NM_001350748.2:c.3657T>C

HGVS Expressions

  • NG_053176.1:g.338483T>C
  • NM_001350748.2:c.3657T>C
  • NP_001337677.1:p.Leu1219=
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Genomic Location

chr13:101083724

Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

686141

Clinvar

262260

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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