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 | L822V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM L822V does not lie within any known functional domains of the Atm protein (UniProt.org). L822V has not been characterized in the scientific literature and therefore, its effect on Atm protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM L822V |
Transcript | NM_000051.4 |
gDNA | chr11:g.108259073T>G |
cDNA | c.2464T>G |
Protein | p.L822V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011542843 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017792 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017792.2 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017791 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_047426981.1 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108259073T>G | c.2464T>G | p.L822V | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
ATM L822V | unknown |