NM_000903.2:c.559C>T

HGVS Expressions

  • NG_011504.1:g.20389C>T
  • NM_000903.2:c.559C>T
  • NP_000894.1:p.Pro187Ser
  • NC_000016.10:g.69711242G>A
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Clinvar Clinical Significance

Drug Response, Pathogenic, Risk factor

Variant Type

Substitution

dbSNP

1800566

Clinvar

16809

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
109800.G.1LebanonYassine et al. 2012 54 cases with bladder cancer and 106 con...
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