NM_153704.5:c.2952A>G

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  2. NM_153704.5:c.2952A>G

HGVS Expressions

  • NG_009190.1:g.66573A>G
  • NM_153704.5:c.2952A>G
  • NP_714915.3:p.Ala984=
  • NC_000008.11:g.93816416A>G

Associated Genes

Transmembrane Protein 67
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Clinvar Clinical Significance

Benign, Likely Benign, Uncertain Significance

CTGA Clinical Significance

Benign, Likely Benign

Variant Type

Substitution

dbSNP

115967793

Clinvar

262749

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
607361.11Morocco2Benign, Likely BenignKhaddour et al. 2007 Individual was healthy
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Contributors

  • Sami Bizzari: 25.06.2020

Edit History

  • Pratibha Nair: 21.11.2022
  • Sami Bizzari: 25.06.2020
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.