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Gene | TSC2 |
Variant | R1329P |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TSC2 R1329P does not lie within any known functional domains of the Tsc2 protein (UniProt.org). R1329P has been identified in sequencing studies (J Thorac Oncol. Vol 13, Issue 10, S512-S513), but has not been biochemically characterized and therefore, its effect on Tsc2 protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 R1329P |
Transcript | NM_000548.5 |
gDNA | chr16:g.2083797G>C |
cDNA | c.3986G>C |
Protein | p.R1329P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000548.4 | chr16:g.2083797G>C | c.3986G>C | p.R1329P | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.2084285_2084286delAGinsCC | c.3985_3986delAGinsCC | p.R1329P | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.2083797G>C | c.3986G>C | p.R1329P | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2083797G>C | c.3986G>C | p.R1329P | RefSeq | GRCh38/hg38 |
XM_011522640 | chr16:g.2084285_2084286delAGinsCC | c.3985_3986delAGinsCC | p.R1329P | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.2084285_2084286delAGinsCC | c.3985_3986delAGinsCC | p.R1329P | RefSeq | GRCh38/hg38 |
NM_001406680.1 | chr16:g.2085246G>C | c.3986G>C | p.R1329P | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
TSC2 R1329P | unknown |