NM_018125.4(ARHGEF10L):c.2353T>C (p.Cys785Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 13, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004241751.1
Allele description [Variation Report for NM_018125.4(ARHGEF10L):c.2353T>C (p.Cys785Arg)]
NM_018125.4(ARHGEF10L):c.2353T>C (p.Cys785Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens chromosome 16 clone RP11-486L19, complete sequence
Homo sapiens chromosome 16 clone RP11-486L19, complete sequencegi|16195198|gnl|lanlchgs|486L19|gb| 123.7|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024