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Gene | ATM |
Variant | V2119fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ATM V2119fs results in a change in the amino acid sequence of the Atm protein beginning at 2119 of 3056, likely resulting in premature truncation of the functional protein (UniProt.org). V2119fs has not been characterized, however, due to the effects of other truncation mutations downstream of V2119 (PMID: 16603769), is predicted to lead to a loss of Atm protein function. |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM V2119fs |
Transcript | NM_000051.4 |
gDNA | chr11:g.(108319960_108319961) |
cDNA | c.(6355_6354) |
Protein | p.V2119fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011542844 | chr11:g.108330306_108330309delTTGA | c.6356_6359delTTGA | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542844.3 | chr11:g.(108330304_108330305) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_017017791 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542844.4 | chr11:g.(108330304_108330305) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108319961dupG | c.6355dupG | p.V2119fs*8 | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.(108319960_108319961) | c.(6355_6354) | p.V2119fs | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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