R0047:1110002E22Rik UTSW 3 138,066,264 (GRCm38) missense probably damaging 0.97
R0102:1110002E22Rik UTSW 3 138,068,113 (GRCm38) missense probably damaging 1.00
R0102:1110002E22Rik UTSW 3 138,068,113 (GRCm38) missense probably damaging 1.00
R0197:1110002E22Rik UTSW 3 138,069,871 (GRCm38) missense probably damaging 1.00
R0239:1110002E22Rik UTSW 3 138,065,834 (GRCm38) small deletion probably benign
R0394:1110002E22Rik UTSW 3 138,067,304 (GRCm38) missense probably damaging 0.99
R0401:1110002E22Rik UTSW 3 138,070,306 (GRCm38) missense possibly damaging 0.73
R0496:1110002E22Rik UTSW 3 138,068,244 (GRCm38) missense probably damaging 1.00
R0591:1110002E22Rik UTSW 3 138,068,943 (GRCm38) nonsense probably null
R0711:1110002E22Rik UTSW 3 138,068,225 (GRCm38) missense probably damaging 0.99
R0908:1110002E22Rik UTSW 3 138,070,077 (GRCm38) missense probably damaging 0.99
R0968:1110002E22Rik UTSW 3 138,067,206 (GRCm38) missense probably damaging 0.99
R1023:1110002E22Rik UTSW 3 138,066,871 (GRCm38) missense probably damaging 1.00
R1168:1110002E22Rik UTSW 3 138,067,900 (GRCm38) missense probably benign 0.20
R1472:1110002E22Rik UTSW 3 138,067,552 (GRCm38) missense possibly damaging 0.95
R1538:1110002E22Rik UTSW 3 138,065,401 (GRCm38) missense probably benign 0.02
R1648:1110002E22Rik UTSW 3 138,069,420 (GRCm38) missense probably benign 0.18
R1800:1110002E22Rik UTSW 3 138,066,718 (GRCm38) missense probably damaging 1.00
R1919:1110002E22Rik UTSW 3 138,067,270 (GRCm38) missense probably damaging 0.99
R1974:1110002E22Rik UTSW 3 138,067,267 (GRCm38) missense probably damaging 1.00
R1990:1110002E22Rik UTSW 3 138,065,658 (GRCm38) nonsense probably null
R1991:1110002E22Rik UTSW 3 138,065,658 (GRCm38) nonsense probably null
R2102:1110002E22Rik UTSW 3 138,065,173 (GRCm38) missense probably damaging 0.99
R2761:1110002E22Rik UTSW 3 138,067,780 (GRCm38) missense probably damaging 0.99
R2899:1110002E22Rik UTSW 3 138,065,682 (GRCm38) missense probably benign 0.00
R3618:1110002E22Rik UTSW 3 138,068,407 (GRCm38) missense probably damaging 1.00
R3904:1110002E22Rik UTSW 3 138,066,639 (GRCm38) missense probably benign 0.15
R3955:1110002E22Rik UTSW 3 138,068,073 (GRCm38) missense probably benign 0.00
R4520:1110002E22Rik UTSW 3 138,070,266 (GRCm38) missense probably damaging 0.99
R4619:1110002E22Rik UTSW 3 138,069,759 (GRCm38) missense probably damaging 0.99
R4736:1110002E22Rik UTSW 3 138,068,485 (GRCm38) missense probably damaging 0.99
R4752:1110002E22Rik UTSW 3 138,069,990 (GRCm38) missense possibly damaging 0.91
R4777:1110002E22Rik UTSW 3 138,065,742 (GRCm38) missense probably benign 0.09
R4780:1110002E22Rik UTSW 3 138,065,370 (GRCm38) missense probably benign 0.02
R4824:1110002E22Rik UTSW 3 138,065,676 (GRCm38) missense probably benign 0.00
R4829:1110002E22Rik UTSW 3 138,069,019 (GRCm38) missense probably damaging 0.99
R4965:1110002E22Rik UTSW 3 138,069,672 (GRCm38) missense probably benign
R5206:1110002E22Rik UTSW 3 138,066,511 (GRCm38) missense probably benign 0.00
R5212:1110002E22Rik UTSW 3 138,065,850 (GRCm38) missense possibly damaging 0.85
R5373:1110002E22Rik UTSW 3 138,067,635 (GRCm38) missense probably benign
R5374:1110002E22Rik UTSW 3 138,067,635 (GRCm38) missense probably benign
R5506:1110002E22Rik UTSW 3 138,067,947 (GRCm38) missense probably damaging 1.00
R5528:1110002E22Rik UTSW 3 138,066,499 (GRCm38) missense probably benign
R5536:1110002E22Rik UTSW 3 138,066,388 (GRCm38) missense possibly damaging 0.89
R5587:1110002E22Rik UTSW 3 138,065,409 (GRCm38) missense probably benign
R5759:1110002E22Rik UTSW 3 138,068,658 (GRCm38) missense probably benign
R5933:1110002E22Rik UTSW 3 138,070,348 (GRCm38) missense probably damaging 1.00
R5957:1110002E22Rik UTSW 3 138,070,161 (GRCm38) missense probably benign
R6092:1110002E22Rik UTSW 3 138,068,940 (GRCm38) missense probably benign 0.02
R6305:1110002E22Rik UTSW 3 138,067,980 (GRCm38) missense probably damaging 1.00
R6457:1110002E22Rik UTSW 3 138,066,622 (GRCm38) missense probably damaging 1.00
R6469:1110002E22Rik UTSW 3 138,066,975 (GRCm38) missense probably damaging 0.97
R6499:1110002E22Rik UTSW 3 138,068,800 (GRCm38) missense probably damaging 1.00
R6527:1110002E22Rik UTSW 3 138,067,527 (GRCm38) missense probably damaging 0.99
R6580:1110002E22Rik UTSW 3 138,066,625 (GRCm38) missense probably benign 0.00
R6693:1110002E22Rik UTSW 3 138,069,154 (GRCm38) missense probably benign 0.00
R6751:1110002E22Rik UTSW 3 138,066,210 (GRCm38) missense probably damaging 1.00
R6852:1110002E22Rik UTSW 3 138,065,169 (GRCm38) nonsense probably null
R6920:1110002E22Rik UTSW 3 138,068,050 (GRCm38) missense probably damaging 1.00
R7001:1110002E22Rik UTSW 3 138,065,511 (GRCm38) missense probably benign
R7145:1110002E22Rik UTSW 3 138,070,059 (GRCm38) missense probably damaging 1.00
R7238:1110002E22Rik UTSW 3 138,069,951 (GRCm38) missense probably damaging 1.00
R7278:1110002E22Rik UTSW 3 138,065,476 (GRCm38) missense probably benign
R7425:1110002E22Rik UTSW 3 138,065,695 (GRCm38) missense probably benign 0.00
R7487:1110002E22Rik UTSW 3 138,066,868 (GRCm38) missense probably damaging 1.00
R7557:1110002E22Rik UTSW 3 138,068,283 (GRCm38) nonsense probably null
R7663:1110002E22Rik UTSW 3 138,066,126 (GRCm38) missense probably damaging 0.98
R7743:1110002E22Rik UTSW 3 138,068,755 (GRCm38) missense probably damaging 1.00
R7799:1110002E22Rik UTSW 3 138,069,601 (GRCm38) missense probably benign 0.33
R8181:1110002E22Rik UTSW 3 138,068,395 (GRCm38) missense probably damaging 0.99
R8264:1110002E22Rik UTSW 3 138,067,782 (GRCm38) missense probably damaging 0.99
R8273:1110002E22Rik UTSW 3 138,066,450 (GRCm38) missense probably benign
R8434:1110002E22Rik UTSW 3 138,067,260 (GRCm38) missense probably damaging 0.97
R8530:1110002E22Rik UTSW 3 138,068,825 (GRCm38) missense probably damaging 0.99
R8754:1110002E22Rik UTSW 3 138,066,037 (GRCm38) missense probably benign
R8808:1110002E22Rik UTSW 3 138,070,113 (GRCm38) missense probably benign 0.01
R8891:1110002E22Rik UTSW 3 138,066,759 (GRCm38) nonsense probably null
R9026:1110002E22Rik UTSW 3 138,065,148 (GRCm38) missense possibly damaging 0.53
R9177:1110002E22Rik UTSW 3 138,069,916 (GRCm38) missense probably damaging 1.00
R9250:1110002E22Rik UTSW 3 138,066,628 (GRCm38) missense probably damaging 1.00
R9291:1110002E22Rik UTSW 3 138,066,703 (GRCm38) missense probably benign 0.02
R9293:1110002E22Rik UTSW 3 138,066,078 (GRCm38) missense possibly damaging 0.93
R9307:1110002E22Rik UTSW 3 138,065,422 (GRCm38) missense probably benign 0.04
R9439:1110002E22Rik UTSW 3 138,066,287 (GRCm38) missense probably benign 0.00
R9509:1110002E22Rik UTSW 3 138,065,834 (GRCm38) small deletion probably benign
R9582:1110002E22Rik UTSW 3 138,067,005 (GRCm38) missense probably damaging 0.99
R9599:1110002E22Rik UTSW 3 138,068,506 (GRCm38) missense probably benign 0.16
R9613:1110002E22Rik UTSW 3 138,065,365 (GRCm38) missense probably damaging 0.98
R9670:1110002E22Rik UTSW 3 138,065,133 (GRCm38) missense probably benign
X0003:1110002E22Rik UTSW 3 138,069,096 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATCTCAGGTCAGTGGAACCAGCAG -3'
(R):5'- TCCAGGATAGATCATGTAGGTGGGC -3'

Sequencing Primer
(F):5'- AGAAACAGTCGTTGCTGCC -3'
(R):5'- CCCATAGGCCCCAGGAC -3'
Posted On 2013-11-07