USA/GS_00H0L4P.1/2026-01-16
W. E. Gruner, V. S. Hogan, D. M. Muehleman, A. C. Fries, J. F. Hanson, D. L. Kramer, L. S. Demarcus, P. M. Wasik, E. A. Macias, J. M. Garcia, C. A. Smetana & T. R. Hartless

United States Air Force School of Aerospace Medicine Public Health Submission Group, 711th Human Performance Wing

Submission details

Submission ID
PX989229.1.seg4/PX989385.1.seg5/PX989334.1.seg6/PX989285.1.seg7/PX989435.1.seg8
Date submitted
2026-02-14 04:24:10 UTC
Date released
2026-02-14 04:25:49 UTC

Clade

Clade HA
D.3.1
Clade NA
D.1

Sample details

Collection country
USA
Collection subdivision level 1
Rhode Island
Collection date
2026-01-16
Isolate name
A/Rhode Island/USAFSAM-16798/2026

Host

INSDC

INSDC accession seg4
INSDC accession seg5
INSDC accession seg6
INSDC accession seg7
INSDC accession seg8
NCBI release date
2026-02-11

INSDC seg4

Subtype seg4
H1

INSDC seg6

Subtype seg6
N1

Alignment and QC

Length seg4
1701 (97.1%)
Total SNPs seg4
107
Length seg5
1497 (100%)
Total SNPs seg5
63
Length seg6
1410 (98.4%)
Total SNPs seg6
26
Length seg7
982 (100%)
Total SNPs seg7
31
Length seg8
838 (97.1%)
Total SNPs seg8
33

Nucleotide mutations

Mutations called relative to the NC_026438.1, NC_026435.1, NC_026437.1, CY121680.1, NC_026436.1, MW626056.1, NC_026431.1 & NC_026432.1 references

Substitutions

seg4

  • seg4:A38G
  • seg4:C42A
  • seg4:A47G
  • seg4:G57A
  • seg4:A119G
  • seg4:T161C
  • seg4:C164T
  • seg4:G188A
  • seg4:A231C
  • seg4:C281A
  • seg4:C293G
  • seg4:C318T
  • seg4:G322A
  • seg4:G360A
  • seg4:G409A
  • seg4:G416A
  • seg4:C443T
  • seg4:A456G
  • seg5

  • seg5:A33G
  • seg5:G42T
  • seg5:C87T
  • seg5:A97G
  • seg5:C141A
  • seg5:A168G
  • seg5:C171T
  • seg5:T177C
  • seg5:C180T
  • seg5:C249A
  • seg5:A288C
  • seg5:G296A
  • seg5:G298A
  • seg5:C303T
  • seg5:G309A
  • seg5:T314C
  • seg5:G315A
  • seg5:R341A
  • seg6

  • seg6:C20T
  • seg6:A179G
  • seg6:C285T
  • seg6:C301T
  • seg6:C452A
  • seg6:C571T
  • seg6:G607A
  • seg6:A785G
  • seg6:T799C
  • seg6:A818G
  • seg6:G867A
  • seg6:C874T
  • seg6:C893T
  • seg6:G914T
  • seg6:G950A
  • seg6:A999G
  • seg6:A1049G
  • seg6:C1187T
  • seg7

  • seg7:G48A
  • seg7:G75A
  • seg7:T123C
  • seg7:C124A
  • seg7:G238A
  • seg7:G258A
  • seg7:A293G
  • seg7:G306A
  • seg7:G339A
  • seg7:G342A
  • seg7:C375A
  • seg7:T432C
  • seg7:G441T
  • seg7:G492A
  • seg7:C507A
  • seg7:A574G
  • seg7:C622A
  • seg7:G660A
  • seg8

  • seg8:C6A
  • seg8:C42T
  • seg8:C54T
  • seg8:G60A
  • seg8:T99C
  • seg8:C108A
  • seg8:T159C
  • seg8:G163A
  • seg8:C192T
  • seg8:C204T
  • seg8:A238G
  • seg8:G250A
  • seg8:C264T
  • seg8:C268A
  • seg8:C315T
  • seg8:A367G
  • seg8:A375T
  • seg8:A391G
  • Deletions
    None
    Insertions
    None

    Amino acid mutations

    Mutations called relative to the NC_026438.1, NC_026435.1, NC_026437.1, CY121680.1, NC_026436.1, MW626056.1, NC_026431.1 & NC_026432.1 references

    Substitutions

    HA1

  • HA1:K54Q
  • HA1:S74R
  • HA1:P83S
  • HA1:S84N
  • HA1:D97N
  • HA1:R113K
  • HA1:N129D
  • HA1:K130N
  • HA1:P137S
  • HA1:A139D
  • HA1:K142R
  • HA1:N156K
  • HA1:L161I
  • HA1:S162N
  • HA1:K163Q
  • HA1:S164T
  • HA1:S183P
  • HA1:S185I
  • HA2

  • HA2:E29D
  • HA2:I45V
  • HA2:E47K
  • HA2:I91V
  • HA2:S124H
  • HA2:I133T
  • HA2:E172K
  • HA2:E179D
  • HA2:V193A
  • M1

  • M1:L42I
  • M1:V80I
  • M1:K98R
  • M1:M192V
  • M1:Q208K
  • M1:K230R
  • M2

  • M2:R18K
  • M2:D21G
  • M2:S23N
  • M2:I28T
  • M2:G89S
  • NA

  • NA:P93S
  • NA:A98V
  • NA:T188I
  • NA:S200N
  • NA:I264T
  • NA:E287K
  • NA:T289I
  • NA:M314I
  • NA:K331E
  • NA:I396M
  • NA:V453M
  • NA:K469N
  • NEP

  • NEP:D2E
  • NEP:N29S
  • NEP:T48A
  • NEP:M83I
  • NP

  • NP:E14D
  • NP:I33V
  • NP:R99K
  • NP:V100I
  • NP:M105T
  • NP:X114E
  • NP:L122Q
  • NP:I136L
  • NP:V217I
  • NP:V425I
  • NP:S498N
  • NS1

  • NS1:D2E
  • NS1:E55K
  • NS1:T80A
  • NS1:V84I
  • NS1:L90I
  • NS1:I123V
  • NS1:E125D
  • NS1:K131E
  • NS1:A155T
  • NS1:N205S
  • SigPep

  • SigPep:L8M
  • SigPep:A13T
  • Deletions
    None
    Insertions
    None