Display Name: Pakistan/PP_000SNLL.2/2024-07-12
M. Umair, R. Hakim, Z. Jamal & M. Salman

Sample details

Collection date
2024-07-12
Country
Pakistan
Admin level 1
Punjab
Isolate name
CCHF/NIHPAK-37/2024

Data use terms

Data use terms
OPEN

Authors

Author affiliations
National Institute of Health, Department of Virology

INSDC

INSDC accession L
INSDC accession M
INSDC accession S
NCBI release date
2024-11-12

Host

Host taxon ID
Host name - scientific
Homo sapiens

Alignment and QC metrics L

Length L
12140
Completeness L
99.88%
# of SNPs L
1631
# of inserted bases L
47
# of deleted bases L
0
# of ambiguous bases L
0
# of unknown bases L
0
# of frame shifts L
0
# of stop codons L
0

Alignment and QC metrics M

Length M
5345
Completeness M
99.27%
# of SNPs M
1562
# of inserted bases M
48
# of deleted bases M
30
# of ambiguous bases M
0
# of unknown bases M
0
# of frame shifts M
0
# of stop codons M
0

Alignment and QC metrics S

Length S
1655
Completeness S
98.92%
# of SNPs S
213
# of inserted bases S
1
# of deleted bases S
0
# of ambiguous bases S
0
# of unknown bases S
0
# of frame shifts S
0
# of stop codons S
0

Submission details

Submission ID
PQ523728.1.L/PQ523725.1.M/PQ523721.1.S
Date submitted
2025-09-24 17:35:10 UTC
Date released
2025-09-24 18:29:12 UTC
Earliest release date
2024-11-12

Lineage

Segment S Lineage
IV.2

Nucleotide mutations

Mutations called relative to the NC_005301.3, NC_005300.2 & NC_005302.1 references

Substitutions

L

  • L:G23T
  • L:A35G
  • L:G43T
  • L:T49C
  • L:C63G
  • L:C64T
  • L:T65C
  • L:T66C
  • L:T68C
  • L:G69A
  • L:G71C
  • L:C85T
  • L:G88A
  • L:G93A
  • L:A109G
  • L:C117A
  • L:A124G
  • L:T131A
  • M

  • M:G50C
  • M:A51G
  • M:A52T
  • M:G56T
  • M:T58A
  • M:T59A
  • M:T65A
  • M:C66T
  • M:T67C
  • M:A69G
  • M:A70T
  • M:T71G
  • M:T72A
  • M:G76A
  • M:A80G
  • M:C81T
  • M:C82T
  • M:T83G
  • S

  • S:T48C
  • S:G54A
  • S:A61G
  • S:C64T
  • S:G67A
  • S:G99A
  • S:A118G
  • S:C142T
  • S:T157C
  • S:C166T
  • S:G169A
  • S:C178A
  • S:T182C
  • S:C217T
  • S:G229A
  • S:C235T
  • S:T250A
  • S:G262A
  • Deletions
    M:795-809, M:5172-5186
    Insertions
    ins_L:58:T, ins_L:11917:CA, ins_L:12053:CTAC, ins_L:12086:CTACTATTCCAC, ins_L:12108:TTTATTATTTCTGGGGTGTGGGGGGAAC, ins_M:236:CCGTCAACAGACACTGCC, ins_M:313:CACTGATCCCTC, ins_M:457:CAACTCGCCTACACT, ins_M:5202:CA, ins_M:5248:C, ins_S:1581:C

    Amino acid mutations

    Mutations called relative to the NC_005301.3, NC_005300.2 & NC_005302.1 references

    Substitutions

    GPC

  • GPC:M1S
  • GPC:H2M
  • GPC:I3L
  • GPC:S4L
  • GPC:L5T
  • GPC:M6N
  • GPC:Y7F
  • GPC:A8I
  • GPC:I9L
  • GPC:L10C
  • GPC:C11Q
  • GPC:Q13F
  • GPC:L14W
  • GPC:C15S
  • GPC:L17S
  • GPC:E19V
  • GPC:H21S
  • GPC:S23G
  • NP

  • NP:R15K
  • NP:D116E
  • NP:T124A
  • NP:G125N
  • NP:N150H
  • NP:H195R
  • NP:D199E
  • NP:I246V
  • NP:R270K
  • NP:S275N
  • NP:S301G
  • NP:V436I
  • RdRp

  • RdRp:S6N
  • RdRp:A14D
  • RdRp:S19T
  • RdRp:Y60N
  • RdRp:R63H
  • RdRp:S67V
  • RdRp:R80K
  • RdRp:V82I
  • RdRp:I114V
  • RdRp:T163A
  • RdRp:A168T
  • RdRp:M172V
  • RdRp:R174K
  • RdRp:A202V
  • RdRp:S205P
  • RdRp:N206Y
  • RdRp:I223V
  • RdRp:K275R
  • Deletions
    GPC:176-210
    Insertions
    ins_GPC:77:ESSTDPSVTNKDTSP, ins_GPC:229:NTTGQTYPTTLETSPKTQMIQGQQTTTPVT

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