NM_001171.5:c.3803G>A

HGVS Expressions

  • NG_007558.2:g.70730G>A
  • NM_001171.5:c.3803G>A
  • NP_001162.4:p.Arg1268Gln
  • NC_000016.10:g.16157742C>T
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Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

2238472

Clinvar

6570

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
114480.G.5LebanonDrug ResponseBreast CancerAwada et al. 2013 Case-control study observed 12 SNPs to b...
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