Display Name: South_Africa/PP_004JWHW.1/2025-10-01
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
2025-10-01
Sample received date
2025-10-01
Country
South Africa
Admin level 1
Western Cape
Admin level 2
Cape Town
City
Cape Town
Site
Tokai

Data use terms

Data use terms
OPEN

Lineage

Lineage
B2

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

INSDC accession
BioProject accession
BioSample accession
GCA accession

Sampling

Sample type
Sputum

Host

Host name - scientific
Homo sapiens
Host name - common
Human
Host age
2
Host gender
F
Host origin country
South Africa

Sequencing

Purpose of sequencing
Surveillance
Sequencing instrument
Illumina NextSeq
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
Reference genome accession
NC_039199.1
Consensus sequence software name
Genome Detective
Consensus sequence software version
Pan-viral (2.21.4)
Depth of coverage
71
Breadth of coverage
89

Alignment and QC metrics

Length
13151
Completeness
88.66%
# of SNPs
1942
# of inserted bases
3
# of deleted bases
40
# of ambiguous bases
0
# of unknown bases
1352
# of frame shifts
0
# of stop codons
0

Submission details

Submission ID
hMPV/B/SouthAfrica/PATH-CERI-C070897/2025
Date submitted
2026-02-13 05:29:58 UTC
Date released
2026-02-13 05:30:04 UTC
Earliest release date
2026-02-13

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • G11A
  • A20C
  • T24A
  • A25C
  • T26G
  • G29A
  • A30C
  • C31A
  • G34T
  • T35A
  • G36A
  • G63A
  • T70C
  • A72G
  • C78T
  • G81A
  • G99A
  • G105A
  • Deletions
    3006, 4684-4722
    Insertions
    ins_5813:AGA

    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:K143T
  • F:D167E
  • F:R175S
  • F:T223N
  • F:N233Y
  • F:F258I
  • F:D280N
  • F:V286I
  • F:G294E
  • F:K296D
  • F:Q312K
  • G

  • G:K4R
  • G:T10A
  • G:L14F
  • G:R17K
  • G:V18M
  • G:V22I
  • G:A23R
  • G:R24N
  • G:F28Y
  • G:K29R
  • G:S32T
  • G:V34I
  • G:I38L
  • G:T40A
  • G:I43M
  • G:Y48F
  • G:N52D
  • G:K54A
  • L

  • L:L4F
  • L:N5C
  • L:N42K
  • L:A46S
  • 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
  • L:R282K
  • M

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

  • M2-1:I37L
  • M2-1:R52K
  • M2-1:S88G
  • M2-1:V108I
  • 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
  • M2-2:C56Y
  • N

  • N:A54T
  • N:A57T
  • N:S71C
  • N:R96K
  • N:I103G
  • N:N106S
  • N:D110E
  • N:A136V
  • 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:K60R
  • P:P61S
  • P:T62S
  • P:I63T
  • P:S65L
  • P:T72A
  • P:K74S
  • P:G75S
  • P:E81T
  • P:I82E
  • SH

  • SH:T17N
  • SH:H18Q
  • SH:D25N
  • SH:V30L
  • SH:V33A
  • SH:L44F
  • SH:I50V
  • SH:I61A
  • SH:S64L
  • SH:T66N
  • SH:S73T
  • SH:S74K
  • SH:S75L
  • SH:V80T
  • SH:T82I
  • SH:T84P
  • SH:T85I
  • SH:L86P
  • Deletions
    None
    Insertions
    ins_SH:108:R

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