This is a demonstration environment. It may contain non-accurate test data and should not be used for real-world applications. Data will be deleted regularly.

Display Name: Pakistan/LOC_000P79W.1/2024-07-16
Umair, M.; Hakim, R.; Jamal, Z.; Salman, M.

Submission details

Submission ID
PQ523729.1.L/PQ523726.1.M/PQ523722.1.S
Date submitted
2024-12-20 08:39:34 UTC
Date released
2024-12-20 08:43:49 UTC

Data use terms

Data use terms
OPEN
Data use terms URL

Authors

Author affiliations
National Institute of Health, Department of Virology

Alignment states and QC metrics L

Completeness L
97.56%
Frame shifts L
RdRp:792-795(nt:2450-2461)
Length L
12104
Total ambiguous nucs L
0
Total deleted nucs L
12
Total frame shifts L
1
Total inserted nucs L
38
Total SNPs L
1563
Total unknown nucs L
266

Alignment states and QC metrics M

Completeness M
95.75%
Length M
5287
Total ambiguous nucs M
0
Total deleted nucs M
0
Total frame shifts M
0
Total inserted nucs M
0
Total SNPs M
622
Total unknown nucs M
149

Alignment states and QC metrics S

Completeness S
91.93%
Length S
1590
Total ambiguous nucs S
0
Total deleted nucs S
11
Total frame shifts S
0
Total inserted nucs S
4
Total SNPs S
196
Total unknown nucs S
60

Sample details

Earliest release date
2024-11-12
Collection subdivision level 1
Punjab
Collection country
Pakistan
Collection date
2024-07-16
Collection date (lower bound)
2024-07-16
Collection date (upper bound)
2024-07-16
Isolate name
CCHF/NIHPAK-41/2024

Host

Host name scientific
Homo sapiens
Host taxon id

INSDC

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

Nucleotide mutations

Substitutions

L

  • 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
  • L:T139C
  • M

  • M:C82T
  • M:C85T
  • M:T86C
  • M:A107G
  • M:A117G
  • M:C119T
  • M:C120T
  • M:T122C
  • M:C126T
  • M:A128G
  • M:T137C
  • M:G143A
  • M:A146G
  • M:G147A
  • M:G149A
  • M:T159C
  • M:A169G
  • M:A170G
  • S

  • S:A50G
  • S:G54A
  • S:G67A
  • S:T79C
  • S:A81G
  • S:G99A
  • S:A109G
  • S:C115T
  • S:A118G
  • S:C166T
  • S:G169A
  • S:T172C
  • S:C178A
  • S:T182C
  • S:G190A
  • S:C208T
  • S:C217T
  • S:G229A
  • Deletions
    L:2449, L:11920-11924, L:11981, L:11982, L:12054, L:12058, L:12059, L:12073, S:1541-1543, S:1611-1618
    Insertions
    ins_S:1532:CCA, ins_S:1584:C, ins_L:12096:GTTC, ins_L:11977:CA, ins_L:12101:CGT, ins_L:11917:CATTATC, ins_L:12085:ACTATCCTACTATTCCA, ins_L:58:T, ins_L:2461:G, ins_L:12080:TAA

    Amino acid mutations

    Substitutions

    GPC

  • GPC:I9V
  • GPC:L10F
  • GPC:E19K
  • GPC:S23P
  • GPC:E26G
  • GPC:R28E
  • GPC:K31N
  • GPC:D33H
  • GPC:T34A
  • GPC:G39D
  • GPC:N41S
  • GPC:P42Q
  • GPC:S44P
  • GPC:S53P
  • GPC:I54A
  • GPC:L56P
  • GPC:S59P
  • GPC:P80S
  • NP

  • NP:N9S
  • NP:R15K
  • NP:V83A
  • NP:D186N
  • NP:H195R
  • NP:D199E
  • NP:I246V
  • NP:R270K
  • NP:S301G
  • NP:A307V
  • NP:E322D
  • NP:Q405L
  • NP:V436I
  • RdRp

  • RdRp:S6N
  • RdRp:A14D
  • RdRp:S19T
  • RdRp:Y60N
  • RdRp:R63H
  • RdRp:S67V
  • RdRp:V82I
  • RdRp:I114V
  • RdRp:T163A
  • RdRp:A168T
  • RdRp:M172V
  • RdRp:R174K
  • RdRp:S205P
  • RdRp:N206Y
  • RdRp:I223V
  • RdRp:K275R
  • RdRp:I279V
  • RdRp:R302K
  • Deletions
    None
    Insertions
    None