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: Greece/LOC_000PBBN.1/1975
D'Addiego, J.; Shah, S.; Elaldi, N.; Allen, D.; Hewson, R.

Submission details

Submission ID
PP735375.1.L/PP735373.1.S
Date submitted
2025-03-11 18:18:53 UTC
Date released
2025-03-11 18:23:22 UTC

Data use terms

Data use terms
OPEN
Data use terms URL

Authors

Author affiliations
UK Health Security Agency, Research & Evaluation

Alignment and QC metrics L

Completeness L
41.65%
Frame shifts L
RdRp:768-771(nt:2376-2387),RdRp:778-781(nt:2406-2419),RdRp:786-789(nt:2432-2442)
Length L
5062
Total ambiguous nucs L
19
Total deleted nucs L
23
Total frame shifts L
3
Total inserted nucs L
23
Total SNPs L
1095
Total unknown nucs L
0

Alignment and QC metrics S

Completeness S
90.25%
Length S
1498
Total ambiguous nucs S
8
Total deleted nucs S
41
Total frame shifts S
0
Total inserted nucs S
1
Total SNPs S
260
Total unknown nucs S
21

Sample details

Earliest release date
2024-10-26
Collection country
Greece
Collection date
1975
Collection date (lower bound)
1975-01-01
Collection date (upper bound)
1975-12-31
Isolate name
CCHFV_AP92

Host

Host name scientific
Homo sapiens
Host taxon id

INSDC

INSDC accession L
INSDC accession S
NCBI release date
2024-10-26

Nucleotide mutations

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

Substitutions

L

  • L:T253C
  • L:T254A
  • L:A262G
  • L:G264A
  • L:C266A
  • L:C271T
  • L:G272A
  • L:G274A
  • L:T275A
  • L:G277A
  • L:G285A
  • L:G289A
  • L:T292C
  • L:C295T
  • L:C296T
  • L:A297T
  • L:A298G
  • L:G301T
  • S

  • S:T79C
  • S:A81G
  • S:T88C
  • S:G91T
  • S:A92C
  • S:A109G
  • S:A118G
  • S:A130G
  • S:C154A
  • S:C160T
  • S:C166T
  • S:G169A
  • S:G171A
  • S:T175G
  • S:C178G
  • S:T181C
  • S:G190A
  • S:T198A
  • Deletions
    L:2375, L:2388, L:2389, L:2401-2405, L:2420-2423, L:2443-2447, L:2453-2455, L:3172-3174, S:1544-1569, S:1579-1586, S:1597-1603
    Insertions
    ins_S:1572:G, ins_L:2391:CAC, ins_L:3178:GCA, ins_L:2413:CTACTT, ins_L:2431:GAGCCCGAAAG

    Amino acid mutations

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

    Substitutions

    NP

  • NP:N9S
  • NP:E12D
  • NP:M13L
  • NP:S39N
  • NP:F48Y
  • NP:F73Y
  • NP:A100T
  • NP:G101S
  • NP:V117I
  • NP:T124S
  • NP:G125S
  • NP:V141I
  • NP:A146T
  • NP:V163L
  • NP:M164V
  • NP:S165P
  • NP:L179I
  • NP:V198I
  • RdRp

  • RdRp:Y60N
  • RdRp:R63H
  • RdRp:L64I
  • RdRp:E66K
  • RdRp:S67T
  • RdRp:R70Q
  • RdRp:Q74L
  • RdRp:E75D
  • RdRp:R80K
  • RdRp:K91Q
  • RdRp:L94S
  • RdRp:A122T
  • RdRp:S124N
  • RdRp:D135E
  • RdRp:I157V
  • RdRp:F161L
  • RdRp:T165A
  • RdRp:E167G
  • Deletions
    RdRp:767, RdRp:776, RdRp:777, RdRp:782, RdRp:783, RdRp:790, RdRp:791
    Insertions
    None

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