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Gene | CTNNB1 |
Variant | E396D |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CTNNB1 E396D does not lie within any functional domains of the Ctnnb1 protein (UniProt.org). E396D has not been characterized and therefore, its effect on Ctnnb1 protein function is unknown (PubMed, Sep 2024). |
Associated Drug Resistance | |
Category Variants Paths |
CTNNB1 mutant CTNNB1 E396D |
Transcript | NM_001098210.2 |
gDNA | chr3:g.41233531A>C |
cDNA | c.1188A>C |
Protein | p.E396D |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047447477.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_006712985.2 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_047447480.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_024453356.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_024453358.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098209 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098209.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_024453357.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_005264886 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_006712985 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_024453356.2 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_006712985.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098210.2 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_047447483.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098210 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_017005738.2 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_047447478.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_047447481.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_047447479.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001904 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098210.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001904.3 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_017005738.1 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
XM_017005738 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001904.4 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
NM_001098209.2 | chr3:g.41233531A>C | c.1188A>C | p.E396D | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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