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Gene | ARID2 |
Variant | S635* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ARID2 S635* results in a premature truncation of the Arid2 protein at amino acid 635 of 1835 (UniProt.org). Due to the loss of the C2H2-type zinc finger domain (PMID: 32071245), S635* is predicted to lead to a loss of Arid2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
ARID2 mutant ARID2 inact mut ARID2 S635* |
Transcript | NM_152641.4 |
gDNA | chr12:g.45849768C>A |
cDNA | c.1904C>A |
Protein | p.S635* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_152641.3 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
XM_047428489.1 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
NM_001347839.2 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
NM_001347839.1 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
XM_006719272.4 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
NM_152641.4 | chr12:g.45849768C>A | c.1904C>A | p.S635* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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