NM_199242.2:c.610A>G

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HGVS Expressions

  • NG_007266.1:g.8757A>G
  • NM_199242.2:c.610A>G
  • NP_954712.1:p.Met204Val
  • NC_000017.11:g.75840961T>C

Associated Genes

UNC13 Homolog D
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Clinvar Clinical Significance

Likely Benign, Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

144722609

Clinvar

574872

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
249100.6Lebanon1Uncertain SignificanceUmar et al, 2020
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Contributors

  • Sayeeda Hana: 03.02.2021

Edit History

  • Sayeeda Hana: 14.02.2021
  • Sayeeda Hana: 03.02.2021
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.