NM_001350748.2:c.4503A>C

HGVS Expressions

  • NG_053176.1:g.354259A>C
  • NM_001350748.2:c.4503A>C
  • NP_001337677.1:p.Ile1501=
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Genomic Location

chr13:101067948

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

1289556

Clinvar

262263

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
615419.13Morocco1BenignBramswig et al. 2018
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