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Gene | TSC1 |
Variant | R424fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TSC1 R424fs results in a change in the amino acid sequence of the Tsc1 protein beginning at aa 424 of 1164, likely resulting in premature truncation of the functional protein (UniProt.org). R424fs has not been characterized however, due to the effects of other truncation mutations downstream of R424 (PMID: 11875047, PMID: 20547222), is predicted to lead to a loss of Tsc1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TSC1 mutant TSC1 inact mut TSC1 R424fs |
Transcript | NM_000368.5 |
gDNA | chr9:g.(132907364_132907365) |
cDNA | c.(1270_1269) |
Protein | p.R424fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006717271.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.(132907364_132907365) | c.(1270_1269) | p.R424fs | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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