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Display Name: USA/PPD_000B27W.1/2024-12-12
E. B. Nunley, S. Goya, C. Varela, D. Y. Kim & A. L. Greninger

Sample details

Collection date
2024-12-12
Country
USA
Admin level 1
WA
Isolate name
hMPV/181717/USA/2024

Data use terms

Data use terms
OPEN

Lineage

Lineage
B2

Authors

Author affiliations
University of Washington, University of Washington

INSDC

INSDC accession
BioProject accession
BioSample accession
NCBI release date
2025-02-05
NCBI update date
2025-02-05
Raw reads accession

Host

Host taxon ID
Host name - scientific
Homo sapiens

Alignment and QC metrics

Length
13065
# of SNPs
2311
# of inserted bases
15
# of deleted bases
101
# of ambiguous bases
1
# of unknown bases
558
# of frame shifts
2
Frame shifts
G:149-154(nt:6691-6707),G:207-224(nt:6865-6918)
Completeness
94.32%

Submission details

Submission ID
PV052155.1
Date submitted
2025-09-17 10:45:53 UTC
Date released
2025-09-17 12:00:38 UTC
Earliest release date
2025-02-05

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • G195T
  • T198C
  • G199A
  • G208A
  • C209A
  • C213T
  • A231G
  • A237G
  • T248A
  • A250T
  • A255G
  • T259C
  • G270A
  • G276A
  • G279A
  • C286T
  • G288A
  • G291A
  • Deletions
    2963, 3006, 4684-4722, 6126-6130, 6196, 6210-6215, 6864, 6919, 6920, 6977-6984, 7031-7039, 7123, 7133-7135, 13188, 13204, 13205, 13283-13289, 13300-13313
    Insertions
    ins_2981:C, ins_5813:AGA, ins_6690:A, ins_6707:GGAGCAAC, ins_7080:T, ins_13229:G

    Amino acid mutations

    Mutations called relative to the NC_039199.1 reference

    Substitutions

    F

  • F:V6M
  • F:F9I
  • F:L36Q
  • F:A61T
  • F:R82K
  • F:V122I
  • F:T135N
  • F:N139G
  • F:K143T
  • F:D167E
  • F:R175S
  • F:T223N
  • F:N233Y
  • F:F258I
  • F:D280N
  • F:V286I
  • F:G294E
  • F:K296D
  • G

  • G:K4R
  • G:T10A
  • G:L14F
  • G:R17K
  • G:V18M
  • G:V22I
  • G:A23R
  • G:R24S
  • G:F28Y
  • G:K29R
  • G:S32T
  • G:V34I
  • G:I38L
  • G:Y48F
  • G:N52D
  • G:K54A
  • G:M55K
  • G:Q56L
  • L

  • L:L4F
  • L:N5C
  • L:V89T
  • L:T109S
  • L:N113S
  • L:S123T
  • L:D127N
  • L:S132N
  • L:S141V
  • L:K162R
  • L:V182I
  • L:I189V
  • L:V198I
  • L:S228N
  • L:E231K
  • L:L238F
  • L:I245M
  • L:C262S
  • M

  • M:I23V
  • M:E103D
  • M:E111D
  • M:T156I
  • M:K237R
  • M:T241S
  • M2-1

  • M2-1:K4R
  • M2-1:I37L
  • M2-1:R52K
  • M2-1:S88G
  • M2-1:V108I
  • M2-1:S121N
  • M2-1:V130I
  • M2-1:R149K
  • M2-1:K160R
  • M2-1:A169T
  • M2-1:E170D
  • M2-2

  • M2-2:E18K
  • M2-2:V22K
  • M2-2:V28A
  • M2-2:D37E
  • M2-2:A41T
  • M2-2:N55S
  • N

  • N:A54T
  • N:A57N
  • N:I70N
  • N:S71C
  • N:R96K
  • N:I103G
  • N:N106S
  • N:D110E
  • N:A136V
  • N:A173R
  • N:M201V
  • N:D212E
  • N:H220Y
  • N:K356R
  • N:V385M
  • N:S389N
  • N:N391D
  • P

  • P:L19I
  • P:R28K
  • P:K29R
  • P:P30S
  • P:S35T
  • P:I39V
  • P:N44T
  • P:V46I
  • P:R57K
  • P:K60R
  • P:P61S
  • P:T62S
  • P:I63T
  • P:S65L
  • P:T72A
  • P:K74S
  • P:G75S
  • P:E81T
  • SH

  • SH:I2K
  • SH:T17N
  • SH:H18Q
  • SH:L19I
  • SH:D25N
  • SH:V30L
  • SH:V33A
  • SH:L44F
  • SH:I50V
  • SH:I61A
  • SH:S64L
  • SH:T66N
  • SH:S73T
  • SH:S74K
  • SH:S75P
  • SH:V80T
  • SH:T82I
  • SH:K83R
  • Deletions
    G:225
    Insertions
    ins_G:137:R, ins_G:187:A, ins_SH:108:R

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