Display Name: South_Africa/PP_004JVJV.1/2025-09-29
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
2025-09-29
Sample received date
2025-09-30
Country
South Africa
Admin level 1
Northern Cape
Admin level 2
Upington
City
Upington
Site
Upington

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

BioProject accession
BioSample accession

Sampling

Sample type
Swab

Host

Host name - scientific
Homo sapiens
Host name - common
Human
Host age bin
4 - 5
Host gender
M
Host origin country
South Africa

Sequencing

Purpose of sequencing
Surveillance
Sequencing instrument
Illumina NextSeq
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
915
Breadth of coverage
99

Alignment and QC metrics

Length
13261
Completeness
99.98%
# of SNPs
2468
# of inserted bases
23
# of deleted bases
109
# of ambiguous bases
0
# of unknown bases
0
# of frame shifts
2
# of stop codons
2
Frame shifts
G:149-159(nt:6691-6723),G:207-223(nt:6865-6915)
Stop Codons
SH:177,G:227

Submission details

Submission ID
hMPV/B/SouthAfrica/PATH-CERI-C070880/2025
Date submitted
2026-02-13 05:15:39 UTC
Date released
2026-02-13 05:15:49 UTC
Earliest release date
2026-02-13

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • G11A
  • C16A
  • A20C
  • T26C
  • G34A
  • G36A
  • G63A
  • T70C
  • A72G
  • C78T
  • G81A
  • G99A
  • G105A
  • G126A
  • A132C
  • A162G
  • A168G
  • G177T
  • Deletions
    24, 2934, 3006, 4684-4722, 6025-6027, 6112-6114, 6166, 6196, 6210-6215, 6864, 6916, 6917, 6977-6984, 7009-7015, 7034-7037, 7144-7147, 13188, 13204-13208, 13285-13304, 13313
    Insertions
    ins_2981:C, ins_5813:AGA, ins_6690:A, ins_6723:AAGGAAAAGAA, ins_6767:ACT, ins_7065:TT, ins_7080:T, ins_13230: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: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:I50V
  • L:K61R
  • L:V64I
  • L:N65M
  • L:S66T
  • L:I75V
  • L:V79I
  • L:V89T
  • L:T109S
  • L:N113S
  • L:S123T
  • L:D127N
  • L:S132N
  • L:S141V
  • 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
  • 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:E380G
  • 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:I2K
  • 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
  • Deletions
    G:201, G:224
    Insertions
    ins_G:141:RQT, ins_G:187:AT, ins_SH:108:R

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