Incidental Mutation 'R6261:Scn9a'
ID 506674
Institutional Source Beutler Lab
Gene Symbol Scn9a
Ensembl Gene ENSMUSG00000075316
Gene Name sodium channel, voltage-gated, type IX, alpha
Synonyms PN1
MMRRC Submission 044404-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6261 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 66480080-66634962 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 66483896 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Leucine to Glutamine at position 1815 (L1815Q)
Ref Sequence ENSEMBL: ENSMUSP00000131711 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100063] [ENSMUST00000100064] [ENSMUST00000112354] [ENSMUST00000164384] [ENSMUST00000169900]
AlphaFold Q62205
Predicted Effect probably damaging
Transcript: ENSMUST00000100063
AA Change: L1817Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000097641
Gene: ENSMUSG00000075316
AA Change: L1817Q

DomainStartEndE-ValueType
low complexity region 29 49 N/A INTRINSIC
Pfam:Ion_trans 154 403 9.5e-78 PFAM
coiled coil region 404 442 N/A INTRINSIC
Pfam:DUF3451 465 685 1.3e-62 PFAM
Pfam:Ion_trans 768 957 9.9e-48 PFAM
Pfam:Na_trans_assoc 972 1191 2.9e-72 PFAM
low complexity region 1203 1214 N/A INTRINSIC
Pfam:Ion_trans 1217 1445 2.8e-55 PFAM
PDB:1BYY|A 1447 1499 9e-27 PDB
Pfam:Ion_trans 1538 1748 3.4e-52 PFAM
Pfam:PKD_channel 1599 1755 1.1e-7 PFAM
IQ 1877 1899 1.03e-3 SMART
low complexity region 1956 1972 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000100064
AA Change: L1826Q

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000097642
Gene: ENSMUSG00000075316
AA Change: L1826Q

DomainStartEndE-ValueType
low complexity region 29 49 N/A INTRINSIC
Pfam:Ion_trans 125 412 2.2e-84 PFAM
low complexity region 433 446 N/A INTRINSIC
Pfam:Na_trans_cytopl 483 693 7.5e-76 PFAM
Pfam:Ion_trans 742 977 4.1e-57 PFAM
Pfam:Na_trans_assoc 981 1185 1.4e-58 PFAM
Pfam:Ion_trans 1189 1466 7e-67 PFAM
Pfam:Ion_trans 1512 1769 1e-55 PFAM
Pfam:PKD_channel 1605 1763 2.6e-7 PFAM
IQ 1886 1908 1.03e-3 SMART
low complexity region 1965 1981 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000112354
AA Change: L1815Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000107973
Gene: ENSMUSG00000075316
AA Change: L1815Q

DomainStartEndE-ValueType
low complexity region 29 49 N/A INTRINSIC
Pfam:Ion_trans 154 401 1.2e-77 PFAM
coiled coil region 402 449 N/A INTRINSIC
Pfam:DUF3451 463 683 1.3e-62 PFAM
Pfam:Ion_trans 766 955 9.9e-48 PFAM
Pfam:Na_trans_assoc 970 1189 2.9e-72 PFAM
low complexity region 1201 1212 N/A INTRINSIC
Pfam:Ion_trans 1215 1443 2.8e-55 PFAM
PDB:1BYY|A 1445 1497 7e-29 PDB
Pfam:Ion_trans 1536 1746 3.4e-52 PFAM
Pfam:PKD_channel 1597 1753 1.1e-7 PFAM
IQ 1875 1897 1.03e-3 SMART
low complexity region 1954 1970 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141149
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152740
Predicted Effect probably damaging
Transcript: ENSMUST00000164384
AA Change: L1826Q

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000126528
Gene: ENSMUSG00000075316
AA Change: L1826Q

DomainStartEndE-ValueType
low complexity region 29 49 N/A INTRINSIC
Pfam:Ion_trans 154 401 1.1e-77 PFAM
coiled coil region 402 449 N/A INTRINSIC
Pfam:DUF3451 463 694 4.2e-66 PFAM
Pfam:Ion_trans 777 966 8.8e-48 PFAM
Pfam:Na_trans_assoc 981 1200 6e-72 PFAM
low complexity region 1212 1223 N/A INTRINSIC
Pfam:Ion_trans 1226 1454 2.5e-55 PFAM
PDB:1BYY|A 1456 1508 6e-29 PDB
Pfam:Ion_trans 1547 1757 3e-52 PFAM
Pfam:PKD_channel 1608 1764 8.1e-8 PFAM
IQ 1886 1908 1.03e-3 SMART
low complexity region 1965 1981 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000169900
AA Change: L1815Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000131711
Gene: ENSMUSG00000075316
AA Change: L1815Q

DomainStartEndE-ValueType
low complexity region 29 49 N/A INTRINSIC
Pfam:Ion_trans 154 401 3.7e-78 PFAM
coiled coil region 402 449 N/A INTRINSIC
Pfam:DUF3451 463 683 1.3e-62 PFAM
Pfam:Ion_trans 766 955 9.9e-48 PFAM
Pfam:Na_trans_assoc 970 1189 2.9e-72 PFAM
low complexity region 1201 1212 N/A INTRINSIC
Pfam:Ion_trans 1215 1443 2.8e-55 PFAM
PDB:1BYY|A 1445 1497 7e-29 PDB
Pfam:Ion_trans 1536 1746 3.4e-52 PFAM
Pfam:PKD_channel 1597 1753 1.1e-7 PFAM
IQ 1875 1897 1.03e-3 SMART
low complexity region 1954 1970 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.7%
Validation Efficiency 100% (65/65)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a voltage-gated sodium channel which plays a significant role in nociception signaling. Mutations in this gene have been associated with primary erythermalgia, channelopathy-associated insensitivity to pain, and paroxysmal extreme pain disorder. [provided by RefSeq, Aug 2009]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit prenatal/neonatal lethality. Mice homozygous for a knock-in allele exhibit increased susceptibility to electrically induced seizures. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot8 T C 2: 164,795,059 (GRCm38) D257G probably damaging Het
Adamtsl1 T C 4: 86,336,878 (GRCm38) V736A probably benign Het
Anln A G 9: 22,364,046 (GRCm38) L521S probably damaging Het
Arfgap2 T G 2: 91,270,282 (GRCm38) S311A probably benign Het
Brdt A T 5: 107,348,503 (GRCm38) E160D probably benign Het
Ccdc187 A G 2: 26,276,203 (GRCm38) I738T probably damaging Het
Cd59a G C 2: 104,104,205 (GRCm38) G6A probably damaging Het
Cd5l C T 3: 87,368,608 (GRCm38) P295L probably benign Het
Cdhr17 T C 5: 16,812,185 (GRCm38) noncoding transcript Het
Cnot1 A G 8: 95,741,921 (GRCm38) S1432P probably benign Het
Cnot8 T A 11: 58,114,051 (GRCm38) I192N probably damaging Het
Col4a1 G T 8: 11,207,409 (GRCm38) probably null Het
Cuta A G 17: 26,939,327 (GRCm38) L11P possibly damaging Het
Cyp2c39 G A 19: 39,568,019 (GRCm38) R433H probably damaging Het
Cyp4a12b T A 4: 115,414,543 (GRCm38) Y150* probably null Het
Dcaf15 G A 8: 84,099,105 (GRCm38) A291V probably benign Het
Dcstamp A T 15: 39,754,735 (GRCm38) H180L possibly damaging Het
Egfr A G 11: 16,889,964 (GRCm38) I659M probably benign Het
Fzd8 A G 18: 9,214,598 (GRCm38) E560G possibly damaging Het
Gm5111 A T 6: 48,589,592 (GRCm38) probably benign Het
Gm7945 T C 14: 41,382,823 (GRCm38) T214A unknown Het
Gpi1 T C 7: 34,220,745 (GRCm38) T168A possibly damaging Het
Gys2 T C 6: 142,459,408 (GRCm38) I218V probably benign Het
Gzmf T A 14: 56,206,492 (GRCm38) I74L probably benign Het
Hacl1 G A 14: 31,635,771 (GRCm38) A70V probably damaging Het
Herc2 T A 7: 56,197,072 (GRCm38) L3590* probably null Het
Idh2 GGTCCCAG GG 7: 80,098,329 (GRCm38) probably benign Het
Igfals G T 17: 24,881,365 (GRCm38) V477F possibly damaging Het
Igkv8-28 A T 6: 70,143,890 (GRCm38) V23E probably benign Het
Isg20l2 T A 3: 87,932,088 (GRCm38) V202E probably damaging Het
Jakmip2 A G 18: 43,575,534 (GRCm38) I288T probably benign Het
Kansl3 A G 1: 36,365,605 (GRCm38) V88A probably benign Het
Kcna3 A G 3: 107,037,950 (GRCm38) T510A possibly damaging Het
Map2k5 G T 9: 63,338,098 (GRCm38) L140I probably benign Het
Map3k19 A G 1: 127,822,599 (GRCm38) I1005T possibly damaging Het
Mmp25 G A 17: 23,630,794 (GRCm38) A541V possibly damaging Het
Ms4a14 T A 19: 11,304,020 (GRCm38) E391D probably benign Het
Mtrf1l A G 10: 5,815,550 (GRCm38) probably null Het
Myom1 A G 17: 71,126,137 (GRCm38) N1591S probably damaging Het
Nos1 G A 5: 117,936,570 (GRCm38) V1060M probably benign Het
Nsun5 C T 5: 135,371,531 (GRCm38) T142M probably damaging Het
Odc1 A G 12: 17,550,654 (GRCm38) E430G probably benign Het
Or8g36 C A 9: 39,510,809 (GRCm38) V304F probably benign Het
P2ry12 T C 3: 59,217,907 (GRCm38) I116V probably null Het
Patl1 T A 19: 11,920,331 (GRCm38) V94E probably damaging Het
Plin3 A T 17: 56,281,488 (GRCm38) Y255* probably null Het
Pou6f1 T C 15: 100,579,946 (GRCm38) T439A probably damaging Het
Prdm13 T C 4: 21,678,366 (GRCm38) K708R probably damaging Het
Prr14l A G 5: 32,829,404 (GRCm38) S916P possibly damaging Het
Rab34 T A 11: 78,191,202 (GRCm38) probably null Het
Rps7 A G 12: 28,635,594 (GRCm38) S21P possibly damaging Het
Sesn3 A G 9: 14,321,163 (GRCm38) Y244C probably benign Het
Slc15a2 A G 16: 36,761,611 (GRCm38) F284L probably benign Het
Slc25a44 C T 3: 88,420,911 (GRCm38) G72D probably damaging Het
Slco6d1 A G 1: 98,499,863 (GRCm38) T640A probably benign Het
Sspo A T 6: 48,462,191 (GRCm38) E1591V possibly damaging Het
Tbata C A 10: 61,175,865 (GRCm38) T60K possibly damaging Het
Tbc1d2 T A 4: 46,637,692 (GRCm38) T185S possibly damaging Het
Tlcd4 T A 3: 121,235,059 (GRCm38) I60F possibly damaging Het
Tmem87a A G 2: 120,404,021 (GRCm38) S14P possibly damaging Het
Tnnt2 C A 1: 135,850,554 (GRCm38) probably null Het
Trex1 A G 9: 109,058,641 (GRCm38) V94A probably benign Het
Ubtfl1 A C 9: 18,409,296 (GRCm38) D40A possibly damaging Het
Zc3hav1 A T 6: 38,333,000 (GRCm38) Y296N probably benign Het
Zfp521 T A 18: 13,844,627 (GRCm38) N910Y probably damaging Het
Zfp53 A G 17: 21,508,713 (GRCm38) E336G possibly damaging Het
Other mutations in Scn9a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00514:Scn9a APN 2 66,563,601 (GRCm38) missense probably damaging 1.00
IGL00570:Scn9a APN 2 66,484,142 (GRCm38) missense probably damaging 1.00
IGL00809:Scn9a APN 2 66,483,935 (GRCm38) missense probably damaging 1.00
IGL00977:Scn9a APN 2 66,484,301 (GRCm38) missense probably damaging 0.99
IGL01120:Scn9a APN 2 66,526,972 (GRCm38) missense probably benign 0.00
IGL01134:Scn9a APN 2 66,504,968 (GRCm38) missense probably damaging 1.00
IGL01300:Scn9a APN 2 66,488,053 (GRCm38) nonsense probably null
IGL01452:Scn9a APN 2 66,527,072 (GRCm38) missense probably damaging 1.00
IGL01531:Scn9a APN 2 66,537,378 (GRCm38) missense probably benign 0.11
IGL01572:Scn9a APN 2 66,493,886 (GRCm38) missense probably benign 0.00
IGL01645:Scn9a APN 2 66,487,642 (GRCm38) missense possibly damaging 0.62
IGL01823:Scn9a APN 2 66,484,042 (GRCm38) missense probably damaging 1.00
IGL01965:Scn9a APN 2 66,484,433 (GRCm38) missense probably damaging 1.00
IGL02127:Scn9a APN 2 66,494,826 (GRCm38) missense probably damaging 1.00
IGL02127:Scn9a APN 2 66,547,135 (GRCm38) missense probably damaging 1.00
IGL02166:Scn9a APN 2 66,493,103 (GRCm38) missense possibly damaging 0.95
IGL02183:Scn9a APN 2 66,484,611 (GRCm38) splice site probably benign
IGL02640:Scn9a APN 2 66,536,096 (GRCm38) critical splice donor site probably null
IGL02685:Scn9a APN 2 66,537,293 (GRCm38) missense probably damaging 1.00
IGL02798:Scn9a APN 2 66,540,559 (GRCm38) missense possibly damaging 0.52
IGL02832:Scn9a APN 2 66,568,029 (GRCm38) missense probably damaging 1.00
IGL03008:Scn9a APN 2 66,562,511 (GRCm38) missense probably damaging 1.00
IGL03270:Scn9a APN 2 66,484,014 (GRCm38) missense probably damaging 1.00
IGL03408:Scn9a APN 2 66,526,747 (GRCm38) missense probably benign 0.00
BB007:Scn9a UTSW 2 66,504,849 (GRCm38) missense probably damaging 0.99
BB017:Scn9a UTSW 2 66,504,849 (GRCm38) missense probably damaging 0.99
R0039:Scn9a UTSW 2 66,562,444 (GRCm38) missense probably damaging 0.98
R0173:Scn9a UTSW 2 66,533,093 (GRCm38) missense probably damaging 1.00
R0323:Scn9a UTSW 2 66,568,131 (GRCm38) missense probably damaging 1.00
R0344:Scn9a UTSW 2 66,505,010 (GRCm38) missense probably damaging 0.99
R0421:Scn9a UTSW 2 66,543,277 (GRCm38) missense probably benign
R0465:Scn9a UTSW 2 66,526,996 (GRCm38) missense probably damaging 1.00
R0514:Scn9a UTSW 2 66,483,678 (GRCm38) missense probably damaging 1.00
R0599:Scn9a UTSW 2 66,526,799 (GRCm38) missense probably damaging 0.96
R0627:Scn9a UTSW 2 66,537,377 (GRCm38) missense probably benign 0.00
R0644:Scn9a UTSW 2 66,533,061 (GRCm38) critical splice donor site probably null
R0653:Scn9a UTSW 2 66,533,377 (GRCm38) missense probably damaging 1.00
R0685:Scn9a UTSW 2 66,483,499 (GRCm38) missense probably benign 0.02
R0718:Scn9a UTSW 2 66,547,112 (GRCm38) missense probably damaging 1.00
R0827:Scn9a UTSW 2 66,536,124 (GRCm38) nonsense probably null
R0890:Scn9a UTSW 2 66,483,735 (GRCm38) missense probably damaging 1.00
R1139:Scn9a UTSW 2 66,504,997 (GRCm38) missense probably benign 0.02
R1385:Scn9a UTSW 2 66,563,542 (GRCm38) missense probably damaging 1.00
R1398:Scn9a UTSW 2 66,484,586 (GRCm38) missense probably benign 0.11
R1496:Scn9a UTSW 2 66,526,888 (GRCm38) missense probably benign
R1511:Scn9a UTSW 2 66,526,813 (GRCm38) missense probably benign 0.01
R1517:Scn9a UTSW 2 66,505,027 (GRCm38) splice site probably benign
R1564:Scn9a UTSW 2 66,484,304 (GRCm38) missense probably damaging 1.00
R1634:Scn9a UTSW 2 66,488,017 (GRCm38) missense probably damaging 1.00
R1662:Scn9a UTSW 2 66,483,459 (GRCm38) missense probably benign 0.00
R1695:Scn9a UTSW 2 66,504,876 (GRCm38) nonsense probably null
R1709:Scn9a UTSW 2 66,483,506 (GRCm38) missense probably damaging 1.00
R1741:Scn9a UTSW 2 66,487,594 (GRCm38) missense probably damaging 0.99
R1755:Scn9a UTSW 2 66,501,716 (GRCm38) missense probably benign 0.38
R1914:Scn9a UTSW 2 66,566,250 (GRCm38) missense probably damaging 1.00
R1962:Scn9a UTSW 2 66,484,311 (GRCm38) missense probably damaging 1.00
R1970:Scn9a UTSW 2 66,515,380 (GRCm38) missense probably damaging 0.97
R2017:Scn9a UTSW 2 66,515,321 (GRCm38) missense probably damaging 0.99
R2092:Scn9a UTSW 2 66,533,376 (GRCm38) missense probably damaging 0.99
R2105:Scn9a UTSW 2 66,568,183 (GRCm38) missense probably benign 0.25
R2114:Scn9a UTSW 2 66,484,052 (GRCm38) missense probably damaging 1.00
R2115:Scn9a UTSW 2 66,484,052 (GRCm38) missense probably damaging 1.00
R2128:Scn9a UTSW 2 66,526,654 (GRCm38) missense probably damaging 1.00
R2157:Scn9a UTSW 2 66,536,325 (GRCm38) missense probably damaging 1.00
R2162:Scn9a UTSW 2 66,534,229 (GRCm38) missense probably damaging 0.98
R2350:Scn9a UTSW 2 66,504,968 (GRCm38) missense probably damaging 1.00
R3694:Scn9a UTSW 2 66,562,405 (GRCm38) missense probably benign
R3771:Scn9a UTSW 2 66,483,648 (GRCm38) missense probably benign 0.26
R3772:Scn9a UTSW 2 66,483,648 (GRCm38) missense probably benign 0.26
R3773:Scn9a UTSW 2 66,483,648 (GRCm38) missense probably benign 0.26
R3922:Scn9a UTSW 2 66,526,873 (GRCm38) missense possibly damaging 0.88
R3926:Scn9a UTSW 2 66,526,873 (GRCm38) missense possibly damaging 0.88
R4258:Scn9a UTSW 2 66,565,054 (GRCm38) intron probably benign
R4385:Scn9a UTSW 2 66,484,556 (GRCm38) missense probably damaging 1.00
R4415:Scn9a UTSW 2 66,526,693 (GRCm38) missense probably damaging 1.00
R4570:Scn9a UTSW 2 66,483,558 (GRCm38) missense possibly damaging 0.85
R4682:Scn9a UTSW 2 66,547,018 (GRCm38) missense probably benign
R4783:Scn9a UTSW 2 66,540,623 (GRCm38) missense probably benign 0.01
R4822:Scn9a UTSW 2 66,483,749 (GRCm38) missense possibly damaging 0.55
R4829:Scn9a UTSW 2 66,551,713 (GRCm38) missense probably benign
R4908:Scn9a UTSW 2 66,526,743 (GRCm38) missense probably benign 0.03
R4983:Scn9a UTSW 2 66,566,270 (GRCm38) missense probably benign 0.02
R5047:Scn9a UTSW 2 66,562,480 (GRCm38) missense probably damaging 1.00
R5100:Scn9a UTSW 2 66,534,119 (GRCm38) missense probably damaging 1.00
R5140:Scn9a UTSW 2 66,565,167 (GRCm38) missense possibly damaging 0.81
R5398:Scn9a UTSW 2 66,488,043 (GRCm38) missense probably damaging 1.00
R5557:Scn9a UTSW 2 66,547,103 (GRCm38) missense probably damaging 0.99
R5582:Scn9a UTSW 2 66,565,029 (GRCm38) intron probably benign
R6108:Scn9a UTSW 2 66,484,049 (GRCm38) missense probably damaging 1.00
R6115:Scn9a UTSW 2 66,563,629 (GRCm38) missense possibly damaging 0.70
R6143:Scn9a UTSW 2 66,487,524 (GRCm38) missense probably benign 0.00
R6335:Scn9a UTSW 2 66,568,264 (GRCm38) start codon destroyed possibly damaging 0.91
R6429:Scn9a UTSW 2 66,526,963 (GRCm38) missense possibly damaging 0.95
R6632:Scn9a UTSW 2 66,483,502 (GRCm38) missense probably benign 0.23
R6681:Scn9a UTSW 2 66,563,342 (GRCm38) missense possibly damaging 0.90
R6830:Scn9a UTSW 2 66,568,029 (GRCm38) missense probably damaging 1.00
R7102:Scn9a UTSW 2 66,549,015 (GRCm38) missense probably damaging 1.00
R7186:Scn9a UTSW 2 66,534,223 (GRCm38) missense probably damaging 1.00
R7243:Scn9a UTSW 2 66,540,530 (GRCm38) missense probably damaging 1.00
R7311:Scn9a UTSW 2 66,484,404 (GRCm38) missense possibly damaging 0.54
R7328:Scn9a UTSW 2 66,484,587 (GRCm38) missense probably benign
R7386:Scn9a UTSW 2 66,540,550 (GRCm38) missense probably damaging 1.00
R7438:Scn9a UTSW 2 66,547,187 (GRCm38) missense possibly damaging 0.81
R7483:Scn9a UTSW 2 66,533,348 (GRCm38) missense probably damaging 0.99
R7485:Scn9a UTSW 2 66,534,217 (GRCm38) missense probably damaging 1.00
R7526:Scn9a UTSW 2 66,483,646 (GRCm38) missense probably benign
R7617:Scn9a UTSW 2 66,540,549 (GRCm38) missense possibly damaging 0.55
R7642:Scn9a UTSW 2 66,536,236 (GRCm38) missense probably benign 0.02
R7653:Scn9a UTSW 2 66,527,080 (GRCm38) missense probably damaging 1.00
R7747:Scn9a UTSW 2 66,484,298 (GRCm38) missense probably damaging 1.00
R7823:Scn9a UTSW 2 66,483,791 (GRCm38) missense probably damaging 1.00
R7864:Scn9a UTSW 2 66,484,560 (GRCm38) missense possibly damaging 0.73
R7890:Scn9a UTSW 2 66,543,112 (GRCm38) missense probably benign 0.00
R7930:Scn9a UTSW 2 66,504,849 (GRCm38) missense probably damaging 0.99
R7975:Scn9a UTSW 2 66,484,253 (GRCm38) missense probably damaging 1.00
R8057:Scn9a UTSW 2 66,515,430 (GRCm38) missense probably benign 0.06
R8145:Scn9a UTSW 2 66,487,410 (GRCm38) missense probably damaging 1.00
R8163:Scn9a UTSW 2 66,484,401 (GRCm38) missense probably damaging 1.00
R8165:Scn9a UTSW 2 66,540,530 (GRCm38) missense probably damaging 1.00
R8342:Scn9a UTSW 2 66,536,282 (GRCm38) missense probably benign
R8345:Scn9a UTSW 2 66,494,622 (GRCm38) missense probably damaging 0.96
R8464:Scn9a UTSW 2 66,566,281 (GRCm38) missense probably damaging 0.99
R8467:Scn9a UTSW 2 66,501,671 (GRCm38) missense probably damaging 1.00
R8698:Scn9a UTSW 2 66,536,284 (GRCm38) missense probably benign 0.00
R8810:Scn9a UTSW 2 66,501,666 (GRCm38) missense probably damaging 1.00
R8822:Scn9a UTSW 2 66,540,635 (GRCm38) missense probably damaging 0.99
R8829:Scn9a UTSW 2 66,483,617 (GRCm38) missense probably benign
R9009:Scn9a UTSW 2 66,508,583 (GRCm38) missense probably damaging 1.00
R9038:Scn9a UTSW 2 66,494,803 (GRCm38) missense probably damaging 1.00
R9126:Scn9a UTSW 2 66,484,400 (GRCm38) missense probably damaging 1.00
R9205:Scn9a UTSW 2 66,533,313 (GRCm38) missense probably damaging 1.00
R9300:Scn9a UTSW 2 66,504,892 (GRCm38) missense probably benign 0.39
R9373:Scn9a UTSW 2 66,483,917 (GRCm38) missense probably benign 0.00
R9404:Scn9a UTSW 2 66,526,696 (GRCm38) missense probably benign 0.02
R9443:Scn9a UTSW 2 66,565,209 (GRCm38) missense probably damaging 1.00
R9590:Scn9a UTSW 2 66,483,984 (GRCm38) missense probably benign 0.05
R9612:Scn9a UTSW 2 66,533,364 (GRCm38) missense probably damaging 1.00
R9617:Scn9a UTSW 2 66,562,465 (GRCm38) missense probably damaging 1.00
R9717:Scn9a UTSW 2 66,526,658 (GRCm38) missense probably benign
X0003:Scn9a UTSW 2 66,508,647 (GRCm38) missense probably benign 0.02
X0062:Scn9a UTSW 2 66,568,077 (GRCm38) missense probably damaging 1.00
Z1176:Scn9a UTSW 2 66,540,592 (GRCm38) missense probably benign 0.00
Z1177:Scn9a UTSW 2 66,494,685 (GRCm38) missense possibly damaging 0.68
Predicted Primers PCR Primer
(F):5'- TAGTCGCAGATACATCCTCTTG -3'
(R):5'- GAACTTCAGCGTTGCCACAG -3'

Sequencing Primer
(F):5'- GCAGATACATCCTCTTGTTTTCG -3'
(R):5'- CTTCAGCGTTGCCACAGAAGAAAG -3'
Posted On 2018-03-15