Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | ATM |
Variant | S3027I |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM S3027I lies within the FATC domain of the Atm protein (UniProt.org). S3027I has been identified in the scientific literature (PMID: 32265839), but has not been biochemically characterized and therefore, its effect on Atm protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM S3027I |
Transcript | NM_000051.4 |
gDNA | chr11:g.108365417G>T |
cDNA | c.9080G>T |
Protein | p.S3027I |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005271562 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108365417G>T | c.9080G>T | p.S3027I | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|