Display Name: GS_001DY6X.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
PQ585624.1.seg5/PQ585625.1.seg7/PQ585626.1.seg8
Date submitted
2024-11-21 13:24:26 UTC
Date released
2024-11-21 13:56:34 UTC

Data use terms

Data use terms
OPEN

Authors

Author affiliations
University of Washington, Laboratory Medicine and Pathology

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 seg7

Completeness seg7
100.00%
Length seg7
1027
Total ambiguous nucs seg7
0
Total deleted nucs seg7
0
Total frame shifts seg7
0
Total inserted nucs seg7
0
Total SNPs seg7
57
Total unknown nucs seg7
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
UW56071

Host

Host name scientific
Homo sapiens
Host taxon id

INSDC

INSDC accession seg5
INSDC accession seg7
INSDC accession seg8
NCBI release date
2024-11-13

Nucleotide mutations

Substitutions

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
  • seg7

  • seg7:A25G
  • seg7:A76G
  • seg7:C142T
  • seg7:A196G
  • seg7:A205G
  • seg7:G268A
  • seg7:C274T
  • seg7:T275C
  • seg7:T292C
  • seg7:T301C
  • seg7:T307C
  • seg7:T316C
  • seg7:G319A
  • seg7:A322G
  • seg7:A327G
  • seg7:G331A
  • seg7:C332T
  • seg7:A337G
  • 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

    M2

  • M2:E14G
  • M2:K18N
  • M2:V28I
  • M2:I51V
  • 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
  • Deletions
    None
    Insertions
    None