Gene Variant Detail

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Gene TP53
Variant S90fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 S90fs results in a change in the amino acid sequence of the Tp53 protein beginning at 90 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). S90fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of S90 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon4 TP53 S90fs

TP53 mutant TP53 inact mut TP53 S90fs

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Transcript NM_000546.6
gDNA chr17:g.(7676101_7676102)
cDNA c.(268_267)
Protein p.S90fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000546.5 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.7676106delG c.267delC p.S90fs*33 RefSeq GRCh38/hg38
NM_001126113 chr17:g.7676106delG c.267delC p.S90fs*33 RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.7676106delG c.267delC p.S90fs*33 RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_000546 chr17:g.7676106delG c.267delC p.S90fs*33 RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7676101_7676102) c.(268_267) p.S90fs RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References