NM_018139.3(DNAAF2):c.186G>C (p.Glu62Asp) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jul 22, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000081941.26
Allele description [Variation Report for NM_018139.3(DNAAF2):c.186G>C (p.Glu62Asp)]
NM_018139.3(DNAAF2):c.186G>C (p.Glu62Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens chromosome 3, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 3, GRCh38.p14 Primary Assemblygi|568815595|gnl|ASM:GCF_000001305| |NC_000003.12||gpp|GPC_000001295.1||gnl|NCBI_GENOMES|3Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 8, 2024