NM_198236.3(ARHGEF11):c.4349C>T (p.Pro1450Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004424918.1
Allele description [Variation Report for NM_198236.3(ARHGEF11):c.4349C>T (p.Pro1450Leu)]
NM_198236.3(ARHGEF11):c.4349C>T (p.Pro1450Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Mus musculus myomixer, myoblast fusion factor (Mymx), transcript variant 2, mRNA
Mus musculus myomixer, myoblast fusion factor (Mymx), transcript variant 2, mRNAgi|294489329|ref|NM_001177469.1|Nucleotide
-
DNA repair protein REV1 isoform X7 [Mus musculus]
DNA repair protein REV1 isoform X7 [Mus musculus]gi|1907069849|ref|XP_036008375.1|Protein
-
Homo sapiens mRNA for ubiquitin specific proteinase 45 (USP45 gene)
Homo sapiens mRNA for ubiquitin specific proteinase 45 (USP45 gene)gi|40788178|emb|AJ583819.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024