TP53 R273H
genetic variant
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TP53 R273H
Summary
TP53 R273H is a missense mutation[1].
Key Facts
- TP53 R273H's instance of is recorded as missense mutation[2].
- TP53 R273H's genomic start is recorded as 7577120[3].
- TP53 R273H's genomic end is recorded as 7577120[4].
- TP53 R273H's chromosome is recorded as human chromosome 17[5].
- TP53 R273H's CIViC variant ID is recorded as 122[6].
- TP53 R273H's HGVS nomenclature is recorded as NM_000546.5:c.818G>A[7].
- TP53 R273H's HGVS nomenclature is recorded as NP_000537.3:p.Arg273His[8].
- TP53 R273H's HGVS nomenclature is recorded as NC_000017.10:g.7577120C>T[9].
- TP53 R273H's HGVS nomenclature is recorded as ENST00000269305.4:c.818G>A[10].
- TP53 R273H's negative therapeutic predictor for is recorded as methotrexate[11].
- TP53 R273H's negative therapeutic predictor for is recorded as doxorubicin[12].
- TP53 R273H's negative prognostic predictor for is recorded as breast cancer[13].
- TP53 R273H's biological variant of is recorded as TP53[14].
- TP53 R273H's dbSNP Reference SNP number is recorded as rs28934576[15].