NM_014862.4(ARNT2):c.2035G>A (p.Gly679Ser) AND ARNT2-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 1, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003980499.2
Allele description [Variation Report for NM_014862.4(ARNT2):c.2035G>A (p.Gly679Ser)]
NM_014862.4(ARNT2):c.2035G>A (p.Gly679Ser)
Condition(s)
- Name:
- ARNT2-related disorder
- Synonyms:
- ARNT2-related condition
- Identifiers:
-
Homo sapiens uncharacterized LOC105373757 (LOC105373757), transcript variant 4, ...
Homo sapiens uncharacterized LOC105373757 (LOC105373757), transcript variant 4, long non-coding RNAgi|2575989385|ref|NR_187989.1|Nucleotide
-
Homo sapiens uncharacterized LOC105373757 (LOC105373757), transcript variant 7, ...
Homo sapiens uncharacterized LOC105373757 (LOC105373757), transcript variant 7, long non-coding RNAgi|2575989406|ref|NR_187992.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024