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Gene | ATM |
Variant | P2665T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM P2665T does not lie within any known functional domains of the Atm protein (UniProt.org). P2665T 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 P2665T |
Transcript | NM_000051.4 |
gDNA | chr11:g.108333951C>A |
cDNA | c.7993C>A |
Protein | p.P2665T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000051.3 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108333951C>A | c.7993C>A | p.P2665T | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
ATM P2665T | unknown |