PP_004JVG0.1

Display Name: South_Africa/PP_004JVG0.1/2025-09-25
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
2025-09-25
Sample received date
2025-09-25
Country
South Africa
Admin level 1
Western Cape
Admin level 2
Cape Town
City
Cape Town
Site
Worcester

Data use terms

Data use terms
OPEN

Data use terms history

ChangedUserData use terms
2026-02-13 05:06stepfandvOPEN
Data use terms URL

Lineage

Lineage
A2.2.2

Authors

Author affiliations
Centre for Epidemic Response and Innovation (CERI), BMRI building, Tygerberg, Stellenbosch University, Francie Van Zjil Drive, Cape Town, South Africa; PathCare Molecular Lab, PathCare Reference Laboratory, Neels Bothma Street, 7460, Cape Town, South Africa

INSDC

BioProject accession
BioSample accession

Sampling

Sample type
Swab

Host

Host name - scientific
Homo sapiens
Host name - common
Human
Host age bin
0 - 1
Host gender
M
Host origin country
South Africa

Sequencing

Purpose of sequencing
Surveillance
Sequencing date
2025-01-01
Sequencing instrument
Illumina MiSeq
Sequencing assay type
WGS
Sequenced by - organization
Centre for Epidemic Response and Innovation (CERI), BMRI building, Tygerberg, Stellenbosch University, Francie Van Zjil Drive, Cape Town, South Africa
Sequenced by - contact name
Stepfan de Villiers
Sequenced by - contact email
stepfan@sun.ac.za
Consensus sequence software name
Genome Detective
Consensus sequence software version
Pan-viral (2.21.4)
Depth of coverage
35
Breadth of coverage
96

Alignment and QC metrics

Length
13177
Completeness
96.26%
# of SNPs
1016
# of inserted bases
112
# of deleted bases
57
# of ambiguous bases
0
# of unknown bases
271
# of frame shifts
1
# of stop codons
1
Frame shifts
G:228-237(nt:6927-6957)
Stop Codons
G:220

Submission details

Submission ID
hMPV/A/SouthAfrica/PATH-CERI-C070371/2025
Submitting group
Date submitted
2026-02-13 05:06:55 UTC
Date released
2026-02-13 05:07:02 UTC
Earliest release date
2026-02-13

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • A51G
  • T70C
  • A117G
  • G126A
  • T129C
  • T138A
  • G180A
  • G195A
  • A204G
  • G208A
  • C213T
  • T249C
  • T259C
  • A264G
  • T265A
  • G276A
  • T285C
  • G288A
    • Deletions
    4692-4719, 6224, 6907-6926, 7024-7031
    Insertions
    ins_6705:TCAAGCACAGTCTCCAAAACACAACTCCCATCACGGGCAACAACGAAGGCGGCCTCCAGAGCCACCACCCTCAGAATAAAAACAAAATCGACAGCCCACAGAAGAAACATC, ins_7133:T

    Amino acid mutations

    Mutations called relative to the NC_039199.1 reference

    Substitutions

    F

  • F:R82K
  • F:P98L
  • F:A185D
  • F:F258I
  • F:G294E
  • F:S466N
  • F:T504S
  • F:V510I
  • F:K518R
  • F:N539S

    • G

  • G:T10A
  • G:K29R
  • G:V34I
  • G:T40A
  • G:L41M
  • G:I43V
  • G:K54T
  • G:M55I
  • G:N58T
  • G:T59A
  • G:E61K
  • G:S69P
  • G:M71T
  • G:S74N
  • G:R75K
  • G:P78S
  • G:V80I
  • G:T82I

    • L

  • L:I75V
  • L:T95K
  • L:S132G
  • L:K162R
  • L:V182I
  • L:I245M
  • L:W390L
  • L:K496T
  • L:T505A
  • L:K530R
  • L:S534N
  • L:K538R
  • L:D546E
  • L:G760D
  • L:S769R
  • L:S895T
  • L:R951K
  • L:A954T

    • M

  • M:I23V
  • M:N66S
  • M:K87R

    • M2-1

  • M2-1:V130I
  • M2-1:E170D

    • M2-2

  • M2-2:H35Q
  • M2-2:D37E

    • N

  • N:A57T
  • N:S76T
  • N:V92A
  • N:I103V
  • N:H220Y

    • P

  • P:G31S
  • P:N44S
  • P:A59T
  • P:T78I
  • P:K79R
  • P:I82A
  • P:A85T
  • P:V88I
  • P:V214I
  • P:K227R
  • P:S239N
  • P:S242T
  • P:T280L
  • P:S284N

    • SH

  • SH:S9N
  • SH:V33A
  • SH:L44F
  • SH:S68P
  • SH:K71E
  • SH:S74P
  • SH:N87D
  • SH:S96R
  • SH:N103D
  • SH:A105V
  • SH:S108K
  • SH:N115S
  • SH:S132P
  • SH:T135S
  • SH:T137I
  • SH:N139S
  • SH:K142R
  • SH:P151S
    • Deletions
    G:221-227
    Insertions
    ins_G:153:SSTVSKTQLPSRATTKAASRATTLRIKTKSTAHRRNI

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