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Display Name: South_Africa/PPD_000NXFW.1/2025-09-30
J. Maritz, D. Goedhals, J. Pekeur, T. Maponga, M. Claassen, T. Stander, G. van Zyl, W. Preiser, L. M. Hofstra, L. Chabuka, K. W. Liedeman, S. De Villiers, V. Wentzel, L. Singh, T. Ramakutoane, H. Tegally, E. Wilkinson & T. de Oliveira

Sample details

Collection date
2025-09-30
Country
South Africa
Admin level 1
Eastern Cape; Kariega (Uitenhage); Kariega (Uitenhage)
Isolate name
hMPV/B/SouthAfrica/PATH-CERI-C071077/2025

Data use terms

Data use terms
OPEN

Lineage

Lineage
B1

Authors

Author affiliations
S, Cape Town, Western Cape

INSDC

INSDC accession
BioProject accession
BioSample accession
NCBI release date
2026-02-17
NCBI update date
2026-02-18

Host

Host taxon ID
Host name - scientific
Homo sapiens

Alignment and QC metrics

Length
13004
Completeness
92.86%
# of SNPs
2182
# of inserted bases
26
# of deleted bases
80
# of ambiguous bases
0
# of unknown bases
661
# of frame shifts
2
# of stop codons
0
Frame shifts
G:149-160(nt:6689-6725),G:216-237(nt:6890-6957)

Submission details

Submission ID
OZ412853.1
Date submitted
2026-02-23 16:49:20 UTC
Date released
2026-02-23 18:28:29 UTC
Earliest release date
2026-02-17

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • G34A
  • G36A
  • G63A
  • T70C
  • A72G
  • G81A
  • G105A
  • G126A
  • T129C
  • C150T
  • G177T
  • G195T
  • T198C
  • G199A
  • T207C
  • G208A
  • A228T
  • A231G
  • Deletions
    3009, 4684-4722, 6196, 6210-6215, 6688, 6889, 6981-6983, 6990-7009, 7041-7044, 7144-7147
    Insertions
    ins_6696:GAA, ins_6725:GGGGAAGAGGAAAAGA, ins_6945:AT, ins_6965:CC, ins_7060:AG, ins_7073:G

    Amino acid mutations

    Mutations called relative to the NC_039199.1 reference

    Substitutions

    F

  • F:V6M
  • F:F9I
  • F:A61T
  • F:R82K
  • F:V122I
  • F:T135N
  • F:N139G
  • F:K143Q
  • F:D167E
  • F:R175S
  • F:K179R
  • F:N233Y
  • F:F258I
  • F:V286I
  • F:G294E
  • F:K296N
  • F:Q312K
  • F:K348R
  • G

  • G:K4R
  • G:T10A
  • G:L14F
  • G:R17K
  • G:V18I
  • G:V22I
  • G:A23R
  • G:R24S
  • G:K26R
  • G:F28Y
  • G:K29R
  • G:N30Y
  • G:S32T
  • G:V34I
  • G:I38L
  • G:I43M
  • G:Y48F
  • G:I50V
  • L

  • L:L4F
  • L:N5C
  • L:I50V
  • L:I55V
  • L:K61R
  • L:N65M
  • L:S66T
  • L:I75V
  • L:V89M
  • L:T109S
  • L:I115M
  • L:S141V
  • L:K162R
  • L:V182I
  • L:I189V
  • L:S228N
  • L:E231K
  • L:I245M
  • M

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

  • M2-1:A5T
  • M2-1:E20D
  • M2-1:I37L
  • M2-1:R52K
  • M2-1:S88G
  • M2-1:V108T
  • M2-1:V130I
  • M2-1:R149K
  • M2-1:K160R
  • M2-1:A169T
  • M2-1:E170D
  • M2-1:S173P
  • M2-2

  • M2-2:E18K
  • M2-2:V22K
  • M2-2:V28S
  • M2-2:D37E
  • M2-2:A41T
  • M2-2:N55S
  • M2-2:A68T
  • N

  • N:A54T
  • N:A57T
  • N:I67M
  • N:S71C
  • N:R96K
  • N:I103G
  • N:N106S
  • N:D110E
  • N:A136V
  • N:M201V
  • N:D212E
  • N:H220Y
  • N:M258L
  • N:A280S
  • N:K356R
  • N:V385M
  • N:D387G
  • N:S389N
  • N:N391D
  • P

  • P:L19I
  • P:R28K
  • P:P30S
  • P:S35T
  • P:I39V
  • P:V46I
  • P:R57K
  • P:K60R
  • P:P61S
  • P:T62S
  • P:I63T
  • P:P64L
  • P:S65L
  • P:T72A
  • P:K74N
  • P:G75S
  • P:A77T
  • P:T80I
  • SH

  • SH:I2K
  • Deletions
    G:148, G:215
    Insertions
    ins_G:143:ITQT, ins_G:189:TT

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