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Display Name: GS_001EAX0.1/2024-10-18
Roychoudhury, P.; Xie, H.; Ellis, S. E.; Dang, T.; Murray, T.; Hiatt, B.; Black, A.; Greninger, A.

Submission details

Submission ID
PQ585622.1.seg1/PQ585621.1.seg5/PQ585623.1.seg8
Date submitted
2024-12-11 16:47:38 UTC
Date released
2024-12-11 17:24:58 UTC

Data use terms

Data use terms
OPEN

Authors

Author affiliations
University of Washington, Laboratory Medicine and Pathology

Alignment states and QC metrics seg1

Completeness seg1
98.93%
Length seg1
2316
Total ambiguous nucs seg1
0
Total deleted nucs seg1
0
Total frame shifts seg1
0
Total inserted nucs seg1
0
Total SNPs seg1
366
Total unknown nucs seg1
0

Alignment states and QC metrics seg5

Completeness seg5
99.49%
Length seg5
1557
Total ambiguous nucs seg5
0
Total deleted nucs seg5
0
Total frame shifts seg5
0
Total inserted nucs seg5
0
Total SNPs seg5
173
Total unknown nucs seg5
0

Alignment states and QC metrics seg8

Completeness seg8
96.88%
Length seg8
838
Total ambiguous nucs seg8
0
Total deleted nucs seg8
5
Total frame shifts seg8
0
Total inserted nucs seg8
5
Total SNPs seg8
237
Total unknown nucs seg8
0

Sample details

Collection country
USA
Collection subdivision level 1
Washington
Collection date
2024-10-18
Isolate name
UW63494

Host

Host name scientific
Homo sapiens
Host taxon id

INSDC

INSDC accession seg1
INSDC accession seg5
INSDC accession seg8
NCBI release date
2024-11-13

Nucleotide mutations

Substitutions

seg1

  • seg1:T17A
  • seg1:A33G
  • seg1:A48G
  • seg1:G63A
  • seg1:C69T
  • seg1:A90C
  • seg1:G102T
  • seg1:T105C
  • seg1:T108C
  • seg1:A126G
  • seg1:A141G
  • seg1:G147A
  • seg1:T159A
  • seg1:A165G
  • seg1:T192C
  • seg1:A211C
  • seg1:G222A
  • seg1:T228C
  • seg5

  • seg5:A40C
  • seg5:G57A
  • seg5:T72C
  • seg5:G81A
  • seg5:A96G
  • seg5:T111C
  • seg5:G117A
  • seg5:T147C
  • seg5:T153C
  • seg5:G159A
  • seg5:T162C
  • seg5:T165C
  • seg5:A183G
  • seg5:C195T
  • seg5:C198T
  • seg5:T201C
  • seg5:A207G
  • seg5:T216C
  • seg8

  • seg8:G29T
  • seg8:A30G
  • seg8:A32G
  • seg8:A33T
  • seg8:C35A
  • seg8:T36A
  • seg8:C37G
  • seg8:G38C
  • seg8:T50C
  • seg8:T53C
  • seg8:A55T
  • seg8:A59T
  • seg8:C65T
  • seg8:A66G
  • seg8:A68C
  • seg8:A69C
  • seg8:A71C
  • seg8:G74A
  • Deletions
    seg8:90, seg8:93, seg8:226-228
    Insertions
    ins_seg8:221:G, ins_seg8:231:AT, ins_seg8:79:TG

    Amino acid mutations

    Substitutions

    NP

  • NP:V105M
  • NP:M136L
  • NP:A353V
  • NP:S450N
  • NP:S451A
  • NS2

  • NS2:I6V
  • NS2:T7S
  • NS2:Q14M
  • NS2:E22G
  • NS2:V26E
  • NS2:E36K
  • NS2:R37S
  • NS2:I40L
  • NS2:S48A
  • NS2:M49V
  • NS2:N60S
  • NS2:A63E
  • NS2:T64K
  • NS2:N67G
  • NS2:E68Q
  • NS2:A81E
  • NS2:C83V
  • NS2:N85H
  • PB2

  • PB2:D153G
  • PB2:N334S
  • PB2:K340R
  • PB2:K355R
  • PB2:A471T
  • PB2:V478I
  • PB2:Q508R
  • PB2:S579P
  • PB2:S590G
  • PB2:P628Q
  • PB2:R699K
  • PB2:M727G
  • PB2:F741S
  • Deletions
    None
    Insertions
    None