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PPD_006U1PR.1

Display Name: France/PPD_006U1PR.1/2024
M. Gasparine

Sample details

Collection date
2024
Country
France
Isolate name
590

Data use terms

Data use terms
OPEN

Data use terms history

ChangedUserData use terms
2025-09-19 09:57insdc_ingest_userOPEN
Data use terms URL

Authors

Author affiliations
University of Corsica, Unite des Virus Emergents

INSDC

INSDC accession L
NCBI release date
2025-08-10

Host

Host taxon ID
Host name - scientific
Ixodoidea

Alignment and QC metrics L

Length L
10913
Completeness L
73.11%
# of SNPs L
527
# of inserted bases L
130
# of deleted bases L
86
# of ambiguous bases L
0
# of unknown bases L
2017
# of frame shifts L
32
# of stop codons L
0
Frame shifts L
RdRp:563-634(nt:1763-1976),RdRp:642-690(nt:2000-2146),RdRp:699-708(nt:2169-2200),RdRp:717-1033(nt:2225-3175),RdRp:1048-1636(nt:3216-4983),RdRp:1645-1652(nt:5009-5031),RdRp:1666-1683(nt:5070-5125),RdRp:1695-1723(nt:5159-5245),RdRp:1746-1754(nt:5311-5336),RdRp:1761-1780(nt:5357-5416),RdRp:1789-1837(nt:5440-5587),RdRp:1854-2040(nt:5636-6196),RdRp:2047-2058(nt:6213-6249),...

Submission details

Submission ID
PV976882.1.L
Submitting group
Date submitted
2025-09-19 09:57:06 UTC
Date released
2025-09-19 09:59:00 UTC
Earliest release date
2025-08-10

Nucleotide mutations

Mutations called relative to the NC_005301.3, NC_005300.2 & NC_005302.1 references

Substitutions

L

  • L:A1375G
  • L:G1408A
  • L:T1420C
  • L:C1435T
  • L:C1495T
  • L:T1590C
  • L:C1591T
  • L:A1641G
  • L:T1710C
  • L:T1732C
  • L:T1802G
  • L:T1877C
  • L:A1879G
  • L:C1927T
  • L:G1990A
  • L:C1999T
  • L:G2000T
  • L:C2006T
    • Deletions
    L:1977, L:2069, L:2168, L:2186, L:2201, L:2224, L:2234, L:3176, L:3212-3215, L:4396, L:4822, L:4823, L:5086, L:5099, L:5100, L:5126, L:5127, L:5158, L:5198-5200, L:5237, L:5246, L:5309, L:5310, L:5337, L:5390-5392, L:5417, L:5480, L:5498, L:5499, L:5588, L:5635, L:6047, L:6197, L:6212, L:6506, L:6586, L:6620, L:6670, L:6682, L:6725, L:6959-6962, L:6987, L:6988, L:7037, L:7038, L:7076,...
    Insertions
    ins_L:1762:G, ins_L:1999:T, ins_L:2032:A, ins_L:2116:A, ins_L:2146:TGGA, ins_L:4983:C, ins_L:5008:CT, ins_L:5031:C, ins_L:5069:AT, ins_L:5257:TTG, ins_L:5356:A, ins_L:5439:T, ins_L:5458:AGCT, ins_L:5549:TTACC, ins_L:6249:CACT, ins_L:6304:TGCAG, ins_L:6320:G, ins_L:6345:GCCTAAG, ins_L:6364:T, ins_L:6391:AC, ins_L:6482:CAC, ins_L:6526:C, ins_L:6553:T, ins_L:6714:ATG, ins_L:6771:C,...

    Amino acid mutations

    Mutations called relative to the NC_005301.3, NC_005300.2 & NC_005302.1 references

    Substitutions

    RdRp

  • RdRp:I505T
  • RdRp:K522R
  • RdRp:L545P
  • RdRp:I1035K
  • RdRp:K1037I
  • RdRp:V1039D
  • RdRp:D1040N
  • RdRp:E1041R
  • RdRp:T1042S
  • RdRp:A1043I
  • RdRp:N1044A
  • RdRp:E1643G
  • RdRp:P1660T
  • RdRp:L1665H
  • RdRp:T1692I
  • RdRp:P1725E
  • RdRp:F1726L
  • RdRp:Y1755T
    • Deletions
    RdRp:698, RdRp:709, RdRp:1034, RdRp:1046, RdRp:1047, RdRp:1637, RdRp:1684, RdRp:1724, RdRp:1727, RdRp:1745, RdRp:1781, RdRp:1838, RdRp:2041, RdRp:2046, RdRp:2144, RdRp:2182, RdRp:2217, RdRp:2295-2297, RdRp:2361, RdRp:2364, RdRp:2365, RdRp:2474, RdRp:2478, RdRp:2531, RdRp:2681, RdRp:2735, RdRp:2891, RdRp:2892, RdRp:2919, RdRp:2934, RdRp:3372, RdRp:3453, RdRp:3900
    Insertions
    ins_RdRp:691:GL, ins_RdRp:1643:T, ins_RdRp:2087:HYKAMP, ins_RdRp:2774:M, ins_RdRp:2838:XXP, ins_RdRp:3539:M, ins_RdRp:3583:XX

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