NM_003001.5:c.31C>T

HGVS Expressions

  • NG_012767.1:g.14249C>T
  • NM_003001.5:c.31C>T
  • NP_002992.1:p.Arg11Cys
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Genomic Location

chr1:161323624

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

577853

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.52LebanonUncertain SignificanceBreast CancerJalkh et al, 2017 Patient 'B48' from family 38 in the publ...
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