NM_014681.6(DHX34):c.1897C>T (p.Arg633Trp) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 13, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004614199.1
Allele description [Variation Report for NM_014681.6(DHX34):c.1897C>T (p.Arg633Trp)]
NM_014681.6(DHX34):c.1897C>T (p.Arg633Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
03p241 - Chromosomal Variation in Man
03p241 - Chromosomal Variation in Man
-
cytochrome c oxidase subunit I, partial (mitochondrion) [Devario aequipinnatus]
cytochrome c oxidase subunit I, partial (mitochondrion) [Devario aequipinnatus]gi|1441481316|gb|AXJ97878.1|Protein
-
cytochrome c oxidase subunit I, partial (mitochondrion) [Puntius chola]
cytochrome c oxidase subunit I, partial (mitochondrion) [Puntius chola]gi|1441481340|gb|AXJ97890.1|Protein
-
cytochrome c oxidase subunit I, partial (mitochondrion) [Neolissochilus hexastic...
cytochrome c oxidase subunit I, partial (mitochondrion) [Neolissochilus hexastichus]gi|1441481312|gb|AXJ97876.1|Protein
-
03 - Chromosomal Variation in Man
03 - Chromosomal Variation in Man
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024