This is a demo instance. You can upload any data you like, including test data to try things out. You can find test data to upload in the example data repository. This instance should not be used for analysis.
Display Name: USA/PPD_0070ZJR.1/2025-03-08
A. S. Lauring & L. K. Papalambros

Sample details

Collection date
2025-03-08
Country
USA
Isolate name
hMPV-G25Y82Q7

Data use terms

Data use terms
OPEN

Lineage

Lineage
B2

Authors

Author affiliations
University Of Michigan, Internal Medicine - Infectious Disease

INSDC

INSDC accession
BioProject accession
NCBI release date
2025-10-11
NCBI update date
2025-10-11

Host

Host taxon ID
Host name - scientific
Homo sapiens

Alignment and QC metrics

Length
13168
Completeness
97.14%
# of SNPs
2357
# of inserted bases
13
# of deleted bases
94
# of ambiguous bases
0
# of unknown bases
281
# of frame shifts
1
# of stop codons
0
Frame shifts
G:207-224(nt:6865-6918)

Submission details

Submission ID
PX444143.1
Date submitted
2025-10-12 02:57:21 UTC
Date released
2025-10-12 02:59:53 UTC
Earliest release date
2025-10-11

Nucleotide mutations

Mutations called relative to the NC_039199.1 reference

Substitutions

  • A21C
  • T24A
  • T26C
  • G34A
  • G36A
  • G63A
  • T70C
  • A72G
  • C78T
  • G105A
  • G126A
  • T129C
  • A132C
  • C150T
  • A162G
  • A168G
  • G177T
  • A189G
  • Deletions
    1593-1598, 2930, 3006, 4684-4722, 6046-6048, 6109, 6110, 6196, 6210-6215, 6864, 6919, 6920, 6977-6984, 6997, 6998, 7012-7016, 7035-7037, 7144-7147, 13188, 13204, 13205, 13224-13230
    Insertions
    ins_2975:C, ins_5813:GGA, ins_6759:GCAACC, ins_7065:TT, ins_7080:T

    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:K142R
  • 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:R17K
  • G:V22I
  • G:A23R
  • G:R24S
  • G:F28Y
  • G:K29R
  • G:S32T
  • G:V34I
  • G:I38L
  • G:T40A
  • G:I43M
  • G:Y48F
  • G:N52D
  • G:K54A
  • G:Q56L
  • G:T59M
  • L

  • L:L4F
  • L:N5C
  • L:N42K
  • L:I50V
  • L:K61R
  • L:N65M
  • L:S66T
  • L:I75V
  • L:V89T
  • L:T109S
  • L:N113S
  • L:S123T
  • L:D127N
  • L:S132N
  • L:S141V
  • L:K162R
  • L:V182I
  • L:I189V
  • 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: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: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:L19V
  • 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:D25N
  • SH:V30L
  • SH:V33A
  • SH:L44F
  • SH:I50V
  • SH:I61A
  • SH:S64L
  • SH:T66N
  • SH:S73T
  • SH:S74K
  • SH:S75L
  • SH:T82I
  • SH:K83R
  • SH:T84P
  • SH:T85I
  • SH:L86P
  • Deletions
    G:163-166, G:189, G:201, G:225, P:119, P:120
    Insertions
    ins_G:141:RQTTQTT, ins_SH:108:R

    Report an issue with this sequence or metadata

    Create GitHub issue